Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MEEEG others(439): Show |
chr7 | 44995201 | 45081453 |
| a0002 | 0/0 | 444 | 41 | 1 | 13 | 18 | 2 | 7 | 13 | CCM2_chr7_44995201_45081453 | CCM2 | MEEEG others(439): Show |
chr7 | 44995201 | 45081453 |
| a0003 | 0/0 | 444 | 13 | 1 | 10 | 2 | 0 | 0 | 2 | CCM2_chr7_44995201_45081453 | CCM2 | MEEEG others(439): Show |
chr7 | 44995201 | 45081453 |
| a0004 | 0/0 | 444 | 5 | 0 | 2 | 0 | 3 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | MEEEG others(439): Show |
chr7 | 44995201 | 45081453 |
| a0005 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | MEEEG others(439): Show |
chr7 | 44995201 | 45081453 |
| a0006 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | MEEEG others(439): Show |
chr7 | 44995201 | 45081453 |
| a0007 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | MEEEG others(439): Show |
chr7 | 44995201 | 45081453 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1332 | 164 | 47 | 28 | 56 | 8 | 24 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0001c0002 | 0/1 | 1332 | 77 | 19 | 19 | 30 | 3 | 5 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0001c0006 | 0/0 | 1332 | 7 | 7 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0001c0008 | 0/0 | 1332 | 5 | 5 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0001c0013 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0002c0003 | 0/0 | 1332 | 30 | 1 | 12 | 8 | 2 | 7 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0002c0005 | 0/0 | 1332 | 8 | 0 | 0 | 8 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0002c0009 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0002c0010 | 0/0 | 1332 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0002c0015 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0003c0004 | 0/0 | 1332 | 13 | 1 | 10 | 2 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0004c0007 | 0/0 | 1332 | 5 | 0 | 2 | 0 | 3 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0005c0014 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0006c0012 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
chr7 | 44995201 | 45081453 | ||
| a0007c0011 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | ATGGA others(1327): Show |
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 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0001t0004 | 0/0 | 1864 | 2 | 0 | 2 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0001t0005 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0001t0006 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0002t0001 | 0/1 | 1864 | 37 | 0 | 4 | 28 | 1 | 3 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0002t0002 | 0/0 | 1864 | 40 | 19 | 15 | 2 | 2 | 2 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0006t0001 | 0/0 | 1864 | 4 | 4 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0006t0003 | 0/0 | 1864 | 2 | 2 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0006t0007 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0008t0001 | 0/0 | 1864 | 5 | 5 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0001c0013t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0002c0003t0002 | 0/0 | 1864 | 30 | 1 | 12 | 8 | 2 | 7 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0002c0005t0002 | 0/0 | 1864 | 8 | 0 | 0 | 8 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0002c0009t0002 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0002c0010t0002 | 0/0 | 1864 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0002c0015t0002 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0003c0004t0001 | 0/0 | 1864 | 13 | 1 | 10 | 2 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0004c0007t0001 | 0/0 | 1864 | 5 | 0 | 2 | 0 | 3 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0005c0014t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0006c0012t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| a0007c0011t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | GGAGA others(1859): Show |
chr7 | 44995201 | 45081453 |
| actghapid | grch38/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 |
| a0005c0014t0001g0165 | 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 |
| a0007c0011t0001g0190 | 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 | a0005 | 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 | a0007 | 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 | a0001 | c0002 | t0001 | g0098 | REF | REF | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0049 | REF | REF | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| view | 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 | a0005 | 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 | a0007 | 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 |
| view | 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 | a0001c0002 a0005c0014 a0006c0012 |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0002c0005 a0002c0009 |
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 |
| view | 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 | a0001c0002t0002 a0002c0003t0002 a0002c0005t0002 others(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 |
| view | 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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | 35 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(32): Show |
35 | HG00323.hp2 HG00558.hp2 HG00735.hp1 others(32): 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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0004g0003 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0002t0001g0314 a0001c0002t0002g0305 a0001c0002t0002g0306 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0164 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0302 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0088 a0001c0006t0001g0059 a0001c0006t0001g0060 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0296 a0003c0004t0001g0297 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0088 a0001c0006t0001g0059 a0001c0006t0001g0060 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
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 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.30+3329T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003692 | |||||||
| chr7:45003728 | CA | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0179 a0001c0001t0001g0186 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0074 a0001c0001t0001g0118 a0001c0001t0001g0119 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0103 |
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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0156 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0004g0003 a0001c0001t0004g0004 |
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 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0006t0001g0060 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 59 | a0001c0001t0001g0069 a0001c0002t0001g0013 a0001c0002t0001g0014 others(56): Show |
59 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(56): 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 | a0001c0001t0001g0069 a0001c0002t0002g0120 a0001c0002t0002g0121 others(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 | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0202 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 51 | a0001c0001t0001g0020 a0001c0002t0001g0013 a0001c0002t0001g0014 others(48): Show |
51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.30+7928T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008291 | |||||||
| chr7:45008293 | C | T | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.30+7930C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008293 | |||||||
| chr7:45008320 | T | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0088 a0001c0006t0001g0059 a0001c0006t0001g0060 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0140 |
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 | a0001c0002t0002g0089 a0001c0002t0002g0100 a0001c0002t0002g0139 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): 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 | a0001c0001t0001g0291 a0001c0002t0002g0089 a0001c0002t0002g0100 others(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 | a0001c0001t0001g0209 a0001c0001t0001g0288 |
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 | 48 | a0001c0001t0001g0088 a0001c0002t0001g0013 a0001c0002t0001g0014 others(45): Show |
48 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(45): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0275 a0003c0004t0001g0193 |
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 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0276 |
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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0145 a0001c0002t0001g0141 a0001c0002t0002g0012 others(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 | a0001c0001t0001g0215 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0088 a0001c0006t0007g0162 |
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 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0153 |
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 | a0001c0006t0001g0061 a0001c0006t0001g0161 a0002c0003t0002g0029 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0176 |
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 | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): 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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0221 a0001c0002t0001g0195 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0215 a0001c0001t0001g0277 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0001g0181 others(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 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0003c0004t0001g0169 a0003c0004t0001g0201 a0003c0004t0001g0208 others(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 | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0210 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0303 |
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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0002t0001g0125 a0001c0002t0001g0128 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0002t0002g0089 a0001c0002t0002g0092 a0001c0002t0002g0100 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0002t0001g0125 a0001c0002t0001g0128 |
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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0002c0003t0002g0031 a0002c0003t0002g0036 a0002c0003t0002g0079 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0164 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0088 a0001c0006t0001g0061 a0001c0006t0001g0161 others(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 | a0001c0001t0001g0034 a0002c0003t0002g0030 a0002c0003t0002g0037 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.30+15153T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015516 | |||||||
| chr7:45015615 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0178 a0001c0001t0001g0221 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0088 a0001c0006t0001g0060 a0001c0006t0001g0061 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0002c0003t0002g0046 a0002c0003t0002g0047 |
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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 |
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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0088 a0001c0006t0007g0162 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-18613T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019640 | |||||||
| chr7:45019648 | T | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.31-18605T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019648 | |||||||
| chr7:45019740 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0164 a0001c0001t0001g0179 a0001c0001t0001g0186 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
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 | 69 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(66): Show |
70 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.31-17417C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020836 | |||||||
| chr7:45020859 | T | TAG | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0145 a0001c0001t0001g0234 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0025 a0001c0002t0002g0026 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0107 others(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 | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): 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 | a0001c0001t0001g0071 a0001c0001t0001g0104 a0001c0001t0005g0235 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0088 a0001c0006t0007g0162 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0002t0001g0125 a0001c0002t0001g0128 |
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 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0006t0001g0061 a0001c0006t0001g0161 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0154 a0001c0001t0001g0177 others(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 | 66 | a0001c0001t0001g0088 a0001c0001t0001g0166 a0001c0001t0001g0188 others(63): Show |
66 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(63): 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 | a0001c0001t0001g0021 a0001c0001t0001g0075 a0001c0001t0001g0107 others(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 | 205 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0022 others(202): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0108 others(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 | a0002c0003t0002g0030 a0002c0003t0002g0037 a0002c0003t0002g0048 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0075 a0001c0001t0001g0107 others(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 | 202 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0021 others(199): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | 192 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0034 others(189): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0296 others(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 | a0001c0001t0001g0034 a0001c0002t0002g0120 a0001c0002t0002g0121 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0152 |
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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-13812G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024441 | |||||||
| chr7:45024588 | T | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 81 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(78): Show |
82 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.31-12930C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025323 | |||||||
| chr7:45025534 | CT | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): 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 | a0001c0002t0001g0096 a0001c0002t0001g0136 |
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 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 49 | a0001c0001t0001g0021 a0001c0001t0001g0071 a0001c0001t0001g0171 others(46): Show |
49 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(46): 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 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0002t0001g0068 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0170 a0001c0001t0001g0187 others(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 | 39 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(36): Show |
39 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(36): 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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0088 a0001c0006t0007g0162 |
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 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0144 others(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 | 309 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(306): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): 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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | 81 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(78): Show |
82 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(79): 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 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0004g0003 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-9068T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029185 | |||||||
| chr7:45029228 | G | A | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0002t0001g0141 a0001c0002t0001g0142 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | a0001c0001t0004g0003 a0001c0001t0004g0004 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0088 a0001c0006t0001g0059 a0001c0006t0001g0060 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | 19 | a0001c0001t0001g0019 a0001c0001t0001g0071 a0001c0001t0001g0106 others(16): Show |
19 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(16): 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 | a0001c0001t0001g0069 a0001c0001t0001g0108 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0209 a0001c0001t0001g0288 |
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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0112 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0107 a0001c0001t0001g0144 a0001c0001t0001g0163 |
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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0020 a0001c0001t0001g0117 a0001c0001t0001g0147 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | a0002c0003t0002g0030 a0002c0003t0002g0080 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): 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 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0182 others(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 | a0001c0006t0001g0061 a0001c0006t0001g0161 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0164 a0001c0001t0001g0170 others(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 | a0007c0011t0001g0190 | 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 | a0001c0001t0001g0249 a0001c0001t0001g0280 |
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 | a0001c0006t0001g0061 a0001c0006t0001g0161 |
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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0002t0002g0089 a0001c0002t0002g0092 a0001c0002t0002g0100 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0088 a0001c0006t0001g0060 a0001c0006t0001g0061 others(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 | a0001c0002t0001g0014 a0001c0002t0001g0017 a0001c0002t0001g0137 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0033 a0002c0003t0002g0038 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0219 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0181 a0001c0001t0001g0213 a0001c0001t0001g0234 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0004c0007t0001g0242 a0004c0007t0001g0248 |
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 | a0003c0004t0001g0201 a0003c0004t0001g0225 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0034 a0002c0003t0002g0030 a0002c0003t0002g0037 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0178 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0004c0007t0001g0200 a0004c0007t0001g0279 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0186 |
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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | a0001c0001t0001g0204 a0001c0013t0001g0245 |
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 | a0001c0001t0001g0204 a0002c0003t0002g0045 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0103 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0182 a0001c0001t0001g0183 others(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 | 5 | a0001c0002t0001g0093 a0001c0002t0001g0096 a0001c0002t0001g0097 others(2): Show |
5 | HG00323.hp2 NA18952.hp2 NA18968.hp2 others(2): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0254 a0001c0001t0001g0275 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0001t0001g0107 others(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 |
51 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(48): Show |
51 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(48): 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 | a0001c0002t0001g0068 a0001c0002t0001g0091 a0001c0002t0001g0096 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0009 a0001c0008t0001g0010 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0001t0001g0088 a0001c0006t0001g0059 a0001c0006t0001g0060 others(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 | a0001c0001t0001g0088 a0001c0006t0001g0059 a0001c0006t0001g0060 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0006t0001g0061 a0001c0006t0001g0161 |
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 | a0001c0001t0001g0172 a0001c0001t0001g0178 a0001c0001t0001g0216 others(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 | 164 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(161): Show |
165 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(162): 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 | a0001c0001t0004g0003 a0001c0001t0004g0004 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0002c0003t0002g0046 a0002c0003t0002g0047 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
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 | a0001c0002t0002g0089 a0001c0002t0002g0100 a0001c0002t0002g0139 |
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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0002c0003t0002g0031 a0002c0003t0002g0035 a0002c0003t0002g0036 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(201): Show |
205 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.204+5864C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044290 | |||||||
| chr7:45044457 | G | A | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0001t0004g0003 a0001c0001t0004g0004 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0140 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0176 others(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 | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0002t0002g0122 a0001c0002t0002g0157 a0001c0002t0002g0159 |
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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 278 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.204+7870T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046296 | |||||||
| chr7:45046337 | T | C | 166 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(163): Show |
167 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.204+7911T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046337 | |||||||
| chr7:45046439 | C | T | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | 70 | a0001c0001t0001g0177 a0001c0001t0001g0207 a0001c0001t0001g0257 others(67): Show |
71 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(68): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0145 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0002c0003t0002g0029 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0206 a0001c0002t0002g0001 a0001c0002t0002g0024 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0153 a0001c0001t0001g0155 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 129 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(126): Show |
130 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(127): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0002c0003t0002g0046 a0002c0003t0002g0047 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0069 a0001c0008t0001g0007 a0001c0008t0001g0008 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0001t0001g0107 a0001c0001t0001g0144 a0001c0001t0001g0163 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0004c0007t0001g0242 a0004c0007t0001g0248 |
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 | a0001c0008t0001g0010 a0001c0008t0001g0011 |
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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0118 a0001c0001t0001g0146 |
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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0179 a0001c0001t0001g0186 |
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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0002c0003t0002g0053 a0002c0003t0002g0084 |
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 | a0001c0001t0001g0209 a0001c0001t0001g0288 |
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 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0001g0244 |
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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0103 |
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 | a0001c0002t0002g0122 a0001c0002t0002g0157 a0001c0002t0002g0159 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0156 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0237 a0001c0001t0001g0281 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0002t0001g0015 a0001c0002t0001g0016 |
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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0253 a0001c0001t0001g0271 a0001c0001t0001g0294 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0303 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0152 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0032 a0002c0003t0002g0033 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0241 a0001c0001t0001g0259 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0001t0001g0189 a0001c0001t0001g0238 a0001c0001t0001g0241 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0145 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0147 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 144 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(141): Show |
144 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(141): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0003c0004t0001g0169 a0003c0004t0001g0193 a0003c0004t0001g0201 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0003c0004t0001g0169 a0003c0004t0001g0193 a0003c0004t0001g0201 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0147 others(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 | 204 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(201): Show |
205 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(202): 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 | a0001c0001t0001g0209 a0001c0001t0001g0288 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0002t0002g0305 a0001c0002t0002g0306 a0001c0002t0002g0307 others(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 | a0001c0001t0001g0117 a0001c0001t0001g0202 a0001c0008t0001g0007 others(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 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(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 | a0001c0006t0001g0059 a0001c0006t0001g0060 a0001c0006t0001g0061 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0063 others(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 | 78 | a0001c0001t0001g0155 a0001c0002t0001g0013 a0001c0002t0001g0014 others(75): Show |
79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0205 others(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 | 75 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(72): Show |
76 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(73): 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 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0001g0097 a0002c0003t0002g0029 a0002c0003t0002g0030 others(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 | a0001c0006t0001g0061 a0001c0006t0001g0161 |
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 | a0001c0006t0001g0060 a0001c0006t0001g0061 a0001c0006t0001g0161 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.205-36A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063882 | |||||||
| chr7:45064172 | C | T | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0002c0003t0002g0040 a0002c0003t0002g0053 a0002c0003t0002g0058 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 119 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(116): Show |
120 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(117): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(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 | 50 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(47): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0006t0001g0061 a0001c0006t0001g0161 |
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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0301 |
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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0154 others(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 | 76 | a0001c0001t0001g0183 a0001c0002t0001g0013 a0001c0002t0001g0014 others(73): Show |
77 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(74): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 176 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(173): Show |
177 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(174): 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 | 175 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(172): Show |
176 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(173): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0001t0001g0020 a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0214 a0001c0001t0001g0276 |
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 | a0001c0001t0001g0295 a0001c0001t0001g0304 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0001c0001t0001g0020 a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 124 | a0001c0001t0001g0020 a0001c0001t0001g0069 a0001c0002t0001g0013 others(121): Show |
125 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.610-547C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069279 | |||||||
| chr7:45069373 | A | G | 70 | a0001c0001t0001g0069 a0001c0002t0001g0013 a0001c0002t0001g0014 others(67): Show |
71 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.610-453A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069373 | |||||||
| chr7:45069442 | T | C | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0001c0001t0001g0020 a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0002c0003t0002g0032 a0002c0003t0002g0046 a0002c0003t0002g0047 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0025 a0001c0002t0002g0026 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0033 a0002c0003t0002g0038 others(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 | a0001c0002t0002g0120 a0001c0002t0002g0121 a0001c0002t0002g0123 others(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 | a0001c0001t0001g0020 a0001c0006t0001g0059 a0001c0006t0003g0076 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0153 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0152 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(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 | a0002c0003t0002g0040 a0002c0003t0002g0053 a0002c0003t0002g0058 others(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 | 118 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(115): Show |
119 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(116): 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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0025 others(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 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0140 |
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 | a0001c0002t0002g0122 a0001c0002t0002g0157 a0001c0002t0002g0159 |
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 | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.746-382A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072344 | |||||||
| chr7:45072471 | T | G | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | a0001c0001t0001g0295 a0001c0001t0001g0304 |
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 | a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.803+330A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073113 | |||||||
| chr7:45073174 | T | C | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | |||||||
| chr7:45073412 | 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 | a0001c0006t0001g0059 a0001c0006t0003g0076 a0001c0006t0003g0077 |
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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0002t0002g0012 a0001c0002t0002g0063 a0001c0002t0002g0305 others(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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
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 | a0002c0005t0002g0041 a0002c0005t0002g0043 |
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 | a0001c0002t0002g0101 a0001c0002t0002g0102 a0001c0002t0002g0140 |
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 | 77 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0015 others(74): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): 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 | a0001c0008t0001g0007 a0001c0008t0001g0008 a0001c0008t0001g0009 others(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 | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.1055-333T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075444 | |||||||
| chr7:45075445 | C | A | 177 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(174): Show |
178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): 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 | a0001c0006t0001g0061 a0001c0006t0001g0161 |
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 |