| geneid | 26005 |
|---|---|
| ensemblid | ENSG00000168014.18 |
| hgncid | 24564 |
| symbol | C2CD3 |
| name | C2 domain containing 3 centriole elongation regulator |
| refseq_nuc | NM_001286577.2 |
| refseq_prot | NP_001273506.1 |
| ensembl_nuc | ENST00000334126.12 |
| ensembl_prot | ENSP00000334379.7 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 74012718 |
| end | 74171002 |
| strand | - |
| ver | v1.2 |
| region | chr11:74012718-74171002 |
| region5000 | chr11:74007718-74176002 |
| regionname0 | C2CD3_chr11_74012718_74171002 |
| regionname5000 | C2CD3_chr11_74007718_74176002 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2353 | 78 | 5 | 15 | 41 | 4 | 11 | 27 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002 | 0/0 | 2353 | 69 | 16 | 18 | 23 | 6 | 6 | 19 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003 | 0/0 | 2353 | 60 | 4 | 5 | 41 | 3 | 7 | 28 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0004 | 0/0 | 2353 | 20 | 19 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0005 | 0/0 | 2353 | 13 | 7 | 3 | 0 | 0 | 3 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0006 | 0/0 | 2353 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0007 | 0/0 | 2353 | 10 | 9 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0008 | 0/0 | 2353 | 8 | 0 | 1 | 5 | 0 | 2 | 5 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0009 | 0/0 | 2353 | 6 | 1 | 0 | 4 | 0 | 1 | 4 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0010 | 0/0 | 2353 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0011 | 0/0 | 2353 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0012 | 0/0 | 2353 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0013 | 0/0 | 2353 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0014 | 0/0 | 2353 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0015 | 0/0 | 1123 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0016 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0017 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0018 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0019 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0020 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0021 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0022 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0023 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0024 | 0/0 | 2353 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0025 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0026 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0027 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0028 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0029 | 0/0 | 2353 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0030 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0031 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0032 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0033 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0034 | 0/0 | 2353 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0035 | 0/0 | 2353 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0036 | 0/0 | 2353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 7062 | 77 | 5 | 14 | 41 | 4 | 11 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0002 | 0/0 | 7062 | 56 | 1 | 5 | 40 | 3 | 7 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0003 | 0/0 | 7062 | 49 | 15 | 16 | 6 | 6 | 6 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0004 | 0/0 | 7062 | 20 | 19 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0005 | 0/0 | 7062 | 19 | 0 | 2 | 17 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0006 | 0/0 | 7062 | 12 | 7 | 3 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0007 | 0/0 | 7062 | 8 | 0 | 1 | 5 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0008 | 0/0 | 7062 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0009 | 0/0 | 7062 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0010 | 0/0 | 7062 | 6 | 1 | 0 | 4 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0011 | 0/0 | 7062 | 6 | 0 | 0 | 6 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0012 | 0/0 | 7062 | 5 | 5 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0013 | 0/0 | 7062 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0014 | 0/0 | 7062 | 3 | 0 | 1 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0015 | 0/0 | 7062 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0016 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0017 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0018 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0019 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0020 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0021 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0022 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0023 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0024 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0025 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0026 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0027 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0028 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0029 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0030 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0031 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0032 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0033 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0034 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0035 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0036 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0037 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0038 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0039 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0040 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0041 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0042 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0043 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0044 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0045 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0046 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| c0047 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 878 | 303 | 85 | 47 | 123 | 12 | 34 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| t0002 | 0/0 | 878 | 9 | 9 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| t0003 | 0/0 | 878 | 3 | 0 | 1 | 0 | 2 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| t0004 | 0/0 | 878 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| t0005 | 0/0 | 878 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 7062 | 77 | 5 | 14 | 41 | 4 | 11 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0001c0030 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002c0003 | 0/0 | 7062 | 49 | 15 | 16 | 6 | 6 | 6 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002c0005 | 0/0 | 7062 | 19 | 0 | 2 | 17 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002c0028 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0002 | 0/0 | 7062 | 56 | 1 | 5 | 40 | 3 | 7 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0016 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0034 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0041 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0004c0004 | 0/0 | 7062 | 20 | 19 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0005c0006 | 0/0 | 7062 | 12 | 7 | 3 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0005c0027 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0006c0008 | 0/0 | 7062 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0006c0012 | 0/0 | 7062 | 5 | 5 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0007c0009 | 0/0 | 7062 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0007c0017 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0007c0026 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0008c0007 | 0/0 | 7062 | 8 | 0 | 1 | 5 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0009c0010 | 0/0 | 7062 | 6 | 1 | 0 | 4 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0010c0011 | 0/0 | 7062 | 6 | 0 | 0 | 6 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0011c0015 | 0/0 | 7062 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0011c0018 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0012c0013 | 0/0 | 7062 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0013c0014 | 0/0 | 7062 | 3 | 0 | 1 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0014c0020 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0015c0019 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0016c0021 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0017c0043 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0018c0044 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0019c0045 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0020c0040 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0021c0023 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0022c0035 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0023c0037 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0024c0038 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0025c0036 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0026c0025 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0027c0047 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0028c0046 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0029c0029 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0030c0031 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0031c0032 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0032c0024 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0033c0022 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0034c0033 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0035c0039 | 0/0 | 7062 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0036c0042 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7939 | 77 | 5 | 14 | 41 | 4 | 11 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0001c0030t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002c0003t0001 | 0/0 | 7939 | 48 | 15 | 16 | 5 | 6 | 6 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002c0003t0005 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002c0005t0001 | 0/0 | 7939 | 19 | 0 | 2 | 17 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0002c0028t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0002t0001 | 0/0 | 7939 | 53 | 1 | 4 | 40 | 1 | 7 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0002t0003 | 0/0 | 7939 | 3 | 0 | 1 | 0 | 2 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0016t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0034t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0003c0041t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0004c0004t0001 | 0/0 | 7939 | 20 | 19 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0005c0006t0001 | 0/0 | 7939 | 12 | 7 | 3 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0005c0027t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0006c0008t0001 | 0/0 | 7939 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0006c0012t0001 | 0/0 | 7939 | 5 | 5 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0007c0009t0002 | 0/0 | 7939 | 7 | 7 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0007c0017t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0007c0026t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0008c0007t0001 | 0/0 | 7939 | 8 | 0 | 1 | 5 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0009c0010t0001 | 0/0 | 7939 | 6 | 1 | 0 | 4 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0010c0011t0001 | 0/0 | 7939 | 6 | 0 | 0 | 6 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0011c0015t0001 | 0/0 | 7939 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0011c0018t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0012c0013t0001 | 0/0 | 7939 | 3 | 3 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0013c0014t0001 | 0/0 | 7939 | 3 | 0 | 1 | 0 | 0 | 2 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0014c0020t0004 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0015c0019t0001 | 0/0 | 7939 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0016c0021t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0017c0043t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0018c0044t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0019c0045t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0020c0040t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0021c0023t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0022c0035t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0023c0037t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0024c0038t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0025c0036t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0026c0025t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0027c0047t0002 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0028c0046t0002 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0029c0029t0001 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0030c0031t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0031c0032t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0032c0024t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0033c0022t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0034c0033t0001 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0035c0039t0001 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| a0036c0042t0001 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | copy fasta | chr11 | 74007718 | 74176002 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0001c0030t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0003t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0005t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0002c0028t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0002t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0016t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0016t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0034t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0003c0041t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0004c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0005c0027t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0008t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0008t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0008t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0008t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0008t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0012t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0012t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0012t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0012t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0006c0012t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0009t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0009t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0009t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0009t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0009t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0009t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0009t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0017t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0017t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0007c0026t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0008c0007t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0009c0010t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0009c0010t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0009c0010t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0009c0010t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0009c0010t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0009c0010t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0010c0011t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0010c0011t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0010c0011t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0010c0011t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0010c0011t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0010c0011t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0011c0015t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0011c0015t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0011c0018t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0011c0018t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0012c0013t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0012c0013t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0012c0013t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0013c0014t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0013c0014t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0013c0014t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0014c0020t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0014c0020t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0015c0019t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0015c0019t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0016c0021t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0017c0043t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0018c0044t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0019c0045t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0020c0040t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0021c0023t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0022c0035t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0023c0037t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0024c0038t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0025c0036t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0026c0025t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0027c0047t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0028c0046t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0029c0029t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0030c0031t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0031c0032t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0032c0024t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0033c0022t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0034c0033t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0035c0039t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| a0036c0042t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0209 | EUR | GBR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00280 | hp1 | a0003 | c0002 | t0001 | g0269 | EUR | FIN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0205 | EUR | FIN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00408 | hp1 | a0003 | c0002 | t0001 | g0259 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00423 | hp1 | a0003 | c0002 | t0001 | g0260 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00438 | hp2 | a0003 | c0002 | t0001 | g0257 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00544 | hp2 | a0003 | c0002 | t0001 | g0280 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00558 | hp2 | a0003 | c0002 | t0001 | g0285 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00597 | hp2 | a0003 | c0002 | t0001 | g0261 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00609 | hp1 | a0003 | c0002 | t0001 | g0291 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00639 | hp1 | a0021 | c0023 | t0001 | g0132 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0208 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00642 | hp1 | a0005 | c0006 | t0001 | g0013 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00642 | hp2 | a0003 | c0002 | t0003 | g0004 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00673 | hp1 | a0003 | c0002 | t0001 | g0265 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00733 | hp1 | a0003 | c0002 | t0001 | g0270 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00733 | hp2 | a0002 | c0005 | t0001 | g0008 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00738 | hp1 | a0002 | c0005 | t0001 | g0049 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00738 | hp2 | a0003 | c0002 | t0001 | g0298 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0081 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01074 | hp1 | a0008 | c0007 | t0001 | g0177 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01074 | hp2 | a0004 | c0004 | t0001 | g0036 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0196 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01081 | hp2 | a0003 | c0002 | t0001 | g0247 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01099 | hp1 | a0005 | c0006 | t0001 | g0015 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01099 | hp2 | a0018 | c0044 | t0001 | g0089 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01106 | hp2 | a0005 | c0006 | t0001 | g0025 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0187 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01169 | hp2 | a0029 | c0029 | t0001 | g0198 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0168 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0059 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0060 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01261 | hp2 | a0017 | c0043 | t0001 | g0084 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0171 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01361 | hp1 | a0013 | c0014 | t0001 | g0153 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0202 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0075 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01433 | hp2 | a0001 | c0030 | t0001 | g0192 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01515 | hp1 | a0034 | c0033 | t0001 | g0178 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01516 | hp1 | a0003 | c0002 | t0003 | g0002 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0210 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01517 | hp1 | a0003 | c0002 | t0003 | g0003 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01884 | hp1 | a0006 | c0008 | t0001 | g0240 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01884 | hp2 | a0011 | c0015 | t0001 | g0001 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0170 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0169 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0172 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0167 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02015 | hp1 | a0002 | c0005 | t0001 | g0069 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02015 | hp2 | a0023 | c0037 | t0001 | g0276 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02040 | hp2 | a0003 | c0002 | t0001 | g0241 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02055 | hp1 | a0012 | c0013 | t0001 | g0227 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0197 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02056 | hp1 | a0003 | c0002 | t0001 | g0290 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02074 | hp1 | a0003 | c0002 | t0001 | g0292 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02074 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02083 | hp2 | a0010 | c0011 | t0001 | g0079 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02129 | hp1 | a0002 | c0003 | t0005 | g0080 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0070 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02145 | hp1 | a0005 | c0006 | t0001 | g0024 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02145 | hp2 | a0007 | c0009 | t0002 | g0313 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02257 | hp2 | a0006 | c0008 | t0001 | g0236 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02258 | hp1 | a0004 | c0004 | t0001 | g0037 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02258 | hp2 | a0006 | c0008 | t0001 | g0237 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02280 | hp1 | a0007 | c0017 | t0001 | g0194 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02280 | hp2 | a0009 | c0010 | t0001 | g0303 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0050 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02451 | hp2 | a0007 | c0017 | t0001 | g0195 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02523 | hp1 | a0003 | c0002 | t0001 | g0288 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02523 | hp2 | a0016 | c0021 | t0001 | g0220 | EAS | KHV | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02572 | hp1 | a0006 | c0008 | t0001 | g0230 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02572 | hp2 | a0002 | c0028 | t0001 | g0011 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0030 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02615 | hp1 | a0006 | c0012 | t0001 | g0233 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02615 | hp2 | a0032 | c0024 | t0001 | g0200 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02622 | hp1 | a0020 | c0040 | t0001 | g0301 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0048 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02630 | hp2 | a0004 | c0004 | t0001 | g0183 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0090 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02647 | hp2 | a0004 | c0004 | t0001 | g0032 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02717 | hp1 | a0027 | c0047 | t0002 | g0311 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02717 | hp2 | a0006 | c0012 | t0001 | g0231 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02723 | hp1 | a0006 | c0012 | t0001 | g0232 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02723 | hp2 | a0014 | c0020 | t0004 | g0219 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02735 | hp1 | a0005 | c0027 | t0001 | g0012 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02738 | hp1 | a0013 | c0014 | t0001 | g0134 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0215 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0056 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02809 | hp2 | a0004 | c0004 | t0001 | g0033 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02818 | hp1 | a0003 | c0002 | t0001 | g0274 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02818 | hp2 | a0004 | c0004 | t0001 | g0046 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02886 | hp1 | a0005 | c0006 | t0001 | g0020 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02886 | hp2 | a0003 | c0016 | t0001 | g0242 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02895 | hp1 | a0004 | c0004 | t0001 | g0042 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02895 | hp2 | a0005 | c0006 | t0001 | g0014 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02896 | hp2 | a0015 | c0019 | t0001 | g0028 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02897 | hp1 | a0015 | c0019 | t0001 | g0022 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02897 | hp2 | a0004 | c0004 | t0001 | g0045 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0199 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0044 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02965 | hp1 | a0011 | c0018 | t0001 | g0126 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02965 | hp2 | a0004 | c0004 | t0001 | g0038 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02970 | hp1 | a0006 | c0008 | t0001 | g0239 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02976 | hp1 | a0004 | c0004 | t0001 | g0043 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02976 | hp2 | a0006 | c0008 | t0001 | g0229 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03041 | hp1 | a0014 | c0020 | t0004 | g0218 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03041 | hp2 | a0007 | c0009 | t0002 | g0314 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03098 | hp1 | a0003 | c0034 | t0001 | g0185 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0054 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03130 | hp1 | a0011 | c0015 | t0001 | g0223 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03130 | hp2 | a0005 | c0006 | t0001 | g0023 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03139 | hp1 | a0011 | c0018 | t0001 | g0127 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03139 | hp2 | a0025 | c0036 | t0001 | g0287 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03195 | hp1 | a0007 | c0009 | t0002 | g0316 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03195 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03209 | hp1 | a0004 | c0004 | t0001 | g0040 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03209 | hp2 | a0019 | c0045 | t0001 | g0224 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03239 | hp1 | a0003 | c0002 | t0001 | g0272 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0065 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0213 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0034 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0206 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03486 | hp2 | a0006 | c0008 | t0001 | g0238 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03490 | hp2 | a0003 | c0002 | t0001 | g0264 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03491 | hp1 | a0024 | c0038 | t0001 | g0293 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03491 | hp2 | a0005 | c0006 | t0001 | g0007 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03492 | hp1 | a0005 | c0006 | t0001 | g0006 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03492 | hp2 | a0003 | c0002 | t0001 | g0271 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03516 | hp1 | a0006 | c0012 | t0001 | g0234 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03516 | hp2 | a0012 | c0013 | t0001 | g0226 | AFR | ESN | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03540 | hp1 | a0007 | c0009 | t0002 | g0315 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03540 | hp2 | a0005 | c0006 | t0001 | g0021 | AFR | GWD | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03579 | hp1 | a0004 | c0004 | t0001 | g0035 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03654 | hp1 | a0003 | c0002 | t0001 | g0254 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03669 | hp2 | a0008 | c0007 | t0001 | g0076 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03704 | hp1 | a0003 | c0002 | t0001 | g0299 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0031 | SAS | PJL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03831 | hp2 | a0007 | c0026 | t0001 | g0005 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0214 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03927 | hp1 | a0003 | c0002 | t0001 | g0277 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03942 | hp2 | a0008 | c0007 | t0001 | g0217 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG04184 | hp2 | a0003 | c0002 | t0001 | g0273 | SAS | BEB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG04228 | hp2 | a0009 | c0010 | t0001 | g0304 | SAS | STU | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18522 | hp1 | a0026 | c0025 | t0001 | g0222 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18522 | hp2 | a0028 | c0046 | t0002 | g0309 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18747 | hp2 | a0003 | c0002 | t0001 | g0289 | EAS | CHB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18906 | hp1 | a0012 | c0013 | t0001 | g0225 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18941 | hp1 | a0003 | c0002 | t0001 | g0262 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18941 | hp2 | a0002 | c0005 | t0001 | g0074 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18942 | hp2 | a0002 | c0005 | t0001 | g0092 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18943 | hp2 | a0009 | c0010 | t0001 | g0305 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18945 | hp1 | a0002 | c0005 | t0001 | g0062 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18946 | hp2 | a0002 | c0005 | t0001 | g0058 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18948 | hp1 | a0002 | c0005 | t0001 | g0189 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18948 | hp2 | a0003 | c0002 | t0001 | g0279 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18949 | hp2 | a0003 | c0002 | t0001 | g0256 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18950 | hp1 | a0003 | c0002 | t0001 | g0268 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18950 | hp2 | a0008 | c0007 | t0001 | g0221 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18956 | hp1 | a0008 | c0007 | t0001 | g0216 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18957 | hp1 | a0003 | c0041 | t0001 | g0296 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18960 | hp2 | a0003 | c0002 | t0001 | g0283 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18962 | hp1 | a0003 | c0002 | t0001 | g0253 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18962 | hp2 | a0002 | c0005 | t0001 | g0063 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18963 | hp1 | a0008 | c0007 | t0001 | g0211 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18963 | hp2 | a0003 | c0002 | t0001 | g0246 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18966 | hp1 | a0002 | c0005 | t0001 | g0086 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18967 | hp1 | a0002 | c0005 | t0001 | g0188 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18970 | hp2 | a0003 | c0002 | t0001 | g0275 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18972 | hp1 | a0003 | c0002 | t0001 | g0284 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18979 | hp1 | a0002 | c0005 | t0001 | g0087 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18979 | hp2 | a0010 | c0011 | t0001 | g0077 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18980 | hp2 | a0003 | c0002 | t0001 | g0286 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18982 | hp1 | a0002 | c0005 | t0001 | g0085 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18982 | hp2 | a0003 | c0002 | t0001 | g0248 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18984 | hp2 | a0009 | c0010 | t0001 | g0308 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18988 | hp1 | a0003 | c0002 | t0001 | g0267 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18989 | hp2 | a0003 | c0002 | t0001 | g0297 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18991 | hp2 | a0003 | c0002 | t0001 | g0294 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18993 | hp2 | a0008 | c0007 | t0001 | g0082 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18995 | hp1 | a0003 | c0002 | t0001 | g0251 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18998 | hp1 | a0003 | c0002 | t0001 | g0266 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18998 | hp2 | a0010 | c0011 | t0001 | g0067 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA18999 | hp2 | a0009 | c0010 | t0001 | g0306 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19003 | hp1 | a0002 | c0005 | t0001 | g0072 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19003 | hp2 | a0009 | c0010 | t0001 | g0307 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19005 | hp1 | a0003 | c0002 | t0001 | g0281 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19009 | hp2 | a0002 | c0005 | t0001 | g0064 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19010 | hp2 | a0003 | c0002 | t0001 | g0258 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19011 | hp2 | a0003 | c0002 | t0001 | g0244 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19030 | hp1 | a0004 | c0004 | t0001 | g0181 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19030 | hp2 | a0007 | c0009 | t0002 | g0312 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19043 | hp1 | a0022 | c0035 | t0001 | g0228 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19043 | hp2 | a0005 | c0006 | t0001 | g0026 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19058 | hp1 | a0003 | c0002 | t0001 | g0263 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19060 | hp1 | a0003 | c0002 | t0001 | g0250 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19062 | hp1 | a0010 | c0011 | t0001 | g0066 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19064 | hp2 | a0002 | c0005 | t0001 | g0166 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19068 | hp1 | a0030 | c0031 | t0001 | g0184 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19068 | hp2 | a0003 | c0002 | t0001 | g0278 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19070 | hp1 | a0008 | c0007 | t0001 | g0212 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19070 | hp2 | a0003 | c0002 | t0001 | g0252 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19074 | hp1 | a0003 | c0002 | t0001 | g0243 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19074 | hp2 | a0010 | c0011 | t0001 | g0068 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19078 | hp1 | a0002 | c0005 | t0001 | g0088 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19078 | hp2 | a0035 | c0039 | t0001 | g0122 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19080 | hp1 | a0002 | c0005 | t0001 | g0073 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19080 | hp2 | a0003 | c0002 | t0001 | g0282 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19081 | hp1 | a0002 | c0005 | t0001 | g0093 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19081 | hp2 | a0003 | c0002 | t0001 | g0255 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19083 | hp1 | a0003 | c0002 | t0001 | g0245 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19085 | hp1 | a0010 | c0011 | t0001 | g0053 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19240 | hp1 | a0004 | c0004 | t0001 | g0041 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA19240 | hp2 | a0007 | c0009 | t0002 | g0317 | AFR | YRI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20129 | hp2 | a0007 | c0009 | t0002 | g0310 | AFR | ASW | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0201 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0204 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20805 | hp2 | a0002 | c0003 | t0001 | g0051 | EUR | TSI | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0207 | SAS | GIH | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20905 | hp2 | a0013 | c0014 | t0001 | g0130 | SAS | GIH | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0203 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG01123 | hp2 | a0003 | c0002 | t0001 | g0300 | AMR | CLM | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02109 | hp1 | a0031 | c0032 | t0001 | g0176 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02486 | hp1 | a0004 | c0004 | t0001 | g0186 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02486 | hp2 | a0011 | c0015 | t0001 | g0001 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0055 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03471 | hp1 | a0005 | c0006 | t0001 | g0027 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG03471 | hp2 | a0004 | c0004 | t0001 | g0047 | AFR | MSL | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG06807 | hp1 | a0036 | c0042 | t0001 | g0302 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0057 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20300 | hp1 | a0006 | c0012 | t0001 | g0235 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA20300 | hp2 | a0033 | c0022 | t0001 | g0295 | AFR | USA | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA21309 | hp1 | a0003 | c0016 | t0001 | g0249 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0052 | AFR | LWK | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0098 | REF | REF | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0107 | REF | REF | C2CD3_chr11_74007718_74176002 | C2CD3 | chr11 | 74007718 | 74176002 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74013467
|
T | C | 1 | a0028 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.6980A>G | p.Asn2327Ser | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 7190/7939 | 6980/7062 | 2327/2353 | chr11 | 74013467 | ||
| chr11:74013495
|
A | C | 1 | a0030 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.6952T>G | p.Ser2318Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 7162/7939 | 6952/7062 | 2318/2353 | chr11 | 74013495 | ||
| chr11:74033588
|
C | G | 1 | a0010 | 6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
missense_variant | MODERATE | c.6572G>C | p.Gly2191Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6782/7939 | 6572/7062 | 2191/2353 | chr11 | 74033588 | ||
| chr11:74033924
|
G | A | 1 | a0013 | 3 | HG01361.hp1 HG02738.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.6236C>T | p.Thr2079Met | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6446/7939 | 6236/7062 | 2079/2353 | chr11 | 74033924 | ||
| chr11:74033969
|
T | C | 1 | a0027 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.6191A>G | p.Tyr2064Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6401/7939 | 6191/7062 | 2064/2353 | chr11 | 74033969 | ||
| chr11:74034102
|
A | G | 15 | a0004a0006a0007others(12): Show | 66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
missense_variant | MODERATE | c.6058T>C | p.Ser2020Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/33 | 6268/7939 | 6058/7062 | 2020/2353 | chr11 | 74034102 | ||
| chr11:74048206
|
T | C | 3 | a0004a0014a0031 | 23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
missense_variant&splice_region_variant | MODERATE | c.5494A>G | p.Arg1832Gly | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/33 | 5704/7939 | 5494/7062 | 1832/2353 | chr11 | 74048206 | ||
| chr11:74048209
|
C | A | 3 | a0004a0014a0031 | 23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
missense_variant | MODERATE | c.5491G>T | p.Gly1831Trp | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/33 | 5701/7939 | 5491/7062 | 1831/2353 | chr11 | 74048209 | ||
| chr11:74049368
|
G | T | 3 | a0009a0026a0036 | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
missense_variant | MODERATE | c.5330C>A | p.Ala1777Glu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/33 | 5540/7939 | 5330/7062 | 1777/2353 | chr11 | 74049368 | ||
| chr11:74057443
|
T | C | 1 | a0020 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.5053A>G | p.Thr1685Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/33 | 5263/7939 | 5053/7062 | 1685/2353 | chr11 | 74057443 | ||
| chr11:74057508
|
C | T | 2 | a0005a0015 | 15 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(12): Show |
missense_variant | MODERATE | c.4988G>A | p.Ser1663Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/33 | 5198/7939 | 4988/7062 | 1663/2353 | chr11 | 74057508 | ||
| chr11:74074519
|
G | C | 1 | a0023 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.4685C>G | p.Ser1562Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/33 | 4895/7939 | 4685/7062 | 1562/2353 | chr11 | 74074519 | ||
| chr11:74078681
|
T | G | 1 | a0022 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.4037A>C | p.Asp1346Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/33 | 4247/7939 | 4037/7062 | 1346/2353 | chr11 | 74078681 | ||
| chr11:74085638
|
T | C | 2 | a0004a0014 | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
missense_variant | MODERATE | c.3890A>G | p.Tyr1297Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 4100/7939 | 3890/7062 | 1297/2353 | chr11 | 74085638 | ||
| chr11:74085782
|
C | T | 1 | a0026 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.3746G>A | p.Arg1249Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3956/7939 | 3746/7062 | 1249/2353 | chr11 | 74085782 | ||
| chr11:74085833
|
T | C | 1 | a0024 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.3695A>G | p.Asn1232Ser | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3905/7939 | 3695/7062 | 1232/2353 | chr11 | 74085833 | ||
| chr11:74085857
|
T | C | 1 | a0029 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.3671A>G | p.Gln1224Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3881/7939 | 3671/7062 | 1224/2353 | chr11 | 74085857 | ||
| chr11:74085872
|
C | T | 17 | a0002a0004a0005others(14): Show | 144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
missense_variant | MODERATE | c.3656G>A | p.Arg1219Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 3866/7939 | 3656/7062 | 1219/2353 | chr11 | 74085872 | ||
| chr11:74092422
|
A | T | 1 | a0032 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.3511T>A | p.Ser1171Thr | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/33 | 3721/7939 | 3511/7062 | 1171/2353 | chr11 | 74092422 | ||
| chr11:74092563
|
G | A | 1 | a0015 | 2 | HG02896.hp2 HG02897.hp1 |
stop_gained | HIGH | c.3370C>T | p.Gln1124* | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/33 | 3580/7939 | 3370/7062 | 1124/2353 | chr11 | 74092563 | ||
| chr11:74095240
|
A | G | 1 | a0025 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.3148T>C | p.Phe1050Leu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/33 | 3358/7939 | 3148/7062 | 1050/2353 | chr11 | 74095240 | ||
| chr11:74095398
|
C | T | 9 | a0003a0006a0012others(6): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
missense_variant | MODERATE | c.2990G>A | p.Arg997Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/33 | 3200/7939 | 2990/7062 | 997/2353 | chr11 | 74095398 | ||
| chr11:74098055
|
C | T | 1 | a0034 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2933G>A | p.Arg978Lys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/33 | 3143/7939 | 2933/7062 | 978/2353 | chr11 | 74098055 | ||
| chr11:74100598
|
C | T | 1 | a0021 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2659G>A | p.Val887Met | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/33 | 2869/7939 | 2659/7062 | 887/2353 | chr11 | 74100598 | ||
| chr11:74103210
|
C | T | 1 | a0033 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2501G>A | p.Cys834Tyr | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2711/7939 | 2501/7062 | 834/2353 | chr11 | 74103210 | ||
| chr11:74103367
|
C | T | 1 | a0020 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.2344G>A | p.Val782Ile | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2554/7939 | 2344/7062 | 782/2353 | chr11 | 74103367 | ||
| chr11:74103393
|
G | C | 3 | a0008a0010a0034 | 15 | HG01074.hp1 HG01515.hp1 HG02083.hp2 others(12): Show |
missense_variant | MODERATE | c.2318C>G | p.Pro773Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2528/7939 | 2318/7062 | 773/2353 | chr11 | 74103393 | ||
| chr11:74114579
|
T | C | 1 | a0035 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.1535A>G | p.Gln512Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/33 | 1745/7939 | 1535/7062 | 512/2353 | chr11 | 74114579 | ||
| chr11:74118334
|
C | T | 1 | a0019 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1414G>A | p.Val472Ile | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/33 | 1624/7939 | 1414/7062 | 472/2353 | chr11 | 74118334 | ||
| chr11:74132892
|
C | T | 1 | a0012 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1169G>A | p.Arg390Lys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/33 | 1379/7939 | 1169/7062 | 390/2353 | chr11 | 74132892 | ||
| chr11:74133555
|
G | C | 1 | a0036 | 1 | HG06807.hp1 | missense_variant&splice_region_variant | MODERATE | c.958C>G | p.Leu320Val | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/33 | 1168/7939 | 958/7062 | 320/2353 | chr11 | 74133555 | ||
| chr11:74138957
|
G | C | 2 | a0017a0018 | 2 | HG01099.hp2 HG01261.hp2 |
missense_variant | MODERATE | c.718C>G | p.His240Asp | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/33 | 928/7939 | 718/7062 | 240/2353 | chr11 | 74138957 | ||
| chr11:74161421
|
G | C | 1 | a0014 | 2 | HG02723.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.461C>G | p.Ser154Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/33 | 671/7939 | 461/7062 | 154/2353 | chr11 | 74161421 | ||
| chr11:74168380
|
G | A | 1 | a0014 | 2 | HG02723.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.289C>T | p.Arg97Cys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/33 | 499/7939 | 289/7062 | 97/2353 | chr11 | 74168380 | ||
| chr11:74168538
|
G | T | 1 | a0016 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.131C>A | p.Thr44Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/33 | 341/7939 | 131/7062 | 44/2353 | chr11 | 74168538 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74013403
|
C | T | 3 | a0007c0009a0011c0018a0027c0047 | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
synonymous_variant | LOW | c.7044G>A | p.Gln2348Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 7254/7939 | 7044/7062 | 2348/2353 | chr11 | 74013403 | ||
| chr11:74028389
|
G | A | 1 | a0005c0027 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.6819C>T | p.Pro2273Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/33 | 7029/7939 | 6819/7062 | 2273/2353 | chr11 | 74028389 | ||
| chr11:74048297
|
C | T | 1 | a0002c0028 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.5403G>A | p.Thr1801Thr | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/33 | 5613/7939 | 5403/7062 | 1801/2353 | chr11 | 74048297 | ||
| chr11:74074281
|
T | C | 22 | a0002c0003a0002c0005a0002c0028others(19): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
synonymous_variant | LOW | c.4923A>G | p.Val1641Val | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/33 | 5133/7939 | 4923/7062 | 1641/2353 | chr11 | 74074281 | ||
| chr11:74078287
|
C | T | 3 | a0009c0010a0026c0025a0036c0042 | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
synonymous_variant | LOW | c.4431G>A | p.Arg1477Arg | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/33 | 4641/7939 | 4431/7062 | 1477/2353 | chr11 | 74078287 | ||
| chr11:74085664
|
C | T | 1 | a0001c0030 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.3864G>A | p.Glu1288Glu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 4074/7939 | 3864/7062 | 1288/2353 | chr11 | 74085664 | ||
| chr11:74085715
|
C | T | 2 | a0003c0016a0033c0022 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.3813G>A | p.Leu1271Leu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/33 | 4023/7939 | 3813/7062 | 1271/2353 | chr11 | 74085715 | ||
| chr11:74093908
|
T | C | 2 | a0011c0015a0019c0045 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.3252A>G | p.Pro1084Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/33 | 3462/7939 | 3252/7062 | 1084/2353 | chr11 | 74093908 | ||
| chr11:74098233
|
G | A | 1 | a0002c0005 | 19 | HG00733.hp2 HG00738.hp1 HG02015.hp1 others(16): Show |
synonymous_variant | LOW | c.2755C>T | p.Leu919Leu | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/33 | 2965/7939 | 2755/7062 | 919/2353 | chr11 | 74098233 | ||
| chr11:74103431
|
T | G | 5 | a0003c0034a0006c0008a0006c0012others(2): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
synonymous_variant | LOW | c.2280A>C | p.Ala760Ala | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2490/7939 | 2280/7062 | 760/2353 | chr11 | 74103431 | ||
| chr11:74103560
|
G | A | 1 | a0006c0008 | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
synonymous_variant | LOW | c.2151C>T | p.Asn717Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/33 | 2361/7939 | 2151/7062 | 717/2353 | chr11 | 74103560 | ||
| chr11:74114458
|
T | C | 5 | a0003c0002a0003c0041a0023c0037others(2): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
synonymous_variant | LOW | c.1656A>G | p.Pro552Pro | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/33 | 1866/7939 | 1656/7062 | 552/2353 | chr11 | 74114458 | ||
| chr11:74123102
|
C | A | 1 | a0020c0040 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1251G>T | p.Gly417Gly | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/33 | 1461/7939 | 1251/7062 | 417/2353 | chr11 | 74123102 | ||
| chr11:74123120
|
T | C | 1 | a0003c0041 | 1 | NA18957.hp1 | synonymous_variant | LOW | c.1233A>G | p.Gln411Gln | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/33 | 1443/7939 | 1233/7062 | 411/2353 | chr11 | 74123120 | ||
| chr11:74139628
|
G | A | 2 | a0011c0015a0019c0045 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.684C>T | p.Asn228Asn | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/33 | 894/7939 | 684/7062 | 228/2353 | chr11 | 74139628 | ||
| chr11:74168543
|
T | C | 3 | a0007c0009a0027c0047a0028c0046 | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
synonymous_variant | LOW | c.126A>G | p.Lys42Lys | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/33 | 336/7939 | 126/7062 | 42/2353 | chr11 | 74168543 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74012801
|
T | C | 1 | a0002c0003t0005 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 584 | chr11 | 74012801 | |||||
| chr11:74013301
|
G | A | 1 | a0014c0020t0004 | 2 | HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*84C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 33/33 | 84 | chr11 | 74013301 | |||||
| chr11:74170803
|
A | G | 1 | a0003c0002t0003 | 3 | HG00642.hp2 HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-11T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/33 | 11 | chr11 | 74170803 | |||||
| chr11:74170832
|
C | A | 3 | a0007c0009t0002a0027c0047t0002a0028c0046t0002 | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-40G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/33 | 40 | chr11 | 74170832 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74013657
|
G | A | 4 | a0002c0003t0001g0052a0012c0013t0001g0225a0012c0013t0001g0226others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6922-132C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74013657 | ||||||
| chr11:74013790
|
C | T | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-265G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74013790 | ||||||
| chr11:74013818
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.6922-293C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74013818 | ||||||
| chr11:74014012
|
G | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.6922-487C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014012 | ||||||
| chr11:74014206
|
A | G | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-681T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014206 | ||||||
| chr11:74014207
|
G | A | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-682C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014207 | ||||||
| chr11:74014347
|
T | G | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6922-822A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014347 | ||||||
| chr11:74014399
|
A | G | 1 | a0019c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6922-874T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014399 | ||||||
| chr11:74014519
|
G | GGCCCAGC others(9): Show |
1 | a0001c0001t0001g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6922-1010_6922-995 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014519 | ||||||
| chr11:74014519
|
GGCCCAGC others(9): Show |
G | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-1010_6922-995 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014519 | ||||||
| chr11:74014632
|
T | C | 2 | a0009c0010t0001g0303a0036c0042t0001g0302 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6922-1107A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74014632 | ||||||
| chr11:74015079
|
C | T | 14 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-1554G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015079 | ||||||
| chr11:74015100
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.6922-1575T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015100 | ||||||
| chr11:74015255
|
G | C | 4 | a0002c0003t0001g0205a0002c0003t0001g0208a0002c0003t0001g0209others(1): Show | 4 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.6922-1730C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015255 | ||||||
| chr11:74015278
|
T | C | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-1753A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015278 | ||||||
| chr11:74015498
|
C | T | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-1973G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015498 | ||||||
| chr11:74015532
|
C | T | 1 | a0002c0005t0001g0062 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6922-2007G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015532 | ||||||
| chr11:74015887
|
G | A | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-2362C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015887 | ||||||
| chr11:74015900
|
C | CA | 18 | a0003c0002t0001g0299a0005c0006t0001g0015a0006c0008t0001g0229others(15): Show | 19 | HG01099.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.6922-2376dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015900 | ||||||
| chr11:74015916
|
G | A | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6922-2391C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015916 | ||||||
| chr11:74015917
|
GA | G | 20 | a0001c0001t0001g0112a0002c0003t0001g0196a0002c0003t0001g0197others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.6922-2393delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015917 | ||||||
| chr11:74015918
|
A | G | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6922-2393T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74015918 | ||||||
| chr11:74016046
|
C | G | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6922-2521G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016046 | ||||||
| chr11:74016105
|
T | C | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-2580A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016105 | ||||||
| chr11:74016311
|
C | CA | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-2787dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016311 | ||||||
| chr11:74016511
|
C | T | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6922-2986G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016511 | ||||||
| chr11:74016573
|
G | A | 4 | a0001c0001t0001g0115a0001c0001t0001g0160a0003c0002t0001g0290others(1): Show | 4 | HG01952.hp1 HG02056.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.6922-3048C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016573 | ||||||
| chr11:74016678
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.6922-3153G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016678 | ||||||
| chr11:74016783
|
T | C | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-3258A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016783 | ||||||
| chr11:74016796
|
G | A | 1 | a0003c0016t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6922-3271C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016796 | ||||||
| chr11:74016851
|
T | C | 1 | a0002c0005t0001g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.6922-3326A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016851 | ||||||
| chr11:74016921
|
G | A | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-3396C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016921 | ||||||
| chr11:74016940
|
G | A | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6922-3415C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016940 | ||||||
| chr11:74016972
|
G | A | 12 | a0001c0001t0001g0098a0003c0016t0001g0242a0003c0016t0001g0249others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6922-3447C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74016972 | ||||||
| chr11:74017110
|
G | C | 1 | a0029c0029t0001g0198 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6922-3585C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017110 | ||||||
| chr11:74017114
|
A | G | 123 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0144others(120): Show | 124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.6922-3589T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017114 | ||||||
| chr11:74017115
|
C | T | 1 | a0003c0002t0001g0279 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.6922-3590G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017115 | ||||||
| chr11:74017138
|
G | A | 14 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-3613C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017138 | ||||||
| chr11:74017214
|
C | T | 2 | a0012c0013t0001g0226a0012c0013t0001g0227 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.6922-3689G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017214 | ||||||
| chr11:74017264
|
G | A | 1 | a0002c0003t0001g0172 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.6922-3739C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017264 | ||||||
| chr11:74017383
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6922-3858C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017383 | ||||||
| chr11:74017477
|
A | G | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-3952T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017477 | ||||||
| chr11:74017552
|
A | G | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4027T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017552 | ||||||
| chr11:74017627
|
C | A | 1 | a0006c0008t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6922-4102G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017627 | ||||||
| chr11:74017659
|
T | C | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4134A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017659 | ||||||
| chr11:74017777
|
A | C | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4252T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017777 | ||||||
| chr11:74017797
|
TC | T | 12 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6922-4273delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74017797 | ||||||
| chr11:74018011
|
C | T | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4486G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018011 | ||||||
| chr11:74018097
|
G | A | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6922-4572C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018097 | ||||||
| chr11:74018155
|
A | G | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-4630T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018155 | ||||||
| chr11:74018174
|
CG | C | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-4650delC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018174 | ||||||
| chr11:74018175
|
G | A | 14 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-4650C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018175 | ||||||
| chr11:74018177
|
G | A | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-4652C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018177 | ||||||
| chr11:74018290
|
C | T | 2 | a0009c0010t0001g0303a0036c0042t0001g0302 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6922-4765G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018290 | ||||||
| chr11:74018307
|
C | A | 1 | a0003c0002t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.6922-4782G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018307 | ||||||
| chr11:74018336
|
C | T | 43 | a0001c0030t0001g0192a0002c0003t0001g0030a0002c0003t0001g0031others(40): Show | 43 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.6922-4811G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018336 | ||||||
| chr11:74018344
|
C | T | 33 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(30): Show | 34 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(31): Show |
intron_variant | MODIFIER | c.6922-4819G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018344 | ||||||
| chr11:74018603
|
C | T | 12 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6922-5078G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018603 | ||||||
| chr11:74018674
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6922-5149T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018674 | ||||||
| chr11:74018714
|
C | T | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6922-5189G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018714 | ||||||
| chr11:74018724
|
T | C | 19 | a0002c0005t0001g0049a0002c0005t0001g0058a0002c0005t0001g0062others(16): Show | 19 | HG00733.hp1 HG00738.hp1 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.6922-5199A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018724 | ||||||
| chr11:74018846
|
A | G | 1 | a0016c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6922-5321T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018846 | ||||||
| chr11:74018929
|
A | T | 1 | a0036c0042t0001g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6922-5404T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018929 | ||||||
| chr11:74018957
|
C | T | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6922-5432G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74018957 | ||||||
| chr11:74019124
|
G | T | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-5599C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019124 | ||||||
| chr11:74019234
|
G | A | 1 | a0002c0003t0001g0205 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.6922-5709C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019234 | ||||||
| chr11:74019235
|
C | T | 12 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.6922-5710G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019235 | ||||||
| chr11:74019316
|
T | TG | 46 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0032others(43): Show | 47 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.6922-5792dupC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019316 | ||||||
| chr11:74019465
|
T | C | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-5940A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019465 | ||||||
| chr11:74019563
|
T | G | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-6038A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019563 | ||||||
| chr11:74019683
|
A | ATTTT | 23 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(20): Show | 23 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.6922-6162_6922-615 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019683 | ||||||
| chr11:74019683
|
A | ATTTTT | 11 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(8): Show | 12 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.6922-6163_6922-615 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019683 | ||||||
| chr11:74019695
|
C | T | 46 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0032others(43): Show | 47 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.6922-6170G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019695 | ||||||
| chr11:74019704
|
T | G | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-6179A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019704 | ||||||
| chr11:74019715
|
C | T | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-6190G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019715 | ||||||
| chr11:74019787
|
A | G | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6922-6262T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74019787 | ||||||
| chr11:74020203
|
A | G | 61 | a0002c0003t0001g0052a0003c0016t0001g0242a0003c0016t0001g0249others(58): Show | 62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.6922-6678T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020203 | ||||||
| chr11:74020377
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0146 | 2 | HG01109.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.6922-6852T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020377 | ||||||
| chr11:74020401
|
C | G | 14 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.6922-6876G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020401 | ||||||
| chr11:74020531
|
T | G | 46 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0032others(43): Show | 47 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.6922-7006A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020531 | ||||||
| chr11:74020538
|
C | A | 2 | a0005c0006t0001g0006a0024c0038t0001g0293 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.6922-7013G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020538 | ||||||
| chr11:74020539
|
G | C | 34 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(31): Show | 35 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(32): Show |
intron_variant | MODIFIER | c.6922-7014C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020539 | ||||||
| chr11:74020553
|
C | T | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6922-7028G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020553 | ||||||
| chr11:74020619
|
C | T | 209 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0112others(206): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.6922-7094G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020619 | ||||||
| chr11:74020817
|
A | G | 3 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195 | 3 | HG02280.hp1 HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.6922-7292T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020817 | ||||||
| chr11:74020889
|
G | A | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6922-7364C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020889 | ||||||
| chr11:74020919
|
G | C | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6921+7368C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020919 | ||||||
| chr11:74020946
|
C | A | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.6921+7341G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020946 | ||||||
| chr11:74020998
|
G | C | 26 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(23): Show | 27 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.6921+7289C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74020998 | ||||||
| chr11:74021048
|
T | C | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(8): Show | 11 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.6921+7239A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021048 | ||||||
| chr11:74021055
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0151 | 2 | HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.6921+7232C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021055 | ||||||
| chr11:74021138
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.6921+7149G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021138 | ||||||
| chr11:74021198
|
C | G | 2 | a0002c0005t0001g0086a0002c0005t0001g0092 | 2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.6921+7089G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021198 | ||||||
| chr11:74021246
|
A | AAAAC | 23 | a0003c0002t0001g0278a0003c0002t0001g0279a0004c0004t0001g0032others(20): Show | 23 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.6921+7037_6921+704 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021246 | ||||||
| chr11:74021480
|
G | T | 27 | a0003c0016t0001g0242a0003c0016t0001g0249a0004c0004t0001g0036others(24): Show | 28 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.6921+6807C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021480 | ||||||
| chr11:74021644
|
C | T | 16 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(13): Show | 16 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.6921+6643G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021644 | ||||||
| chr11:74021767
|
C | T | 1 | a0002c0003t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6921+6520G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021767 | ||||||
| chr11:74021811
|
G | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6921+6476C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021811 | ||||||
| chr11:74021836
|
G | T | 2 | a0008c0007t0001g0076a0008c0007t0001g0217 | 2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.6921+6451C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021836 | ||||||
| chr11:74021854
|
A | G | 2 | a0008c0007t0001g0177a0034c0033t0001g0178 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.6921+6433T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021854 | ||||||
| chr11:74021861
|
T | C | 40 | a0002c0003t0001g0054a0002c0003t0001g0055a0002c0003t0001g0056others(37): Show | 41 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(38): Show |
intron_variant | MODIFIER | c.6921+6426A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021861 | ||||||
| chr11:74021896
|
C | T | 1 | a0002c0003t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.6921+6391G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021896 | ||||||
| chr11:74021998
|
C | T | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.6921+6289G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74021998 | ||||||
| chr11:74022062
|
G | A | 3 | a0012c0013t0001g0226a0012c0013t0001g0227a0022c0035t0001g0228 | 3 | HG02055.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.6921+6225C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022062 | ||||||
| chr11:74022115
|
T | A | 18 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(15): Show | 18 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.6921+6172A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022115 | ||||||
| chr11:74022116
|
T | C | 157 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0112others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.6921+6171A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022116 | ||||||
| chr11:74022127
|
G | GA | 6 | a0001c0001t0001g0193a0006c0008t0001g0230a0007c0017t0001g0194others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.6921+6159dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022127 | ||||||
| chr11:74022238
|
T | C | 1 | a0002c0005t0001g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.6921+6049A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022238 | ||||||
| chr11:74022317
|
G | A | 1 | a0004c0004t0001g0186 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6921+5970C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022317 | ||||||
| chr11:74022418
|
C | T | 8 | a0002c0003t0001g0213a0005c0006t0001g0024a0006c0008t0001g0238others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.6921+5869G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022418 | ||||||
| chr11:74022449
|
G | A | 5 | a0002c0003t0001g0196a0002c0003t0001g0204a0002c0003t0001g0206others(2): Show | 5 | HG01081.hp1 HG02738.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.6921+5838C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022449 | ||||||
| chr11:74022461
|
G | A | 1 | a0003c0002t0001g0288 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.6921+5826C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022461 | ||||||
| chr11:74022468
|
G | A | 12 | a0003c0034t0001g0185a0006c0008t0001g0238a0006c0008t0001g0239others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.6921+5819C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022468 | ||||||
| chr11:74022516
|
T | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0164a0013c0014t0001g0130others(2): Show | 5 | HG01361.hp1 HG02109.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.6921+5771A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022516 | ||||||
| chr11:74022575
|
G | A | 2 | a0009c0010t0001g0303a0036c0042t0001g0302 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5712C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022575 | ||||||
| chr11:74022611
|
ACTGCCGT others(25): Show |
A | 1 | a0002c0003t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6921+5644_6921+567 others(36): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022611 | ||||||
| chr11:74022626
|
G | A | 2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.6921+5661C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022626 | ||||||
| chr11:74022856
|
G | A | 2 | a0009c0010t0001g0303a0036c0042t0001g0302 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5431C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74022856 | ||||||
| chr11:74023013
|
A | G | 39 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(36): Show | 40 | HG01074.hp2 HG01884.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.6921+5274T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023013 | ||||||
| chr11:74023044
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6921+5243G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023044 | ||||||
| chr11:74023161
|
T | C | 60 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(57): Show | 61 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(58): Show |
intron_variant | MODIFIER | c.6921+5126A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023161 | ||||||
| chr11:74023162
|
G | A | 3 | a0007c0026t0001g0005a0009c0010t0001g0303a0036c0042t0001g0302 | 3 | HG02280.hp2 HG03831.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5125C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023162 | ||||||
| chr11:74023189
|
C | T | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+5098G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023189 | ||||||
| chr11:74023229
|
C | T | 3 | a0007c0026t0001g0005a0009c0010t0001g0303a0036c0042t0001g0302 | 3 | HG02280.hp2 HG03831.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+5058G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023229 | ||||||
| chr11:74023329
|
A | C | 80 | a0001c0001t0001g0150a0001c0001t0001g0179a0001c0030t0001g0192others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.6921+4958T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023329 | ||||||
| chr11:74023355
|
T | A | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6921+4932A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023355 | ||||||
| chr11:74023468
|
T | C | 2 | a0009c0010t0001g0303a0036c0042t0001g0302 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6921+4819A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023468 | ||||||
| chr11:74023542
|
T | G | 2 | a0001c0001t0001g0182a0003c0002t0001g0255 | 2 | NA18949.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.6921+4745A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023542 | ||||||
| chr11:74023639
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6921+4648G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023639 | ||||||
| chr11:74023655
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.6921+4632G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023655 | ||||||
| chr11:74023666
|
T | C | 1 | a0007c0009t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6921+4621A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023666 | ||||||
| chr11:74023688
|
T | TC | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+4598dupG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023688 | ||||||
| chr11:74023774
|
C | T | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6921+4513G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023774 | ||||||
| chr11:74023782
|
C | T | 1 | a0002c0003t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6921+4505G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023782 | ||||||
| chr11:74023860
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0174 | 2 | NA18747.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.6921+4427A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74023860 | ||||||
| chr11:74024009
|
G | A | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6921+4278C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024009 | ||||||
| chr11:74024043
|
G | A | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6921+4244C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024043 | ||||||
| chr11:74024044
|
T | G | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6921+4243A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024044 | ||||||
| chr11:74024114
|
C | T | 1 | a0003c0002t0001g0245 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6921+4173G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024114 | ||||||
| chr11:74024179
|
C | T | 60 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(57): Show | 61 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(58): Show |
intron_variant | MODIFIER | c.6921+4108G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024179 | ||||||
| chr11:74024282
|
A | G | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+4005T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024282 | ||||||
| chr11:74024330
|
A | G | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6921+3957T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024330 | ||||||
| chr11:74024767
|
G | A | 4 | a0002c0003t0001g0054a0002c0003t0001g0055a0002c0003t0001g0056others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.6921+3520C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024767 | ||||||
| chr11:74024780
|
G | A | 41 | a0001c0001t0001g0150a0001c0001t0001g0179a0002c0003t0001g0052others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.6921+3507C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024780 | ||||||
| chr11:74024839
|
T | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.6921+3448A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74024839 | ||||||
| chr11:74025114
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0160 | 2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.6921+3173A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025114 | ||||||
| chr11:74025176
|
A | G | 7 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6921+3111T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025176 | ||||||
| chr11:74025336
|
G | A | 1 | a0002c0003t0001g0201 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.6921+2951C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025336 | ||||||
| chr11:74025373
|
G | A | 7 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6921+2914C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025373 | ||||||
| chr11:74025457
|
G | A | 2 | a0006c0008t0001g0239a0006c0008t0001g0240 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6921+2830C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025457 | ||||||
| chr11:74025468
|
A | T | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6921+2819T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025468 | ||||||
| chr11:74025547
|
C | G | 24 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(21): Show | 24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.6921+2740G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025547 | ||||||
| chr11:74025620
|
G | A | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.6921+2667C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025620 | ||||||
| chr11:74025643
|
G | A | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+2644C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025643 | ||||||
| chr11:74025696
|
G | A | 2 | a0006c0008t0001g0239a0006c0008t0001g0240 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6921+2591C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025696 | ||||||
| chr11:74025702
|
G | C | 2 | a0005c0006t0001g0026a0005c0006t0001g0027 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.6921+2585C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025702 | ||||||
| chr11:74025725
|
G | T | 7 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(4): Show | 7 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6921+2562C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025725 | ||||||
| chr11:74025756
|
C | A | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.6921+2531G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025756 | ||||||
| chr11:74025830
|
T | C | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.6921+2457A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025830 | ||||||
| chr11:74025897
|
G | A | 2 | a0006c0008t0001g0239a0006c0008t0001g0240 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6921+2390C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74025897 | ||||||
| chr11:74026012
|
C | T | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6921+2275G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026012 | ||||||
| chr11:74026043
|
A | T | 1 | a0008c0007t0001g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6921+2244T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026043 | ||||||
| chr11:74026200
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6921+2087G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026200 | ||||||
| chr11:74026231
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.6921+2056G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026231 | ||||||
| chr11:74026268
|
C | T | 1 | a0002c0003t0001g0210 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.6921+2019G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026268 | ||||||
| chr11:74026310
|
GA | G | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+1976delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026310 | ||||||
| chr11:74026321
|
A | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6921+1966T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026321 | ||||||
| chr11:74026443
|
G | A | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.6921+1844C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026443 | ||||||
| chr11:74026692
|
G | A | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6921+1595C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026692 | ||||||
| chr11:74026735
|
T | C | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6921+1552A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026735 | ||||||
| chr11:74026791
|
A | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6921+1496T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026791 | ||||||
| chr11:74026822
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0103 | 2 | HG01192.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.6921+1465C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026822 | ||||||
| chr11:74026870
|
C | G | 4 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.6921+1417G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026870 | ||||||
| chr11:74026962
|
C | CA | 178 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0156others(175): Show | 179 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.6921+1324dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026962 | ||||||
| chr11:74026962
|
C | CAA | 14 | a0003c0002t0001g0283a0003c0002t0001g0286a0003c0002t0003g0002others(11): Show | 14 | HG01516.hp1 HG01517.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.6921+1323_6921+132 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74026962 | ||||||
| chr11:74027074
|
A | T | 3 | a0003c0016t0001g0242a0003c0016t0001g0249a0033c0022t0001g0295 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6921+1213T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027074 | ||||||
| chr11:74027112
|
T | C | 6 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(3): Show | 6 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.6921+1175A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027112 | ||||||
| chr11:74027210
|
G | A | 1 | a0007c0009t0002g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6921+1077C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027210 | ||||||
| chr11:74027239
|
A | T | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+1048T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027239 | ||||||
| chr11:74027244
|
C | T | 229 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0150others(226): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.6921+1043G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027244 | ||||||
| chr11:74027254
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.6921+1033C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027254 | ||||||
| chr11:74027296
|
T | C | 1 | a0002c0003t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6921+991A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027296 | ||||||
| chr11:74027431
|
A | G | 1 | a0006c0012t0001g0235 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.6921+856T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027431 | ||||||
| chr11:74027451
|
A | C | 1 | a0005c0027t0001g0012 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6921+836T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027451 | ||||||
| chr11:74027507
|
A | G | 24 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(21): Show | 24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.6921+780T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027507 | ||||||
| chr11:74027671
|
C | T | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.6921+616G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027671 | ||||||
| chr11:74027755
|
AT | A | 3 | a0003c0002t0001g0298a0003c0002t0001g0299a0003c0002t0001g0300 | 3 | HG00738.hp2 HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.6921+531delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027755 | ||||||
| chr11:74027840
|
C | T | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+447G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027840 | ||||||
| chr11:74027896
|
C | T | 2 | a0002c0003t0001g0050a0002c0003t0001g0051 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.6921+391G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027896 | ||||||
| chr11:74027897
|
G | A | 1 | a0003c0002t0001g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6921+390C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027897 | ||||||
| chr11:74027941
|
G | A | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6921+346C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027941 | ||||||
| chr11:74027999
|
T | C | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6921+288A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74027999 | ||||||
| chr11:74028014
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6921+273A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028014 | ||||||
| chr11:74028045
|
T | C | 31 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(28): Show | 31 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.6921+242A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028045 | ||||||
| chr11:74028245
|
T | G | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6921+42A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028245 | ||||||
| chr11:74028256
|
T | C | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6921+31A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 32/32 | chr11 | 74028256 | ||||||
| chr11:74028608
|
C | G | 36 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(33): Show | 36 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.6810-210G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028608 | ||||||
| chr11:74028636
|
T | C | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6810-238A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028636 | ||||||
| chr11:74028712
|
T | A | 1 | a0003c0002t0001g0283 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.6810-314A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028712 | ||||||
| chr11:74028864
|
G | A | 36 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(33): Show | 36 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.6810-466C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74028864 | ||||||
| chr11:74029119
|
G | A | 65 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(62): Show | 66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.6810-721C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029119 | ||||||
| chr11:74029208
|
C | A | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-810G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029208 | ||||||
| chr11:74029210
|
C | A | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.6810-812G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029210 | ||||||
| chr11:74029217
|
G | A | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-819C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029217 | ||||||
| chr11:74029355
|
G | A | 1 | a0002c0003t0001g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.6810-957C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029355 | ||||||
| chr11:74029530
|
C | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6810-1132G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029530 | ||||||
| chr11:74029606
|
CCAGA | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG00544.hp1 HG02129.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.6810-1212_6810-120 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029606 | ||||||
| chr11:74029630
|
G | A | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.6810-1232C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029630 | ||||||
| chr11:74029722
|
C | G | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.6810-1324G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029722 | ||||||
| chr11:74029953
|
G | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.6810-1555C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74029953 | ||||||
| chr11:74030050
|
C | A | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6810-1652G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030050 | ||||||
| chr11:74030220
|
C | T | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-1822G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030220 | ||||||
| chr11:74030253
|
T | C | 36 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(33): Show | 36 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.6810-1855A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030253 | ||||||
| chr11:74030282
|
T | C | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6810-1884A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030282 | ||||||
| chr11:74030351
|
T | C | 1 | a0002c0003t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6810-1953A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030351 | ||||||
| chr11:74030354
|
T | C | 55 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(52): Show | 56 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(53): Show |
intron_variant | MODIFIER | c.6810-1956A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030354 | ||||||
| chr11:74030377
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0103 | 2 | HG01192.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.6810-1979A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030377 | ||||||
| chr11:74030472
|
C | T | 1 | a0002c0003t0001g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6810-2074G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030472 | ||||||
| chr11:74030550
|
C | T | 6 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.6810-2152G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030550 | ||||||
| chr11:74030703
|
A | G | 23 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(20): Show | 23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.6810-2305T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030703 | ||||||
| chr11:74030744
|
ACTCCTCC others(5): Show |
A | 1 | a0001c0001t0001g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6810-2358_6810-234 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030744 | ||||||
| chr11:74030794
|
G | A | 3 | a0002c0003t0001g0201a0002c0003t0001g0202a0002c0003t0001g0203 | 3 | HG01123.hp1 HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.6810-2396C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030794 | ||||||
| chr11:74030954
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0151 | 2 | HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.6809+2397G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74030954 | ||||||
| chr11:74031219
|
T | G | 26 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(23): Show | 26 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.6809+2132A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031219 | ||||||
| chr11:74031365
|
C | T | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.6809+1986G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031365 | ||||||
| chr11:74031392
|
C | T | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.6809+1959G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031392 | ||||||
| chr11:74031919
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6809+1432C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74031919 | ||||||
| chr11:74032284
|
T | C | 11 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.6809+1067A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032284 | ||||||
| chr11:74032368
|
G | A | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6809+983C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032368 | ||||||
| chr11:74032487
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.6809+864G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032487 | ||||||
| chr11:74032490
|
CCT | C | 39 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(36): Show | 40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.6809+859_6809+860d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032490 | ||||||
| chr11:74032590
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.6809+761C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032590 | ||||||
| chr11:74032596
|
C | T | 1 | a0003c0002t0001g0278 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.6809+755G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032596 | ||||||
| chr11:74032640
|
G | A | 1 | a0002c0003t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6809+711C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032640 | ||||||
| chr11:74032732
|
C | G | 41 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(38): Show | 42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.6809+619G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032732 | ||||||
| chr11:74032735
|
C | T | 8 | a0001c0001t0001g0182a0003c0002t0001g0251a0003c0002t0001g0253others(5): Show | 8 | HG00438.hp2 HG03654.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.6809+616G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032735 | ||||||
| chr11:74032817
|
G | A | 41 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(38): Show | 42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.6809+534C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032817 | ||||||
| chr11:74032839
|
T | C | 2 | a0003c0002t0001g0281a0003c0002t0001g0282 | 2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6809+512A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032839 | ||||||
| chr11:74032863
|
T | TA | 8 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.6809+487dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74032863 | ||||||
| chr11:74033056
|
T | G | 3 | a0006c0008t0001g0238a0006c0008t0001g0239a0006c0008t0001g0240 | 3 | HG01884.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6809+295A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74033056 | ||||||
| chr11:74033118
|
G | T | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.6809+233C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 31/32 | chr11 | 74033118 | ||||||
| chr11:74034350
|
T | C | 41 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(38): Show | 42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.5882-72A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034350 | ||||||
| chr11:74034482
|
A | C | 1 | a0004c0004t0001g0036 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5882-204T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034482 | ||||||
| chr11:74034499
|
G | A | 11 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5882-221C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034499 | ||||||
| chr11:74034579
|
G | A | 1 | a0003c0002t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5882-301C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034579 | ||||||
| chr11:74034633
|
T | C | 1 | a0003c0002t0001g0288 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5882-355A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034633 | ||||||
| chr11:74034765
|
T | G | 1 | a0033c0022t0001g0295 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5882-487A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034765 | ||||||
| chr11:74034794
|
G | A | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5882-516C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034794 | ||||||
| chr11:74034843
|
T | C | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5882-565A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034843 | ||||||
| chr11:74034890
|
A | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5882-612T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034890 | ||||||
| chr11:74034942
|
T | G | 1 | a0012c0013t0001g0225 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5882-664A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74034942 | ||||||
| chr11:74035022
|
G | A | 2 | a0004c0004t0001g0042a0004c0004t0001g0045 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5882-744C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035022 | ||||||
| chr11:74035119
|
G | T | 1 | a0013c0014t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5882-841C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035119 | ||||||
| chr11:74035143
|
A | G | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5882-865T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035143 | ||||||
| chr11:74035236
|
C | T | 3 | a0007c0009t0002g0310a0007c0009t0002g0312a0027c0047t0002g0311 | 3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5882-958G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035236 | ||||||
| chr11:74035244
|
A | G | 65 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(62): Show | 66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.5882-966T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035244 | ||||||
| chr11:74035402
|
G | A | 63 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(60): Show | 64 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(61): Show |
intron_variant | MODIFIER | c.5882-1124C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035402 | ||||||
| chr11:74035421
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5882-1143C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035421 | ||||||
| chr11:74035635
|
T | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5882-1357A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035635 | ||||||
| chr11:74035709
|
G | GT | 12 | a0001c0001t0001g0094a0007c0009t0002g0310a0007c0009t0002g0312others(9): Show | 12 | HG01255.hp2 HG02145.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5882-1432dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035709 | ||||||
| chr11:74035748
|
T | C | 11 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5882-1470A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035748 | ||||||
| chr11:74035816
|
T | C | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5882-1538A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035816 | ||||||
| chr11:74035859
|
C | CT | 17 | a0003c0002t0001g0251a0005c0027t0001g0012a0006c0008t0001g0229others(14): Show | 18 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.5882-1582dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035859 | ||||||
| chr11:74035859
|
C | G | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5882-1581G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035859 | ||||||
| chr11:74035908
|
C | T | 8 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(5): Show | 9 | HG01884.hp2 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.5881+1570G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035908 | ||||||
| chr11:74035970
|
G | C | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5881+1508C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74035970 | ||||||
| chr11:74036110
|
C | G | 1 | a0017c0043t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5881+1368G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036110 | ||||||
| chr11:74036175
|
C | T | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5881+1303G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036175 | ||||||
| chr11:74036216
|
G | C | 6 | a0010c0011t0001g0053a0010c0011t0001g0066a0010c0011t0001g0067others(3): Show | 6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.5881+1262C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036216 | ||||||
| chr11:74036349
|
A | G | 5 | a0003c0002t0001g0260a0003c0002t0001g0261a0003c0002t0001g0262others(2): Show | 5 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.5881+1129T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036349 | ||||||
| chr11:74036452
|
A | G | 1 | a0003c0002t0001g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5881+1026T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036452 | ||||||
| chr11:74036582
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5881+896C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74036582 | ||||||
| chr11:74037100
|
T | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5881+378A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037100 | ||||||
| chr11:74037115
|
C | T | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5881+363G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037115 | ||||||
| chr11:74037134
|
T | C | 39 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(36): Show | 40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5881+344A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037134 | ||||||
| chr11:74037163
|
T | C | 1 | a0013c0014t0001g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5881+315A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037163 | ||||||
| chr11:74037208
|
C | T | 41 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(38): Show | 42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.5881+270G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037208 | ||||||
| chr11:74037336
|
T | TA | 13 | a0001c0001t0001g0140a0002c0003t0001g0197a0005c0006t0001g0015others(10): Show | 13 | HG00597.hp1 HG01099.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.5881+141dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 30/32 | chr11 | 74037336 | ||||||
| chr11:74037711
|
G | A | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5661-13C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74037711 | ||||||
| chr11:74037752
|
A | T | 5 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.5661-54T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74037752 | ||||||
| chr11:74037841
|
C | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0148others(1): Show | 4 | HG00140.hp1 HG01106.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.5661-143G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74037841 | ||||||
| chr11:74038364
|
A | G | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5661-666T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038364 | ||||||
| chr11:74038507
|
C | T | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5661-809G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038507 | ||||||
| chr11:74038670
|
A | G | 4 | a0009c0010t0001g0305a0009c0010t0001g0306a0009c0010t0001g0307others(1): Show | 4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.5661-972T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038670 | ||||||
| chr11:74038923
|
C | T | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5661-1225G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74038923 | ||||||
| chr11:74039064
|
C | T | 11 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5661-1366G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039064 | ||||||
| chr11:74039183
|
T | C | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5661-1485A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039183 | ||||||
| chr11:74039187
|
C | T | 41 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(38): Show | 42 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.5661-1489G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039187 | ||||||
| chr11:74039204
|
G | T | 1 | a0004c0004t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5661-1506C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039204 | ||||||
| chr11:74039388
|
T | C | 11 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5661-1690A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039388 | ||||||
| chr11:74039391
|
C | T | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5661-1693G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039391 | ||||||
| chr11:74039392
|
G | A | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5661-1694C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039392 | ||||||
| chr11:74039504
|
C | G | 6 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5661-1806G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039504 | ||||||
| chr11:74039506
|
T | C | 1 | a0003c0002t0001g0254 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5661-1808A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039506 | ||||||
| chr11:74039556
|
G | A | 4 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.5661-1858C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039556 | ||||||
| chr11:74039657
|
T | C | 24 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(21): Show | 24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5661-1959A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039657 | ||||||
| chr11:74039759
|
C | T | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5661-2061G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74039759 | ||||||
| chr11:74040122
|
G | A | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5660+1932C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040122 | ||||||
| chr11:74040369
|
C | T | 11 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5660+1685G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040369 | ||||||
| chr11:74040436
|
G | T | 55 | a0001c0030t0001g0192a0002c0003t0001g0030a0002c0003t0001g0031others(52): Show | 55 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.5660+1618C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040436 | ||||||
| chr11:74040457
|
G | A | 1 | a0002c0003t0001g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5660+1597C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040457 | ||||||
| chr11:74040572
|
T | C | 1 | a0017c0043t0001g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5660+1482A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040572 | ||||||
| chr11:74040657
|
G | C | 1 | a0003c0002t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5660+1397C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040657 | ||||||
| chr11:74040884
|
C | G | 1 | a0006c0012t0001g0234 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5660+1170G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040884 | ||||||
| chr11:74040899
|
C | T | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5660+1155G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040899 | ||||||
| chr11:74040908
|
GCA | G | 39 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(36): Show | 40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5660+1144_5660+114 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040908 | ||||||
| chr11:74040925
|
C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5660+1129G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040925 | ||||||
| chr11:74040964
|
A | AT | 78 | a0001c0001t0001g0193a0001c0030t0001g0192a0002c0003t0001g0030others(75): Show | 78 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.5660+1089dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040964 | ||||||
| chr11:74040964
|
ATT | A | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5660+1088_5660+108 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040964 | ||||||
| chr11:74040964
|
ATTT | A | 29 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(26): Show | 30 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.5660+1087_5660+108 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74040964 | ||||||
| chr11:74041015
|
A | T | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5660+1039T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041015 | ||||||
| chr11:74041095
|
T | C | 39 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(36): Show | 40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5660+959A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041095 | ||||||
| chr11:74041158
|
C | T | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5660+896G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041158 | ||||||
| chr11:74041176
|
C | T | 39 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(36): Show | 40 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.5660+878G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041176 | ||||||
| chr11:74041339
|
C | T | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5660+715G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041339 | ||||||
| chr11:74041746
|
A | C | 65 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(62): Show | 66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.5660+308T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041746 | ||||||
| chr11:74041866
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0103 | 2 | HG01192.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.5660+188A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041866 | ||||||
| chr11:74041879
|
A | G | 11 | a0006c0008t0001g0230a0007c0017t0001g0194a0007c0017t0001g0195others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.5660+175T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74041879 | ||||||
| chr11:74042024
|
T | C | 2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.5660+30A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 29/32 | chr11 | 74042024 | ||||||
| chr11:74042223
|
C | CA | 23 | a0002c0003t0001g0018a0004c0004t0001g0047a0006c0008t0001g0229others(20): Show | 23 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(20): Show |
splice_region_variant&intron_variant | LOW | c.5496-6dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042223 | ||||||
| chr11:74042223
|
CA | C | 9 | a0002c0005t0001g0063a0002c0005t0001g0069a0002c0005t0001g0072others(6): Show | 9 | HG01074.hp2 HG02015.hp1 HG02886.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.5496-6delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042223 | ||||||
| chr11:74042243
|
G | A | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.5496-25C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042243 | ||||||
| chr11:74042360
|
C | CT | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5496-143dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042360 | ||||||
| chr11:74042490
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.5496-272G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042490 | ||||||
| chr11:74042564
|
T | C | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5496-346A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042564 | ||||||
| chr11:74042574
|
G | A | 1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.5496-356C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042574 | ||||||
| chr11:74042626
|
G | A | 41 | a0001c0030t0001g0192a0002c0003t0001g0030a0002c0003t0001g0031others(38): Show | 41 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.5496-408C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042626 | ||||||
| chr11:74042677
|
T | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5496-459A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042677 | ||||||
| chr11:74042752
|
TA | T | 65 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0193others(62): Show | 66 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.5496-535delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042752 | ||||||
| chr11:74042787
|
A | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5496-569T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042787 | ||||||
| chr11:74042812
|
C | T | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-594G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042812 | ||||||
| chr11:74042992
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0191 | 2 | HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5496-774G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74042992 | ||||||
| chr11:74043025
|
A | G | 5 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.5496-807T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043025 | ||||||
| chr11:74043034
|
T | C | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.5496-816A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043034 | ||||||
| chr11:74043405
|
G | A | 5 | a0004c0004t0001g0037a0004c0004t0001g0038a0004c0004t0001g0039others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.5496-1187C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043405 | ||||||
| chr11:74043470
|
T | C | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5496-1252A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043470 | ||||||
| chr11:74043509
|
A | AT | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5496-1292dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043509 | ||||||
| chr11:74043585
|
T | A | 5 | a0010c0011t0001g0053a0010c0011t0001g0066a0010c0011t0001g0067others(2): Show | 5 | HG02083.hp2 NA18998.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.5496-1367A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043585 | ||||||
| chr11:74043591
|
C | T | 23 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(20): Show | 23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.5496-1373G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043591 | ||||||
| chr11:74043603
|
A | T | 1 | a0002c0003t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5496-1385T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043603 | ||||||
| chr11:74043619
|
T | G | 9 | a0005c0006t0001g0020a0005c0006t0001g0021a0005c0006t0001g0023others(6): Show | 9 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.5496-1401A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043619 | ||||||
| chr11:74043663
|
C | G | 9 | a0003c0002t0001g0246a0003c0002t0001g0248a0003c0002t0001g0258others(6): Show | 9 | NA18948.hp2 NA18950.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.5496-1445G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043663 | ||||||
| chr11:74043689
|
T | C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5496-1471A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043689 | ||||||
| chr11:74043762
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5496-1544C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043762 | ||||||
| chr11:74043999
|
T | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5496-1781A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74043999 | ||||||
| chr11:74044072
|
G | A | 3 | a0004c0004t0001g0035a0004c0004t0001g0043a0004c0004t0001g0044 | 3 | HG02922.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5496-1854C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044072 | ||||||
| chr11:74044091
|
C | T | 4 | a0002c0003t0001g0054a0002c0003t0001g0055a0002c0003t0001g0056others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5496-1873G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044091 | ||||||
| chr11:74044137
|
C | T | 1 | a0003c0002t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5496-1919G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044137 | ||||||
| chr11:74044205
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5496-1987G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044205 | ||||||
| chr11:74044253
|
C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5496-2035G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044253 | ||||||
| chr11:74044287
|
C | G | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-2069G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044287 | ||||||
| chr11:74044338
|
C | T | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5496-2120G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044338 | ||||||
| chr11:74044353
|
G | A | 13 | a0002c0003t0001g0196a0002c0003t0001g0204a0002c0003t0001g0205others(10): Show | 13 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.5496-2135C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044353 | ||||||
| chr11:74044392
|
T | C | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-2174A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044392 | ||||||
| chr11:74044444
|
A | ACT | 60 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(57): Show | 61 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(58): Show |
intron_variant | MODIFIER | c.5496-2228_5496-222 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044444 | ||||||
| chr11:74044451
|
C | CA | 11 | a0001c0001t0001g0157a0003c0002t0001g0277a0004c0004t0001g0037others(8): Show | 11 | HG00639.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.5496-2234dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044451 | ||||||
| chr11:74044468
|
G | T | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5496-2250C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044468 | ||||||
| chr11:74044494
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.5496-2276T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044494 | ||||||
| chr11:74044746
|
A | C | 38 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(35): Show | 39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.5496-2528T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044746 | ||||||
| chr11:74044865
|
C | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5496-2647G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74044865 | ||||||
| chr11:74045144
|
C | T | 62 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(59): Show | 63 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(60): Show |
intron_variant | MODIFIER | c.5496-2926G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045144 | ||||||
| chr11:74045181
|
C | T | 1 | a0001c0001t0001g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5496-2963G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045181 | ||||||
| chr11:74045254
|
C | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+2951G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045254 | ||||||
| chr11:74045511
|
G | C | 38 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(35): Show | 39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.5495+2694C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045511 | ||||||
| chr11:74045524
|
T | C | 1 | a0003c0002t0001g0258 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5495+2681A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045524 | ||||||
| chr11:74045575
|
TC | T | 30 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(27): Show | 31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5495+2629delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045575 | ||||||
| chr11:74045577
|
CT | C | 191 | a0001c0001t0001g0101a0001c0001t0001g0104a0001c0001t0001g0148others(188): Show | 191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.5495+2627delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045577 | ||||||
| chr11:74045719
|
G | A | 1 | a0009c0010t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5495+2486C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74045719 | ||||||
| chr11:74046160
|
C | CATTA | 30 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(27): Show | 31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5495+2041_5495+204 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046160 | ||||||
| chr11:74046194
|
C | A | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+2011G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046194 | ||||||
| chr11:74046271
|
C | A | 12 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(9): Show | 12 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.5495+1934G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046271 | ||||||
| chr11:74046331
|
A | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0160 | 2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.5495+1874T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046331 | ||||||
| chr11:74046415
|
C | G | 1 | a0001c0001t0001g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5495+1790G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046415 | ||||||
| chr11:74046491
|
G | A | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.5495+1714C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046491 | ||||||
| chr11:74046650
|
G | GCT | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+1553_5495+155 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046650 | ||||||
| chr11:74046659
|
C | T | 1 | a0036c0042t0001g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5495+1546G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046659 | ||||||
| chr11:74046678
|
A | G | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.5495+1527T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046678 | ||||||
| chr11:74046755
|
C | T | 9 | a0003c0002t0001g0246a0003c0002t0001g0248a0003c0002t0001g0258others(6): Show | 9 | NA18948.hp2 NA18950.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.5495+1450G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046755 | ||||||
| chr11:74046956
|
A | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+1249T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74046956 | ||||||
| chr11:74047065
|
G | C | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5495+1140C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047065 | ||||||
| chr11:74047302
|
C | A | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5495+903G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047302 | ||||||
| chr11:74047315
|
A | G | 2 | a0003c0002t0001g0262a0003c0002t0001g0263 | 2 | NA18941.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.5495+890T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047315 | ||||||
| chr11:74047426
|
A | G | 1 | a0002c0003t0001g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5495+779T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047426 | ||||||
| chr11:74047647
|
C | T | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5495+558G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047647 | ||||||
| chr11:74047699
|
C | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5495+506G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047699 | ||||||
| chr11:74047846
|
G | A | 10 | a0004c0004t0001g0036a0004c0004t0001g0037a0004c0004t0001g0038others(7): Show | 10 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.5495+359C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 28/32 | chr11 | 74047846 | ||||||
| chr11:74048411
|
G | A | 38 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(35): Show | 39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.5362-73C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048411 | ||||||
| chr11:74048499
|
T | C | 6 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5362-161A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048499 | ||||||
| chr11:74048574
|
T | C | 43 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(40): Show | 43 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.5362-236A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048574 | ||||||
| chr11:74048619
|
T | G | 6 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5362-281A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048619 | ||||||
| chr11:74048780
|
G | A | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5362-442C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048780 | ||||||
| chr11:74048867
|
C | T | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5361+470G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048867 | ||||||
| chr11:74048889
|
A | ATTC | 220 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0101others(217): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.5361+445_5361+447d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048889 | ||||||
| chr11:74048894
|
T | TC | 4 | a0002c0003t0001g0215a0003c0002t0001g0261a0003c0002t0001g0280others(1): Show | 4 | HG00544.hp2 HG00597.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.5361+442_5361+443i others(3): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048894 | ||||||
| chr11:74048927
|
C | T | 1 | a0032c0024t0001g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5361+410G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74048927 | ||||||
| chr11:74049032
|
TAG | T | 5 | a0004c0004t0001g0033a0004c0004t0001g0034a0004c0004t0001g0042others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5361+303_5361+304d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049032 | ||||||
| chr11:74049058
|
C | T | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5361+279G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049058 | ||||||
| chr11:74049086
|
T | C | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.5361+251A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049086 | ||||||
| chr11:74049209
|
A | G | 4 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.5361+128T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 27/32 | chr11 | 74049209 | ||||||
| chr11:74049570
|
A | G | 2 | a0008c0007t0001g0082a0008c0007t0001g0221 | 2 | NA18950.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.5156-28T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049570 | ||||||
| chr11:74049641
|
A | G | 62 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(59): Show | 63 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(60): Show |
intron_variant | MODIFIER | c.5156-99T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049641 | ||||||
| chr11:74049700
|
C | A | 1 | a0032c0024t0001g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5156-158G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049700 | ||||||
| chr11:74049744
|
G | A | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5156-202C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049744 | ||||||
| chr11:74049765
|
A | G | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5156-223T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049765 | ||||||
| chr11:74049771
|
TTC | T | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5156-231_5156-230d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049771 | ||||||
| chr11:74049891
|
C | CCAAGTAG others(19): Show |
18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5156-350_5156-349i others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049891 | ||||||
| chr11:74049894
|
C | A | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5156-352G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049894 | ||||||
| chr11:74049895
|
T | C | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.5156-353A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049895 | ||||||
| chr11:74049944
|
C | T | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5156-402G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049944 | ||||||
| chr11:74049986
|
G | T | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5156-444C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049986 | ||||||
| chr11:74049992
|
G | A | 3 | a0006c0008t0001g0238a0006c0008t0001g0239a0006c0008t0001g0240 | 3 | HG01884.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5156-450C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74049992 | ||||||
| chr11:74050046
|
T | C | 3 | a0003c0016t0001g0242a0003c0016t0001g0249a0033c0022t0001g0295 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5156-504A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050046 | ||||||
| chr11:74050121
|
A | T | 1 | a0002c0003t0001g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5156-579T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050121 | ||||||
| chr11:74050216
|
A | G | 6 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5156-674T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050216 | ||||||
| chr11:74050282
|
T | C | 30 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(27): Show | 31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5156-740A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050282 | ||||||
| chr11:74050383
|
T | C | 3 | a0003c0002t0001g0298a0003c0002t0001g0299a0003c0002t0001g0300 | 3 | HG00738.hp2 HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.5156-841A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050383 | ||||||
| chr11:74050390
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.5156-848C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050390 | ||||||
| chr11:74050428
|
A | G | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5156-886T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050428 | ||||||
| chr11:74050566
|
A | G | 7 | a0002c0003t0001g0197a0002c0003t0001g0199a0002c0003t0001g0201others(4): Show | 7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.5156-1024T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050566 | ||||||
| chr11:74050711
|
GTTTGGAC others(559): Show |
G | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5156-1735_5156-117 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050711 | ||||||
| chr11:74050715
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.5156-1173C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050715 | ||||||
| chr11:74050830
|
T | C | 1 | a0003c0002t0001g0283 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5156-1288A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74050830 | ||||||
| chr11:74051013
|
C | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5156-1471G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051013 | ||||||
| chr11:74051015
|
G | T | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5156-1473C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051015 | ||||||
| chr11:74051125
|
A | AAAAAC | 7 | a0001c0001t0001g0119a0001c0001t0001g0182a0003c0002t0001g0251others(4): Show | 7 | NA18949.hp1 NA18949.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.5156-1588_5156-158 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051125 | ||||||
| chr11:74051301
|
G | GA | 25 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(22): Show | 26 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.5156-1760dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051301 | ||||||
| chr11:74051571
|
T | A | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5156-2029A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051571 | ||||||
| chr11:74051590
|
C | A | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5156-2048G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74051590 | ||||||
| chr11:74052068
|
G | A | 2 | a0007c0026t0001g0005a0028c0046t0002g0309 | 2 | HG03831.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.5156-2526C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052068 | ||||||
| chr11:74052237
|
C | T | 1 | a0003c0002t0001g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.5155+2370G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052237 | ||||||
| chr11:74052443
|
T | C | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5155+2164A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052443 | ||||||
| chr11:74052562
|
T | A | 8 | a0004c0004t0001g0036a0004c0004t0001g0037a0004c0004t0001g0038others(5): Show | 8 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.5155+2045A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052562 | ||||||
| chr11:74052664
|
G | A | 5 | a0004c0004t0001g0033a0004c0004t0001g0034a0004c0004t0001g0042others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.5155+1943C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052664 | ||||||
| chr11:74052988
|
G | T | 1 | a0002c0003t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5155+1619C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052988 | ||||||
| chr11:74052998
|
G | A | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+1609C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74052998 | ||||||
| chr11:74053034
|
A | C | 53 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(50): Show | 54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+1573T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053034 | ||||||
| chr11:74053049
|
A | G | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5155+1558T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053049 | ||||||
| chr11:74053124
|
G | A | 1 | a0004c0004t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5155+1483C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053124 | ||||||
| chr11:74053284
|
A | C | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+1323T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053284 | ||||||
| chr11:74053468
|
A | G | 1 | a0007c0009t0002g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5155+1139T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053468 | ||||||
| chr11:74053687
|
C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5155+920G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053687 | ||||||
| chr11:74053705
|
G | A | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5155+902C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053705 | ||||||
| chr11:74053789
|
A | T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+818T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053789 | ||||||
| chr11:74053882
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5155+725G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053882 | ||||||
| chr11:74053885
|
AGGCAGGA others(6): Show |
A | 53 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(50): Show | 54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+709_5155+721d others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74053885 | ||||||
| chr11:74054039
|
G | A | 14 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.5155+568C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054039 | ||||||
| chr11:74054043
|
C | A | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5155+564G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054043 | ||||||
| chr11:74054069
|
G | C | 1 | a0003c0002t0001g0274 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5155+538C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054069 | ||||||
| chr11:74054078
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.5155+529G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054078 | ||||||
| chr11:74054145
|
G | A | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5155+462C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054145 | ||||||
| chr11:74054190
|
T | G | 1 | a0002c0003t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5155+417A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054190 | ||||||
| chr11:74054226
|
C | G | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5155+381G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054226 | ||||||
| chr11:74054271
|
C | CA | 8 | a0001c0001t0001g0150a0001c0001t0001g0158a0001c0001t0001g0182others(5): Show | 8 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.5155+335dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | ||||||
| chr11:74054271
|
C | CAA | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5155+334_5155+335d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | ||||||
| chr11:74054271
|
CA | C | 37 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0116others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.5155+335delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | ||||||
| chr11:74054271
|
CAA | C | 78 | a0001c0001t0001g0114a0002c0003t0001g0030a0002c0003t0001g0031others(75): Show | 78 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.5155+334_5155+335d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | ||||||
| chr11:74054271
|
CAAA | C | 11 | a0002c0005t0001g0072a0007c0009t0002g0310a0007c0009t0002g0312others(8): Show | 11 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.5155+333_5155+335d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054271 | ||||||
| chr11:74054312
|
T | C | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5155+295A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054312 | ||||||
| chr11:74054314
|
T | C | 53 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(50): Show | 54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+293A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054314 | ||||||
| chr11:74054395
|
C | CA | 24 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(21): Show | 24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5155+211dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054395 | ||||||
| chr11:74054407
|
T | A | 53 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(50): Show | 54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5155+200A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054407 | ||||||
| chr11:74054441
|
C | T | 2 | a0007c0009t0002g0316a0007c0009t0002g0317 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5155+166G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054441 | ||||||
| chr11:74054449
|
T | C | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.5155+158A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054449 | ||||||
| chr11:74054507
|
G | GA | 25 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0109others(22): Show | 25 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.5155+99dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | ||||||
| chr11:74054507
|
GA | G | 27 | a0001c0001t0001g0114a0002c0005t0001g0058a0003c0002t0001g0263others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.5155+99delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | ||||||
| chr11:74054507
|
GAA | G | 8 | a0004c0004t0001g0186a0009c0010t0001g0303a0009c0010t0001g0304others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.5155+98_5155+99del others(2): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | ||||||
| chr11:74054507
|
GAAA | G | 24 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(21): Show | 24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5155+97_5155+99del others(3): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | ||||||
| chr11:74054507
|
GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0105 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5155+87_5155+99del others(13): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054507 | ||||||
| chr11:74054546
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5155+61C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | 74054546 | ||||||
| chr11:74054686
|
A | C | 15 | a0008c0007t0001g0076a0008c0007t0001g0082a0008c0007t0001g0177others(12): Show | 15 | HG01074.hp1 HG01515.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.5091-15T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054686 | ||||||
| chr11:74054710
|
G | C | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5091-39C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054710 | ||||||
| chr11:74054742
|
G | A | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5091-71C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054742 | ||||||
| chr11:74054767
|
T | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.5091-96A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054767 | ||||||
| chr11:74054854
|
G | A | 1 | a0014c0020t0004g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5091-183C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054854 | ||||||
| chr11:74054943
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.5091-272C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74054943 | ||||||
| chr11:74055047
|
G | A | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5091-376C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055047 | ||||||
| chr11:74055098
|
C | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0099a0001c0001t0001g0103others(2): Show | 5 | HG01192.hp2 HG01975.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.5091-427G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055098 | ||||||
| chr11:74055143
|
G | A | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5091-472C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055143 | ||||||
| chr11:74055190
|
A | G | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5091-519T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055190 | ||||||
| chr11:74055251
|
C | A | 2 | a0002c0003t0001g0055a0002c0003t0001g0057 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5091-580G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055251 | ||||||
| chr11:74055251
|
C | T | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5091-580G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055251 | ||||||
| chr11:74055373
|
TATATATT others(2): Show |
T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5091-711_5091-703d others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055373 | ||||||
| chr11:74055545
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.5091-874G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055545 | ||||||
| chr11:74055645
|
T | C | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5091-974A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055645 | ||||||
| chr11:74055741
|
A | G | 53 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(50): Show | 54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.5091-1070T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74055741 | ||||||
| chr11:74056023
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.5091-1352T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056023 | ||||||
| chr11:74056107
|
T | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.5090+1299A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056107 | ||||||
| chr11:74056228
|
G | A | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5090+1178C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056228 | ||||||
| chr11:74056452
|
G | A | 123 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(120): Show | 124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.5090+954C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056452 | ||||||
| chr11:74056527
|
A | G | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5090+879T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056527 | ||||||
| chr11:74056612
|
A | G | 4 | a0005c0006t0001g0006a0005c0006t0001g0007a0005c0006t0001g0013others(1): Show | 4 | HG00642.hp1 HG02735.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.5090+794T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056612 | ||||||
| chr11:74056618
|
G | C | 24 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(21): Show | 24 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.5090+788C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056618 | ||||||
| chr11:74056630
|
G | A | 57 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(54): Show | 57 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.5090+776C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056630 | ||||||
| chr11:74056901
|
A | AT | 125 | a0001c0001t0001g0104a0001c0001t0001g0123a0001c0001t0001g0133others(122): Show | 125 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.5090+504dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056901 | ||||||
| chr11:74056901
|
AT | A | 20 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(17): Show | 20 | HG02258.hp1 HG02486.hp1 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.5090+504delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056901 | ||||||
| chr11:74056901
|
ATT | A | 30 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(27): Show | 31 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.5090+503_5090+504d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74056901 | ||||||
| chr11:74057009
|
AC | A | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(13): Show | 16 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.5090+396delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057009 | ||||||
| chr11:74057112
|
C | G | 3 | a0003c0002t0001g0298a0003c0002t0001g0299a0003c0002t0001g0300 | 3 | HG00738.hp2 HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.5090+294G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057112 | ||||||
| chr11:74057180
|
G | A | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.5090+226C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057180 | ||||||
| chr11:74057185
|
A | G | 1 | a0002c0003t0001g0201 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5090+221T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057185 | ||||||
| chr11:74057393
|
G | A | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5090+13C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 25/32 | chr11 | 74057393 | ||||||
| chr11:74057954
|
G | GTCAA | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-414_4952-411d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74057954 | ||||||
| chr11:74058096
|
A | C | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4952-552T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058096 | ||||||
| chr11:74058392
|
C | G | 1 | a0003c0002t0001g0270 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4952-848G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058392 | ||||||
| chr11:74058490
|
A | G | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-946T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058490 | ||||||
| chr11:74058672
|
C | T | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-1128G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058672 | ||||||
| chr11:74058731
|
G | C | 1 | a0002c0003t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4952-1187C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058731 | ||||||
| chr11:74058860
|
T | C | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4952-1316A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058860 | ||||||
| chr11:74058944
|
C | T | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-1400G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058944 | ||||||
| chr11:74058980
|
T | C | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4952-1436A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74058980 | ||||||
| chr11:74059027
|
C | T | 61 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(58): Show | 62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.4952-1483G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059027 | ||||||
| chr11:74059075
|
G | A | 23 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(20): Show | 23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.4952-1531C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059075 | ||||||
| chr11:74059219
|
C | G | 43 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(40): Show | 44 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.4952-1675G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059219 | ||||||
| chr11:74059250
|
C | A | 53 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(50): Show | 54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.4952-1706G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059250 | ||||||
| chr11:74059271
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4952-1727G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059271 | ||||||
| chr11:74059298
|
C | G | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4952-1754G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059298 | ||||||
| chr11:74059319
|
G | A | 3 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237 | 3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4952-1775C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059319 | ||||||
| chr11:74059343
|
G | A | 1 | a0012c0013t0001g0225 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4952-1799C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059343 | ||||||
| chr11:74059398
|
G | A | 1 | a0003c0002t0001g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4952-1854C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059398 | ||||||
| chr11:74059410
|
C | CA | 23 | a0001c0001t0001g0009a0001c0001t0001g0096a0001c0001t0001g0106others(20): Show | 23 | HG01081.hp2 HG01255.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.4952-1867dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | ||||||
| chr11:74059410
|
C | CAA | 6 | a0006c0008t0001g0240a0006c0012t0001g0232a0006c0012t0001g0235others(3): Show | 7 | HG01884.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.4952-1868_4952-186 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | ||||||
| chr11:74059410
|
C | CAAA | 17 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(14): Show | 17 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.4952-1869_4952-186 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | ||||||
| chr11:74059410
|
C | CAAAAA | 8 | a0004c0004t0001g0036a0004c0004t0001g0037a0004c0004t0001g0038others(5): Show | 8 | HG01074.hp2 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4952-1871_4952-186 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | ||||||
| chr11:74059410
|
C | CAAAAAA | 6 | a0004c0004t0001g0045a0004c0004t0001g0181a0004c0004t0001g0186others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4952-1872_4952-186 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | ||||||
| chr11:74059410
|
C | CAAAAAAA | 7 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(4): Show | 7 | HG02630.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4952-1873_4952-186 others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | ||||||
| chr11:74059410
|
CA | C | 8 | a0001c0001t0001g0103a0001c0001t0001g0105a0002c0003t0001g0091others(5): Show | 8 | HG01516.hp2 HG01975.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.4952-1867delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059410 | ||||||
| chr11:74059462
|
C | T | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4952-1918G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059462 | ||||||
| chr11:74059496
|
C | G | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-1952G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059496 | ||||||
| chr11:74059672
|
G | A | 4 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4952-2128C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059672 | ||||||
| chr11:74059711
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4952-2167G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059711 | ||||||
| chr11:74059729
|
C | T | 2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4952-2185G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059729 | ||||||
| chr11:74059809
|
C | T | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-2265G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059809 | ||||||
| chr11:74059928
|
A | C | 10 | a0003c0002t0001g0243a0003c0002t0001g0244a0003c0002t0001g0245others(7): Show | 10 | HG00558.hp2 HG02056.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.4952-2384T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059928 | ||||||
| chr11:74059968
|
G | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4952-2424C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059968 | ||||||
| chr11:74059976
|
C | T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-2432G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74059976 | ||||||
| chr11:74060008
|
C | G | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-2464G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060008 | ||||||
| chr11:74060012
|
G | A | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-2468C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060012 | ||||||
| chr11:74060078
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-2534G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060078 | ||||||
| chr11:74060284
|
C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-2740G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060284 | ||||||
| chr11:74060493
|
C | T | 3 | a0007c0009t0002g0310a0007c0009t0002g0312a0027c0047t0002g0311 | 3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4952-2949G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060493 | ||||||
| chr11:74060661
|
T | C | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4952-3117A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060661 | ||||||
| chr11:74060672
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4952-3128G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060672 | ||||||
| chr11:74060708
|
G | T | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4952-3164C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060708 | ||||||
| chr11:74060714
|
C | T | 61 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(58): Show | 62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.4952-3170G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060714 | ||||||
| chr11:74060740
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4952-3196C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060740 | ||||||
| chr11:74060749
|
G | A | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4952-3205C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060749 | ||||||
| chr11:74060753
|
C | T | 5 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0160others(2): Show | 5 | HG01952.hp1 HG02056.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.4952-3209G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060753 | ||||||
| chr11:74060764
|
G | A | 1 | a0003c0002t0001g0270 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4952-3220C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060764 | ||||||
| chr11:74060780
|
G | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4952-3236C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060780 | ||||||
| chr11:74060798
|
T | C | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-3254A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060798 | ||||||
| chr11:74060814
|
T | A | 7 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(4): Show | 7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.4952-3270A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060814 | ||||||
| chr11:74060891
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4952-3347C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74060891 | ||||||
| chr11:74061045
|
A | T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-3501T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061045 | ||||||
| chr11:74061155
|
G | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4952-3611C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061155 | ||||||
| chr11:74061322
|
T | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0154others(1): Show | 4 | HG02083.hp1 HG04184.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.4952-3778A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061322 | ||||||
| chr11:74061591
|
C | T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-4047G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061591 | ||||||
| chr11:74061659
|
C | T | 1 | a0003c0002t0001g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4952-4115G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061659 | ||||||
| chr11:74061728
|
T | C | 61 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.4952-4184A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061728 | ||||||
| chr11:74061827
|
G | A | 7 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(4): Show | 7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.4952-4283C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061827 | ||||||
| chr11:74061982
|
T | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0175others(1): Show | 4 | HG02040.hp1 NA18966.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.4952-4438A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74061982 | ||||||
| chr11:74062130
|
C | T | 1 | a0005c0006t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4952-4586G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062130 | ||||||
| chr11:74062218
|
G | A | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4952-4674C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062218 | ||||||
| chr11:74062270
|
G | A | 26 | a0002c0003t0001g0171a0004c0004t0001g0032a0004c0004t0001g0033others(23): Show | 26 | HG01074.hp2 HG01358.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.4952-4726C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062270 | ||||||
| chr11:74062456
|
C | T | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4952-4912G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062456 | ||||||
| chr11:74062717
|
G | A | 43 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(40): Show | 44 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.4952-5173C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062717 | ||||||
| chr11:74062736
|
C | T | 4 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4952-5192G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062736 | ||||||
| chr11:74062738
|
T | C | 36 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(33): Show | 37 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.4952-5194A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062738 | ||||||
| chr11:74062757
|
G | C | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-5213C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062757 | ||||||
| chr11:74062784
|
T | C | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-5240A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062784 | ||||||
| chr11:74062792
|
G | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0151a0004c0004t0001g0032others(24): Show | 27 | HG01074.hp2 HG01358.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4952-5248C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062792 | ||||||
| chr11:74062814
|
C | A | 1 | a0002c0005t0001g0069 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4952-5270G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062814 | ||||||
| chr11:74062830
|
T | C | 2 | a0008c0007t0001g0177a0034c0033t0001g0178 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.4952-5286A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74062830 | ||||||
| chr11:74063061
|
C | T | 18 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(15): Show | 18 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(15): Show |
intron_variant | MODIFIER | c.4952-5517G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063061 | ||||||
| chr11:74063160
|
C | A | 4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4952-5616G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063160 | ||||||
| chr11:74063171
|
T | C | 123 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(120): Show | 124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.4952-5627A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063171 | ||||||
| chr11:74063373
|
T | C | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4952-5829A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063373 | ||||||
| chr11:74063374
|
C | G | 5 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4952-5830G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063374 | ||||||
| chr11:74063409
|
A | ATGGATTC others(3): Show |
1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5866_4952-586 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063409 | ||||||
| chr11:74063410
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5866G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063410 | ||||||
| chr11:74063416
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5872T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063416 | ||||||
| chr11:74063418
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4952-5874T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063418 | ||||||
| chr11:74063730
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4952-6186A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063730 | ||||||
| chr11:74063768
|
A | T | 123 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(120): Show | 124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.4952-6224T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74063768 | ||||||
| chr11:74064143
|
C | T | 1 | a0002c0003t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4952-6599G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064143 | ||||||
| chr11:74064145
|
G | T | 3 | a0003c0002t0001g0254a0003c0002t0001g0257a0003c0041t0001g0296 | 3 | HG00438.hp2 HG03654.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.4952-6601C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064145 | ||||||
| chr11:74064166
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4952-6622G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064166 | ||||||
| chr11:74064261
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4952-6717G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064261 | ||||||
| chr11:74064381
|
T | C | 2 | a0003c0002t0001g0259a0003c0002t0001g0292 | 2 | HG00408.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.4952-6837A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064381 | ||||||
| chr11:74064430
|
T | A | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4952-6886A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064430 | ||||||
| chr11:74064477
|
G | A | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4952-6933C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064477 | ||||||
| chr11:74064540
|
A | C | 3 | a0005c0006t0001g0006a0005c0006t0001g0007a0005c0006t0001g0013 | 3 | HG00642.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4952-6996T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064540 | ||||||
| chr11:74064568
|
C | T | 5 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4952-7024G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064568 | ||||||
| chr11:74064604
|
G | A | 1 | a0005c0006t0001g0025 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4952-7060C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064604 | ||||||
| chr11:74064620
|
C | A | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4952-7076G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064620 | ||||||
| chr11:74064629
|
A | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4952-7085T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064629 | ||||||
| chr11:74064889
|
C | T | 1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4952-7345G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064889 | ||||||
| chr11:74064989
|
C | T | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4952-7445G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74064989 | ||||||
| chr11:74065129
|
C | T | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-7585G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065129 | ||||||
| chr11:74065137
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4952-7593A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065137 | ||||||
| chr11:74065145
|
A | C | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4952-7601T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065145 | ||||||
| chr11:74065317
|
C | T | 1 | a0002c0005t0001g0166 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4952-7773G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065317 | ||||||
| chr11:74065428
|
G | A | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4952-7884C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065428 | ||||||
| chr11:74065552
|
C | A | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4952-8008G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065552 | ||||||
| chr11:74065613
|
C | T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-8069G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065613 | ||||||
| chr11:74065734
|
TA | T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4952-8191delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065734 | ||||||
| chr11:74065831
|
G | A | 1 | a0009c0010t0001g0304 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4952-8287C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065831 | ||||||
| chr11:74065913
|
G | A | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4951+8340C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74065913 | ||||||
| chr11:74066134
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4951+8119G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066134 | ||||||
| chr11:74066135
|
G | A | 2 | a0003c0002t0003g0002a0003c0002t0003g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4951+8118C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066135 | ||||||
| chr11:74066153
|
T | C | 3 | a0007c0009t0002g0313a0007c0009t0002g0314a0007c0009t0002g0315 | 3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4951+8100A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066153 | ||||||
| chr11:74066214
|
A | G | 53 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(50): Show | 54 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.4951+8039T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066214 | ||||||
| chr11:74066264
|
A | AGGAGGGG others(42): Show |
295 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(292): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.4951+7988_4951+798 others(53): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066264 | ||||||
| chr11:74066264
|
A | AGGAGGGG others(43): Show |
16 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0117others(13): Show | 16 | HG00544.hp1 HG00609.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4951+7988_4951+798 others(54): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066264 | ||||||
| chr11:74066264
|
A | AGGAGGGG others(44): Show |
1 | a0001c0001t0001g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4951+7988_4951+798 others(55): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066264 | ||||||
| chr11:74066267
|
A | AGGGGGAA others(43): Show |
2 | a0002c0003t0001g0071a0032c0024t0001g0200 | 2 | HG02615.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.4951+7985_4951+798 others(54): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066267 | ||||||
| chr11:74066267
|
A | AGGGGGAA others(45): Show |
1 | a0001c0001t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4951+7985_4951+798 others(56): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066267 | ||||||
| chr11:74066267
|
A | AGGGGGAA others(44): Show |
1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.4951+7985_4951+798 others(55): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066267 | ||||||
| chr11:74066292
|
TA | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+7960delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066292 | ||||||
| chr11:74066342
|
CA | C | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4951+7910delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066342 | ||||||
| chr11:74066436
|
A | AAAAG | 87 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.4951+7813_4951+781 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066436 | ||||||
| chr11:74066447
|
A | G | 28 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(25): Show | 29 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.4951+7806T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066447 | ||||||
| chr11:74066502
|
T | C | 57 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(54): Show | 57 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.4951+7751A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066502 | ||||||
| chr11:74066592
|
A | C | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+7661T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066592 | ||||||
| chr11:74066601
|
A | G | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4951+7652T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066601 | ||||||
| chr11:74066654
|
C | CT | 207 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(204): Show | 208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.4951+7598dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066654 | ||||||
| chr11:74066725
|
C | G | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4951+7528G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066725 | ||||||
| chr11:74066937
|
A | G | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4951+7316T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74066937 | ||||||
| chr11:74067054
|
T | C | 1 | a0002c0003t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4951+7199A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067054 | ||||||
| chr11:74067091
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.4951+7162A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067091 | ||||||
| chr11:74067311
|
G | T | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4951+6942C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067311 | ||||||
| chr11:74067407
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4951+6846A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067407 | ||||||
| chr11:74067535
|
C | CA | 61 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(58): Show | 62 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(59): Show |
intron_variant | MODIFIER | c.4951+6717dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067535 | ||||||
| chr11:74067576
|
AATGGTAG others(35): Show |
A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6635_4951+667 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067576 | ||||||
| chr11:74067578
|
T | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+6675A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067578 | ||||||
| chr11:74067619
|
A | T | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6634T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067619 | ||||||
| chr11:74067627
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6626A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067627 | ||||||
| chr11:74067632
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6621G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067632 | ||||||
| chr11:74067633
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6620A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067633 | ||||||
| chr11:74067634
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4951+6619T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067634 | ||||||
| chr11:74067898
|
A | G | 211 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(208): Show | 212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.4951+6355T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74067898 | ||||||
| chr11:74068118
|
C | G | 2 | a0003c0016t0001g0242a0033c0022t0001g0295 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4951+6135G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068118 | ||||||
| chr11:74068519
|
C | A | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4951+5734G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068519 | ||||||
| chr11:74068523
|
A | G | 1 | a0027c0047t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4951+5730T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068523 | ||||||
| chr11:74068567
|
C | T | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+5686G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068567 | ||||||
| chr11:74068595
|
G | T | 10 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4951+5658C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068595 | ||||||
| chr11:74068752
|
A | G | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4951+5501T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068752 | ||||||
| chr11:74068875
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4951+5378C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068875 | ||||||
| chr11:74068887
|
C | T | 1 | a0007c0009t0002g0310 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4951+5366G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068887 | ||||||
| chr11:74068934
|
T | C | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4951+5319A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74068934 | ||||||
| chr11:74069078
|
A | G | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+5175T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069078 | ||||||
| chr11:74069079
|
T | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+5174A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069079 | ||||||
| chr11:74069122
|
G | A | 123 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(120): Show | 124 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.4951+5131C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069122 | ||||||
| chr11:74069241
|
T | C | 1 | a0003c0002t0001g0254 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4951+5012A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069241 | ||||||
| chr11:74069262
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4951+4991C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069262 | ||||||
| chr11:74069689
|
G | A | 3 | a0006c0008t0001g0238a0006c0008t0001g0239a0006c0008t0001g0240 | 3 | HG01884.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4951+4564C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069689 | ||||||
| chr11:74069750
|
C | T | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4951+4503G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069750 | ||||||
| chr11:74069798
|
A | G | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4951+4455T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069798 | ||||||
| chr11:74069933
|
C | G | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+4320G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069933 | ||||||
| chr11:74069961
|
A | C | 2 | a0002c0003t0001g0196a0002c0003t0001g0204 | 2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4951+4292T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74069961 | ||||||
| chr11:74070046
|
T | G | 1 | a0002c0005t0001g0088 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4951+4207A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070046 | ||||||
| chr11:74070085
|
A | G | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4951+4168T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070085 | ||||||
| chr11:74070109
|
T | C | 1 | a0003c0002t0001g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4951+4144A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070109 | ||||||
| chr11:74070169
|
A | T | 18 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4951+4084T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070169 | ||||||
| chr11:74070190
|
A | G | 25 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(22): Show | 25 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.4951+4063T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070190 | ||||||
| chr11:74070446
|
G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+3807C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070446 | ||||||
| chr11:74070460
|
C | G | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4951+3793G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070460 | ||||||
| chr11:74070555
|
T | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+3698A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070555 | ||||||
| chr11:74070669
|
G | A | 176 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(173): Show | 176 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.4951+3584C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070669 | ||||||
| chr11:74070716
|
G | A | 35 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(32): Show | 35 | HG01074.hp2 HG02109.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.4951+3537C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070716 | ||||||
| chr11:74070717
|
C | G | 35 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(32): Show | 35 | HG01074.hp2 HG02109.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.4951+3536G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070717 | ||||||
| chr11:74070718
|
A | G | 23 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(20): Show | 23 | HG01074.hp2 HG02109.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.4951+3535T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070718 | ||||||
| chr11:74070948
|
A | G | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4951+3305T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070948 | ||||||
| chr11:74070953
|
T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4951+3300A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74070953 | ||||||
| chr11:74071137
|
T | C | 1 | a0009c0010t0001g0307 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4951+3116A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071137 | ||||||
| chr11:74071264
|
A | G | 23 | a0002c0003t0001g0056a0004c0004t0001g0032a0004c0004t0001g0033others(20): Show | 23 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.4951+2989T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071264 | ||||||
| chr11:74071502
|
G | A | 2 | a0008c0007t0001g0076a0008c0007t0001g0217 | 2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.4951+2751C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071502 | ||||||
| chr11:74071588
|
A | G | 12 | a0006c0012t0001g0235a0007c0009t0002g0310a0007c0009t0002g0312others(9): Show | 12 | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.4951+2665T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071588 | ||||||
| chr11:74071832
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.4951+2421C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071832 | ||||||
| chr11:74071918
|
T | G | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4951+2335A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071918 | ||||||
| chr11:74071920
|
G | A | 209 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(206): Show | 209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4951+2333C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071920 | ||||||
| chr11:74071951
|
G | A | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4951+2302C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74071951 | ||||||
| chr11:74072033
|
C | T | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4951+2220G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072033 | ||||||
| chr11:74072178
|
A | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4951+2075T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072178 | ||||||
| chr11:74072232
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4951+2021G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072232 | ||||||
| chr11:74072248
|
C | T | 11 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0059others(8): Show | 11 | HG01192.hp1 HG01255.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4951+2005G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072248 | ||||||
| chr11:74072293
|
T | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+1960A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072293 | ||||||
| chr11:74072392
|
T | C | 169 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4951+1861A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072392 | ||||||
| chr11:74072433
|
A | T | 177 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.4951+1820T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072433 | ||||||
| chr11:74072439
|
G | C | 1 | a0001c0001t0001g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4951+1814C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072439 | ||||||
| chr11:74072716
|
C | CT | 177 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.4951+1536dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072716 | ||||||
| chr11:74072716
|
C | CTT | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4951+1535_4951+153 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072716 | ||||||
| chr11:74072840
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4951+1413A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072840 | ||||||
| chr11:74072953
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4951+1300A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74072953 | ||||||
| chr11:74073102
|
G | C | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4951+1151C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073102 | ||||||
| chr11:74073112
|
CTCTGGCA others(8): Show |
C | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4951+1126_4951+114 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073112 | ||||||
| chr11:74073325
|
G | A | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4951+928C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073325 | ||||||
| chr11:74073352
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4951+901A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073352 | ||||||
| chr11:74073384
|
C | T | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4951+869G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073384 | ||||||
| chr11:74073535
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.4951+718G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073535 | ||||||
| chr11:74073561
|
T | A | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4951+692A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073561 | ||||||
| chr11:74073565
|
C | T | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4951+688G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073565 | ||||||
| chr11:74073571
|
A | G | 169 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4951+682T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073571 | ||||||
| chr11:74073586
|
CA | C | 170 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0150others(167): Show | 170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.4951+666delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073586 | ||||||
| chr11:74073586
|
CAA | C | 29 | a0003c0002t0001g0247a0003c0002t0001g0263a0003c0002t0001g0298others(26): Show | 29 | HG00738.hp2 HG01074.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.4951+665_4951+666d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073586 | ||||||
| chr11:74073605
|
A | G | 9 | a0003c0002t0001g0246a0003c0002t0001g0248a0003c0002t0001g0258others(6): Show | 9 | NA18948.hp2 NA18950.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.4951+648T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073605 | ||||||
| chr11:74073709
|
C | T | 1 | a0003c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4951+544G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073709 | ||||||
| chr11:74073725
|
T | C | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4951+528A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74073725 | ||||||
| chr11:74074074
|
A | C | 169 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4951+179T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 24/32 | chr11 | 74074074 | ||||||
| chr11:74074694
|
C | T | 2 | a0003c0002t0001g0252a0003c0002t0001g0253 | 2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.4604-94G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074694 | ||||||
| chr11:74074841
|
C | T | 12 | a0005c0006t0001g0014a0005c0006t0001g0015a0005c0006t0001g0020others(9): Show | 12 | HG01099.hp1 HG01106.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.4604-241G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074841 | ||||||
| chr11:74074918
|
TACAAAAA others(2): Show |
T | 43 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(40): Show | 43 | HG01074.hp2 HG02055.hp1 HG02145.hp2 others(40): Show |
intron_variant | MODIFIER | c.4604-327_4604-319d others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074918 | ||||||
| chr11:74074953
|
G | A | 1 | a0008c0007t0001g0211 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4604-353C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74074953 | ||||||
| chr11:74075040
|
C | T | 63 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.4604-440G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075040 | ||||||
| chr11:74075135
|
A | C | 1 | a0002c0003t0001g0197 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4604-535T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075135 | ||||||
| chr11:74075198
|
C | T | 11 | a0007c0009t0002g0310a0007c0009t0002g0312a0009c0010t0001g0303others(8): Show | 11 | HG02280.hp2 HG02717.hp1 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.4604-598G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075198 | ||||||
| chr11:74075354
|
C | T | 1 | a0006c0008t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4604-754G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075354 | ||||||
| chr11:74075358
|
C | T | 1 | a0009c0010t0001g0304 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4604-758G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075358 | ||||||
| chr11:74075366
|
TG | T | 304 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(301): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.4604-767delC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075366 | ||||||
| chr11:74075369
|
G | T | 20 | a0001c0001t0001g0128a0001c0001t0001g0164a0002c0003t0001g0196others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.4604-769C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075369 | ||||||
| chr11:74075377
|
G | C | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4604-777C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075377 | ||||||
| chr11:74075417
|
C | T | 222 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(219): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.4604-817G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075417 | ||||||
| chr11:74075466
|
G | A | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4604-866C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075466 | ||||||
| chr11:74075480
|
T | C | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4604-880A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075480 | ||||||
| chr11:74075482
|
C | G | 2 | a0003c0002t0001g0281a0003c0002t0001g0282 | 2 | NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4604-882G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075482 | ||||||
| chr11:74075577
|
G | C | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4604-977C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075577 | ||||||
| chr11:74075808
|
T | G | 6 | a0010c0011t0001g0053a0010c0011t0001g0066a0010c0011t0001g0067others(3): Show | 6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.4604-1208A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075808 | ||||||
| chr11:74075956
|
C | T | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4604-1356G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74075956 | ||||||
| chr11:74076031
|
C | A | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4604-1431G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076031 | ||||||
| chr11:74076154
|
T | C | 10 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4604-1554A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076154 | ||||||
| chr11:74076279
|
C | T | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4604-1679G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076279 | ||||||
| chr11:74076336
|
G | A | 209 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(206): Show | 209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4604-1736C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076336 | ||||||
| chr11:74076337
|
A | G | 1 | a0003c0002t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4604-1737T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076337 | ||||||
| chr11:74076549
|
T | C | 1 | a0003c0002t0001g0291 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4603+1566A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076549 | ||||||
| chr11:74076584
|
A | G | 1 | a0003c0002t0001g0297 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4603+1531T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076584 | ||||||
| chr11:74076728
|
T | G | 1 | a0001c0001t0001g0119 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4603+1387A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74076728 | ||||||
| chr11:74077043
|
G | A | 1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4603+1072C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077043 | ||||||
| chr11:74077112
|
A | G | 3 | a0003c0016t0001g0242a0003c0016t0001g0249a0033c0022t0001g0295 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4603+1003T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077112 | ||||||
| chr11:74077210
|
G | C | 4 | a0003c0002t0001g0265a0003c0002t0001g0266a0003c0002t0001g0267others(1): Show | 4 | HG00544.hp2 HG00673.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.4603+905C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077210 | ||||||
| chr11:74077442
|
T | G | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4603+673A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077442 | ||||||
| chr11:74077546
|
G | A | 1 | a0032c0024t0001g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4603+569C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077546 | ||||||
| chr11:74077725
|
T | A | 4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4603+390A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077725 | ||||||
| chr11:74077771
|
GTATA | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0111 | 3 | HG00423.hp2 HG00544.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.4603+340_4603+343d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(1): Show |
G | 7 | a0001c0001t0001g0101a0001c0001t0001g0114a0001c0001t0001g0136others(4): Show | 7 | HG00408.hp2 HG00639.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.4603+336_4603+343d others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(3): Show |
G | 11 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0108others(8): Show | 11 | HG01261.hp1 HG01952.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.4603+334_4603+343d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(5): Show |
G | 10 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0109others(7): Show | 10 | HG00438.hp1 HG01975.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.4603+332_4603+343d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(7): Show |
G | 7 | a0001c0001t0001g0125a0001c0001t0001g0135a0001c0001t0001g0152others(4): Show | 7 | HG00558.hp1 HG00741.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.4603+330_4603+343d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(9): Show |
G | 5 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0131others(2): Show | 5 | HG01433.hp2 HG02602.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.4603+328_4603+343d others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(11): Show |
G | 5 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0143others(2): Show | 5 | HG01099.hp2 HG02040.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.4603+326_4603+343d others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(13): Show |
G | 1 | a0001c0001t0001g0145 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4603+324_4603+343d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(15): Show |
G | 3 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0142 | 3 | HG01255.hp2 HG02300.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.4603+322_4603+343d others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(17): Show |
G | 2 | a0001c0001t0001g0095a0001c0001t0001g0138 | 2 | HG01169.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.4603+320_4603+343d others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4603+318_4603+343d others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(23): Show |
G | 3 | a0001c0001t0001g0120a0001c0001t0001g0182a0031c0032t0001g0176 | 3 | HG02109.hp1 NA18949.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.4603+314_4603+343d others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(25): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4603+312_4603+343d others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(29): Show |
G | 2 | a0001c0001t0001g0099a0001c0001t0001g0158 | 2 | HG00609.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.4603+308_4603+343d others(38): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(33): Show |
G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0140others(3): Show | 6 | HG00597.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4603+304_4603+343d others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(35): Show |
G | 2 | a0001c0001t0001g0147a0001c0001t0001g0161 | 2 | HG02559.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.4603+302_4603+343d others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(37): Show |
G | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4603+300_4603+343d others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(39): Show |
G | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4603+298_4603+343d others(48): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(41): Show |
G | 3 | a0001c0001t0001g0139a0001c0001t0001g0148a0001c0001t0001g0165 | 3 | HG01106.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.4603+296_4603+343d others(50): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(51): Show |
G | 3 | a0001c0001t0001g0096a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | NA18967.hp2 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.4603+286_4603+343d others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077771
|
GTATATAT others(55): Show |
G | 1 | a0035c0039t0001g0122 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.4603+282_4603+343d others(64): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077771 | ||||||
| chr11:74077793
|
ATATATAT others(47): Show |
A | 7 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(4): Show | 7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.4603+268_4603+321d others(56): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077793 | ||||||
| chr11:74077795
|
A | G | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.4603+320T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077795 | ||||||
| chr11:74077795
|
ATATATAT others(45): Show |
A | 7 | a0002c0003t0001g0061a0002c0003t0001g0070a0002c0003t0001g0071others(4): Show | 7 | HG02129.hp1 HG02132.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.4603+268_4603+319d others(54): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077795 | ||||||
| chr11:74077797
|
A | G | 6 | a0007c0009t0002g0310a0007c0009t0002g0313a0007c0009t0002g0314others(3): Show | 6 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.4603+318T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077797 | ||||||
| chr11:74077797
|
ATATATAT others(43): Show |
A | 3 | a0006c0008t0001g0230a0006c0008t0001g0238a0006c0008t0001g0240 | 3 | HG01884.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4603+268_4603+317d others(52): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077797 | ||||||
| chr11:74077799
|
A | G | 8 | a0007c0009t0002g0310a0007c0009t0002g0313a0007c0009t0002g0314others(5): Show | 8 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.4603+316T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077799 | ||||||
| chr11:74077799
|
ATATATAT others(41): Show |
A | 8 | a0005c0006t0001g0006a0005c0006t0001g0007a0005c0006t0001g0013others(5): Show | 8 | HG00642.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4603+268_4603+315d others(50): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077799 | ||||||
| chr11:74077801
|
A | G | 4 | a0007c0009t0002g0314a0007c0009t0002g0317a0007c0026t0001g0005others(1): Show | 4 | HG03041.hp2 HG03831.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.4603+314T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077801 | ||||||
| chr11:74077803
|
ATATATAT others(37): Show |
A | 1 | a0003c0002t0001g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.4603+268_4603+311d others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077803 | ||||||
| chr11:74077805
|
ATATATAT others(35): Show |
A | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4603+268_4603+309d others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077805 | ||||||
| chr11:74077807
|
ATATATAT others(33): Show |
A | 3 | a0002c0003t0001g0213a0003c0016t0001g0249a0005c0006t0001g0014 | 3 | HG02895.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4603+268_4603+307d others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077807 | ||||||
| chr11:74077811
|
ATATATAT others(29): Show |
A | 3 | a0003c0002t0001g0254a0003c0002t0001g0294a0003c0034t0001g0185 | 3 | HG03098.hp1 HG03654.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.4603+268_4603+303d others(38): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077811 | ||||||
| chr11:74077813
|
ATATATAT others(27): Show |
A | 5 | a0003c0002t0001g0273a0003c0002t0001g0278a0003c0002t0001g0297others(2): Show | 5 | HG02015.hp2 HG03139.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.4603+268_4603+301d others(36): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077813 | ||||||
| chr11:74077815
|
ATATATAT others(25): Show |
A | 26 | a0002c0003t0001g0052a0002c0003t0001g0081a0002c0003t0001g0214others(23): Show | 26 | HG00280.hp1 HG00438.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.4603+268_4603+299d others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077815 | ||||||
| chr11:74077817
|
ATATATAT others(23): Show |
A | 46 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0056others(43): Show | 46 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.4603+268_4603+297d others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077817 | ||||||
| chr11:74077819
|
ATATATAT others(21): Show |
A | 15 | a0002c0003t0001g0018a0002c0003t0001g0170a0002c0003t0001g0187others(12): Show | 15 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.4603+268_4603+295d others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077819 | ||||||
| chr11:74077821
|
ATATATAT others(19): Show |
A | 17 | a0001c0001t0001g0133a0002c0003t0001g0051a0002c0003t0001g0168others(14): Show | 17 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.4603+268_4603+293d others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077821 | ||||||
| chr11:74077823
|
ATATATAT others(16): Show |
A | 1 | a0002c0003t0001g0196 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4603+269_4603+291d others(25): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077823 | ||||||
| chr11:74077823
|
ATATATAT others(17): Show |
A | 25 | a0002c0003t0001g0059a0002c0003t0001g0202a0002c0003t0001g0208others(22): Show | 25 | HG00597.hp2 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.4603+268_4603+291d others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077823 | ||||||
| chr11:74077825
|
ATATATAT others(15): Show |
A | 27 | a0002c0003t0001g0019a0002c0003t0001g0030a0002c0003t0001g0031others(24): Show | 28 | HG01074.hp1 HG01123.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.4603+268_4603+289d others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077825 | ||||||
| chr11:74077827
|
ATATATAT others(13): Show |
A | 12 | a0001c0001t0001g0151a0001c0001t0001g0179a0002c0005t0001g0062others(9): Show | 12 | HG01358.hp2 HG02717.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.4603+268_4603+287d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077827 | ||||||
| chr11:74077829
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4603+269_4603+285d others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077829 | ||||||
| chr11:74077829
|
ATATATAT others(11): Show |
A | 6 | a0001c0001t0001g0180a0002c0005t0001g0074a0002c0005t0001g0092others(3): Show | 6 | NA18941.hp2 NA18942.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.4603+268_4603+285d others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077829 | ||||||
| chr11:74077831
|
ATATATAT others(9): Show |
A | 4 | a0002c0003t0001g0083a0002c0005t0001g0189a0010c0011t0001g0068others(1): Show | 4 | HG02074.hp2 HG02622.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.4603+268_4603+283d others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077831 | ||||||
| chr11:74077833
|
ATATATAT others(7): Show |
A | 5 | a0002c0003t0001g0210a0002c0005t0001g0085a0002c0005t0001g0086others(2): Show | 5 | HG01516.hp2 HG02717.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.4603+268_4603+281d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077833 | ||||||
| chr11:74077835
|
ATATATAT others(5): Show |
A | 2 | a0002c0003t0001g0197a0002c0005t0001g0058 | 2 | HG02055.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.4603+268_4603+279d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077835 | ||||||
| chr11:74077847
|
T | A | 2 | a0007c0009t0002g0312a0007c0026t0001g0005 | 2 | HG03831.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.4603+268A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077847 | ||||||
| chr11:74077848
|
A | G | 60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.4603+267T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077848 | ||||||
| chr11:74077868
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0150 | 2 | NA18956.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.4603+247G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077868 | ||||||
| chr11:74077931
|
A | G | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4603+184T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077931 | ||||||
| chr11:74077983
|
A | T | 1 | a0009c0010t0001g0304 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4603+132T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74077983 | ||||||
| chr11:74078100
|
A | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4603+15T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 23/32 | chr11 | 74078100 | ||||||
| chr11:74078732
|
T | G | 228 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(225): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.4001-15A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078732 | ||||||
| chr11:74078832
|
C | T | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-115G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078832 | ||||||
| chr11:74078920
|
G | C | 1 | a0002c0005t0001g0093 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4001-203C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078920 | ||||||
| chr11:74078980
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4001-263A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74078980 | ||||||
| chr11:74079107
|
A | AGT | 209 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(206): Show | 209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4001-392_4001-391d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079107 | ||||||
| chr11:74079162
|
T | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001-445A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079162 | ||||||
| chr11:74079198
|
C | T | 169 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4001-481G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079198 | ||||||
| chr11:74079304
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4001-587A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079304 | ||||||
| chr11:74079364
|
G | A | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4001-647C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079364 | ||||||
| chr11:74079427
|
G | C | 4 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001-710C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079427 | ||||||
| chr11:74079782
|
C | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0104others(6): Show | 9 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.4001-1065G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079782 | ||||||
| chr11:74079879
|
A | G | 5 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0148others(2): Show | 5 | HG00140.hp1 HG01106.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.4001-1162T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079879 | ||||||
| chr11:74079913
|
C | T | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-1196G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079913 | ||||||
| chr11:74079931
|
T | C | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-1214A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079931 | ||||||
| chr11:74079993
|
C | A | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4001-1276G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74079993 | ||||||
| chr11:74080226
|
T | A | 1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4001-1509A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080226 | ||||||
| chr11:74080299
|
T | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4001-1582A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080299 | ||||||
| chr11:74080349
|
T | G | 32 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(29): Show | 32 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.4001-1632A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080349 | ||||||
| chr11:74080423
|
T | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4001-1706A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080423 | ||||||
| chr11:74080501
|
G | A | 4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001-1784C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080501 | ||||||
| chr11:74080700
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4001-1983C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080700 | ||||||
| chr11:74080781
|
G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4001-2064C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74080781 | ||||||
| chr11:74081214
|
T | C | 1 | a0027c0047t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4001-2497A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081214 | ||||||
| chr11:74081268
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4001-2551G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081268 | ||||||
| chr11:74081329
|
C | G | 2 | a0008c0007t0001g0211a0008c0007t0001g0212 | 2 | NA18963.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.4001-2612G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081329 | ||||||
| chr11:74081482
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4001-2765A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081482 | ||||||
| chr11:74081499
|
A | C | 2 | a0002c0003t0001g0090a0002c0003t0001g0091 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4001-2782T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081499 | ||||||
| chr11:74081604
|
TTCA | T | 200 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(197): Show | 200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.4001-2890_4001-288 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081604 | ||||||
| chr11:74081604
|
TTCATCA | T | 9 | a0005c0006t0001g0020a0005c0006t0001g0021a0005c0006t0001g0023others(6): Show | 9 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.4001-2893_4001-288 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081604 | ||||||
| chr11:74081629
|
T | C | 1 | a0005c0027t0001g0012 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4001-2912A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081629 | ||||||
| chr11:74081678
|
T | C | 209 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(206): Show | 209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4001-2961A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081678 | ||||||
| chr11:74081904
|
T | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4000+2977A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081904 | ||||||
| chr11:74081970
|
T | C | 1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4000+2911A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081970 | ||||||
| chr11:74081995
|
T | A | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4000+2886A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74081995 | ||||||
| chr11:74082094
|
G | A | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4000+2787C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082094 | ||||||
| chr11:74082123
|
A | AT | 163 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(160): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4000+2757dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082123 | ||||||
| chr11:74082123
|
A | T | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.4000+2758T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082123 | ||||||
| chr11:74082172
|
G | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4000+2709C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082172 | ||||||
| chr11:74082238
|
C | G | 3 | a0003c0016t0001g0242a0003c0016t0001g0249a0033c0022t0001g0295 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4000+2643G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082238 | ||||||
| chr11:74082501
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4000+2380A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082501 | ||||||
| chr11:74082602
|
T | C | 2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4000+2279A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082602 | ||||||
| chr11:74082698
|
C | A | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4000+2183G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082698 | ||||||
| chr11:74082797
|
C | T | 2 | a0002c0003t0001g0090a0002c0003t0001g0091 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4000+2084G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082797 | ||||||
| chr11:74082830
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4000+2051A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082830 | ||||||
| chr11:74082865
|
C | A | 4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4000+2016G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082865 | ||||||
| chr11:74082987
|
C | A | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.4000+1894G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74082987 | ||||||
| chr11:74083024
|
G | A | 84 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.4000+1857C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083024 | ||||||
| chr11:74083029
|
C | T | 1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4000+1852G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083029 | ||||||
| chr11:74083056
|
C | T | 1 | a0036c0042t0001g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4000+1825G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083056 | ||||||
| chr11:74083107
|
A | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4000+1774T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083107 | ||||||
| chr11:74083108
|
G | GA | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4000+1772dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083108 | ||||||
| chr11:74083164
|
G | C | 1 | a0009c0010t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4000+1717C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083164 | ||||||
| chr11:74083213
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4000+1668A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083213 | ||||||
| chr11:74083214
|
A | G | 209 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(206): Show | 209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.4000+1667T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083214 | ||||||
| chr11:74083580
|
T | G | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4000+1301A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083580 | ||||||
| chr11:74083751
|
T | C | 5 | a0004c0004t0001g0037a0004c0004t0001g0038a0004c0004t0001g0039others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4000+1130A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083751 | ||||||
| chr11:74083886
|
G | A | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4000+995C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083886 | ||||||
| chr11:74083986
|
A | T | 1 | a0018c0044t0001g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4000+895T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74083986 | ||||||
| chr11:74084006
|
C | T | 5 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4000+875G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084006 | ||||||
| chr11:74084096
|
T | C | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4000+785A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084096 | ||||||
| chr11:74084162
|
A | C | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4000+719T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084162 | ||||||
| chr11:74084261
|
C | T | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4000+620G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084261 | ||||||
| chr11:74084366
|
G | A | 169 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4000+515C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084366 | ||||||
| chr11:74084423
|
AAAGTAT | A | 40 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(37): Show | 40 | HG01074.hp2 HG02145.hp2 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.4000+452_4000+457d others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084423 | ||||||
| chr11:74084432
|
TA | T | 169 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(166): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.4000+448delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084432 | ||||||
| chr11:74084495
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4000+386G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084495 | ||||||
| chr11:74084571
|
T | C | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4000+310A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084571 | ||||||
| chr11:74084615
|
TCAA | T | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4000+263_4000+265d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084615 | ||||||
| chr11:74084728
|
A | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.4000+153T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084728 | ||||||
| chr11:74084741
|
A | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.4000+140T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084741 | ||||||
| chr11:74084786
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4000+95A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 22/32 | chr11 | 74084786 | ||||||
| chr11:74085142
|
A | AT | 83 | a0001c0001t0001g0106a0001c0001t0001g0109a0002c0005t0001g0088others(80): Show | 84 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.3911-173dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085142 | ||||||
| chr11:74085391
|
C | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3910+227G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085391 | ||||||
| chr11:74085392
|
G | A | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3910+226C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085392 | ||||||
| chr11:74085563
|
T | C | 315 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(312): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.3910+55A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 21/32 | chr11 | 74085563 | ||||||
| chr11:74085942
|
T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3642-56A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74085942 | ||||||
| chr11:74086148
|
T | C | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3642-262A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086148 | ||||||
| chr11:74086153
|
C | G | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3642-267G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086153 | ||||||
| chr11:74086202
|
A | G | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3642-316T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086202 | ||||||
| chr11:74086431
|
C | A | 1 | a0024c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3642-545G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086431 | ||||||
| chr11:74086450
|
C | T | 1 | a0006c0012t0001g0234 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3642-564G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086450 | ||||||
| chr11:74086459
|
T | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3642-573A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086459 | ||||||
| chr11:74086472
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3642-586A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086472 | ||||||
| chr11:74086475
|
C | T | 144 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(141): Show | 144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.3642-589G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086475 | ||||||
| chr11:74086839
|
T | C | 4 | a0003c0034t0001g0185a0011c0015t0001g0001a0011c0015t0001g0223others(1): Show | 5 | HG01884.hp2 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3642-953A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086839 | ||||||
| chr11:74086862
|
C | G | 126 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.3642-976G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086862 | ||||||
| chr11:74086942
|
T | C | 1 | a0003c0002t0001g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3642-1056A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74086942 | ||||||
| chr11:74087131
|
A | G | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3642-1245T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087131 | ||||||
| chr11:74087478
|
C | T | 8 | a0005c0006t0001g0021a0005c0006t0001g0023a0005c0006t0001g0024others(5): Show | 8 | HG01106.hp2 HG02145.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3642-1592G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087478 | ||||||
| chr11:74087592
|
T | G | 3 | a0003c0002t0001g0258a0003c0002t0001g0268a0003c0002t0001g0294 | 3 | NA18950.hp1 NA18991.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3642-1706A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087592 | ||||||
| chr11:74087721
|
A | G | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3642-1835T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087721 | ||||||
| chr11:74087723
|
C | A | 2 | a0003c0002t0001g0246a0003c0002t0001g0248 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3642-1837G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087723 | ||||||
| chr11:74087814
|
A | C | 3 | a0003c0016t0001g0242a0003c0016t0001g0249a0033c0022t0001g0295 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3642-1928T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74087814 | ||||||
| chr11:74088255
|
C | T | 229 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(226): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.3642-2369G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088255 | ||||||
| chr11:74088269
|
G | C | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3642-2383C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088269 | ||||||
| chr11:74088280
|
T | G | 144 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(141): Show | 144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.3642-2394A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088280 | ||||||
| chr11:74088352
|
G | A | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.3641+2461C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088352 | ||||||
| chr11:74088394
|
A | G | 12 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3641+2419T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088394 | ||||||
| chr11:74088849
|
G | A | 144 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(141): Show | 144 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.3641+1964C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088849 | ||||||
| chr11:74088956
|
T | C | 135 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(132): Show |
intron_variant | MODIFIER | c.3641+1857A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74088956 | ||||||
| chr11:74089034
|
G | T | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3641+1779C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089034 | ||||||
| chr11:74089046
|
A | C | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3641+1767T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089046 | ||||||
| chr11:74089067
|
G | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.3641+1746C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089067 | ||||||
| chr11:74089437
|
A | C | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3641+1376T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089437 | ||||||
| chr11:74089842
|
C | T | 104 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.3641+971G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089842 | ||||||
| chr11:74089951
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3641+862T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74089951 | ||||||
| chr11:74090107
|
G | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3641+706C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090107 | ||||||
| chr11:74090134
|
C | A | 2 | a0003c0002t0001g0246a0003c0002t0001g0248 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3641+679G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090134 | ||||||
| chr11:74090186
|
A | G | 1 | a0003c0002t0001g0258 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3641+627T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090186 | ||||||
| chr11:74090220
|
T | C | 229 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(226): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.3641+593A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090220 | ||||||
| chr11:74090257
|
A | G | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3641+556T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090257 | ||||||
| chr11:74090305
|
G | C | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3641+508C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090305 | ||||||
| chr11:74090315
|
G | A | 18 | a0002c0005t0001g0008a0002c0005t0001g0058a0002c0005t0001g0062others(15): Show | 18 | HG00733.hp2 HG02015.hp1 NA18941.hp2 others(15): Show |
intron_variant | MODIFIER | c.3641+498C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090315 | ||||||
| chr11:74090327
|
G | C | 5 | a0007c0009t0002g0313a0007c0009t0002g0314a0007c0009t0002g0315others(2): Show | 5 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3641+486C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090327 | ||||||
| chr11:74090617
|
G | C | 212 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(209): Show | 213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.3641+196C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090617 | ||||||
| chr11:74090727
|
C | T | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3641+86G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 20/32 | chr11 | 74090727 | ||||||
| chr11:74090966
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3518-30A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74090966 | ||||||
| chr11:74091059
|
A | T | 7 | a0002c0003t0001g0197a0002c0003t0001g0199a0002c0003t0001g0201others(4): Show | 7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.3518-123T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091059 | ||||||
| chr11:74091188
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3518-252G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091188 | ||||||
| chr11:74091453
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3518-517G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091453 | ||||||
| chr11:74091691
|
A | G | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3517+725T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091691 | ||||||
| chr11:74091734
|
C | A | 1 | a0005c0006t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3517+682G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091734 | ||||||
| chr11:74091791
|
T | C | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3517+625A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091791 | ||||||
| chr11:74091970
|
G | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.3517+446C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74091970 | ||||||
| chr11:74092008
|
A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3517+408T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092008 | ||||||
| chr11:74092032
|
A | ATG | 8 | a0002c0003t0001g0061a0003c0034t0001g0185a0007c0009t0002g0313others(5): Show | 9 | HG01884.hp2 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3517+382_3517+383d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092032 | ||||||
| chr11:74092060
|
A | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0159a0006c0012t0001g0231others(3): Show | 6 | HG00438.hp1 HG00558.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3517+356T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092060 | ||||||
| chr11:74092062
|
T | A | 144 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0052others(141): Show | 145 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3517+354A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092062 | ||||||
| chr11:74092095
|
C | G | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3517+321G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092095 | ||||||
| chr11:74092216
|
C | T | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3517+200G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092216 | ||||||
| chr11:74092235
|
G | A | 12 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3517+181C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092235 | ||||||
| chr11:74092243
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3517+173G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092243 | ||||||
| chr11:74092244
|
G | A | 2 | a0002c0003t0001g0061a0002c0003t0001g0071 | 2 | NA18980.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.3517+172C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092244 | ||||||
| chr11:74092344
|
C | T | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3517+72G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092344 | ||||||
| chr11:74092350
|
C | T | 1 | a0025c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3517+66G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092350 | ||||||
| chr11:74092353
|
C | T | 136 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.3517+63G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092353 | ||||||
| chr11:74092379
|
G | A | 4 | a0003c0034t0001g0185a0011c0015t0001g0001a0011c0015t0001g0223others(1): Show | 5 | HG01884.hp2 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3517+37C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 19/32 | chr11 | 74092379 | ||||||
| chr11:74092775
|
C | CCT | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3345-188_3345-187i others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74092775 | ||||||
| chr11:74093043
|
C | G | 12 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3345-455G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093043 | ||||||
| chr11:74093106
|
A | G | 4 | a0002c0003t0001g0061a0002c0003t0001g0070a0002c0003t0001g0071others(1): Show | 4 | HG02129.hp1 HG02132.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345-518T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093106 | ||||||
| chr11:74093196
|
T | C | 1 | a0003c0002t0001g0268 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3345-608A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093196 | ||||||
| chr11:74093336
|
T | C | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3344+480A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093336 | ||||||
| chr11:74093379
|
A | G | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3344+437T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093379 | ||||||
| chr11:74093464
|
C | G | 12 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3344+352G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093464 | ||||||
| chr11:74093476
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3344+340C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093476 | ||||||
| chr11:74093628
|
T | C | 2 | a0008c0007t0001g0076a0008c0007t0001g0217 | 2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3344+188A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 18/32 | chr11 | 74093628 | ||||||
| chr11:74094199
|
G | GT | 6 | a0001c0001t0001g0116a0001c0001t0001g0191a0002c0003t0001g0054others(3): Show | 6 | HG02559.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3161-201dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094199 | ||||||
| chr11:74094199
|
GT | G | 92 | a0001c0001t0001g0103a0001c0001t0001g0110a0002c0003t0001g0016others(89): Show | 92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.3161-201delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094199 | ||||||
| chr11:74094234
|
G | A | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3161-235C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094234 | ||||||
| chr11:74094351
|
C | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3161-352G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094351 | ||||||
| chr11:74094549
|
G | A | 1 | a0003c0002t0001g0297 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3161-550C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094549 | ||||||
| chr11:74094844
|
T | G | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3160+384A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094844 | ||||||
| chr11:74094926
|
A | G | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.3160+302T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094926 | ||||||
| chr11:74094939
|
T | C | 1 | a0016c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3160+289A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094939 | ||||||
| chr11:74094979
|
A | T | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3160+249T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74094979 | ||||||
| chr11:74095152
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3160+76G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 17/32 | chr11 | 74095152 | ||||||
| chr11:74095430
|
CT | C | 17 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2980-23delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095430 | ||||||
| chr11:74095433
|
G | A | 3 | a0005c0006t0001g0006a0005c0006t0001g0007a0005c0006t0001g0013 | 3 | HG00642.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2980-25C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095433 | ||||||
| chr11:74095508
|
A | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2980-100T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095508 | ||||||
| chr11:74095781
|
G | A | 16 | a0001c0001t0001g0128a0001c0001t0001g0164a0002c0003t0001g0196others(13): Show | 16 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2980-373C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095781 | ||||||
| chr11:74095786
|
T | A | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2980-378A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095786 | ||||||
| chr11:74095997
|
T | G | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-589A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74095997 | ||||||
| chr11:74096196
|
G | A | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2980-788C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096196 | ||||||
| chr11:74096256
|
T | C | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-848A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096256 | ||||||
| chr11:74096482
|
A | T | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-1074T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096482 | ||||||
| chr11:74096485
|
GA | G | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-1078delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096485 | ||||||
| chr11:74096593
|
T | A | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-1185A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096593 | ||||||
| chr11:74096812
|
C | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2979+1197G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096812 | ||||||
| chr11:74096856
|
A | T | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2979+1153T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096856 | ||||||
| chr11:74096867
|
A | G | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2979+1142T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096867 | ||||||
| chr11:74096885
|
T | C | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2979+1124A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096885 | ||||||
| chr11:74096910
|
G | C | 80 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2979+1099C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096910 | ||||||
| chr11:74096910
|
G | T | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2979+1099C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74096910 | ||||||
| chr11:74097149
|
G | A | 2 | a0002c0003t0001g0196a0002c0003t0001g0204 | 2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2979+860C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097149 | ||||||
| chr11:74097149
|
GA | G | 105 | a0001c0001t0001g0191a0002c0005t0001g0189a0003c0002t0001g0241others(102): Show | 106 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2979+859delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097149 | ||||||
| chr11:74097178
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2979+831A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097178 | ||||||
| chr11:74097213
|
C | T | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2979+796G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097213 | ||||||
| chr11:74097659
|
T | G | 17 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2979+350A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 16/32 | chr11 | 74097659 | ||||||
| chr11:74098307
|
T | C | 1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2733-52A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74098307 | ||||||
| chr11:74098529
|
G | A | 1 | a0003c0002t0001g0288 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2733-274C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74098529 | ||||||
| chr11:74098748
|
G | T | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2733-493C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74098748 | ||||||
| chr11:74099011
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2733-756A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099011 | ||||||
| chr11:74099043
|
T | C | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2733-788A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099043 | ||||||
| chr11:74099265
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2733-1010T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099265 | ||||||
| chr11:74099518
|
T | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.2732+1007A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099518 | ||||||
| chr11:74099554
|
G | C | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2732+971C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099554 | ||||||
| chr11:74099614
|
A | G | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2732+911T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099614 | ||||||
| chr11:74099622
|
C | T | 60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.2732+903G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099622 | ||||||
| chr11:74099667
|
C | T | 17 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2732+858G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099667 | ||||||
| chr11:74099713
|
G | A | 17 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2732+812C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099713 | ||||||
| chr11:74099724
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2732+801C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099724 | ||||||
| chr11:74099826
|
A | G | 84 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(81): Show | 85 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2732+699T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099826 | ||||||
| chr11:74099851
|
G | A | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.2732+674C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099851 | ||||||
| chr11:74099852
|
T | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2732+673A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099852 | ||||||
| chr11:74099895
|
CA | C | 80 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2732+629delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099895 | ||||||
| chr11:74099937
|
G | T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2732+588C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099937 | ||||||
| chr11:74099983
|
C | T | 17 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2732+542G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74099983 | ||||||
| chr11:74100131
|
T | C | 1 | a0004c0004t0001g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2732+394A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100131 | ||||||
| chr11:74100196
|
T | C | 1 | a0002c0003t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2732+329A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100196 | ||||||
| chr11:74100268
|
T | G | 1 | a0024c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2732+257A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100268 | ||||||
| chr11:74100336
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2732+189A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 15/32 | chr11 | 74100336 | ||||||
| chr11:74100758
|
T | G | 1 | a0002c0005t0001g0062 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2581-82A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100758 | ||||||
| chr11:74100898
|
G | C | 1 | a0025c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2581-222C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100898 | ||||||
| chr11:74100942
|
G | T | 63 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.2581-266C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100942 | ||||||
| chr11:74100976
|
C | T | 2 | a0002c0003t0001g0090a0002c0003t0001g0091 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2581-300G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74100976 | ||||||
| chr11:74101290
|
A | G | 1 | a0027c0047t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2581-614T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101290 | ||||||
| chr11:74101400
|
G | A | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2581-724C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101400 | ||||||
| chr11:74101911
|
C | T | 2 | a0003c0002t0001g0252a0003c0002t0001g0253 | 2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.2580+1220G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101911 | ||||||
| chr11:74101973
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2580+1158A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101973 | ||||||
| chr11:74101983
|
A | G | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2580+1148T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74101983 | ||||||
| chr11:74102000
|
A | T | 12 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2580+1131T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102000 | ||||||
| chr11:74102119
|
A | C | 81 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2580+1012T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102119 | ||||||
| chr11:74102510
|
C | T | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2580+621G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102510 | ||||||
| chr11:74102519
|
G | A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2580+612C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102519 | ||||||
| chr11:74102620
|
C | T | 67 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(64): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.2580+511G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102620 | ||||||
| chr11:74102747
|
T | C | 1 | a0027c0047t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2580+384A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102747 | ||||||
| chr11:74102749
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2580+382G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 14/32 | chr11 | 74102749 | ||||||
| chr11:74103666
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2086-41A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74103666 | ||||||
| chr11:74103906
|
A | G | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2086-281T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74103906 | ||||||
| chr11:74104102
|
T | C | 67 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(64): Show | 68 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.2086-477A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104102 | ||||||
| chr11:74104263
|
A | G | 2 | a0011c0018t0001g0126a0011c0018t0001g0127 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2086-638T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104263 | ||||||
| chr11:74104493
|
CA | C | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2086-869delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104493 | ||||||
| chr11:74104668
|
A | T | 73 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2086-1043T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104668 | ||||||
| chr11:74104894
|
C | A | 98 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(95): Show | 98 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2086-1269G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74104894 | ||||||
| chr11:74105124
|
T | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2085+1247A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105124 | ||||||
| chr11:74105299
|
C | T | 37 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(34): Show | 38 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.2085+1072G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105299 | ||||||
| chr11:74105381
|
G | C | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2085+990C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105381 | ||||||
| chr11:74105442
|
T | C | 11 | a0002c0003t0001g0196a0002c0003t0001g0204a0002c0003t0001g0205others(8): Show | 11 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.2085+929A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105442 | ||||||
| chr11:74105567
|
G | A | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2085+804C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105567 | ||||||
| chr11:74105608
|
C | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0116 | 3 | NA18970.hp1 NA18984.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2085+763G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105608 | ||||||
| chr11:74105728
|
T | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085+643A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105728 | ||||||
| chr11:74105821
|
G | A | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2085+550C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105821 | ||||||
| chr11:74105886
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2085+485A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74105886 | ||||||
| chr11:74106200
|
C | T | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2085+171G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 13/32 | chr11 | 74106200 | ||||||
| chr11:74106931
|
A | G | 1 | a0002c0003t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1963-438T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74106931 | ||||||
| chr11:74107047
|
C | T | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1963-554G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107047 | ||||||
| chr11:74107322
|
T | TCA | 11 | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0174others(8): Show | 11 | HG01192.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1963-831_1963-830d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCACA | 5 | a0001c0001t0001g0029a0011c0015t0001g0001a0011c0015t0001g0223others(2): Show | 6 | HG01884.hp2 HG02132.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-833_1963-830d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCACACA | 6 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(3): Show | 6 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-835_1963-830d others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCACACAC others(3): Show |
1 | a0016c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1963-839_1963-830d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCACACAC others(7): Show |
1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1963-843_1963-830d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCTCACAC others(7): Show |
6 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(3): Show | 6 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1963-830_1963-829i others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCTCACAC others(9): Show |
2 | a0006c0008t0001g0230a0006c0012t0001g0234 | 2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1963-830_1963-829i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCTCACAC others(11): Show |
8 | a0006c0012t0001g0233a0006c0012t0001g0235a0009c0010t0001g0303others(5): Show | 8 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1963-830_1963-829i others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCTCACAC others(13): Show |
5 | a0009c0010t0001g0304a0009c0010t0001g0306a0009c0010t0001g0307others(2): Show | 5 | HG04228.hp2 NA18984.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1963-830_1963-829i others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCTCACAC others(15): Show |
1 | a0006c0012t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1963-830_1963-829i others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
T | TCTCACAC others(19): Show |
1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1963-830_1963-829i others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107322
|
TCA | T | 59 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(56): Show | 59 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1963-831_1963-830d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107322 | ||||||
| chr11:74107801
|
T | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1962+1233A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107801 | ||||||
| chr11:74107827
|
C | T | 1 | a0006c0012t0001g0234 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1962+1207G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107827 | ||||||
| chr11:74107954
|
T | C | 21 | a0004c0004t0001g0032a0004c0004t0001g0034a0004c0004t0001g0035others(18): Show | 21 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1962+1080A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74107954 | ||||||
| chr11:74108105
|
C | T | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1962+929G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108105 | ||||||
| chr11:74108107
|
C | T | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1962+927G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108107 | ||||||
| chr11:74108115
|
C | T | 3 | a0007c0009t0002g0310a0007c0009t0002g0312a0027c0047t0002g0311 | 3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1962+919G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108115 | ||||||
| chr11:74108130
|
G | A | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1962+904C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108130 | ||||||
| chr11:74108144
|
CTG | C | 90 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(87): Show | 91 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1962+888_1962+889d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108144 | ||||||
| chr11:74108147
|
TG | T | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0009c0010t0001g0303others(8): Show | 11 | HG02280.hp2 HG02886.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.1962+886delC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108147 | ||||||
| chr11:74108149
|
T | C | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0009c0010t0001g0303others(8): Show | 11 | HG02280.hp2 HG02886.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.1962+885A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108149 | ||||||
| chr11:74108150
|
C | A | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0009c0010t0001g0303others(8): Show | 11 | HG02280.hp2 HG02886.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.1962+884G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108150 | ||||||
| chr11:74108481
|
T | C | 8 | a0002c0003t0001g0197a0002c0003t0001g0199a0002c0003t0001g0201others(5): Show | 8 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.1962+553A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108481 | ||||||
| chr11:74108527
|
T | C | 104 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1962+507A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108527 | ||||||
| chr11:74108564
|
C | A | 2 | a0003c0016t0001g0242a0033c0022t0001g0295 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1962+470G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74108564 | ||||||
| chr11:74109028
|
A | T | 1 | a0006c0012t0001g0234 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.1962+6T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 12/32 | chr11 | 74109028 | ||||||
| chr11:74109213
|
C | T | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1844-61G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109213 | ||||||
| chr11:74109653
|
A | G | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1844-501T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109653 | ||||||
| chr11:74109839
|
G | A | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1844-687C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109839 | ||||||
| chr11:74109914
|
T | C | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1844-762A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109914 | ||||||
| chr11:74109919
|
C | CA | 5 | a0003c0041t0001g0296a0011c0015t0001g0001a0011c0015t0001g0223others(2): Show | 6 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1844-768dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109919 | ||||||
| chr11:74109922
|
C | A | 100 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1844-770G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109922 | ||||||
| chr11:74109954
|
G | A | 1 | a0002c0003t0001g0060 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1844-802C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109954 | ||||||
| chr11:74109954
|
G | GCGC | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-803_1844-802i others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109954 | ||||||
| chr11:74109956
|
C | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-804G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109956 | ||||||
| chr11:74109959
|
T | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-807A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109959 | ||||||
| chr11:74109962
|
T | C | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-810A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109962 | ||||||
| chr11:74109963
|
C | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-811G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109963 | ||||||
| chr11:74109964
|
C | CTTGGGAG others(9): Show |
8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-813_1844-812i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109964 | ||||||
| chr11:74109965
|
C | A | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-813G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109965 | ||||||
| chr11:74109966
|
A | G | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-814T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74109966 | ||||||
| chr11:74110005
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG00408.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.1844-853C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110005 | ||||||
| chr11:74110082
|
A | AAAAT | 87 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(84): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.1844-934_1844-931d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | ||||||
| chr11:74110082
|
A | AAAATAAA others(5): Show |
3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844-942_1844-931d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | ||||||
| chr11:74110082
|
A | AAAATAAA others(13): Show |
1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1844-950_1844-931d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | ||||||
| chr11:74110082
|
A | AAAATAAA others(101): Show |
8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1844-931_1844-930i others(110): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110082 | ||||||
| chr11:74110098
|
T | TAAATA | 3 | a0003c0016t0001g0242a0003c0016t0001g0249a0033c0022t0001g0295 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1844-951_1844-947d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110098 | ||||||
| chr11:74110915
|
G | C | 4 | a0006c0008t0001g0230a0006c0008t0001g0238a0006c0008t0001g0239others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844-1763C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74110915 | ||||||
| chr11:74111024
|
T | G | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1844-1872A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111024 | ||||||
| chr11:74111029
|
CCAA | C | 3 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237 | 3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1844-1880_1844-187 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111029 | ||||||
| chr11:74111089
|
C | T | 228 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(225): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1844-1937G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111089 | ||||||
| chr11:74111264
|
C | T | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1844-2112G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111264 | ||||||
| chr11:74111634
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1843+2146A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111634 | ||||||
| chr11:74111641
|
C | T | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1843+2139G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111641 | ||||||
| chr11:74111647
|
T | C | 99 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(96): Show | 99 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1843+2133A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111647 | ||||||
| chr11:74111868
|
G | C | 8 | a0004c0004t0001g0036a0004c0004t0001g0037a0004c0004t0001g0038others(5): Show | 8 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1843+1912C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111868 | ||||||
| chr11:74111919
|
T | TAC | 24 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0095others(21): Show | 24 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1843+1859_1843+186 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
T | TACAC | 4 | a0001c0001t0001g0138a0004c0004t0001g0035a0011c0018t0001g0126others(1): Show | 4 | HG01169.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1843+1857_1843+186 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TAC | T | 28 | a0001c0001t0001g0009a0001c0001t0001g0100a0001c0001t0001g0102others(25): Show | 28 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1843+1859_1843+186 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACAC | T | 22 | a0001c0001t0001g0164a0001c0001t0001g0190a0002c0003t0001g0016others(19): Show | 23 | HG01123.hp1 HG01169.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1843+1857_1843+186 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACACAC | T | 41 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0175others(38): Show | 41 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1843+1855_1843+186 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACACACA others(1): Show |
T | 44 | a0002c0003t0001g0050a0002c0003t0001g0051a0002c0003t0001g0052others(41): Show | 44 | HG00639.hp1 HG01074.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.1843+1853_1843+186 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACACACA others(3): Show |
T | 6 | a0002c0003t0001g0196a0002c0003t0001g0204a0002c0005t0001g0008others(3): Show | 6 | HG00733.hp2 HG01081.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1843+1851_1843+186 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACACACA others(5): Show |
T | 13 | a0002c0003t0001g0197a0002c0005t0001g0049a0003c0034t0001g0185others(10): Show | 13 | HG00738.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1843+1849_1843+186 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACACACA others(7): Show |
T | 12 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1843+1847_1843+186 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACACACA others(11): Show |
T | 2 | a0002c0003t0001g0081a0002c0003t0001g0187 | 2 | HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1843+1843_1843+186 others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111919
|
TACACACA others(27): Show |
T | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1843+1827_1843+186 others(38): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111919 | ||||||
| chr11:74111921
|
C | T | 74 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(71): Show | 74 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1843+1859G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111921 | ||||||
| chr11:74111931
|
C | T | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1843+1849G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111931 | ||||||
| chr11:74111933
|
C | T | 7 | a0003c0034t0001g0185a0006c0012t0001g0233a0009c0010t0001g0304others(4): Show | 7 | HG02615.hp1 HG03098.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.1843+1847G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111933 | ||||||
| chr11:74111935
|
C | T | 9 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237others(6): Show | 9 | HG02257.hp2 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1843+1845G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111935 | ||||||
| chr11:74111955
|
CACACACA others(9): Show |
C | 8 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(5): Show | 8 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1843+1809_1843+182 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111955 | ||||||
| chr11:74111957
|
CACACACA others(7): Show |
C | 3 | a0003c0002t0001g0283a0003c0002t0001g0291a0027c0047t0002g0311 | 3 | HG00609.hp1 HG02717.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1843+1809_1843+182 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111957 | ||||||
| chr11:74111959
|
CACACACA others(5): Show |
C | 20 | a0003c0002t0001g0241a0003c0002t0001g0250a0003c0002t0001g0251others(17): Show | 20 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.1843+1809_1843+182 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111959 | ||||||
| chr11:74111959
|
CACACACA others(7): Show |
C | 1 | a0003c0002t0001g0274 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1843+1807_1843+182 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111959 | ||||||
| chr11:74111961
|
CACACACA others(3): Show |
C | 28 | a0003c0002t0001g0246a0003c0002t0001g0247a0003c0002t0001g0248others(25): Show | 28 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1843+1809_1843+181 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111961 | ||||||
| chr11:74111963
|
CACACACA others(1): Show |
C | 11 | a0002c0003t0001g0090a0002c0003t0001g0091a0003c0002t0001g0243others(8): Show | 11 | HG02647.hp1 HG02896.hp1 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.1843+1809_1843+181 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111963 | ||||||
| chr11:74111965
|
CACACAT | C | 4 | a0003c0002t0001g0288a0003c0002t0001g0289a0003c0002t0001g0290others(1): Show | 4 | HG02056.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1843+1809_1843+181 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111965 | ||||||
| chr11:74111971
|
T | C | 16 | a0001c0001t0001g0106a0001c0001t0001g0145a0001c0001t0001g0150others(13): Show | 16 | HG01099.hp2 HG01433.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.1843+1809A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74111971 | ||||||
| chr11:74112101
|
A | C | 2 | a0003c0002t0001g0272a0003c0002t0001g0273 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1843+1679T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74112101 | ||||||
| chr11:74112486
|
T | C | 1 | a0003c0002t0003g0004 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1843+1294A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74112486 | ||||||
| chr11:74112514
|
G | A | 8 | a0003c0002t0001g0247a0003c0002t0001g0264a0003c0002t0001g0269others(5): Show | 8 | HG00280.hp1 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843+1266C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74112514 | ||||||
| chr11:74113094
|
T | C | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1843+686A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113094 | ||||||
| chr11:74113404
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0175others(1): Show | 4 | HG02040.hp1 NA18966.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1843+376G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113404 | ||||||
| chr11:74113500
|
G | A | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1843+280C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113500 | ||||||
| chr11:74113636
|
C | T | 2 | a0008c0007t0001g0177a0034c0033t0001g0178 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1843+144G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113636 | ||||||
| chr11:74113659
|
G | A | 10 | a0004c0004t0001g0033a0004c0004t0001g0034a0004c0004t0001g0035others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1843+121C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113659 | ||||||
| chr11:74113659
|
G | T | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1843+121C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113659 | ||||||
| chr11:74113679
|
C | CA | 6 | a0001c0001t0001g0123a0002c0005t0001g0188a0003c0002t0001g0246others(3): Show | 6 | HG02145.hp2 HG02622.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1843+100dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113679 | ||||||
| chr11:74113679
|
CA | C | 12 | a0001c0001t0001g0150a0002c0003t0001g0078a0003c0016t0001g0242others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1843+100delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 11/32 | chr11 | 74113679 | ||||||
| chr11:74114103
|
T | C | 1 | a0002c0003t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1731-211A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/32 | chr11 | 74114103 | ||||||
| chr11:74114212
|
ATACT | A | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.1730+168_1730+171d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/32 | chr11 | 74114212 | ||||||
| chr11:74114244
|
G | C | 1 | a0028c0046t0002g0309 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1730+140C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 10/32 | chr11 | 74114244 | ||||||
| chr11:74114707
|
T | C | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1521-114A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114707 | ||||||
| chr11:74114708
|
A | T | 1 | a0010c0011t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1521-115T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114708 | ||||||
| chr11:74114843
|
A | G | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1521-250T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114843 | ||||||
| chr11:74114895
|
T | C | 12 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(9): Show | 12 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1521-302A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74114895 | ||||||
| chr11:74115013
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1521-420G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115013 | ||||||
| chr11:74115100
|
A | T | 3 | a0004c0004t0001g0036a0004c0004t0001g0041a0004c0004t0001g0046 | 3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1521-507T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115100 | ||||||
| chr11:74115195
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0160 | 2 | HG01952.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1521-602G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115195 | ||||||
| chr11:74115319
|
C | T | 4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-726G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115319 | ||||||
| chr11:74115693
|
C | A | 6 | a0010c0011t0001g0053a0010c0011t0001g0066a0010c0011t0001g0067others(3): Show | 6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1521-1100G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115693 | ||||||
| chr11:74115708
|
T | A | 6 | a0010c0011t0001g0053a0010c0011t0001g0066a0010c0011t0001g0067others(3): Show | 6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.1521-1115A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115708 | ||||||
| chr11:74115964
|
A | C | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1521-1371T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74115964 | ||||||
| chr11:74116237
|
C | T | 2 | a0003c0002t0001g0252a0003c0002t0001g0253 | 2 | NA18962.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1521-1644G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116237 | ||||||
| chr11:74116272
|
T | C | 1 | a0023c0037t0001g0276 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1521-1679A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116272 | ||||||
| chr11:74116366
|
A | G | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-1773T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116366 | ||||||
| chr11:74116769
|
CATATATG others(241): Show |
C | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1211_1520+145 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116769 | ||||||
| chr11:74116819
|
CAT | C | 73 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1520+1407_1520+140 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116819 | ||||||
| chr11:74116828
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1520+1400C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116828 | ||||||
| chr11:74116836
|
A | ATATATAC others(13): Show |
1 | a0032c0024t0001g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1520+1372_1520+139 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116836 | ||||||
| chr11:74116841
|
T | TACACGTG others(35): Show |
1 | a0002c0003t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1520+1345_1520+138 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116841 | ||||||
| chr11:74116846
|
G | A | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1520+1382C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116846 | ||||||
| chr11:74116848
|
GTA | G | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+1378_1520+137 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116848 | ||||||
| chr11:74116854
|
GTGTATAT others(11): Show |
G | 1 | a0008c0007t0001g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1520+1356_1520+137 others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116854 | ||||||
| chr11:74116856
|
GTATATAC others(13): Show |
G | 1 | a0002c0003t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1520+1352_1520+137 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116856 | ||||||
| chr11:74116876
|
A | G | 16 | a0003c0002t0001g0260a0003c0002t0001g0261a0003c0002t0001g0262others(13): Show | 16 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.1520+1352T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116876 | ||||||
| chr11:74116887
|
C | T | 2 | a0003c0002t0001g0262a0003c0002t0001g0263 | 2 | NA18941.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1520+1341G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116887 | ||||||
| chr11:74116908
|
A | ATG | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1520+1318_1520+131 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116908 | ||||||
| chr11:74116917
|
T | C | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1311A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116917 | ||||||
| chr11:74116917
|
T | TACATATA others(13): Show |
1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1520+1291_1520+131 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116917 | ||||||
| chr11:74116927
|
C | CGTGTATA others(21): Show |
1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1520+1273_1520+130 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116927 | ||||||
| chr11:74116927
|
CGTGTATA others(21): Show |
C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1520+1273_1520+130 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116927 | ||||||
| chr11:74116935
|
T | TACACATA others(31): Show |
1 | a0016c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1520+1255_1520+129 others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116935 | ||||||
| chr11:74116943
|
TAC | T | 24 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1520+1283_1520+128 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116943 | ||||||
| chr11:74116945
|
C | T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1520+1283G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116945 | ||||||
| chr11:74116948
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1520+1280C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116948 | ||||||
| chr11:74116950
|
A | G | 26 | a0002c0003t0001g0215a0003c0034t0001g0185a0006c0008t0001g0229others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1520+1278T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116950 | ||||||
| chr11:74116958
|
G | A | 27 | a0001c0001t0001g0123a0001c0001t0001g0124a0003c0034t0001g0185others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1520+1270C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116958 | ||||||
| chr11:74116965
|
C | T | 5 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+1263G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116965 | ||||||
| chr11:74116973
|
C | T | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1255G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116973 | ||||||
| chr11:74116978
|
A | G | 26 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1520+1250T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116978 | ||||||
| chr11:74116984
|
A | G | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1244T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116984 | ||||||
| chr11:74116985
|
C | T | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1243G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116985 | ||||||
| chr11:74116987
|
C | CATATACG others(21): Show |
6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0151others(3): Show | 6 | HG01109.hp2 HG01358.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1520+1213_1520+124 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116987 | ||||||
| chr11:74116987
|
C | T | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1241G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116987 | ||||||
| chr11:74116998
|
A | G | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1520+1230T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74116998 | ||||||
| chr11:74117000
|
A | G | 26 | a0002c0003t0001g0070a0003c0034t0001g0185a0006c0008t0001g0229others(23): Show | 26 | HG01884.hp1 HG02055.hp1 HG02132.hp1 others(23): Show |
intron_variant | MODIFIER | c.1520+1228T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117000 | ||||||
| chr11:74117021
|
C | G | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1207G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117021 | ||||||
| chr11:74117024
|
G | A | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1204C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117024 | ||||||
| chr11:74117026
|
A | AT | 10 | a0004c0004t0001g0036a0004c0004t0001g0037a0004c0004t0001g0038others(7): Show | 10 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1201dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117026 | ||||||
| chr11:74117026
|
A | G | 3 | a0003c0016t0001g0242a0003c0016t0001g0249a0033c0022t0001g0295 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1520+1202T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117026 | ||||||
| chr11:74117028
|
A | G | 61 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1520+1200T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117028 | ||||||
| chr11:74117030
|
GTATATAT others(79): Show |
G | 2 | a0003c0016t0001g0242a0033c0022t0001g0295 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1520+1112_1520+119 others(90): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117030 | ||||||
| chr11:74117031
|
T | TATATATA others(3): Show |
3 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0164 | 3 | HG02109.hp2 HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1196_1520+119 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117031 | ||||||
| chr11:74117031
|
TATATATA others(37): Show |
T | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1520+1153_1520+119 others(48): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117031 | ||||||
| chr11:74117039
|
C | CACAT | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1188_1520+118 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117039 | ||||||
| chr11:74117039
|
CGT | C | 16 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(13): Show | 16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1520+1187_1520+118 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117039 | ||||||
| chr11:74117039
|
CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0001g0131a0001c0001t0001g0137 | 2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1179_1520+118 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117039 | ||||||
| chr11:74117040
|
G | A | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1188C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117040 | ||||||
| chr11:74117042
|
G | A | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1186C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117042 | ||||||
| chr11:74117044
|
G | A | 13 | a0001c0001t0001g0098a0001c0001t0001g0128a0001c0001t0001g0129others(10): Show | 13 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1520+1184C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117044 | ||||||
| chr11:74117045
|
T | C | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1183A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117045 | ||||||
| chr11:74117046
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0164 | 3 | HG02109.hp2 HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1182C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117046 | ||||||
| chr11:74117046
|
G | GTATATAT others(3): Show |
1 | a0006c0012t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1520+1181_1520+118 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117046 | ||||||
| chr11:74117046
|
GTGTATAT others(49): Show |
G | 2 | a0003c0034t0001g0185a0026c0025t0001g0222 | 2 | HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1520+1126_1520+118 others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117046 | ||||||
| chr11:74117047
|
T | TATATATA others(149): Show |
1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1520+1180_1520+118 others(160): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117047 | ||||||
| chr11:74117047
|
TGTATATA others(21): Show |
T | 6 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(3): Show | 6 | HG02280.hp2 HG04228.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520+1153_1520+118 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117047 | ||||||
| chr11:74117048
|
G | A | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1520+1180C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
G | GTATATAT others(35): Show |
1 | a0004c0004t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1520+1179_1520+118 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
GTATATAT others(33): Show |
G | 5 | a0001c0001t0001g0155a0002c0003t0001g0016a0002c0003t0001g0017others(2): Show | 5 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1140_1520+117 others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
GTATATAT others(47): Show |
G | 17 | a0001c0001t0001g0096a0001c0001t0001g0154a0002c0003t0001g0018others(14): Show | 17 | HG02083.hp1 HG02083.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1520+1126_1520+117 others(58): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
GTATATAT others(61): Show |
G | 12 | a0002c0003t0001g0057a0002c0003t0001g0205a0002c0003t0001g0208others(9): Show | 13 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1520+1112_1520+117 others(72): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
GTATATAT others(75): Show |
G | 66 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(63): Show | 66 | HG00423.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1520+1098_1520+117 others(86): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
GTATATAT others(89): Show |
G | 51 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(48): Show | 51 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1520+1084_1520+117 others(100): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
GTATATAT others(103): Show |
G | 23 | a0003c0041t0001g0296a0005c0006t0001g0006a0005c0006t0001g0007others(20): Show | 23 | HG01099.hp1 HG01106.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1520+1070_1520+117 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117048
|
GTATATAT others(131): Show |
G | 1 | a0005c0006t0001g0013 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1520+1042_1520+117 others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117048 | ||||||
| chr11:74117049
|
T | A | 1 | a0006c0012t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1520+1179A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117049 | ||||||
| chr11:74117049
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1520+1153_1520+117 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117049 | ||||||
| chr11:74117049
|
TATATATA others(19): Show |
T | 3 | a0003c0002t0001g0261a0007c0017t0001g0194a0031c0032t0001g0176 | 3 | HG00597.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1520+1153_1520+117 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117049 | ||||||
| chr11:74117051
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0137 | 2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1177A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117051 | ||||||
| chr11:74117054
|
A | G | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1174T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117054 | ||||||
| chr11:74117057
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0164 | 2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1171A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117057 | ||||||
| chr11:74117058
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1520+1170T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117058 | ||||||
| chr11:74117059
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0137others(1): Show | 4 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1169A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117059 | ||||||
| chr11:74117059
|
TGA | T | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1167_1520+116 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117059 | ||||||
| chr11:74117060
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0164 | 2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1520+1168C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117060 | ||||||
| chr11:74117061
|
A | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0133others(2): Show | 5 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1167T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117061 | ||||||
| chr11:74117061
|
AATATATA others(21): Show |
A | 1 | a0007c0017t0001g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1520+1139_1520+116 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117061 | ||||||
| chr11:74117062
|
A | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0133a0001c0001t0001g0137 | 3 | HG00140.hp1 HG02735.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1520+1166T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117062 | ||||||
| chr11:74117063
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0120 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1520+1153_1520+116 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117063 | ||||||
| chr11:74117063
|
T | TATATATA others(47): Show |
1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1520+1164_1520+116 others(58): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117063 | ||||||
| chr11:74117063
|
TATATATA others(5): Show |
T | 8 | a0001c0001t0001g0095a0003c0002t0001g0262a0003c0002t0001g0263others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520+1153_1520+116 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117063 | ||||||
| chr11:74117065
|
T | C | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1163A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117065 | ||||||
| chr11:74117066
|
A | G | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1162T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117066 | ||||||
| chr11:74117068
|
A | G | 14 | a0001c0001t0001g0098a0001c0001t0001g0128a0001c0001t0001g0129others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1520+1160T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117068 | ||||||
| chr11:74117070
|
A | G | 10 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(7): Show | 10 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1158T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117070 | ||||||
| chr11:74117072
|
A | G | 13 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0135others(10): Show | 13 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1520+1156T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117072 | ||||||
| chr11:74117073
|
T | A | 3 | a0006c0012t0001g0232a0006c0012t0001g0234a0006c0012t0001g0235 | 3 | HG02723.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1520+1155A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117073 | ||||||
| chr11:74117074
|
G | A | 3 | a0006c0012t0001g0232a0006c0012t0001g0234a0006c0012t0001g0235 | 3 | HG02723.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1520+1154C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117074 | ||||||
| chr11:74117075
|
A | AAT | 27 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(24): Show | 27 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1520+1151_1520+115 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117075
|
A | AATATATA others(7): Show |
3 | a0001c0001t0001g0099a0001c0001t0001g0109a0001c0001t0001g0146 | 3 | HG01109.hp2 HG01192.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1520+1139_1520+115 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117075
|
A | AATATATA others(35): Show |
1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1520+1111_1520+115 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117075
|
A | T | 15 | a0001c0001t0001g0098a0001c0001t0001g0128a0001c0001t0001g0129others(12): Show | 15 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1520+1153T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117075
|
AATATATA others(7): Show |
A | 12 | a0001c0001t0001g0009a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.1520+1139_1520+115 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117075
|
AATATATA others(21): Show |
A | 15 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0121others(12): Show | 15 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.1520+1125_1520+115 others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117075
|
AATATATA others(35): Show |
A | 10 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0001g0104others(7): Show | 10 | HG00673.hp2 HG01099.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1111_1520+115 others(46): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117075
|
AATATATA others(49): Show |
A | 4 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0001g0160others(1): Show | 4 | HG01952.hp1 NA18970.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1097_1520+115 others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117075 | ||||||
| chr11:74117079
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0137 | 2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1149A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117079 | ||||||
| chr11:74117080
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0137 | 2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1148T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117080 | ||||||
| chr11:74117082
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0137 | 2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1520+1146T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117082 | ||||||
| chr11:74117084
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0137others(1): Show | 4 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1144T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117084 | ||||||
| chr11:74117086
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1520+1142C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117086 | ||||||
| chr11:74117087
|
A | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0133others(2): Show | 5 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1141T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117087 | ||||||
| chr11:74117087
|
AATATATA others(23): Show |
A | 2 | a0001c0001t0001g0140a0001c0001t0001g0163 | 2 | HG00597.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1520+1111_1520+114 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117087 | ||||||
| chr11:74117088
|
A | G | 5 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0133others(2): Show | 5 | HG00140.hp1 HG02109.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1140T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117088 | ||||||
| chr11:74117089
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1520+1139A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117089 | ||||||
| chr11:74117089
|
T | TATATATA others(5): Show |
2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1520+1127_1520+113 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117089 | ||||||
| chr11:74117101
|
AAT | A | 24 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0001g0129others(21): Show | 24 | HG00741.hp1 HG01169.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1520+1125_1520+112 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117101 | ||||||
| chr11:74117101
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1520+1111_1520+112 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117101 | ||||||
| chr11:74117114
|
G | A | 3 | a0004c0004t0001g0036a0004c0004t0001g0041a0004c0004t0001g0046 | 3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1114C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117114 | ||||||
| chr11:74117115
|
A | T | 3 | a0004c0004t0001g0036a0004c0004t0001g0041a0004c0004t0001g0046 | 3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1113T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117115 | ||||||
| chr11:74117115
|
AAT | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0137others(2): Show | 5 | HG00140.hp1 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+1111_1520+111 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117115 | ||||||
| chr11:74117115
|
AATATATA others(23): Show |
A | 1 | a0016c0021t0001g0220 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1520+1083_1520+111 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117115 | ||||||
| chr11:74117116
|
A | G | 3 | a0004c0004t0001g0036a0004c0004t0001g0041a0004c0004t0001g0046 | 3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1112T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117116 | ||||||
| chr11:74117117
|
T | A | 3 | a0004c0004t0001g0036a0004c0004t0001g0041a0004c0004t0001g0046 | 3 | HG01074.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1520+1111A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | ||||||
| chr11:74117117
|
T | TATATATA others(5): Show |
3 | a0004c0004t0001g0043a0004c0004t0001g0044a0036c0042t0001g0302 | 3 | HG02922.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1520+1099_1520+111 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | ||||||
| chr11:74117117
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1520+1085_1520+111 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | ||||||
| chr11:74117117
|
T | TATATATA others(3): Show |
4 | a0012c0013t0001g0225a0012c0013t0001g0226a0014c0020t0004g0218others(1): Show | 4 | HG02723.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1110_1520+111 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | ||||||
| chr11:74117117
|
TATATATA others(89): Show |
T | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1520+1015_1520+111 others(100): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117117 | ||||||
| chr11:74117119
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1520+1109A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117119 | ||||||
| chr11:74117129
|
AAT | A | 10 | a0001c0001t0001g0113a0004c0004t0001g0037a0004c0004t0001g0038others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1097_1520+109 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117129 | ||||||
| chr11:74117129
|
AATATATA others(9): Show |
A | 1 | a0001c0030t0001g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1520+1083_1520+109 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117129 | ||||||
| chr11:74117129
|
AATATATA others(23): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1520+1069_1520+109 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117129 | ||||||
| chr11:74117131
|
T | TATATATA others(3): Show |
1 | a0006c0012t0001g0231 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1520+1096_1520+109 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117131 | ||||||
| chr11:74117131
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0010 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1520+1085_1520+109 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117131 | ||||||
| chr11:74117143
|
A | AAT | 3 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237 | 3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1520+1083_1520+108 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | ||||||
| chr11:74117143
|
AAT | A | 4 | a0003c0016t0001g0249a0003c0034t0001g0185a0004c0004t0001g0048others(1): Show | 4 | HG02622.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+1083_1520+108 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | ||||||
| chr11:74117143
|
AATATATA others(23): Show |
A | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1520+1055_1520+108 others(34): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | ||||||
| chr11:74117143
|
AATATATA others(37): Show |
A | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1520+1041_1520+108 others(48): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117143 | ||||||
| chr11:74117145
|
T | TATATATA others(5): Show |
2 | a0004c0004t0001g0043a0004c0004t0001g0044 | 2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1520+1071_1520+108 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | ||||||
| chr11:74117145
|
T | TATATATA others(19): Show |
1 | a0004c0004t0001g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1520+1057_1520+108 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | ||||||
| chr11:74117145
|
T | TATATATA others(33): Show |
4 | a0004c0004t0001g0033a0004c0004t0001g0034a0004c0004t0001g0042others(1): Show | 4 | HG02809.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+1043_1520+108 others(44): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | ||||||
| chr11:74117145
|
T | TATATATA others(47): Show |
1 | a0004c0004t0001g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1520+1029_1520+108 others(58): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | ||||||
| chr11:74117145
|
T | TATATATA others(115): Show |
1 | a0004c0004t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1520+1082_1520+108 others(126): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | ||||||
| chr11:74117145
|
T | TATATATA others(3): Show |
4 | a0006c0012t0001g0232a0006c0012t0001g0233a0006c0012t0001g0234others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+1082_1520+108 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | ||||||
| chr11:74117145
|
TATATATA others(5): Show |
T | 1 | a0019c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1520+1071_1520+108 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117145 | ||||||
| chr11:74117157
|
AAT | A | 14 | a0001c0001t0001g0157a0003c0034t0001g0185a0004c0004t0001g0040others(11): Show | 14 | HG02055.hp1 HG02280.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1520+1069_1520+107 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117157 | ||||||
| chr11:74117159
|
T | TATATATA others(5): Show |
2 | a0006c0012t0001g0233a0036c0042t0001g0302 | 2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1520+1057_1520+106 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117159 | ||||||
| chr11:74117159
|
T | TATATATA others(3): Show |
3 | a0006c0012t0001g0232a0006c0012t0001g0234a0006c0012t0001g0235 | 3 | HG02723.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1520+1068_1520+106 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117159 | ||||||
| chr11:74117168
|
A | T | 10 | a0002c0003t0001g0090a0002c0003t0001g0091a0008c0007t0001g0082others(7): Show | 10 | HG02083.hp2 HG02647.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+1060T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117168 | ||||||
| chr11:74117175
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1520+1053A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117175 | ||||||
| chr11:74117182
|
A | T | 6 | a0002c0003t0001g0167a0002c0003t0001g0168a0002c0003t0001g0169others(3): Show | 6 | HG01192.hp1 HG01358.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520+1046T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117182 | ||||||
| chr11:74117185
|
A | AAT | 4 | a0006c0008t0001g0230a0011c0015t0001g0001a0011c0015t0001g0223others(1): Show | 5 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+1041_1520+104 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117185 | ||||||
| chr11:74117190
|
A | G | 2 | a0006c0008t0001g0239a0006c0008t0001g0240 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1520+1038T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117190 | ||||||
| chr11:74117191
|
T | A | 2 | a0006c0008t0001g0239a0006c0008t0001g0240 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1520+1037A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117191 | ||||||
| chr11:74117196
|
A | T | 74 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1520+1032T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117196 | ||||||
| chr11:74117199
|
A | AATATATA others(11): Show |
3 | a0006c0008t0001g0229a0006c0008t0001g0236a0006c0008t0001g0237 | 3 | HG02257.hp2 HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1520+1028_1520+102 others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117199 | ||||||
| chr11:74117208
|
A | G | 3 | a0006c0008t0001g0239a0006c0008t0001g0240a0019c0045t0001g0224 | 3 | HG01884.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1520+1020T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117208 | ||||||
| chr11:74117209
|
T | A | 3 | a0006c0008t0001g0239a0006c0008t0001g0240a0019c0045t0001g0224 | 3 | HG01884.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1520+1019A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117209 | ||||||
| chr11:74117211
|
TGA | T | 3 | a0006c0008t0001g0239a0006c0008t0001g0240a0019c0045t0001g0224 | 3 | HG01884.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1520+1015_1520+101 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117211 | ||||||
| chr11:74117213
|
A | AAT | 37 | a0003c0016t0001g0242a0003c0016t0001g0249a0003c0034t0001g0185others(34): Show | 38 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(35): Show |
intron_variant | MODIFIER | c.1520+1013_1520+101 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117213 | ||||||
| chr11:74117217
|
T | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1520+1011A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117217 | ||||||
| chr11:74117242
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0148 | 3 | HG00140.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1520+986C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117242 | ||||||
| chr11:74117243
|
T | G | 2 | a0012c0013t0001g0226a0012c0013t0001g0227 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1520+985A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117243 | ||||||
| chr11:74117291
|
C | G | 1 | a0036c0042t0001g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1520+937G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117291 | ||||||
| chr11:74117361
|
A | AAT | 4 | a0001c0001t0001g0097a0002c0003t0001g0018a0011c0018t0001g0126others(1): Show | 4 | HG02965.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+865_1520+866d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATAT | 4 | a0001c0001t0001g0118a0001c0001t0001g0129a0001c0001t0001g0141others(1): Show | 4 | HG01258.hp1 HG01261.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1520+863_1520+866d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATAT | 4 | a0002c0003t0001g0075a0002c0028t0001g0011a0005c0006t0001g0014others(1): Show | 4 | HG01099.hp1 HG01433.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+861_1520+866d others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(1): Show |
35 | a0002c0003t0001g0050a0002c0003t0001g0060a0002c0003t0001g0090others(32): Show | 35 | HG01106.hp2 HG01192.hp1 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.1520+859_1520+866d others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(3): Show |
21 | a0002c0003t0001g0051a0002c0003t0001g0059a0002c0003t0001g0065others(18): Show | 21 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1520+857_1520+866d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(5): Show |
12 | a0002c0003t0001g0187a0002c0003t0001g0206a0002c0003t0001g0207others(9): Show | 12 | HG01109.hp1 HG02630.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1520+855_1520+866d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(7): Show |
15 | a0002c0003t0001g0031a0002c0003t0001g0052a0002c0003t0001g0209others(12): Show | 15 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1520+853_1520+866d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(9): Show |
3 | a0002c0003t0001g0056a0002c0003t0001g0205a0008c0007t0001g0211 | 3 | HG00280.hp2 HG02809.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1520+851_1520+866d others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(11): Show |
10 | a0002c0003t0001g0030a0002c0003t0001g0208a0002c0003t0001g0210others(7): Show | 10 | HG00639.hp2 HG01516.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1520+849_1520+866d others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(13): Show |
8 | a0002c0003t0001g0054a0002c0003t0001g0055a0002c0003t0001g0057others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1520+847_1520+866d others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(15): Show |
2 | a0002c0003t0001g0199a0002c0003t0001g0203 | 2 | HG01123.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1520+845_1520+866d others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(17): Show |
2 | a0002c0003t0001g0202a0029c0029t0001g0198 | 2 | HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1520+843_1520+866d others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(19): Show |
1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1520+841_1520+866d others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(21): Show |
1 | a0002c0003t0001g0078 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1520+839_1520+866d others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(23): Show |
1 | a0004c0004t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1520+837_1520+866d others(32): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(27): Show |
3 | a0002c0003t0001g0061a0002c0003t0001g0070a0002c0003t0001g0071 | 3 | HG02132.hp1 NA18980.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1520+866_1520+867i others(36): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | AATATATA others(33): Show |
1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1520+866_1520+867i others(42): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
A | ATATATAT others(8): Show |
1 | a0002c0003t0001g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1520+866_1520+867i others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
AAT | A | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(59): Show | 62 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1520+865_1520+866d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
AATATATA others(1): Show |
A | 3 | a0001c0001t0001g0161a0014c0020t0004g0218a0014c0020t0004g0219 | 3 | HG02723.hp2 HG03041.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1520+859_1520+866d others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117361
|
AATATATA others(5): Show |
A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1520+855_1520+866d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117361 | ||||||
| chr11:74117472
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1520+756T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117472 | ||||||
| chr11:74117563
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1520+665T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117563 | ||||||
| chr11:74117576
|
T | C | 1 | a0003c0002t0001g0297 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1520+652A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117576 | ||||||
| chr11:74117645
|
G | A | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1520+583C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117645 | ||||||
| chr11:74117731
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1520+497A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117731 | ||||||
| chr11:74117846
|
G | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1520+382C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117846 | ||||||
| chr11:74117900
|
C | T | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1520+328G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117900 | ||||||
| chr11:74117913
|
C | CA | 6 | a0001c0001t0001g0094a0001c0001t0001g0125a0001c0001t0001g0147others(3): Show | 6 | HG01255.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1520+314dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117913 | ||||||
| chr11:74117913
|
CA | C | 9 | a0004c0004t0001g0045a0007c0009t0002g0310a0007c0009t0002g0312others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1520+314delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74117913 | ||||||
| chr11:74118182
|
A | G | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1520+46T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74118182 | ||||||
| chr11:74118187
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1520+41G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 9/32 | chr11 | 74118187 | ||||||
| chr11:74118640
|
C | T | 1 | a0032c0024t0001g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1366-258G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118640 | ||||||
| chr11:74118666
|
T | C | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1366-284A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118666 | ||||||
| chr11:74118715
|
A | C | 3 | a0002c0003t0001g0201a0002c0003t0001g0202a0002c0003t0001g0203 | 3 | HG01123.hp1 HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1366-333T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118715 | ||||||
| chr11:74118736
|
G | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1366-354C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118736 | ||||||
| chr11:74118905
|
A | AT | 106 | a0001c0001t0001g0096a0001c0001t0001g0109a0001c0001t0001g0118others(103): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1366-524dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118905 | ||||||
| chr11:74118905
|
A | ATT | 11 | a0001c0001t0001g0142a0003c0002t0001g0246a0003c0002t0001g0284others(8): Show | 11 | HG02074.hp1 HG02145.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1366-525_1366-524d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118905 | ||||||
| chr11:74118905
|
AT | A | 12 | a0001c0001t0001g0103a0004c0004t0001g0032a0004c0004t0001g0033others(9): Show | 12 | HG00639.hp1 HG01975.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1366-524delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118905 | ||||||
| chr11:74118906
|
T | A | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1366-524A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74118906 | ||||||
| chr11:74119498
|
C | T | 1 | a0002c0003t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1366-1116G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119498 | ||||||
| chr11:74119635
|
CT | C | 14 | a0001c0001t0001g0123a0001c0001t0001g0131a0002c0003t0001g0199others(11): Show | 14 | HG02015.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1366-1254delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119635 | ||||||
| chr11:74119705
|
C | T | 104 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1366-1323G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119705 | ||||||
| chr11:74119712
|
T | C | 2 | a0008c0007t0001g0076a0008c0007t0001g0217 | 2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1366-1330A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119712 | ||||||
| chr11:74119784
|
T | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1366-1402A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119784 | ||||||
| chr11:74119855
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0138 | 2 | HG01169.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1366-1473G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119855 | ||||||
| chr11:74119987
|
C | A | 78 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.1366-1605G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74119987 | ||||||
| chr11:74120093
|
G | C | 3 | a0007c0009t0002g0313a0007c0009t0002g0314a0007c0009t0002g0315 | 3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1366-1711C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120093 | ||||||
| chr11:74120264
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1366-1882G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120264 | ||||||
| chr11:74120402
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1366-2020G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120402 | ||||||
| chr11:74120777
|
T | A | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1365+2211A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120777 | ||||||
| chr11:74120805
|
G | A | 1 | a0029c0029t0001g0198 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1365+2183C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120805 | ||||||
| chr11:74120915
|
T | C | 1 | a0006c0008t0001g0229 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1365+2073A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120915 | ||||||
| chr11:74120993
|
C | A | 1 | a0002c0003t0001g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1365+1995G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120993 | ||||||
| chr11:74120995
|
G | GA | 60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1365+1992dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74120995 | ||||||
| chr11:74121166
|
T | C | 105 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(102): Show | 105 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.1365+1822A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121166 | ||||||
| chr11:74121169
|
A | G | 1 | a0003c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1365+1819T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121169 | ||||||
| chr11:74121263
|
A | G | 1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1365+1725T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121263 | ||||||
| chr11:74121298
|
G | A | 1 | a0023c0037t0001g0276 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1365+1690C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121298 | ||||||
| chr11:74121418
|
C | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1365+1570G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121418 | ||||||
| chr11:74121608
|
C | CA | 70 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0143others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1365+1379dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121608 | ||||||
| chr11:74121608
|
C | CAA | 10 | a0003c0002t0001g0244a0003c0002t0001g0273a0007c0009t0002g0310others(7): Show | 10 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1365+1378_1365+137 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121608 | ||||||
| chr11:74121608
|
CAAAAAAA others(5): Show |
C | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1365+1368_1365+137 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121608 | ||||||
| chr11:74121708
|
C | T | 85 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1365+1280G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121708 | ||||||
| chr11:74121833
|
G | A | 7 | a0003c0002t0001g0243a0003c0002t0001g0244a0003c0002t0001g0245others(4): Show | 7 | HG00558.hp2 NA18980.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+1155C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121833 | ||||||
| chr11:74121995
|
C | T | 2 | a0003c0016t0001g0242a0033c0022t0001g0295 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1365+993G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74121995 | ||||||
| chr11:74122153
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02040.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1365+835G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122153 | ||||||
| chr11:74122276
|
T | C | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1365+712A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122276 | ||||||
| chr11:74122348
|
C | T | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1365+640G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122348 | ||||||
| chr11:74122622
|
T | G | 3 | a0007c0009t0002g0313a0007c0009t0002g0314a0007c0009t0002g0315 | 3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1365+366A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122622 | ||||||
| chr11:74122899
|
G | A | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1365+89C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122899 | ||||||
| chr11:74122912
|
C | CTGTCTGG others(7): Show |
229 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(226): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1365+75_1365+76ins others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122912 | ||||||
| chr11:74122946
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1365+42T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 8/32 | chr11 | 74122946 | ||||||
| chr11:74123400
|
A | G | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218-265T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123400 | ||||||
| chr11:74123460
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1218-325A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123460 | ||||||
| chr11:74123665
|
TA | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0104others(6): Show | 9 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218-531delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123665 | ||||||
| chr11:74123729
|
G | T | 8 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(5): Show | 8 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-594C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123729 | ||||||
| chr11:74123737
|
CT | C | 167 | a0001c0001t0001g0131a0002c0003t0001g0016a0002c0003t0001g0017others(164): Show | 168 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(165): Show |
intron_variant | MODIFIER | c.1218-603delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123737 | ||||||
| chr11:74123771
|
T | A | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-636A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123771 | ||||||
| chr11:74123865
|
A | G | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-730T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123865 | ||||||
| chr11:74123866
|
G | A | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-731C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123866 | ||||||
| chr11:74123911
|
G | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1218-776C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123911 | ||||||
| chr11:74123971
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1218-836A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74123971 | ||||||
| chr11:74124251
|
A | G | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1218-1116T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74124251 | ||||||
| chr11:74124525
|
G | A | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1218-1390C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74124525 | ||||||
| chr11:74124775
|
A | G | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1218-1640T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74124775 | ||||||
| chr11:74125017
|
T | A | 15 | a0005c0006t0001g0006a0005c0006t0001g0007a0005c0006t0001g0013others(12): Show | 15 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1218-1882A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74125017 | ||||||
| chr11:74125040
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1218-1905G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74125040 | ||||||
| chr11:74125479
|
T | G | 8 | a0003c0002t0001g0251a0003c0002t0001g0252a0003c0002t0001g0253others(5): Show | 8 | HG00438.hp2 HG03654.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.1218-2344A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74125479 | ||||||
| chr11:74126006
|
ACT | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0148others(2): Show | 5 | HG00140.hp1 HG01106.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1218-2873_1218-287 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126006 | ||||||
| chr11:74126305
|
T | C | 6 | a0011c0015t0001g0001a0011c0015t0001g0223a0012c0013t0001g0225others(3): Show | 7 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1218-3170A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126305 | ||||||
| chr11:74126517
|
C | T | 1 | a0002c0003t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1218-3382G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126517 | ||||||
| chr11:74126560
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0164 | 2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1218-3425G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126560 | ||||||
| chr11:74126636
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1218-3501G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126636 | ||||||
| chr11:74126637
|
G | A | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1218-3502C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126637 | ||||||
| chr11:74126774
|
T | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-3639A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126774 | ||||||
| chr11:74126791
|
T | C | 2 | a0003c0002t0001g0246a0003c0002t0001g0248 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1218-3656A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126791 | ||||||
| chr11:74126852
|
T | G | 1 | a0002c0003t0001g0075 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1218-3717A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126852 | ||||||
| chr11:74126946
|
T | C | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1218-3811A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126946 | ||||||
| chr11:74126986
|
A | G | 3 | a0003c0002t0003g0002a0003c0002t0003g0003a0003c0002t0003g0004 | 3 | HG00642.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1218-3851T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74126986 | ||||||
| chr11:74127044
|
A | G | 229 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(226): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1218-3909T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127044 | ||||||
| chr11:74127111
|
G | A | 2 | a0003c0002t0001g0272a0003c0002t0001g0273 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1218-3976C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127111 | ||||||
| chr11:74127119
|
T | C | 230 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(227): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1218-3984A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127119 | ||||||
| chr11:74127222
|
G | A | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1218-4087C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127222 | ||||||
| chr11:74127357
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0175others(1): Show | 4 | HG02040.hp1 NA18966.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218-4222T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127357 | ||||||
| chr11:74127476
|
A | AT | 15 | a0001c0001t0001g0125a0001c0030t0001g0192a0002c0003t0001g0168others(12): Show | 15 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1218-4342dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127476 | ||||||
| chr11:74127534
|
T | G | 1 | a0001c0030t0001g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1218-4399A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127534 | ||||||
| chr11:74127559
|
G | A | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1218-4424C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127559 | ||||||
| chr11:74127791
|
G | A | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1218-4656C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127791 | ||||||
| chr11:74127827
|
A | G | 1 | a0007c0009t0002g0310 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1218-4692T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127827 | ||||||
| chr11:74127886
|
G | A | 2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1218-4751C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127886 | ||||||
| chr11:74127926
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1218-4791C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74127926 | ||||||
| chr11:74128106
|
G | A | 1 | a0002c0003t0001g0016 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1217+4738C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128106 | ||||||
| chr11:74128142
|
C | T | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1217+4702G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128142 | ||||||
| chr11:74128168
|
G | T | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1217+4676C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128168 | ||||||
| chr11:74128534
|
TTTTA | T | 3 | a0003c0002t0001g0281a0003c0002t0001g0282a0031c0032t0001g0176 | 3 | HG02109.hp1 NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1217+4306_1217+430 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128534 | ||||||
| chr11:74128589
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1217+4255C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128589 | ||||||
| chr11:74128646
|
A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+4198T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128646 | ||||||
| chr11:74128725
|
A | G | 119 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(116): Show | 119 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.1217+4119T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128725 | ||||||
| chr11:74128735
|
G | T | 2 | a0002c0003t0001g0090a0002c0003t0001g0091 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1217+4109C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128735 | ||||||
| chr11:74128744
|
A | C | 99 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1217+4100T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128744 | ||||||
| chr11:74128752
|
C | G | 125 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(122): Show |
intron_variant | MODIFIER | c.1217+4092G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128752 | ||||||
| chr11:74128785
|
A | G | 1 | a0002c0003t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1217+4059T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128785 | ||||||
| chr11:74128797
|
ACCGCCCT others(4): Show |
A | 1 | a0003c0002t0001g0286 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1217+4036_1217+404 others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128797 | ||||||
| chr11:74128800
|
G | A | 1 | a0005c0006t0001g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1217+4044C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128800 | ||||||
| chr11:74128803
|
C | T | 100 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1217+4041G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128803 | ||||||
| chr11:74128824
|
T | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+4020A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128824 | ||||||
| chr11:74128889
|
A | G | 1 | a0002c0003t0001g0030 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1217+3955T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128889 | ||||||
| chr11:74128906
|
G | A | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1217+3938C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128906 | ||||||
| chr11:74128952
|
C | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1217+3892G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74128952 | ||||||
| chr11:74129041
|
G | A | 1 | a0002c0003t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1217+3803C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129041 | ||||||
| chr11:74129074
|
C | G | 1 | a0003c0002t0001g0258 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1217+3770G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129074 | ||||||
| chr11:74129075
|
A | G | 1 | a0003c0002t0001g0258 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1217+3769T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129075 | ||||||
| chr11:74129082
|
TGGCCGGG others(30): Show |
T | 20 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(17): Show | 20 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1217+3725_1217+376 others(41): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129082 | ||||||
| chr11:74129119
|
C | A | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1217+3725G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129119 | ||||||
| chr11:74129123
|
C | T | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+3721G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129123 | ||||||
| chr11:74129170
|
G | T | 2 | a0008c0007t0001g0076a0008c0007t0001g0217 | 2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1217+3674C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129170 | ||||||
| chr11:74129173
|
A | G | 2 | a0008c0007t0001g0076a0008c0007t0001g0217 | 2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1217+3671T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129173 | ||||||
| chr11:74129183
|
T | C | 2 | a0008c0007t0001g0076a0008c0007t0001g0217 | 2 | HG03669.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1217+3661A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129183 | ||||||
| chr11:74129200
|
G | A | 4 | a0002c0003t0001g0205a0002c0003t0001g0208a0002c0003t0001g0209others(1): Show | 4 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+3644C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129200 | ||||||
| chr11:74129216
|
G | A | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1217+3628C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129216 | ||||||
| chr11:74129279
|
C | T | 1 | a0003c0041t0001g0296 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1217+3565G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129279 | ||||||
| chr11:74129301
|
G | A | 1 | a0003c0002t0001g0277 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1217+3543C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129301 | ||||||
| chr11:74129359
|
G | A | 60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1217+3485C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129359 | ||||||
| chr11:74129367
|
T | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1217+3477A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129367 | ||||||
| chr11:74129377
|
C | T | 1 | a0006c0008t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1217+3467G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129377 | ||||||
| chr11:74129379
|
G | C | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1217+3465C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129379 | ||||||
| chr11:74129384
|
C | T | 1 | a0002c0005t0001g0085 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1217+3460G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129384 | ||||||
| chr11:74129436
|
G | A | 1 | a0019c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1217+3408C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129436 | ||||||
| chr11:74129537
|
C | T | 7 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(4): Show | 7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1217+3307G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129537 | ||||||
| chr11:74129585
|
TCCAGACT others(69): Show |
T | 10 | a0004c0004t0001g0036a0004c0004t0001g0037a0004c0004t0001g0038others(7): Show | 10 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1217+3183_1217+325 others(80): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129585 | ||||||
| chr11:74129612
|
A | C | 114 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(111): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1217+3232T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129612 | ||||||
| chr11:74129628
|
C | T | 58 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(55): Show | 58 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1217+3216G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129628 | ||||||
| chr11:74129661
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1217+3183G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129661 | ||||||
| chr11:74129667
|
C | CG | 9 | a0001c0001t0001g0109a0002c0003t0001g0167a0003c0002t0001g0244others(6): Show | 9 | HG01099.hp1 HG01978.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1217+3176dupC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129667 | ||||||
| chr11:74129680
|
G | A | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1217+3164C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129680 | ||||||
| chr11:74129754
|
T | G | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1217+3090A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129754 | ||||||
| chr11:74129760
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1217+3084C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129760 | ||||||
| chr11:74129765
|
T | G | 60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1217+3079A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129765 | ||||||
| chr11:74129796
|
C | A | 124 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(121): Show | 125 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1217+3048G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129796 | ||||||
| chr11:74129803
|
G | A | 4 | a0009c0010t0001g0305a0009c0010t0001g0306a0009c0010t0001g0307others(1): Show | 4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+3041C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129803 | ||||||
| chr11:74129822
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+3022G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129822 | ||||||
| chr11:74129848
|
G | A | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+2996C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129848 | ||||||
| chr11:74129852
|
C | T | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+2992G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129852 | ||||||
| chr11:74129858
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+2986G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129858 | ||||||
| chr11:74129878
|
G | GC | 316 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(313): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1217+2965dupG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129878 | ||||||
| chr11:74129965
|
T | G | 63 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1217+2879A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129965 | ||||||
| chr11:74129985
|
A | G | 1 | a0002c0005t0001g0087 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1217+2859T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129985 | ||||||
| chr11:74129989
|
A | AG | 316 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(313): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1217+2854dupC | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74129989 | ||||||
| chr11:74130077
|
C | T | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+2767G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130077 | ||||||
| chr11:74130078
|
G | A | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1217+2766C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130078 | ||||||
| chr11:74130122
|
G | GGGGAGA | 11 | a0003c0016t0001g0242a0003c0016t0001g0249a0006c0012t0001g0231others(8): Show | 11 | HG02717.hp1 HG02717.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1217+2716_1217+272 others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130122 | ||||||
| chr11:74130122
|
G | GGGGAGAG others(5): Show |
6 | a0007c0009t0002g0313a0007c0009t0002g0314a0007c0009t0002g0315others(3): Show | 6 | HG02145.hp2 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1217+2710_1217+272 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130122 | ||||||
| chr11:74130140
|
A | AGGGAGAG others(6): Show |
7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+2703_1217+270 others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130140 | ||||||
| chr11:74130226
|
CT | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0114a0001c0001t0001g0133others(6): Show | 9 | HG01169.hp1 HG01517.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+2617delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130226 | ||||||
| chr11:74130281
|
G | A | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1217+2563C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130281 | ||||||
| chr11:74130352
|
A | G | 1 | a0002c0003t0001g0017 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1217+2492T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130352 | ||||||
| chr11:74130535
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1217+2309T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130535 | ||||||
| chr11:74130683
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1217+2161G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130683 | ||||||
| chr11:74130704
|
G | A | 1 | a0003c0002t0001g0284 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1217+2140C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130704 | ||||||
| chr11:74130838
|
A | G | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1217+2006T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130838 | ||||||
| chr11:74130846
|
G | T | 229 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(226): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1217+1998C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74130846 | ||||||
| chr11:74131094
|
G | C | 73 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1217+1750C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131094 | ||||||
| chr11:74131322
|
C | CA | 9 | a0001c0001t0001g0145a0003c0002t0001g0284a0009c0010t0001g0303others(6): Show | 9 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(6): Show |
intron_variant | MODIFIER | c.1217+1521dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131322 | ||||||
| chr11:74131322
|
CA | C | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+1521delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131322 | ||||||
| chr11:74131439
|
A | G | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1217+1405T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131439 | ||||||
| chr11:74131536
|
T | C | 6 | a0003c0002t0001g0241a0003c0002t0001g0260a0003c0002t0001g0261others(3): Show | 6 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.1217+1308A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131536 | ||||||
| chr11:74131564
|
T | A | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1217+1280A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131564 | ||||||
| chr11:74131588
|
C | CT | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1217+1255dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131588 | ||||||
| chr11:74131677
|
C | T | 60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1217+1167G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 7/32 | chr11 | 74131677 | ||||||
| chr11:74133078
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0151 | 2 | HG01358.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1089-106A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/32 | chr11 | 74133078 | ||||||
| chr11:74133182
|
T | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-210A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/32 | chr11 | 74133182 | ||||||
| chr11:74133389
|
A | G | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1088+36T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 6/32 | chr11 | 74133389 | ||||||
| chr11:74133571
|
A | G | 1 | a0005c0006t0001g0014 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.956-14T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74133571 | ||||||
| chr11:74133919
|
C | T | 1 | a0002c0003t0001g0051 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.956-362G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74133919 | ||||||
| chr11:74133964
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.956-407G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74133964 | ||||||
| chr11:74134133
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956-576G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134133 | ||||||
| chr11:74134281
|
T | G | 2 | a0011c0018t0001g0126a0011c0018t0001g0127 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.956-724A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134281 | ||||||
| chr11:74134502
|
G | A | 4 | a0009c0010t0001g0305a0009c0010t0001g0306a0009c0010t0001g0307others(1): Show | 4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-945C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134502 | ||||||
| chr11:74134527
|
T | C | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956-970A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134527 | ||||||
| chr11:74134537
|
C | G | 1 | a0006c0012t0001g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.956-980G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134537 | ||||||
| chr11:74134800
|
G | A | 1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956-1243C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134800 | ||||||
| chr11:74134844
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.956-1287C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134844 | ||||||
| chr11:74134858
|
T | C | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-1301A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134858 | ||||||
| chr11:74134976
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.956-1419G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74134976 | ||||||
| chr11:74135099
|
T | C | 2 | a0004c0004t0001g0033a0004c0004t0001g0034 | 2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.956-1542A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135099 | ||||||
| chr11:74135269
|
C | CT | 8 | a0002c0005t0001g0088a0006c0008t0001g0229a0006c0008t0001g0230others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.956-1713dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135269 | ||||||
| chr11:74135269
|
CTTTTT | C | 6 | a0003c0002t0001g0246a0003c0002t0001g0248a0003c0002t0001g0278others(3): Show | 6 | NA18948.hp2 NA18963.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.956-1717_956-1713d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135269 | ||||||
| chr11:74135326
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.956-1769C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135326 | ||||||
| chr11:74135531
|
G | A | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.956-1974C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135531 | ||||||
| chr11:74135745
|
C | T | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.956-2188G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135745 | ||||||
| chr11:74135800
|
C | G | 230 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(227): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.956-2243G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74135800 | ||||||
| chr11:74136148
|
T | G | 2 | a0015c0019t0001g0022a0015c0019t0001g0028 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.955+2572A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136148 | ||||||
| chr11:74136275
|
G | A | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.955+2445C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136275 | ||||||
| chr11:74136446
|
G | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+2274C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136446 | ||||||
| chr11:74136548
|
A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.955+2172T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136548 | ||||||
| chr11:74136643
|
T | C | 2 | a0004c0004t0001g0042a0004c0004t0001g0045 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.955+2077A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136643 | ||||||
| chr11:74136654
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+2066G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136654 | ||||||
| chr11:74136724
|
T | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+1996A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136724 | ||||||
| chr11:74136772
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.955+1948C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136772 | ||||||
| chr11:74136805
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.955+1915T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136805 | ||||||
| chr11:74136816
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.955+1904C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136816 | ||||||
| chr11:74136964
|
TA | T | 85 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.955+1755delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74136964 | ||||||
| chr11:74137033
|
T | C | 1 | a0002c0003t0001g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.955+1687A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137033 | ||||||
| chr11:74137327
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.955+1393A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137327 | ||||||
| chr11:74137417
|
T | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.955+1303A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137417 | ||||||
| chr11:74137508
|
G | A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+1212C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137508 | ||||||
| chr11:74137535
|
G | GTA | 85 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.955+1183_955+1184d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137535 | ||||||
| chr11:74137535
|
GTA | G | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.955+1183_955+1184d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137535 | ||||||
| chr11:74137567
|
T | TTA | 6 | a0002c0003t0001g0171a0008c0007t0001g0082a0008c0007t0001g0221others(3): Show | 7 | HG01358.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.955+1151_955+1152d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137567 | ||||||
| chr11:74137581
|
A | T | 21 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(18): Show | 21 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.955+1139T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137581 | ||||||
| chr11:74137620
|
C | T | 1 | a0010c0011t0001g0066 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.955+1100G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137620 | ||||||
| chr11:74137866
|
G | A | 106 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(103): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.955+854C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137866 | ||||||
| chr11:74137944
|
T | A | 1 | a0011c0015t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.955+776A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137944 | ||||||
| chr11:74137946
|
T | G | 1 | a0011c0015t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.955+774A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74137946 | ||||||
| chr11:74138282
|
A | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+438T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138282 | ||||||
| chr11:74138421
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.955+299C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138421 | ||||||
| chr11:74138664
|
C | T | 1 | a0013c0014t0001g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.955+56G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138664 | ||||||
| chr11:74138709
|
T | C | 3 | a0002c0003t0001g0050a0002c0003t0001g0051a0002c0003t0001g0065 | 3 | HG02300.hp1 HG03239.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.955+11A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 5/32 | chr11 | 74138709 | ||||||
| chr11:74139173
|
G | A | 6 | a0010c0011t0001g0053a0010c0011t0001g0066a0010c0011t0001g0067others(3): Show | 6 | HG02083.hp2 NA18979.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.708-206C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139173 | ||||||
| chr11:74139199
|
C | T | 2 | a0005c0006t0001g0026a0005c0006t0001g0027 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.708-232G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139199 | ||||||
| chr11:74139448
|
A | C | 1 | a0002c0003t0001g0065 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.707+157T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139448 | ||||||
| chr11:74139595
|
T | A | 4 | a0003c0034t0001g0185a0012c0013t0001g0225a0012c0013t0001g0226others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.707+10A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 4/32 | chr11 | 74139595 | ||||||
| chr11:74139873
|
T | C | 3 | a0004c0004t0001g0035a0004c0004t0001g0043a0004c0004t0001g0044 | 3 | HG02922.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.484-45A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139873 | ||||||
| chr11:74139909
|
T | TAATGTCC others(24): Show |
10 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(7): Show | 10 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(29): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139909
|
T | TAATGTCC others(55): Show |
8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139909
|
T | TAATGTCC others(55): Show |
4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(60): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139909
|
T | TAATGTCC others(86): Show |
3 | a0003c0016t0001g0242a0020c0040t0001g0301a0033c0022t0001g0295 | 3 | HG02622.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.484-82_484-81insCC others(91): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139909
|
T | TAATGTCC others(115): Show |
49 | a0003c0002t0001g0241a0003c0002t0001g0246a0003c0002t0001g0247others(46): Show | 49 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(120): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139909
|
T | TAATGTCC others(146): Show |
10 | a0003c0002t0001g0243a0003c0002t0001g0244a0003c0002t0001g0245others(7): Show | 10 | HG02074.hp1 HG02818.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-82_484-81insCC others(151): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139909
|
T | TAATGTCC others(177): Show |
1 | a0003c0002t0001g0285 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.484-82_484-81insCC others(182): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139909
|
TAATGTCC others(24): Show |
T | 3 | a0008c0007t0001g0211a0008c0007t0001g0212a0008c0007t0001g0216 | 3 | NA18956.hp1 NA18963.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.484-112_484-82delC others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139909 | ||||||
| chr11:74139921
|
T | C | 3 | a0007c0009t0002g0313a0007c0009t0002g0314a0007c0009t0002g0315 | 3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.484-93A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139921 | ||||||
| chr11:74139928
|
C | G | 17 | a0003c0016t0001g0249a0007c0009t0002g0310a0007c0009t0002g0312others(14): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.484-100G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139928 | ||||||
| chr11:74139928
|
CAGGATTG others(24): Show |
C | 2 | a0002c0003t0001g0078a0032c0024t0001g0200 | 2 | HG02615.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.484-131_484-101del others(31): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139928 | ||||||
| chr11:74139959
|
G | C | 92 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(89): Show | 92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.484-131C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | ||||||
| chr11:74139959
|
G | GAGGATTG others(24): Show |
4 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227others(1): Show | 4 | HG02055.hp1 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-132_484-131ins others(31): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | ||||||
| chr11:74139959
|
G | GAGGATTG others(87): Show |
1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-132_484-131ins others(94): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | ||||||
| chr11:74139959
|
GAGGATTG others(55): Show |
G | 5 | a0002c0003t0001g0061a0002c0003t0001g0070a0002c0003t0001g0071others(2): Show | 5 | HG02129.hp1 HG02132.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-193_484-132del others(62): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139959 | ||||||
| chr11:74139990
|
G | C | 267 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.484-162C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139990 | ||||||
| chr11:74139990
|
G | GAGGATTG others(86): Show |
1 | a0003c0016t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484-163_484-162ins others(93): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74139990 | ||||||
| chr11:74140052
|
G | C | 112 | a0001c0001t0001g0140a0001c0001t0001g0163a0002c0003t0001g0061others(109): Show | 112 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.484-224C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | ||||||
| chr11:74140052
|
G | GAGGATTG others(210): Show |
2 | a0011c0015t0001g0001a0011c0015t0001g0223 | 3 | HG01884.hp2 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.484-225_484-224ins others(217): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | ||||||
| chr11:74140052
|
G | GAGGATTG others(241): Show |
1 | a0019c0045t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.484-225_484-224ins others(248): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | ||||||
| chr11:74140052
|
GAGGATTG others(24): Show |
G | 116 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(113): Show | 116 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.484-255_484-225del others(31): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140052 | ||||||
| chr11:74140060
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.484-232A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140060 | ||||||
| chr11:74140083
|
C | G | 5 | a0002c0005t0001g0049a0008c0007t0001g0211a0008c0007t0001g0212others(2): Show | 5 | HG00738.hp1 NA18956.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-255G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140083 | ||||||
| chr11:74140093
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.484-265T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140093 | ||||||
| chr11:74140387
|
T | G | 1 | a0001c0001t0001g0190 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.484-559A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140387 | ||||||
| chr11:74140419
|
T | C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-591A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140419 | ||||||
| chr11:74140830
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | HG00438.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.484-1002C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74140830 | ||||||
| chr11:74141004
|
A | G | 1 | a0004c0004t0001g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.484-1176T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141004 | ||||||
| chr11:74141043
|
G | C | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.484-1215C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141043 | ||||||
| chr11:74141342
|
A | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-1514T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141342 | ||||||
| chr11:74141384
|
T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.484-1556A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141384 | ||||||
| chr11:74141770
|
G | A | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-1942C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141770 | ||||||
| chr11:74141840
|
T | A | 1 | a0002c0003t0005g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.484-2012A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74141840 | ||||||
| chr11:74142038
|
C | T | 2 | a0002c0003t0001g0090a0002c0003t0001g0091 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.484-2210G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142038 | ||||||
| chr11:74142059
|
T | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-2231A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142059 | ||||||
| chr11:74142185
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-2357A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142185 | ||||||
| chr11:74142194
|
A | T | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.484-2366T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142194 | ||||||
| chr11:74142379
|
A | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-2551T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142379 | ||||||
| chr11:74142651
|
TAAA | T | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-2826_484-2824d others(5): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142651 | ||||||
| chr11:74142703
|
G | A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-2875C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142703 | ||||||
| chr11:74142728
|
C | T | 1 | a0003c0002t0001g0299 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.484-2900G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142728 | ||||||
| chr11:74142838
|
C | T | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-3010G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74142838 | ||||||
| chr11:74143049
|
T | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-3221A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143049 | ||||||
| chr11:74143093
|
C | T | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-3265G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143093 | ||||||
| chr11:74143244
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0164 | 2 | HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.484-3416T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143244 | ||||||
| chr11:74143423
|
A | G | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-3595T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143423 | ||||||
| chr11:74143455
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.484-3627A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143455 | ||||||
| chr11:74143535
|
T | TTA | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-3709_484-3708d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143535 | ||||||
| chr11:74143703
|
G | A | 86 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.484-3875C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143703 | ||||||
| chr11:74143822
|
T | G | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.484-3994A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74143822 | ||||||
| chr11:74144344
|
C | T | 17 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.484-4516G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144344 | ||||||
| chr11:74144432
|
T | C | 1 | a0001c0030t0001g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.484-4604A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144432 | ||||||
| chr11:74144444
|
CT | C | 10 | a0003c0002t0001g0283a0005c0006t0001g0020a0005c0006t0001g0021others(7): Show | 10 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-4617delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144444 | ||||||
| chr11:74144474
|
G | A | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-4646C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144474 | ||||||
| chr11:74144617
|
A | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-4789T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144617 | ||||||
| chr11:74144723
|
G | A | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.484-4895C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144723 | ||||||
| chr11:74144803
|
T | C | 1 | a0021c0023t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.484-4975A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144803 | ||||||
| chr11:74144841
|
G | A | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.484-5013C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144841 | ||||||
| chr11:74144973
|
T | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-5145A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74144973 | ||||||
| chr11:74145133
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.484-5305G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74145133 | ||||||
| chr11:74145497
|
T | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-5669A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74145497 | ||||||
| chr11:74145872
|
G | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-6044C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74145872 | ||||||
| chr11:74146350
|
G | A | 1 | a0006c0008t0001g0238 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.484-6522C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146350 | ||||||
| chr11:74146393
|
T | C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-6565A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146393 | ||||||
| chr11:74146539
|
T | C | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-6711A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146539 | ||||||
| chr11:74146572
|
T | C | 4 | a0003c0034t0001g0185a0012c0013t0001g0225a0012c0013t0001g0226others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-6744A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146572 | ||||||
| chr11:74146710
|
C | CACACACA others(16): Show |
1 | a0032c0024t0001g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.484-6883_484-6882i others(25): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
C | CCA | 8 | a0001c0001t0001g0029a0001c0001t0001g0099a0001c0001t0001g0103others(5): Show | 8 | HG01192.hp2 HG01975.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.484-6884_484-6883d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
C | CCACACAC others(5): Show |
59 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(56): Show | 59 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.484-6883_484-6882i others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
C | CCACACAC others(7): Show |
1 | a0003c0002t0001g0297 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.484-6883_484-6882i others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
C | CCACACAC others(9): Show |
4 | a0003c0002t0001g0275a0003c0016t0001g0242a0023c0037t0001g0276others(1): Show | 4 | HG02015.hp2 HG02886.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-6883_484-6882i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
C | CCACACAC others(19): Show |
1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-6883_484-6882i others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
C | CCCCACAC others(5): Show |
1 | a0005c0006t0001g0015 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.484-6883_484-6882i others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
CCA | C | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0095others(33): Show | 36 | HG00140.hp1 HG00597.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.484-6884_484-6883d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
CCACA | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0133a0001c0001t0001g0151others(1): Show | 4 | HG01255.hp2 HG01358.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-6886_484-6883d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146710
|
CCACACAC others(7): Show |
C | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-6896_484-6883d others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146710 | ||||||
| chr11:74146711
|
C | CACACACA others(3): Show |
4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-6884_484-6883i others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146711 | ||||||
| chr11:74146713
|
C | CACACACA others(1): Show |
7 | a0003c0016t0001g0249a0007c0009t0002g0312a0007c0009t0002g0313others(4): Show | 7 | HG02145.hp2 HG03041.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-6886_484-6885i others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146713 | ||||||
| chr11:74146715
|
C | CACACAT | 15 | a0007c0009t0002g0310a0007c0009t0002g0316a0007c0009t0002g0317others(12): Show | 16 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.484-6888_484-6887i others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146715 | ||||||
| chr11:74146717
|
C | CACAT | 11 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(8): Show | 11 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-6890_484-6889i others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146717 | ||||||
| chr11:74146747
|
C | CACACACA others(21): Show |
1 | a0002c0003t0001g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.484-6920_484-6919i others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(17): Show |
2 | a0002c0003t0001g0090a0002c0003t0001g0210 | 2 | HG01516.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.484-6920_484-6919i others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(15): Show |
5 | a0002c0003t0001g0083a0002c0003t0001g0196a0002c0003t0001g0199others(2): Show | 5 | HG01081.hp1 HG01169.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(13): Show |
11 | a0002c0003t0001g0197a0002c0003t0001g0204a0002c0003t0001g0208others(8): Show | 11 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(22): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(11): Show |
22 | a0002c0003t0001g0050a0002c0003t0001g0051a0002c0003t0001g0075others(19): Show | 22 | HG01109.hp1 HG01123.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(9): Show |
10 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0003t0001g0202others(7): Show | 10 | HG00280.hp2 HG01361.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(7): Show |
18 | a0002c0003t0001g0052a0002c0003t0001g0059a0002c0003t0001g0060others(15): Show | 18 | HG00642.hp1 HG01192.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(5): Show |
24 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(21): Show | 24 | HG00738.hp1 HG01106.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(3): Show |
6 | a0002c0003t0001g0065a0005c0006t0001g0006a0005c0006t0001g0007others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACACACA others(1): Show |
3 | a0004c0004t0001g0040a0017c0043t0001g0084a0018c0044t0001g0089 | 3 | HG01099.hp2 HG01261.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.484-6920_484-6919i others(10): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CACAT | 5 | a0004c0004t0001g0037a0004c0004t0001g0038a0004c0004t0001g0039others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | CAT | 15 | a0004c0004t0001g0032a0004c0004t0001g0034a0004c0004t0001g0035others(12): Show | 15 | HG01074.hp2 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.484-6920_484-6919i others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146747
|
C | T | 106 | a0002c0028t0001g0011a0003c0002t0001g0241a0003c0002t0001g0243others(103): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.484-6919G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146747 | ||||||
| chr11:74146850
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-7022G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146850 | ||||||
| chr11:74146911
|
G | A | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-7083C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146911 | ||||||
| chr11:74146912
|
G | C | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-7084C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146912 | ||||||
| chr11:74146948
|
G | A | 2 | a0011c0018t0001g0126a0011c0018t0001g0127 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.484-7120C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146948 | ||||||
| chr11:74146982
|
C | T | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.484-7154G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74146982 | ||||||
| chr11:74147052
|
A | AAAAAT | 60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.484-7229_484-7225d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147052 | ||||||
| chr11:74147052
|
A | AAAAATAA others(3): Show |
3 | a0003c0002t0001g0246a0003c0016t0001g0242a0033c0022t0001g0295 | 3 | HG02886.hp2 NA18963.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.484-7234_484-7225d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147052 | ||||||
| chr11:74147242
|
T | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-7414A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147242 | ||||||
| chr11:74147288
|
C | T | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-7460G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147288 | ||||||
| chr11:74147318
|
G | A | 1 | a0002c0003t0001g0209 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.484-7490C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147318 | ||||||
| chr11:74147412
|
G | A | 12 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(9): Show | 12 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.484-7584C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147412 | ||||||
| chr11:74147444
|
C | A | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-7616G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147444 | ||||||
| chr11:74147548
|
C | G | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-7720G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147548 | ||||||
| chr11:74147685
|
C | T | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.484-7857G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147685 | ||||||
| chr11:74147792
|
T | G | 85 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.484-7964A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147792 | ||||||
| chr11:74147844
|
C | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-8016G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74147844 | ||||||
| chr11:74148020
|
TAAATTTT others(20): Show |
T | 10 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(7): Show | 10 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.484-8219_484-8193d others(29): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148020 | ||||||
| chr11:74148148
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-8320A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148148 | ||||||
| chr11:74148367
|
C | T | 1 | a0001c0001t0001g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.484-8539G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148367 | ||||||
| chr11:74148414
|
T | C | 1 | a0008c0007t0001g0082 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.484-8586A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148414 | ||||||
| chr11:74148744
|
G | C | 38 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(35): Show | 39 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.484-8916C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148744 | ||||||
| chr11:74148956
|
TCAAA | T | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.484-9132_484-9129d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74148956 | ||||||
| chr11:74149027
|
C | T | 1 | a0003c0002t0001g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.484-9199G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149027 | ||||||
| chr11:74149058
|
G | T | 1 | a0025c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.484-9230C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149058 | ||||||
| chr11:74149059
|
T | C | 1 | a0002c0003t0001g0210 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.484-9231A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149059 | ||||||
| chr11:74149089
|
T | C | 85 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.484-9261A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149089 | ||||||
| chr11:74149277
|
A | T | 37 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(34): Show | 38 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.484-9449T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149277 | ||||||
| chr11:74149297
|
AC | A | 3 | a0007c0009t0002g0310a0007c0009t0002g0312a0027c0047t0002g0311 | 3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.484-9470delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149297 | ||||||
| chr11:74149310
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.484-9482A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149310 | ||||||
| chr11:74149312
|
C | T | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-9484G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149312 | ||||||
| chr11:74149358
|
TA | T | 229 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(226): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.484-9531delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149358 | ||||||
| chr11:74149368
|
A | T | 4 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224others(1): Show | 5 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.484-9540T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149368 | ||||||
| chr11:74149425
|
T | C | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.484-9597A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149425 | ||||||
| chr11:74149431
|
G | A | 4 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0234others(1): Show | 4 | HG02717.hp2 HG02723.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-9603C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149431 | ||||||
| chr11:74149586
|
G | A | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.484-9758C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149586 | ||||||
| chr11:74149597
|
CT | C | 20 | a0002c0005t0001g0093a0003c0034t0001g0185a0004c0004t0001g0045others(17): Show | 21 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.484-9770delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149597 | ||||||
| chr11:74149630
|
C | G | 25 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(22): Show | 25 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.484-9802G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149630 | ||||||
| chr11:74149713
|
G | A | 2 | a0006c0012t0001g0233a0020c0040t0001g0301 | 2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.484-9885C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149713 | ||||||
| chr11:74149714
|
G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-9886C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149714 | ||||||
| chr11:74149828
|
G | A | 61 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(58): Show | 61 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.484-10000C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149828 | ||||||
| chr11:74149829
|
G | A | 61 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(58): Show | 61 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.484-10001C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149829 | ||||||
| chr11:74149903
|
G | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484-10075C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74149903 | ||||||
| chr11:74150121
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.484-10293G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150121 | ||||||
| chr11:74150155
|
T | TA | 78 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.484-10328dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150155 | ||||||
| chr11:74150155
|
TA | T | 8 | a0001c0001t0001g0109a0001c0001t0001g0174a0004c0004t0001g0033others(5): Show | 8 | HG02717.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.484-10328delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150155 | ||||||
| chr11:74150206
|
G | A | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.484-10378C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150206 | ||||||
| chr11:74150220
|
G | C | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.484-10392C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150220 | ||||||
| chr11:74150492
|
C | CA | 68 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0110others(65): Show | 68 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.484-10665dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | ||||||
| chr11:74150492
|
C | CAA | 35 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0101others(32): Show | 35 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.484-10666_484-1066 others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | ||||||
| chr11:74150492
|
C | CAAA | 14 | a0001c0001t0001g0096a0001c0001t0001g0104a0001c0001t0001g0105others(11): Show | 14 | HG00544.hp2 HG02040.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.484-10667_484-1066 others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | ||||||
| chr11:74150492
|
C | CAAAA | 9 | a0001c0001t0001g0121a0001c0001t0001g0151a0003c0002t0001g0257others(6): Show | 9 | HG00438.hp2 HG00558.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-10668_484-1066 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | ||||||
| chr11:74150492
|
C | CAAAAA | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0152others(6): Show | 9 | HG02622.hp2 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.484-10669_484-1066 others(9): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | ||||||
| chr11:74150492
|
C | CAAAAAAA others(5): Show |
1 | a0003c0002t0001g0286 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.484-10676_484-1066 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150492 | ||||||
| chr11:74150501
|
AAAAAAAA others(19): Show |
A | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484-10699_484-1067 others(30): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150501 | ||||||
| chr11:74150505
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.484-10677T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150505 | ||||||
| chr11:74150505
|
AAAAAAAA others(4): Show |
A | 1 | a0007c0009t0002g0310 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.484-10688_484-1067 others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150505 | ||||||
| chr11:74150505
|
AAAAAAAA others(15): Show |
A | 5 | a0002c0005t0001g0062a0002c0005t0001g0063a0002c0005t0001g0064others(2): Show | 5 | HG02615.hp2 NA18945.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-10699_484-1067 others(26): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150505 | ||||||
| chr11:74150506
|
AAAAAAAA others(3): Show |
A | 3 | a0007c0009t0002g0312a0027c0047t0002g0311a0028c0046t0002g0309 | 3 | HG02717.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.484-10688_484-1067 others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150506 | ||||||
| chr11:74150506
|
AAAAAAAA others(14): Show |
A | 80 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.484-10699_484-1067 others(25): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150506 | ||||||
| chr11:74150507
|
AAAAAAAA others(13): Show |
A | 6 | a0002c0003t0001g0061a0002c0003t0001g0090a0002c0003t0001g0213others(3): Show | 6 | HG02647.hp1 HG02895.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.484-10699_484-1068 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150507 | ||||||
| chr11:74150509
|
AAAAAAAC | A | 8 | a0004c0004t0001g0181a0006c0008t0001g0229a0006c0008t0001g0237others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.484-10688_484-1068 others(11): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150509 | ||||||
| chr11:74150511
|
AAAAACAA others(9): Show |
A | 3 | a0003c0002t0001g0258a0011c0015t0001g0001a0011c0015t0001g0223 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-10699_484-1068 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150511 | ||||||
| chr11:74150512
|
AAAACAAA others(8): Show |
A | 2 | a0003c0002t0001g0294a0019c0045t0001g0224 | 2 | HG03209.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.484-10699_484-1068 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150512 | ||||||
| chr11:74150515
|
AC | A | 7 | a0003c0016t0001g0249a0005c0006t0001g0020a0005c0006t0001g0027others(4): Show | 7 | HG02886.hp1 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-10688delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150515 | ||||||
| chr11:74150516
|
C | A | 177 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(174): Show | 177 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.484-10688G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150516 | ||||||
| chr11:74150517
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.484-10689T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150517 | ||||||
| chr11:74150527
|
C | A | 106 | a0001c0030t0001g0192a0003c0002t0001g0241a0003c0002t0001g0243others(103): Show | 106 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.484-10699G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150527 | ||||||
| chr11:74150528
|
A | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484-10700T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150528 | ||||||
| chr11:74150546
|
T | TTTTATTA others(7): Show |
102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.484-10719_484-1071 others(18): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150546 | ||||||
| chr11:74150560
|
A | C | 11 | a0002c0003t0001g0196a0002c0003t0001g0204a0002c0003t0001g0205others(8): Show | 11 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.484-10732T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150560 | ||||||
| chr11:74150561
|
A | C | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.484-10733T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150561 | ||||||
| chr11:74150604
|
G | A | 1 | a0024c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.484-10776C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150604 | ||||||
| chr11:74150605
|
C | G | 1 | a0024c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.484-10777G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150605 | ||||||
| chr11:74150896
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.483+10503G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74150896 | ||||||
| chr11:74151171
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.483+10228C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151171 | ||||||
| chr11:74151305
|
C | CTTTA | 6 | a0002c0003t0001g0083a0005c0006t0001g0014a0006c0008t0001g0229others(3): Show | 6 | HG01169.hp2 HG02074.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+10090_483+1009 others(8): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | ||||||
| chr11:74151305
|
C | CTTTATTT others(1): Show |
14 | a0002c0003t0001g0051a0006c0008t0001g0230a0006c0008t0001g0238others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.483+10086_483+1009 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | ||||||
| chr11:74151305
|
C | CTTTATTT others(5): Show |
16 | a0003c0016t0001g0242a0003c0016t0001g0249a0003c0034t0001g0185others(13): Show | 16 | HG02055.hp1 HG02145.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.483+10082_483+1009 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | ||||||
| chr11:74151305
|
C | CTTTATTT others(9): Show |
1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+10078_483+1009 others(20): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | ||||||
| chr11:74151305
|
C | CTTTATTT others(13): Show |
1 | a0007c0009t0002g0316 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.483+10074_483+1009 others(24): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | ||||||
| chr11:74151305
|
C | CTTTATTT others(17): Show |
1 | a0007c0009t0002g0317 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.483+10070_483+1009 others(28): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151305 | ||||||
| chr11:74151312
|
T | TATTTATT others(1): Show |
60 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.483+10086_483+1008 others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151312 | ||||||
| chr11:74151319
|
T | TTATTTAT others(5): Show |
7 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(4): Show | 7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.483+10079_483+1008 others(16): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151319 | ||||||
| chr11:74151591
|
T | A | 1 | a0008c0007t0001g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.483+9808A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151591 | ||||||
| chr11:74151712
|
T | A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+9687A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74151712 | ||||||
| chr11:74152089
|
T | C | 1 | a0003c0002t0001g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.483+9310A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152089 | ||||||
| chr11:74152366
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+9033G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152366 | ||||||
| chr11:74152570
|
A | G | 1 | a0007c0009t0002g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.483+8829T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152570 | ||||||
| chr11:74152635
|
T | C | 1 | a0004c0004t0001g0046 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.483+8764A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152635 | ||||||
| chr11:74152650
|
C | T | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+8749G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152650 | ||||||
| chr11:74152873
|
C | T | 5 | a0006c0012t0001g0231a0006c0012t0001g0232a0006c0012t0001g0233others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.483+8526G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152873 | ||||||
| chr11:74152911
|
A | G | 1 | a0002c0028t0001g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.483+8488T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152911 | ||||||
| chr11:74152949
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG00408.hp2 HG00423.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.483+8450G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74152949 | ||||||
| chr11:74153095
|
G | A | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+8304C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153095 | ||||||
| chr11:74153105
|
T | C | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+8294A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153105 | ||||||
| chr11:74153184
|
G | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+8215C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153184 | ||||||
| chr11:74153210
|
A | AAAAAC | 90 | a0001c0001t0001g0105a0002c0003t0001g0016a0002c0003t0001g0017others(87): Show | 90 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.483+8184_483+8188d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | ||||||
| chr11:74153210
|
A | AAAAACAA others(3): Show |
16 | a0002c0003t0001g0050a0002c0003t0001g0055a0002c0003t0001g0056others(13): Show | 16 | HG00642.hp1 HG01123.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.483+8179_483+8188d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | ||||||
| chr11:74153210
|
A | AAAAACAA others(8): Show |
2 | a0002c0003t0001g0054a0005c0027t0001g0012 | 2 | HG02735.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.483+8174_483+8188d others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | ||||||
| chr11:74153210
|
AAAAAC | A | 80 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(77): Show | 80 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.483+8184_483+8188d others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | ||||||
| chr11:74153210
|
AAAAACAA others(3): Show |
A | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.483+8179_483+8188d others(12): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | ||||||
| chr11:74153210
|
AAAAACAA others(8): Show |
A | 9 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0104others(6): Show | 9 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+8174_483+8188d others(17): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153210 | ||||||
| chr11:74153228
|
A | AACAAG | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+8170_483+8171i others(7): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153228 | ||||||
| chr11:74153334
|
C | T | 2 | a0002c0003t0001g0196a0002c0003t0001g0204 | 2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.483+8065G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153334 | ||||||
| chr11:74153591
|
T | A | 17 | a0003c0034t0001g0185a0006c0008t0001g0229a0006c0008t0001g0230others(14): Show | 17 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.483+7808A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153591 | ||||||
| chr11:74153666
|
TTTTTTAT others(5): Show |
T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+7721_483+7732d others(14): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153666 | ||||||
| chr11:74153721
|
T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+7678A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153721 | ||||||
| chr11:74153952
|
T | G | 7 | a0002c0003t0001g0197a0002c0003t0001g0199a0002c0003t0001g0201others(4): Show | 7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+7447A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74153952 | ||||||
| chr11:74154016
|
GA | G | 8 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(5): Show | 8 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.483+7382delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154016 | ||||||
| chr11:74154129
|
G | A | 1 | a0002c0003t0001g0172 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.483+7270C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154129 | ||||||
| chr11:74154475
|
G | T | 1 | a0002c0003t0001g0090 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.483+6924C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154475 | ||||||
| chr11:74154711
|
T | C | 1 | a0003c0002t0001g0292 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.483+6688A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154711 | ||||||
| chr11:74154733
|
A | G | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+6666T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154733 | ||||||
| chr11:74154737
|
C | A | 230 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(227): Show | 231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.483+6662G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154737 | ||||||
| chr11:74154936
|
T | C | 1 | a0025c0036t0001g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.483+6463A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154936 | ||||||
| chr11:74154993
|
A | G | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.483+6406T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154993 | ||||||
| chr11:74154995
|
G | A | 3 | a0003c0002t0001g0288a0003c0002t0001g0289a0003c0002t0001g0290 | 3 | HG02056.hp1 HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.483+6404C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74154995 | ||||||
| chr11:74155038
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+6361G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155038 | ||||||
| chr11:74155217
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.483+6182C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155217 | ||||||
| chr11:74155321
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.483+6078C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155321 | ||||||
| chr11:74155677
|
C | T | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+5722G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155677 | ||||||
| chr11:74155958
|
T | C | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+5441A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155958 | ||||||
| chr11:74155968
|
C | A | 7 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+5431G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74155968 | ||||||
| chr11:74156025
|
C | T | 1 | a0003c0002t0001g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.483+5374G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156025 | ||||||
| chr11:74156417
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.483+4982G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156417 | ||||||
| chr11:74156440
|
G | A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+4959C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156440 | ||||||
| chr11:74156459
|
C | CA | 28 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(25): Show | 29 | HG00609.hp1 HG01106.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.483+4939dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | ||||||
| chr11:74156459
|
C | G | 1 | a0010c0011t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.483+4940G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | ||||||
| chr11:74156459
|
CA | C | 17 | a0001c0001t0001g0103a0002c0003t0001g0016a0002c0005t0001g0058others(14): Show | 17 | HG01975.hp1 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.483+4939delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | ||||||
| chr11:74156459
|
CAAAAAAA others(6): Show |
C | 1 | a0005c0006t0001g0020 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.483+4927_483+4939d others(15): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156459 | ||||||
| chr11:74156654
|
G | C | 1 | a0005c0006t0001g0027 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.483+4745C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156654 | ||||||
| chr11:74156937
|
C | G | 2 | a0003c0002t0001g0246a0003c0002t0001g0248 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.483+4462G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156937 | ||||||
| chr11:74156941
|
A | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102 | 3 | HG00408.hp2 HG00423.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.483+4458T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156941 | ||||||
| chr11:74156946
|
G | A | 1 | a0004c0004t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.483+4453C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74156946 | ||||||
| chr11:74157020
|
C | A | 79 | a0002c0003t0001g0030a0002c0003t0001g0031a0002c0003t0001g0050others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.483+4379G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157020 | ||||||
| chr11:74157268
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.483+4131G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157268 | ||||||
| chr11:74157397
|
A | T | 1 | a0001c0001t0001g0098 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.483+4002T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157397 | ||||||
| chr11:74157567
|
T | C | 1 | a0003c0016t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.483+3832A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157567 | ||||||
| chr11:74157648
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.483+3751A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157648 | ||||||
| chr11:74157782
|
C | T | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+3617G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157782 | ||||||
| chr11:74157787
|
A | G | 7 | a0002c0003t0001g0197a0002c0003t0001g0199a0002c0003t0001g0201others(4): Show | 7 | HG01123.hp1 HG01169.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+3612T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157787 | ||||||
| chr11:74157806
|
G | A | 1 | a0024c0038t0001g0293 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.483+3593C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157806 | ||||||
| chr11:74157925
|
GTA | G | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+3472_483+3473d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74157925 | ||||||
| chr11:74158225
|
A | G | 1 | a0022c0035t0001g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483+3174T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158225 | ||||||
| chr11:74158506
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+2893G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158506 | ||||||
| chr11:74158667
|
A | T | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.483+2732T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158667 | ||||||
| chr11:74158670
|
C | T | 1 | a0011c0015t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.483+2729G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158670 | ||||||
| chr11:74158709
|
C | A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+2690G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158709 | ||||||
| chr11:74158722
|
CA | C | 94 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(91): Show | 95 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.483+2676delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74158722 | ||||||
| chr11:74159000
|
G | A | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.483+2399C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159000 | ||||||
| chr11:74159056
|
G | C | 63 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(60): Show | 63 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.483+2343C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159056 | ||||||
| chr11:74159061
|
T | C | 1 | a0003c0002t0001g0294 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.483+2338A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159061 | ||||||
| chr11:74159103
|
C | T | 1 | a0003c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.483+2296G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159103 | ||||||
| chr11:74159217
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.483+2182T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159217 | ||||||
| chr11:74159382
|
G | A | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.483+2017C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159382 | ||||||
| chr11:74159511
|
T | C | 2 | a0006c0008t0001g0239a0006c0008t0001g0240 | 2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.483+1888A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159511 | ||||||
| chr11:74159628
|
TTTAA | T | 4 | a0003c0034t0001g0185a0012c0013t0001g0225a0012c0013t0001g0226others(1): Show | 4 | HG02055.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1767_483+1770d others(6): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159628 | ||||||
| chr11:74159642
|
C | T | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.483+1757G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159642 | ||||||
| chr11:74159651
|
A | T | 1 | a0001c0001t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.483+1748T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159651 | ||||||
| chr11:74159657
|
TA | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+1741delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159657 | ||||||
| chr11:74159764
|
G | A | 2 | a0003c0016t0001g0242a0033c0022t0001g0295 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.483+1635C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159764 | ||||||
| chr11:74159968
|
G | A | 15 | a0005c0006t0001g0006a0005c0006t0001g0007a0005c0006t0001g0013others(12): Show | 15 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.483+1431C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74159968 | ||||||
| chr11:74160063
|
T | G | 4 | a0009c0010t0001g0305a0009c0010t0001g0306a0009c0010t0001g0307others(1): Show | 4 | NA18943.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1336A>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160063 | ||||||
| chr11:74160171
|
C | T | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+1228G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160171 | ||||||
| chr11:74160176
|
G | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+1223C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160176 | ||||||
| chr11:74160314
|
C | G | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.483+1085G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160314 | ||||||
| chr11:74160387
|
G | A | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.483+1012C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160387 | ||||||
| chr11:74160400
|
T | C | 1 | a0034c0033t0001g0178 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.483+999A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160400 | ||||||
| chr11:74160406
|
T | C | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.483+993A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160406 | ||||||
| chr11:74160424
|
T | C | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.483+975A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160424 | ||||||
| chr11:74160870
|
C | T | 1 | a0010c0011t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.483+529G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160870 | ||||||
| chr11:74160916
|
T | C | 8 | a0002c0005t0001g0085a0002c0005t0001g0086a0002c0005t0001g0087others(5): Show | 8 | NA18942.hp2 NA18948.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+483A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74160916 | ||||||
| chr11:74161047
|
C | T | 8 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(5): Show | 8 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.483+352G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161047 | ||||||
| chr11:74161116
|
GATTA | G | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.483+279_483+282del others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161116 | ||||||
| chr11:74161221
|
G | A | 3 | a0007c0009t0002g0310a0007c0009t0002g0312a0027c0047t0002g0311 | 3 | HG02717.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.483+178C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161221 | ||||||
| chr11:74161316
|
A | T | 1 | a0009c0010t0001g0304 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.483+83T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 3/32 | chr11 | 74161316 | ||||||
| chr11:74161623
|
T | C | 2 | a0001c0001t0001g0173a0018c0044t0001g0089 | 2 | HG01099.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.326-67A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161623 | ||||||
| chr11:74161706
|
G | A | 2 | a0005c0006t0001g0026a0005c0006t0001g0027 | 2 | HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.326-150C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161706 | ||||||
| chr11:74161723
|
A | G | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.326-167T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161723 | ||||||
| chr11:74161794
|
C | T | 1 | a0002c0003t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.326-238G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161794 | ||||||
| chr11:74161813
|
C | CT | 8 | a0001c0001t0001g0095a0001c0001t0001g0096a0002c0003t0001g0050others(5): Show | 8 | HG01109.hp1 HG02300.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-258dupA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161813 | ||||||
| chr11:74161813
|
CT | C | 14 | a0001c0001t0001g0174a0001c0001t0001g0175a0002c0003t0001g0090others(11): Show | 14 | HG02647.hp1 HG02717.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.326-258delA | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161813 | ||||||
| chr11:74161816
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.326-260A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161816 | ||||||
| chr11:74161971
|
A | G | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.326-415T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161971 | ||||||
| chr11:74161992
|
T | C | 102 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(99): Show | 103 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.326-436A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74161992 | ||||||
| chr11:74162074
|
C | T | 3 | a0003c0002t0001g0243a0003c0002t0001g0244a0003c0002t0001g0245 | 3 | NA19011.hp2 NA19074.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.326-518G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162074 | ||||||
| chr11:74162091
|
C | T | 3 | a0002c0003t0001g0197a0002c0003t0001g0199a0029c0029t0001g0198 | 3 | HG01169.hp2 HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.326-535G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162091 | ||||||
| chr11:74162395
|
G | C | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-839C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162395 | ||||||
| chr11:74162689
|
G | C | 3 | a0007c0009t0002g0313a0007c0009t0002g0314a0007c0009t0002g0315 | 3 | HG02145.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.326-1133C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162689 | ||||||
| chr11:74162691
|
C | A | 100 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.326-1135G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162691 | ||||||
| chr11:74162707
|
T | C | 1 | a0002c0003t0001g0019 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.326-1151A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162707 | ||||||
| chr11:74162764
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.326-1208T>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74162764 | ||||||
| chr11:74163046
|
T | A | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.326-1490A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163046 | ||||||
| chr11:74163051
|
A | C | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-1495T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163051 | ||||||
| chr11:74163229
|
G | A | 1 | a0031c0032t0001g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.326-1673C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163229 | ||||||
| chr11:74163243
|
A | G | 7 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(4): Show | 7 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.326-1687T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163243 | ||||||
| chr11:74163482
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18943.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.326-1926G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163482 | ||||||
| chr11:74163508
|
C | T | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.326-1952G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163508 | ||||||
| chr11:74163636
|
G | T | 9 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(6): Show | 9 | HG02145.hp2 HG02717.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-2080C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163636 | ||||||
| chr11:74163655
|
TTG | T | 3 | a0012c0013t0001g0225a0012c0013t0001g0226a0012c0013t0001g0227 | 3 | HG02055.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.326-2101_326-2100d others(4): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74163655 | ||||||
| chr11:74164030
|
T | C | 4 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(1): Show | 4 | HG02451.hp1 HG02970.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-2474A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164030 | ||||||
| chr11:74164148
|
T | C | 73 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.326-2592A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164148 | ||||||
| chr11:74164258
|
C | G | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.326-2702G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164258 | ||||||
| chr11:74164271
|
C | T | 97 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.326-2715G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164271 | ||||||
| chr11:74164309
|
A | C | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.326-2753T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164309 | ||||||
| chr11:74164425
|
C | T | 1 | a0003c0002t0001g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.326-2869G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164425 | ||||||
| chr11:74164463
|
G | A | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.326-2907C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164463 | ||||||
| chr11:74164502
|
G | C | 24 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.326-2946C>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164502 | ||||||
| chr11:74164527
|
C | G | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.326-2971G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164527 | ||||||
| chr11:74164539
|
C | G | 2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.326-2983G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164539 | ||||||
| chr11:74164572
|
C | T | 1 | a0002c0005t0001g0049 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326-3016G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164572 | ||||||
| chr11:74164695
|
T | C | 2 | a0008c0007t0001g0177a0034c0033t0001g0178 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.326-3139A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164695 | ||||||
| chr11:74164872
|
C | T | 22 | a0004c0004t0001g0032a0004c0004t0001g0033a0004c0004t0001g0034others(19): Show | 22 | HG01074.hp2 HG02258.hp1 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.326-3316G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74164872 | ||||||
| chr11:74165139
|
T | C | 9 | a0005c0006t0001g0020a0005c0006t0001g0021a0005c0006t0001g0023others(6): Show | 9 | HG01106.hp2 HG02145.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.325+3205A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165139 | ||||||
| chr11:74165314
|
C | T | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+3030G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165314 | ||||||
| chr11:74165337
|
G | A | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+3007C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165337 | ||||||
| chr11:74165461
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0193 | 3 | NA18943.hp1 NA18993.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.325+2883C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165461 | ||||||
| chr11:74165488
|
T | C | 1 | a0004c0004t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.325+2856A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165488 | ||||||
| chr11:74165580
|
C | T | 3 | a0011c0015t0001g0001a0011c0015t0001g0223a0019c0045t0001g0224 | 4 | HG01884.hp2 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+2764G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165580 | ||||||
| chr11:74165608
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.325+2736A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165608 | ||||||
| chr11:74165654
|
C | A | 1 | a0004c0004t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.325+2690G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165654 | ||||||
| chr11:74165783
|
T | C | 1 | a0030c0031t0001g0184 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.325+2561A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165783 | ||||||
| chr11:74165805
|
C | T | 2 | a0002c0003t0001g0030a0002c0003t0001g0031 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.325+2539G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74165805 | ||||||
| chr11:74166033
|
G | A | 1 | a0003c0034t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325+2311C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166033 | ||||||
| chr11:74166045
|
T | C | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+2299A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166045 | ||||||
| chr11:74166082
|
G | A | 2 | a0007c0017t0001g0194a0007c0017t0001g0195 | 2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.325+2262C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166082 | ||||||
| chr11:74166126
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.325+2218G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166126 | ||||||
| chr11:74166173
|
C | G | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+2171G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166173 | ||||||
| chr11:74166274
|
G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325+2070C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166274 | ||||||
| chr11:74166316
|
T | TA | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0193others(9): Show | 12 | HG01109.hp1 HG01433.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.325+2027dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166316 | ||||||
| chr11:74166316
|
TA | T | 65 | a0002c0003t0001g0196a0003c0002t0001g0241a0003c0002t0001g0243others(62): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.325+2027delT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166316 | ||||||
| chr11:74166335
|
AC | A | 22 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(19): Show | 22 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.325+2008delG | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166335 | ||||||
| chr11:74166457
|
C | G | 1 | a0003c0016t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.325+1887G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166457 | ||||||
| chr11:74166673
|
A | G | 2 | a0014c0020t0004g0218a0014c0020t0004g0219 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.325+1671T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74166673 | ||||||
| chr11:74167179
|
T | C | 64 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(61): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.325+1165A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167179 | ||||||
| chr11:74167415
|
C | G | 100 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(97): Show | 101 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.325+929G>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167415 | ||||||
| chr11:74167463
|
T | C | 1 | a0020c0040t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.325+881A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167463 | ||||||
| chr11:74167467
|
T | A | 24 | a0006c0008t0001g0229a0006c0008t0001g0230a0006c0008t0001g0236others(21): Show | 24 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.325+877A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167467 | ||||||
| chr11:74167482
|
A | G | 1 | a0003c0002t0001g0241 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.325+862T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167482 | ||||||
| chr11:74167639
|
G | A | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.325+705C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167639 | ||||||
| chr11:74167643
|
G | A | 21 | a0002c0003t0001g0196a0002c0003t0001g0197a0002c0003t0001g0199others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.325+701C>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167643 | ||||||
| chr11:74167796
|
T | C | 73 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(70): Show | 73 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.325+548A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167796 | ||||||
| chr11:74167857
|
A | G | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+487T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167857 | ||||||
| chr11:74167885
|
T | C | 1 | a0008c0007t0001g0217 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.325+459A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74167885 | ||||||
| chr11:74168079
|
C | CA | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.325+264dupT | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 2/32 | chr11 | 74168079 | ||||||
| chr11:74168670
|
T | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.56-57A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168670 | ||||||
| chr11:74168702
|
A | C | 20 | a0002c0003t0001g0016a0002c0003t0001g0017a0002c0003t0001g0018others(17): Show | 20 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.56-89T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168702 | ||||||
| chr11:74168753
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.56-140G>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168753 | ||||||
| chr11:74168792
|
C | A | 7 | a0009c0010t0001g0303a0009c0010t0001g0304a0009c0010t0001g0305others(4): Show | 7 | HG02280.hp2 HG04228.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-179G>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168792 | ||||||
| chr11:74168843
|
A | C | 1 | a0002c0005t0001g0008 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.56-230T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74168843 | ||||||
| chr11:74169194
|
A | C | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.56-581T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74169194 | ||||||
| chr11:74169651
|
G | T | 2 | a0005c0006t0001g0006a0005c0006t0001g0007 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.56-1038C>A | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74169651 | ||||||
| chr11:74170135
|
A | G | 1 | a0026c0025t0001g0222 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.55+603T>C | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170135 | ||||||
| chr11:74170335
|
T | C | 2 | a0008c0007t0001g0221a0016c0021t0001g0220 | 2 | HG02523.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.55+403A>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170335 | ||||||
| chr11:74170535
|
T | A | 101 | a0003c0002t0001g0241a0003c0002t0001g0243a0003c0002t0001g0244others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.55+203A>T | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170535 | ||||||
| chr11:74170716
|
A | C | 1 | a0007c0026t0001g0005 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.55+22T>G | C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 1/32 | chr11 | 74170716 |