| geneid | 84319 |
|---|---|
| ensemblid | ENSG00000184220.12 |
| hgncid | 28666 |
| symbol | CMSS1 |
| name | cms1 ribosomal small subunit homolog |
| refseq_nuc | NM_032359.4 |
| refseq_prot | NP_115735.2 |
| ensembl_nuc | ENST00000421999.8 |
| ensembl_prot | ENSP00000410396.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 99817862 |
| end | 100181732 |
| strand | + |
| ver | v1.2 |
| region | chr3:99817862-100181732 |
| region5000 | chr3:99812862-100186732 |
| regionname0 | CMSS1_chr3_99817862_100181732 |
| regionname5000 | CMSS1_chr3_99812862_100186732 |
| 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 | 0/0 | 279 | 196 | 62 | 33 | 64 | 9 | 28 | 40 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0002 | 0/0 | 279 | 35 | 2 | 13 | 6 | 2 | 12 | 6 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0003 | 0/0 | 279 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| 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 | 0/0 | 840 | 196 | 62 | 33 | 64 | 9 | 28 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| c0002 | 0/0 | 840 | 35 | 2 | 13 | 6 | 2 | 12 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| c0003 | 0/0 | 840 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3463 | 77 | 19 | 16 | 28 | 4 | 10 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0002 | 0/0 | 3462 | 71 | 16 | 13 | 28 | 4 | 10 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0003 | 0/0 | 3457 | 32 | 1 | 13 | 6 | 1 | 11 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0004 | 0/0 | 3463 | 15 | 2 | 1 | 5 | 1 | 6 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0005 | 0/0 | 3463 | 8 | 8 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0006 | 0/0 | 3462 | 7 | 7 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0007 | 0/0 | 3463 | 3 | 2 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0008 | 0/0 | 3462 | 3 | 0 | 0 | 3 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0009 | 0/0 | 3462 | 3 | 3 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0010 | 0/0 | 3462 | 2 | 2 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0011 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0012 | 0/0 | 3463 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0013 | 0/0 | 3463 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0014 | 0/0 | 3463 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0015 | 0/0 | 3463 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0016 | 0/0 | 3463 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0017 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0018 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0019 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0020 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| t0021 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| 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 | 0 | 2 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| 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 | 0/0 | 840 | 196 | 62 | 33 | 64 | 9 | 28 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0002c0002 | 0/0 | 840 | 35 | 2 | 13 | 6 | 2 | 12 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0003c0003 | 0/0 | 840 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4302 | 76 | 19 | 16 | 28 | 3 | 10 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0002 | 0/0 | 4301 | 71 | 16 | 13 | 28 | 4 | 10 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0004 | 0/0 | 4302 | 15 | 2 | 1 | 5 | 1 | 6 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0005 | 0/0 | 4302 | 8 | 8 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0006 | 0/0 | 4301 | 7 | 7 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0007 | 0/0 | 4302 | 3 | 2 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0008 | 0/0 | 4301 | 3 | 0 | 0 | 3 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0009 | 0/0 | 4301 | 3 | 3 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0010 | 0/0 | 4301 | 2 | 2 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0011 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0012 | 0/0 | 4302 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0013 | 0/0 | 4302 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0014 | 0/0 | 4302 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0015 | 0/0 | 4302 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0016 | 0/0 | 4302 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0018 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0001c0001t0021 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0002c0002t0003 | 0/0 | 4296 | 32 | 1 | 13 | 6 | 1 | 11 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0002c0002t0017 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0002c0002t0019 | 0/0 | 4301 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0002c0002t0020 | 0/0 | 4296 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| a0003c0003t0001 | 0/0 | 4302 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | copy fasta | chr3 | 99812862 | 100186732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0013g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0014g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0015g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0016g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0018g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0001c0001t0021g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0017g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0002c0002t0020g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0013 | g0201 | EUR | GBR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0137 | EUR | GBR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0106 | EUR | FIN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00323 | hp2 | a0002 | c0002 | t0020 | g0116 | EUR | FIN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0135 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0138 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01069 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01071 | hp1 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0113 | AMR | PUR | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0231 | EUR | IBS | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0155 | EUR | IBS | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | IBS | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01891 | hp2 | a0001 | c0001 | t0018 | g0002 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01928 | hp2 | a0002 | c0002 | t0003 | g0117 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0110 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01943 | hp1 | a0002 | c0002 | t0003 | g0129 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01943 | hp2 | a0001 | c0001 | t0015 | g0230 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0114 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0032 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01981 | hp1 | a0001 | c0001 | t0016 | g0195 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0089 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0128 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0056 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02273 | hp1 | a0002 | c0002 | t0003 | g0115 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0118 | AMR | PEL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02602 | hp2 | a0001 | c0001 | t0012 | g0036 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02698 | hp1 | a0002 | c0002 | t0003 | g0133 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02738 | hp1 | a0002 | c0002 | t0003 | g0141 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0055 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0184 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0111 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0083 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0040 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03195 | hp2 | a0001 | c0001 | t0021 | g0018 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | MSL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03490 | hp1 | a0002 | c0002 | t0017 | g0131 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0120 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0026 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03654 | hp2 | a0002 | c0002 | t0003 | g0136 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0119 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0223 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0130 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03927 | hp1 | a0002 | c0002 | t0003 | g0134 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0109 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0125 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | YRI | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | YRI | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | CHB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18906 | hp2 | a0001 | c0001 | t0011 | g0169 | AFR | YRI | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18943 | hp2 | a0002 | c0002 | t0003 | g0126 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18959 | hp1 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0127 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18964 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18973 | hp1 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | LWK | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | LWK | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19043 | hp2 | a0002 | c0002 | t0019 | g0012 | AFR | LWK | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19065 | hp2 | a0001 | c0001 | t0008 | g0088 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0087 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19088 | hp1 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | TSI | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | TSI | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | GIH | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | GIH | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0112 | AMR | CLM | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | ACB | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | MSL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0010 | AFR | MSL | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0139 | AFR | LWK | CMSS1_chr3_99812862_100186732 | CMSS1 | chr3 | 99812862 | 100186732 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100166392
|
A | G | 1 | a0003 | 1 | HG01515.hp1 | missense_variant&splice_region_variant | MODERATE | c.413A>G | p.Glu138Gly | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/10 | 531/4302 | 413/840 | 138/279 | chr3 | 100166392 | ||
| chr3:100167818
|
G | A | 1 | a0002 | 35 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(32): Show |
missense_variant | MODERATE | c.496G>A | p.Val166Ile | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/10 | 614/4302 | 496/840 | 166/279 | chr3 | 100167818 |
| 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 |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:99817877
|
C | G | 1 | a0001c0001t0021 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-103C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/10 | 103 | chr3 | 99817877 | |||||
| chr3:100178707
|
C | G | 1 | a0002c0002t0020 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 319 | chr3 | 100178707 | |||||
| chr3:100178933
|
G | A | 1 | a0001c0001t0006 | 7 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*545G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 545 | chr3 | 100178933 | |||||
| chr3:100179178
|
A | C | 1 | a0002c0002t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*790A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 790 | chr3 | 100179178 | |||||
| chr3:100179300
|
C | T | 1 | a0001c0001t0009 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*912C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 912 | chr3 | 100179300 | |||||
| chr3:100179394
|
A | AT | 2 | a0001c0001t0005a0001c0001t0018 | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1007dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1008 | INFO_REALIGN_3_PRIME | chr3 | 100179394 | ||||
| chr3:100179597
|
G | A | 2 | a0001c0001t0005a0001c0001t0018 | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1209G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1209 | chr3 | 100179597 | |||||
| chr3:100179601
|
GCTCCC | G | 3 | a0002c0002t0003a0002c0002t0017a0002c0002t0020 | 34 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1214_*1218delCTCC others(1): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1214 | chr3 | 100179601 | |||||
| chr3:100179607
|
A | G | 3 | a0002c0002t0003a0002c0002t0017a0002c0002t0020 | 34 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1219A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1219 | chr3 | 100179607 | |||||
| chr3:100179639
|
G | T | 2 | a0001c0001t0005a0001c0001t0018 | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1251G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1251 | chr3 | 100179639 | |||||
| chr3:100179746
|
A | T | 1 | a0001c0001t0016 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1358A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1358 | chr3 | 100179746 | |||||
| chr3:100179989
|
G | T | 1 | a0001c0001t0015 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1601 | chr3 | 100179989 | |||||
| chr3:100180042
|
C | G | 3 | a0001c0001t0002a0001c0001t0006a0001c0001t0008 | 81 | HG00280.hp1 HG00423.hp2 HG00738.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1654C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1654 | chr3 | 100180042 | |||||
| chr3:100180147
|
AT | A | 11 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(8): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1766delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 1766 | INFO_REALIGN_3_PRIME | chr3 | 100180147 | ||||
| chr3:100180435
|
C | T | 1 | a0001c0001t0014 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2047C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2047 | chr3 | 100180435 | |||||
| chr3:100180681
|
T | G | 1 | a0001c0001t0008 | 3 | HG02083.hp2 NA19065.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2293T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2293 | chr3 | 100180681 | |||||
| chr3:100180751
|
G | A | 1 | a0001c0001t0018 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2363G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2363 | chr3 | 100180751 | |||||
| chr3:100180849
|
C | T | 1 | a0002c0002t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2461C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2461 | chr3 | 100180849 | |||||
| chr3:100181163
|
C | T | 1 | a0001c0001t0013 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2775C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2775 | chr3 | 100181163 | |||||
| chr3:100181164
|
G | A | 1 | a0001c0001t0011 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2776G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2776 | chr3 | 100181164 | |||||
| chr3:100181252
|
G | A | 13 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(10): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*2864G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2864 | chr3 | 100181252 | |||||
| chr3:100181300
|
T | A | 6 | a0001c0001t0007a0001c0001t0012a0001c0001t0016others(3): Show | 8 | HG01891.hp2 HG01975.hp2 HG01981.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2912T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 10/10 | 2912 | chr3 | 100181300 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:99818093
|
C | T | 49 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0186others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.64+50C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818093 | ||||||
| chr3:99818155
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+112G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818155 | ||||||
| chr3:99818336
|
T | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+293T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818336 | ||||||
| chr3:99818361
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.64+318T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818361 | ||||||
| chr3:99818399
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+356G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818399 | ||||||
| chr3:99818427
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+384A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818427 | ||||||
| chr3:99818461
|
C | T | 69 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(66): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.64+418C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818461 | ||||||
| chr3:99818871
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+828C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818871 | ||||||
| chr3:99818885
|
C | T | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG01928.hp1 HG01952.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+842C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99818885 | ||||||
| chr3:99819502
|
T | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+1459T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99819502 | ||||||
| chr3:99819571
|
T | C | 22 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+1528T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99819571 | ||||||
| chr3:99819626
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+1583G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99819626 | ||||||
| chr3:99819630
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.64+1587T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99819630 | ||||||
| chr3:99819757
|
CT | C | 10 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0111others(7): Show | 10 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+1729delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99819757 | |||||
| chr3:99819847
|
T | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0004g0164 | 3 | HG02809.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.64+1804T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99819847 | ||||||
| chr3:99819857
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.64+1814C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99819857 | ||||||
| chr3:99820017
|
T | C | 1 | a0001c0001t0004g0011 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64+1974T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820017 | ||||||
| chr3:99820155
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+2112A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820155 | ||||||
| chr3:99820178
|
C | T | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+2135C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820178 | ||||||
| chr3:99820222
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.64+2179G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820222 | ||||||
| chr3:99820289
|
T | G | 1 | a0002c0002t0003g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64+2246T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820289 | ||||||
| chr3:99820445
|
C | T | 4 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(1): Show | 4 | HG02523.hp1 NA18969.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2402C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820445 | ||||||
| chr3:99820475
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+2432G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820475 | ||||||
| chr3:99820704
|
G | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+2661G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820704 | ||||||
| chr3:99820820
|
G | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+2777G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820820 | ||||||
| chr3:99820900
|
T | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+2857T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820900 | ||||||
| chr3:99820996
|
T | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+2953T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99820996 | ||||||
| chr3:99821046
|
A | T | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+3003A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821046 | ||||||
| chr3:99821047
|
C | A | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+3004C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821047 | ||||||
| chr3:99821052
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+3009A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821052 | ||||||
| chr3:99821171
|
T | G | 1 | a0001c0001t0002g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.64+3128T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821171 | ||||||
| chr3:99821202
|
C | T | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+3159C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821202 | ||||||
| chr3:99821620
|
T | C | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+3577T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821620 | ||||||
| chr3:99821666
|
C | T | 42 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(39): Show | 42 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(39): Show |
intron_variant | MODIFIER | c.64+3623C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821666 | ||||||
| chr3:99821753
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64+3710G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821753 | ||||||
| chr3:99821958
|
A | G | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.64+3915A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99821958 | ||||||
| chr3:99822469
|
G | A | 9 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+4426G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822469 | ||||||
| chr3:99822502
|
A | G | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+4459A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822502 | ||||||
| chr3:99822592
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+4549C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822592 | ||||||
| chr3:99822686
|
C | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+4643C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822686 | ||||||
| chr3:99822766
|
A | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+4723A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822766 | ||||||
| chr3:99822826
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+4783C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822826 | ||||||
| chr3:99822903
|
G | T | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.64+4860G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822903 | ||||||
| chr3:99822970
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+4927T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99822970 | ||||||
| chr3:99823221
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.64+5178C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99823221 | ||||||
| chr3:99823484
|
CT | C | 3 | a0001c0001t0008g0087a0001c0001t0008g0088a0001c0001t0008g0089 | 3 | HG02083.hp2 NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.64+5442delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99823484 | ||||||
| chr3:99823789
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.64+5746T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99823789 | ||||||
| chr3:99823957
|
C | G | 4 | a0001c0001t0002g0107a0001c0001t0008g0087a0001c0001t0008g0088others(1): Show | 4 | HG02040.hp1 HG02083.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+5914C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99823957 | ||||||
| chr3:99824036
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+5993T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824036 | ||||||
| chr3:99824106
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64+6063A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824106 | ||||||
| chr3:99824123
|
A | G | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+6080A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824123 | ||||||
| chr3:99824129
|
A | G | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+6086A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824129 | ||||||
| chr3:99824217
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0004g0014 | 2 | HG01516.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.64+6174G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824217 | ||||||
| chr3:99824290
|
G | T | 1 | a0001c0001t0002g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.64+6247G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824290 | ||||||
| chr3:99824297
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+6254T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824297 | ||||||
| chr3:99824314
|
T | C | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64+6271T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824314 | ||||||
| chr3:99824566
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.64+6523C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824566 | ||||||
| chr3:99824664
|
A | G | 19 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0093others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.64+6621A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824664 | ||||||
| chr3:99824860
|
C | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+6817C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824860 | ||||||
| chr3:99824920
|
A | G | 109 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.64+6877A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99824920 | ||||||
| chr3:99825187
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+7144G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99825187 | ||||||
| chr3:99825339
|
T | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+7296T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99825339 | ||||||
| chr3:99825364
|
CAG | C | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.64+7322_64+7323del others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99825364 | ||||||
| chr3:99825536
|
A | G | 156 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(153): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.64+7493A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99825536 | ||||||
| chr3:99825550
|
G | A | 3 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0017 | 3 | HG02040.hp2 HG02129.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.64+7507G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99825550 | ||||||
| chr3:99825775
|
C | CT | 36 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0229others(33): Show | 36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.64+7751dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99825775 | |||||
| chr3:99825775
|
CT | C | 7 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+7751delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99825775 | |||||
| chr3:99825863
|
C | T | 40 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(37): Show | 40 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.64+7820C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99825863 | ||||||
| chr3:99825912
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+7869G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99825912 | ||||||
| chr3:99826018
|
C | T | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | HG02015.hp2 HG02071.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.64+7975C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826018 | ||||||
| chr3:99826071
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+8028C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826071 | ||||||
| chr3:99826104
|
T | A | 1 | a0002c0002t0003g0119 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64+8061T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826104 | ||||||
| chr3:99826105
|
C | A | 1 | a0002c0002t0003g0119 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64+8062C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826105 | ||||||
| chr3:99826333
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.64+8290T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826333 | ||||||
| chr3:99826368
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64+8325G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826368 | ||||||
| chr3:99826440
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.64+8397C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826440 | ||||||
| chr3:99826497
|
T | C | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(3): Show | 6 | HG01952.hp1 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+8454T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826497 | ||||||
| chr3:99826742
|
T | G | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+8699T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826742 | ||||||
| chr3:99826997
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+8954C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99826997 | ||||||
| chr3:99827018
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64+8975G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827018 | ||||||
| chr3:99827025
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.64+8982G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827025 | ||||||
| chr3:99827171
|
C | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+9128C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827171 | ||||||
| chr3:99827266
|
A | G | 174 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.64+9223A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827266 | ||||||
| chr3:99827438
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+9395C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827438 | ||||||
| chr3:99827455
|
G | A | 1 | a0001c0001t0004g0011 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64+9412G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827455 | ||||||
| chr3:99827474
|
G | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.64+9431G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827474 | ||||||
| chr3:99827491
|
A | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+9448A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827491 | ||||||
| chr3:99827741
|
G | A | 1 | a0001c0001t0004g0015 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.64+9698G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827741 | ||||||
| chr3:99827795
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+9752A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827795 | ||||||
| chr3:99827824
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0014others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+9781C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827824 | ||||||
| chr3:99827920
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+9877A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99827920 | ||||||
| chr3:99828020
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+9977A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828020 | ||||||
| chr3:99828104
|
G | A | 22 | a0001c0001t0002g0108a0002c0002t0003g0109a0002c0002t0003g0110others(19): Show | 22 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+10061G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828104 | ||||||
| chr3:99828245
|
C | T | 11 | a0001c0001t0001g0069a0001c0001t0002g0062a0001c0001t0002g0063others(8): Show | 11 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+10202C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828245 | ||||||
| chr3:99828272
|
T | C | 1 | a0001c0001t0006g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.64+10229T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828272 | ||||||
| chr3:99828342
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+10299A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828342 | ||||||
| chr3:99828411
|
A | AT | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.64+10381dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99828411 | |||||
| chr3:99828411
|
A | ATT | 41 | a0001c0001t0001g0070a0001c0001t0001g0157a0001c0001t0001g0158others(38): Show | 41 | HG00423.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.64+10380_64+10381d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99828411 | |||||
| chr3:99828411
|
A | ATTT | 123 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(120): Show | 123 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(120): Show |
intron_variant | MODIFIER | c.64+10379_64+10381d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99828411 | |||||
| chr3:99828411
|
A | ATTTT | 10 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0225others(7): Show | 10 | HG00280.hp2 HG01071.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+10378_64+10381d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99828411 | |||||
| chr3:99828450
|
CT | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+10421delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99828450 | |||||
| chr3:99828525
|
A | G | 1 | a0001c0001t0005g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+10482A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828525 | ||||||
| chr3:99828574
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64+10531C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828574 | ||||||
| chr3:99828614
|
C | CT | 15 | a0001c0001t0001g0224a0001c0001t0004g0011a0001c0001t0004g0015others(12): Show | 15 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+10587dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99828614 | |||||
| chr3:99828650
|
C | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+10607C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828650 | ||||||
| chr3:99828680
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+10637T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828680 | ||||||
| chr3:99828916
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+10873T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828916 | ||||||
| chr3:99828916
|
T | TATCATCC others(15): Show |
6 | a0001c0001t0001g0192a0001c0001t0006g0003a0001c0001t0006g0004others(3): Show | 6 | HG02015.hp1 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+10905_64+10926d others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99828916 | |||||
| chr3:99828979
|
G | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+10936G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99828979 | ||||||
| chr3:99829225
|
T | C | 1 | a0002c0002t0003g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.64+11182T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99829225 | ||||||
| chr3:99829228
|
AT | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.64+11192delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99829228 | |||||
| chr3:99829244
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+11201G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99829244 | ||||||
| chr3:99829362
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+11319A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99829362 | ||||||
| chr3:99829430
|
A | G | 140 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.64+11387A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99829430 | ||||||
| chr3:99829762
|
C | G | 5 | a0001c0001t0001g0031a0001c0001t0004g0030a0001c0001t0007g0029others(2): Show | 5 | HG01975.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+11719C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99829762 | ||||||
| chr3:99829864
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64+11821T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99829864 | ||||||
| chr3:99830020
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.64+11977A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830020 | ||||||
| chr3:99830095
|
C | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+12052C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830095 | ||||||
| chr3:99830263
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64+12220C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830263 | ||||||
| chr3:99830387
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+12344T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830387 | ||||||
| chr3:99830513
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.64+12470C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830513 | ||||||
| chr3:99830549
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+12506T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830549 | ||||||
| chr3:99830559
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.64+12516G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830559 | ||||||
| chr3:99830639
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+12596T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830639 | ||||||
| chr3:99830879
|
T | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+12836T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830879 | ||||||
| chr3:99830943
|
G | A | 4 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+12900G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99830943 | ||||||
| chr3:99831055
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+13012A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99831055 | ||||||
| chr3:99831184
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+13141G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99831184 | ||||||
| chr3:99831305
|
A | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+13262A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99831305 | ||||||
| chr3:99831477
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+13434C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99831477 | ||||||
| chr3:99831789
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64+13746A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99831789 | ||||||
| chr3:99832231
|
C | CT | 9 | a0001c0001t0001g0221a0001c0001t0002g0049a0001c0001t0002g0050others(6): Show | 9 | HG02559.hp1 HG02738.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+14205dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99832231 | |||||
| chr3:99832295
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+14252A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832295 | ||||||
| chr3:99832452
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+14409G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832452 | ||||||
| chr3:99832481
|
T | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+14438T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832481 | ||||||
| chr3:99832522
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+14479G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832522 | ||||||
| chr3:99832560
|
A | AAG | 86 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.64+14517_64+14518i others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832560 | ||||||
| chr3:99832560
|
A | AG | 68 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0069others(65): Show | 68 | HG01168.hp1 HG01168.hp2 HG01257.hp1 others(65): Show |
intron_variant | MODIFIER | c.64+14519dupG | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99832560 | |||||
| chr3:99832733
|
T | TG | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+14692dupG | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99832733 | |||||
| chr3:99832774
|
A | T | 1 | a0001c0001t0009g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64+14731A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832774 | ||||||
| chr3:99832838
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.64+14795T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832838 | ||||||
| chr3:99832844
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0004g0164 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.64+14801A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832844 | ||||||
| chr3:99832858
|
G | T | 1 | a0001c0001t0010g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64+14815G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832858 | ||||||
| chr3:99832860
|
TG | T | 6 | a0001c0001t0004g0022a0001c0001t0006g0003a0001c0001t0006g0004others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+14818delG | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832860 | ||||||
| chr3:99832861
|
G | GT | 5 | a0001c0001t0002g0093a0001c0001t0002g0103a0001c0001t0002g0104others(2): Show | 5 | HG00280.hp1 HG02735.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+14832dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99832861 | |||||
| chr3:99832861
|
G | T | 153 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(150): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.64+14818G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832861 | ||||||
| chr3:99832863
|
T | G | 40 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(37): Show | 40 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.64+14820T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832863 | ||||||
| chr3:99832955
|
A | C | 1 | a0001c0001t0004g0011 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64+14912A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832955 | ||||||
| chr3:99832995
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+14952A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99832995 | ||||||
| chr3:99833181
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+15138T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99833181 | ||||||
| chr3:99833653
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64+15610A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99833653 | ||||||
| chr3:99833692
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+15649G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99833692 | ||||||
| chr3:99833801
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+15758C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99833801 | ||||||
| chr3:99833912
|
C | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+15869C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99833912 | ||||||
| chr3:99834067
|
T | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+16024T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834067 | ||||||
| chr3:99834071
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+16028G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834071 | ||||||
| chr3:99834132
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64+16089G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834132 | ||||||
| chr3:99834382
|
T | C | 1 | a0002c0002t0017g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.64+16339T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834382 | ||||||
| chr3:99834683
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.64+16640G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834683 | ||||||
| chr3:99834694
|
A | C | 5 | a0001c0001t0001g0031a0001c0001t0004g0030a0001c0001t0007g0029others(2): Show | 5 | HG01975.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+16651A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834694 | ||||||
| chr3:99834857
|
A | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG00280.hp2 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+16814A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834857 | ||||||
| chr3:99834943
|
G | A | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+16900G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834943 | ||||||
| chr3:99834948
|
A | G | 231 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.64+16905A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99834948 | ||||||
| chr3:99835121
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.64+17078C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99835121 | ||||||
| chr3:99835317
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.64+17274G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99835317 | ||||||
| chr3:99835322
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+17279A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99835322 | ||||||
| chr3:99835525
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+17482G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99835525 | ||||||
| chr3:99835571
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+17528A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99835571 | ||||||
| chr3:99835591
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+17548T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99835591 | ||||||
| chr3:99835773
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+17730G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99835773 | ||||||
| chr3:99836267
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+18224T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99836267 | ||||||
| chr3:99836387
|
T | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+18344T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99836387 | ||||||
| chr3:99836647
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+18604C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99836647 | ||||||
| chr3:99836844
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64+18801C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99836844 | ||||||
| chr3:99837139
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+19096G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99837139 | ||||||
| chr3:99837226
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+19183C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99837226 | ||||||
| chr3:99837316
|
A | T | 157 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(154): Show | 157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.64+19273A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99837316 | ||||||
| chr3:99837404
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+19361A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99837404 | ||||||
| chr3:99837439
|
GA | G | 26 | a0001c0001t0001g0102a0001c0001t0002g0045a0001c0001t0002g0086others(23): Show | 26 | HG00280.hp1 HG00423.hp2 HG01515.hp2 others(23): Show |
intron_variant | MODIFIER | c.64+19408delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99837439 | |||||
| chr3:99837761
|
T | C | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64+19718T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99837761 | ||||||
| chr3:99837952
|
T | A | 7 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+19909T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99837952 | ||||||
| chr3:99838010
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.64+19967G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99838010 | ||||||
| chr3:99838131
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+20088A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99838131 | ||||||
| chr3:99838253
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64+20210G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99838253 | ||||||
| chr3:99838657
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+20614G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99838657 | ||||||
| chr3:99838865
|
C | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+20822C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99838865 | ||||||
| chr3:99839007
|
G | C | 1 | a0001c0001t0002g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.64+20964G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99839007 | ||||||
| chr3:99839074
|
G | A | 7 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(4): Show | 7 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+21031G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99839074 | ||||||
| chr3:99839359
|
G | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+21316G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99839359 | ||||||
| chr3:99839423
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+21380A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99839423 | ||||||
| chr3:99839616
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+21573C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99839616 | ||||||
| chr3:99839737
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+21694A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99839737 | ||||||
| chr3:99839978
|
G | A | 1 | a0001c0001t0005g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64+21935G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99839978 | ||||||
| chr3:99840221
|
C | CT | 140 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0031others(137): Show | 140 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.64+22200dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99840221 | |||||
| chr3:99840221
|
C | CTT | 11 | a0001c0001t0001g0021a0001c0001t0001g0217a0001c0001t0002g0043others(8): Show | 11 | HG01257.hp1 HG01258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+22199_64+22200d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99840221 | |||||
| chr3:99840221
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | HG01934.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.64+22190_64+22200d others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99840221 | |||||
| chr3:99840277
|
G | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG00280.hp2 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64+22234G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99840277 | ||||||
| chr3:99840342
|
G | C | 1 | a0001c0001t0002g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.64+22299G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99840342 | ||||||
| chr3:99840376
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+22333A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99840376 | ||||||
| chr3:99840747
|
C | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+22704C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99840747 | ||||||
| chr3:99840761
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64+22718C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99840761 | ||||||
| chr3:99840958
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+22915T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99840958 | ||||||
| chr3:99840997
|
A | T | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.64+22954A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99840997 | ||||||
| chr3:99841010
|
C | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.64+22967C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99841010 | ||||||
| chr3:99841027
|
C | G | 1 | a0001c0001t0005g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64+22984C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99841027 | ||||||
| chr3:99841089
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64+23046A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99841089 | ||||||
| chr3:99841148
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.64+23105A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99841148 | ||||||
| chr3:99841195
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+23152G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99841195 | ||||||
| chr3:99841987
|
G | T | 1 | a0001c0001t0004g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64+23944G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99841987 | ||||||
| chr3:99842192
|
A | T | 10 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0111others(7): Show | 10 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+24149A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99842192 | ||||||
| chr3:99842229
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+24186A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99842229 | ||||||
| chr3:99842441
|
T | C | 9 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(6): Show | 9 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+24398T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99842441 | ||||||
| chr3:99842504
|
CA | C | 156 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(153): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.64+24477delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99842504 | |||||
| chr3:99842924
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0014others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+24881G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99842924 | ||||||
| chr3:99842967
|
A | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+24924A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99842967 | ||||||
| chr3:99843271
|
G | C | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.64+25228G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843271 | ||||||
| chr3:99843389
|
AAAG | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+25349_64+25351d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99843389 | |||||
| chr3:99843468
|
T | A | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64+25425T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843468 | ||||||
| chr3:99843495
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.64+25452A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843495 | ||||||
| chr3:99843600
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+25557T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843600 | ||||||
| chr3:99843621
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+25578T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843621 | ||||||
| chr3:99843653
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+25610A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843653 | ||||||
| chr3:99843732
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+25689T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843732 | ||||||
| chr3:99843786
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.64+25743G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843786 | ||||||
| chr3:99843911
|
G | A | 1 | a0001c0001t0007g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64+25868G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99843911 | ||||||
| chr3:99844000
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+25957C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99844000 | ||||||
| chr3:99844242
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+26199T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99844242 | ||||||
| chr3:99844297
|
A | G | 3 | a0001c0001t0007g0029a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+26254A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99844297 | ||||||
| chr3:99844727
|
C | A | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+26684C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99844727 | ||||||
| chr3:99845000
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64+26957T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845000 | ||||||
| chr3:99845374
|
G | A | 10 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(7): Show | 10 | HG01975.hp2 HG02027.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+27331G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845374 | ||||||
| chr3:99845477
|
A | G | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+27434A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845477 | ||||||
| chr3:99845597
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+27554G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845597 | ||||||
| chr3:99845647
|
A | T | 1 | a0001c0001t0005g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+27604A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845647 | ||||||
| chr3:99845836
|
T | C | 1 | a0001c0001t0016g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.64+27793T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845836 | ||||||
| chr3:99845846
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.64+27803G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845846 | ||||||
| chr3:99845904
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.64+27861T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99845904 | ||||||
| chr3:99846154
|
C | G | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64+28111C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846154 | ||||||
| chr3:99846156
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+28113C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846156 | ||||||
| chr3:99846157
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+28114G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846157 | ||||||
| chr3:99846327
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+28284A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846327 | ||||||
| chr3:99846624
|
A | G | 1 | a0002c0002t0003g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+28581A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846624 | ||||||
| chr3:99846732
|
T | C | 174 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.64+28689T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846732 | ||||||
| chr3:99846861
|
A | G | 1 | a0001c0001t0004g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64+28818A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846861 | ||||||
| chr3:99846984
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+28941A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99846984 | ||||||
| chr3:99847014
|
T | C | 1 | a0001c0001t0004g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64+28971T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99847014 | ||||||
| chr3:99847372
|
G | C | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG00423.hp1 HG02015.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+29329G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99847372 | ||||||
| chr3:99847485
|
T | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+29442T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99847485 | ||||||
| chr3:99848385
|
G | C | 1 | a0001c0001t0002g0095 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+30342G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99848385 | ||||||
| chr3:99848431
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+30388C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99848431 | ||||||
| chr3:99849303
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+31260G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99849303 | ||||||
| chr3:99849441
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+31398G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99849441 | ||||||
| chr3:99849593
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+31550T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99849593 | ||||||
| chr3:99849783
|
T | G | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.64+31740T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99849783 | ||||||
| chr3:99849893
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+31850A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99849893 | ||||||
| chr3:99850344
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+32301C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99850344 | ||||||
| chr3:99850455
|
C | T | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64+32412C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99850455 | ||||||
| chr3:99851036
|
G | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+32993G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851036 | ||||||
| chr3:99851108
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+33065G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851108 | ||||||
| chr3:99851181
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.64+33138G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851181 | ||||||
| chr3:99851258
|
T | C | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG01928.hp1 HG01952.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+33215T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851258 | ||||||
| chr3:99851595
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.64+33552C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851595 | ||||||
| chr3:99851626
|
CTG | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0037 | 2 | HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.64+33585_64+33586d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99851626 | |||||
| chr3:99851868
|
G | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+33825G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851868 | ||||||
| chr3:99851917
|
G | C | 18 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0011others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+33874G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851917 | ||||||
| chr3:99851930
|
G | A | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.64+33887G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851930 | ||||||
| chr3:99851981
|
A | C | 39 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(36): Show | 39 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.64+33938A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99851981 | ||||||
| chr3:99852458
|
A | AT | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+34421dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99852458 | |||||
| chr3:99852509
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+34466G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99852509 | ||||||
| chr3:99852603
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+34560G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99852603 | ||||||
| chr3:99852643
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64+34600A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99852643 | ||||||
| chr3:99852733
|
C | T | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64+34690C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99852733 | ||||||
| chr3:99852944
|
C | T | 14 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0167others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64+34901C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99852944 | ||||||
| chr3:99853082
|
C | T | 174 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.64+35039C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99853082 | ||||||
| chr3:99853163
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+35120G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99853163 | ||||||
| chr3:99853200
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+35157A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99853200 | ||||||
| chr3:99853232
|
C | A | 1 | a0002c0002t0003g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+35189C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99853232 | ||||||
| chr3:99853278
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64+35235G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99853278 | ||||||
| chr3:99853670
|
A | G | 2 | a0001c0001t0002g0013a0001c0001t0004g0014 | 2 | HG01516.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.64+35627A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99853670 | ||||||
| chr3:99853874
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.64+35831C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99853874 | ||||||
| chr3:99854176
|
G | A | 3 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0135 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+36133G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99854176 | ||||||
| chr3:99854372
|
T | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+36329T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99854372 | ||||||
| chr3:99854414
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+36371T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99854414 | ||||||
| chr3:99854550
|
C | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+36507C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99854550 | ||||||
| chr3:99854684
|
T | TG | 150 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(147): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.64+36647dupG | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99854684 | |||||
| chr3:99854703
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.64+36660G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99854703 | ||||||
| chr3:99854735
|
T | C | 1 | a0002c0002t0003g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.64+36692T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99854735 | ||||||
| chr3:99854994
|
A | G | 1 | a0002c0002t0020g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.64+36951A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99854994 | ||||||
| chr3:99855092
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.64+37049T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855092 | ||||||
| chr3:99855114
|
C | A | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.64+37071C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855114 | ||||||
| chr3:99855347
|
A | G | 1 | a0001c0001t0002g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64+37304A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855347 | ||||||
| chr3:99855388
|
A | G | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG00280.hp2 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64+37345A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855388 | ||||||
| chr3:99855564
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+37521G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855564 | ||||||
| chr3:99855732
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.64+37689T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855732 | ||||||
| chr3:99855794
|
C | T | 1 | a0001c0001t0004g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64+37751C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855794 | ||||||
| chr3:99855875
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+37832G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99855875 | ||||||
| chr3:99856088
|
T | G | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+38045T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856088 | ||||||
| chr3:99856098
|
G | GCTGCT | 12 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0130others(9): Show | 13 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+38094_64+38098d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99856098 | |||||
| chr3:99856098
|
GCTGCTCT others(8): Show |
G | 170 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(167): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.64+38084_64+38098d others(17): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99856098 | |||||
| chr3:99856098
|
GCTGCTCT others(13): Show |
G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+38079_64+38098d others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99856098 | |||||
| chr3:99856312
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.64+38269A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856312 | ||||||
| chr3:99856378
|
C | T | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+38335C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856378 | ||||||
| chr3:99856391
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+38348A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856391 | ||||||
| chr3:99856397
|
C | A | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+38354C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856397 | ||||||
| chr3:99856430
|
T | C | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+38387T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856430 | ||||||
| chr3:99856482
|
C | T | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.64+38439C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856482 | ||||||
| chr3:99856945
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+38902T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99856945 | ||||||
| chr3:99857025
|
T | C | 1 | a0001c0001t0004g0019 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64+38982T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99857025 | ||||||
| chr3:99857147
|
T | G | 1 | a0001c0001t0002g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+39104T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99857147 | ||||||
| chr3:99857196
|
A | ATAT | 42 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(39): Show | 42 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(39): Show |
intron_variant | MODIFIER | c.64+39155_64+39157d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99857196 | |||||
| chr3:99857415
|
C | T | 5 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0211others(2): Show | 5 | HG02071.hp1 HG02080.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+39372C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99857415 | ||||||
| chr3:99857800
|
T | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+39757T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99857800 | ||||||
| chr3:99858152
|
A | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+40109A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99858152 | ||||||
| chr3:99858549
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0004g0030 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.64+40506A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99858549 | ||||||
| chr3:99858616
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.64+40573T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99858616 | ||||||
| chr3:99858664
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+40621A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99858664 | ||||||
| chr3:99858886
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0096others(2): Show | 5 | HG02129.hp1 NA18954.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+40843T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99858886 | ||||||
| chr3:99859077
|
T | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+41034T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99859077 | ||||||
| chr3:99859270
|
A | T | 104 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.64+41227A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99859270 | ||||||
| chr3:99859549
|
A | C | 1 | a0001c0001t0004g0011 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64+41506A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99859549 | ||||||
| chr3:99859732
|
T | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+41689T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99859732 | ||||||
| chr3:99859779
|
T | TA | 231 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.64+41737dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99859779 | |||||
| chr3:99859782
|
C | G | 2 | a0001c0001t0001g0220a0001c0001t0016g0195 | 2 | HG01981.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.64+41739C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99859782 | ||||||
| chr3:99859929
|
G | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+41886G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99859929 | ||||||
| chr3:99860125
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+42082G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99860125 | ||||||
| chr3:99860282
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+42239T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99860282 | ||||||
| chr3:99860412
|
C | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+42369C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99860412 | ||||||
| chr3:99860614
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.64+42571A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99860614 | ||||||
| chr3:99860669
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.64+42626A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99860669 | ||||||
| chr3:99860880
|
G | A | 2 | a0001c0001t0002g0085a0001c0001t0004g0019 | 2 | NA18959.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.64+42837G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99860880 | ||||||
| chr3:99861071
|
C | T | 3 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0135 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+43028C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99861071 | ||||||
| chr3:99861424
|
A | G | 231 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.64+43381A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99861424 | ||||||
| chr3:99861652
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.64+43609C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99861652 | ||||||
| chr3:99862032
|
G | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+43989G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99862032 | ||||||
| chr3:99862218
|
A | T | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+44175A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99862218 | ||||||
| chr3:99862301
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+44258G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99862301 | ||||||
| chr3:99862477
|
T | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+44434T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99862477 | ||||||
| chr3:99862485
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+44442C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99862485 | ||||||
| chr3:99862595
|
A | G | 39 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(36): Show | 39 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.64+44552A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99862595 | ||||||
| chr3:99862684
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+44641T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99862684 | ||||||
| chr3:99863398
|
G | T | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+45355G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99863398 | ||||||
| chr3:99863829
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64+45786C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99863829 | ||||||
| chr3:99863858
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+45815G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99863858 | ||||||
| chr3:99863954
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.64+45911C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99863954 | ||||||
| chr3:99863956
|
G | A | 16 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0166others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.64+45913G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99863956 | ||||||
| chr3:99864205
|
C | T | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64+46162C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864205 | ||||||
| chr3:99864217
|
T | C | 1 | a0001c0001t0004g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64+46174T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864217 | ||||||
| chr3:99864240
|
C | A | 8 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(5): Show | 8 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+46197C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864240 | ||||||
| chr3:99864379
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.64+46336T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864379 | ||||||
| chr3:99864403
|
T | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+46360T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864403 | ||||||
| chr3:99864640
|
C | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.64+46597C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864640 | ||||||
| chr3:99864921
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64+46878C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864921 | ||||||
| chr3:99864969
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+46926C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99864969 | ||||||
| chr3:99865582
|
T | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+47539T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99865582 | ||||||
| chr3:99865585
|
G | A | 28 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0187others(25): Show | 28 | HG00140.hp1 HG00280.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.64+47542G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99865585 | ||||||
| chr3:99865755
|
A | AAT | 6 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(3): Show | 6 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+47727_64+47728d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99865755 | |||||
| chr3:99865770
|
A | C | 2 | a0001c0001t0002g0097a0001c0001t0002g0103 | 2 | HG02129.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.64+47727A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99865770 | ||||||
| chr3:99865786
|
G | T | 12 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0130others(9): Show | 13 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+47743G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99865786 | ||||||
| chr3:99865801
|
CTTA | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+47762_64+47764d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99865801 | |||||
| chr3:99866073
|
TTCCTTTA others(5): Show |
T | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.64+48049_64+48060d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99866073 | |||||
| chr3:99866231
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64+48188T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99866231 | ||||||
| chr3:99866281
|
T | A | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+48238T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99866281 | ||||||
| chr3:99866450
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+48407C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99866450 | ||||||
| chr3:99866538
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64+48495T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99866538 | ||||||
| chr3:99866676
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+48633A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99866676 | ||||||
| chr3:99867188
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+49145C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99867188 | ||||||
| chr3:99867305
|
GT | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+49263delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99867305 | ||||||
| chr3:99867340
|
A | G | 4 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+49297A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99867340 | ||||||
| chr3:99867534
|
A | G | 1 | a0001c0001t0002g0101 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.64+49491A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99867534 | ||||||
| chr3:99868054
|
A | T | 1 | a0002c0002t0003g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.64+50011A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868054 | ||||||
| chr3:99868084
|
G | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+50041G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868084 | ||||||
| chr3:99868251
|
AAATCAAG others(9): Show |
A | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64+50211_64+50226d others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99868251 | |||||
| chr3:99868385
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0002g0209 | 2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.64+50342A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868385 | ||||||
| chr3:99868438
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+50395A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868438 | ||||||
| chr3:99868558
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+50515G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868558 | ||||||
| chr3:99868590
|
C | G | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043 | 3 | HG01952.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.64+50547C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868590 | ||||||
| chr3:99868812
|
C | G | 7 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0014others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+50769C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868812 | ||||||
| chr3:99868880
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.64+50837T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99868880 | ||||||
| chr3:99869226
|
A | G | 80 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(77): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.64+51183A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99869226 | ||||||
| chr3:99869463
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+51420T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99869463 | ||||||
| chr3:99869568
|
C | G | 3 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0135 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+51525C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99869568 | ||||||
| chr3:99869573
|
A | G | 144 | a0001c0001t0001g0031a0001c0001t0001g0069a0001c0001t0001g0070others(141): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.64+51530A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99869573 | ||||||
| chr3:99869796
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64+51753G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99869796 | ||||||
| chr3:99870030
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.64+51987A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99870030 | ||||||
| chr3:99870706
|
T | C | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+52663T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99870706 | ||||||
| chr3:99870938
|
C | G | 7 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0014others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+52895C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99870938 | ||||||
| chr3:99871409
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+53366C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99871409 | ||||||
| chr3:99871468
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64+53425A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99871468 | ||||||
| chr3:99871898
|
G | C | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+53855G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99871898 | ||||||
| chr3:99872232
|
T | A | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.64+54189T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872232 | ||||||
| chr3:99872269
|
C | CTG | 18 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0159others(15): Show | 18 | HG00741.hp1 HG01168.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+54279_64+54280d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
C | CTGTG | 12 | a0001c0001t0001g0189a0001c0001t0001g0200a0001c0001t0001g0202others(9): Show | 12 | HG01515.hp2 HG02148.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+54277_64+54280d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
C | CTGTGTG | 26 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 26 | HG00423.hp1 HG01192.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.64+54275_64+54280d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
C | CTGTGTGT others(1): Show |
20 | a0001c0001t0001g0021a0001c0001t0001g0161a0001c0001t0001g0172others(17): Show | 20 | HG00280.hp1 HG01168.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.64+54273_64+54280d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
C | CTGTGTGT others(3): Show |
11 | a0001c0001t0001g0038a0001c0001t0001g0174a0001c0001t0001g0182others(8): Show | 11 | HG01069.hp1 HG01257.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+54271_64+54280d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
C | CTGTGTGT others(5): Show |
10 | a0001c0001t0001g0020a0001c0001t0001g0102a0001c0001t0001g0157others(7): Show | 10 | HG01261.hp1 HG02040.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+54269_64+54280d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0194a0001c0001t0002g0093 | 2 | HG00323.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.64+54267_64+54280d others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0001g0165a0001c0001t0001g0213a0001c0001t0007g0032 | 3 | HG01975.hp2 HG02809.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.64+54265_64+54280d others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTG | C | 33 | a0001c0001t0001g0132a0001c0001t0001g0176a0001c0001t0001g0179others(30): Show | 34 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+54279_64+54280d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTG | C | 17 | a0001c0001t0001g0070a0001c0001t0002g0090a0001c0001t0002g0091others(14): Show | 17 | HG01192.hp2 HG01891.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.64+54277_64+54280d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTGTG | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0162a0001c0001t0002g0067others(7): Show | 10 | HG00323.hp2 HG01123.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+54275_64+54280d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTGTGT others(1): Show |
C | 4 | a0001c0001t0002g0074a0001c0001t0004g0030a0001c0001t0009g0040others(1): Show | 4 | HG01928.hp2 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+54273_64+54280d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTGTGT others(3): Show |
C | 10 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(7): Show | 10 | HG01952.hp1 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.64+54271_64+54280d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTGTGT others(5): Show |
C | 19 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(16): Show | 19 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+54269_64+54280d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01261.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.64+54267_64+54280d others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64+54263_64+54280d others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872269
|
CTGTGTGT others(15): Show |
C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+54259_64+54280d others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99872269 | |||||
| chr3:99872565
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0221 | 2 | HG00423.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.64+54522C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872565 | ||||||
| chr3:99872672
|
G | C | 2 | a0001c0001t0001g0194a0003c0003t0001g0231 | 2 | HG00323.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.64+54629G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872672 | ||||||
| chr3:99872692
|
G | T | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.64+54649G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872692 | ||||||
| chr3:99872696
|
AC | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+54654delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872696 | ||||||
| chr3:99872794
|
T | C | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+54751T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872794 | ||||||
| chr3:99872898
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0002g0209 | 2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.64+54855G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872898 | ||||||
| chr3:99872930
|
T | A | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.64+54887T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99872930 | ||||||
| chr3:99873079
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+55036A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873079 | ||||||
| chr3:99873080
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+55037G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873080 | ||||||
| chr3:99873152
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+55109A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873152 | ||||||
| chr3:99873259
|
A | G | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | HG01934.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.64+55216A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873259 | ||||||
| chr3:99873589
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+55546T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873589 | ||||||
| chr3:99873752
|
C | T | 144 | a0001c0001t0001g0031a0001c0001t0001g0069a0001c0001t0001g0070others(141): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.64+55709C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873752 | ||||||
| chr3:99873789
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+55746C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873789 | ||||||
| chr3:99873872
|
A | G | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+55829A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99873872 | ||||||
| chr3:99874021
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+55978G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99874021 | ||||||
| chr3:99874640
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+56597A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99874640 | ||||||
| chr3:99874648
|
G | C | 231 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.64+56605G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99874648 | ||||||
| chr3:99875361
|
T | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+57318T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99875361 | ||||||
| chr3:99875674
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+57631C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99875674 | ||||||
| chr3:99875858
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.64+57815C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99875858 | ||||||
| chr3:99876105
|
G | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0073 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.64+58062G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99876105 | ||||||
| chr3:99876108
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+58065C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99876108 | ||||||
| chr3:99876114
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+58071C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99876114 | ||||||
| chr3:99876154
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64+58111G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99876154 | ||||||
| chr3:99876252
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64+58209C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99876252 | ||||||
| chr3:99876264
|
G | A | 11 | a0001c0001t0001g0069a0001c0001t0002g0062a0001c0001t0002g0063others(8): Show | 11 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+58221G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99876264 | ||||||
| chr3:99876383
|
T | TGGTGGGC others(1): Show |
31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+58351_64+58358d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99876383 | |||||
| chr3:99876867
|
G | A | 12 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(9): Show | 12 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+58824G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99876867 | ||||||
| chr3:99877116
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+59073A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99877116 | ||||||
| chr3:99877555
|
C | CTATTT | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+59514_64+59515i others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99877555 | |||||
| chr3:99877688
|
A | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+59645A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99877688 | ||||||
| chr3:99878308
|
A | G | 1 | a0002c0002t0003g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.64+60265A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99878308 | ||||||
| chr3:99878497
|
T | C | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+60454T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99878497 | ||||||
| chr3:99878522
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0014others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+60479G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99878522 | ||||||
| chr3:99878688
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+60645A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99878688 | ||||||
| chr3:99879084
|
A | C | 122 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0102others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.64+61041A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99879084 | ||||||
| chr3:99879345
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+61302G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99879345 | ||||||
| chr3:99879362
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.64+61319A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99879362 | ||||||
| chr3:99879434
|
A | G | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+61391A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99879434 | ||||||
| chr3:99879679
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64+61636G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99879679 | ||||||
| chr3:99879780
|
T | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+61737T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99879780 | ||||||
| chr3:99880040
|
C | T | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+61997C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880040 | ||||||
| chr3:99880075
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64+62032G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880075 | ||||||
| chr3:99880217
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64+62174T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880217 | ||||||
| chr3:99880233
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+62190C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880233 | ||||||
| chr3:99880621
|
C | G | 3 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0135 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+62578C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880621 | ||||||
| chr3:99880716
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.64+62673C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880716 | ||||||
| chr3:99880824
|
C | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+62781C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880824 | ||||||
| chr3:99880873
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+62830T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880873 | ||||||
| chr3:99880882
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.64+62839A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880882 | ||||||
| chr3:99880980
|
G | T | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64+62937G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99880980 | ||||||
| chr3:99881145
|
A | T | 3 | a0001c0001t0008g0087a0001c0001t0008g0088a0001c0001t0008g0089 | 3 | HG02083.hp2 NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.64+63102A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881145 | ||||||
| chr3:99881250
|
A | G | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+63207A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881250 | ||||||
| chr3:99881260
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.64+63217G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881260 | ||||||
| chr3:99881304
|
C | G | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.64+63261C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881304 | ||||||
| chr3:99881392
|
C | A | 5 | a0001c0001t0001g0226a0001c0001t0002g0090a0001c0001t0002g0091others(2): Show | 5 | HG00280.hp2 HG02015.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+63349C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881392 | ||||||
| chr3:99881537
|
C | CT | 10 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG01257.hp2 HG01346.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+63507dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99881537 | |||||
| chr3:99881589
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+63546G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881589 | ||||||
| chr3:99881721
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0077 | 2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.64+63678C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881721 | ||||||
| chr3:99881722
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.64+63679G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881722 | ||||||
| chr3:99881753
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+63710G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99881753 | ||||||
| chr3:99882073
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+64030A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99882073 | ||||||
| chr3:99882280
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+64237T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99882280 | ||||||
| chr3:99882427
|
T | G | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+64384T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99882427 | ||||||
| chr3:99882637
|
C | T | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.64+64594C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99882637 | ||||||
| chr3:99882692
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+64649G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99882692 | ||||||
| chr3:99882822
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+64779G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99882822 | ||||||
| chr3:99882928
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+64885A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99882928 | ||||||
| chr3:99883030
|
AATTCT | A | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+64991_64+64995d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99883030 | |||||
| chr3:99883115
|
C | T | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+65072C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883115 | ||||||
| chr3:99883225
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.64+65182C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883225 | ||||||
| chr3:99883234
|
G | A | 2 | a0001c0001t0004g0022a0001c0001t0004g0024 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.64+65191G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883234 | ||||||
| chr3:99883243
|
A | G | 182 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(179): Show | 183 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.64+65200A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883243 | ||||||
| chr3:99883322
|
G | A | 4 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(1): Show | 4 | HG02040.hp2 HG02129.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+65279G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883322 | ||||||
| chr3:99883452
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+65409A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883452 | ||||||
| chr3:99883473
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.64+65430C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883473 | ||||||
| chr3:99883536
|
T | C | 40 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(37): Show | 40 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.64+65493T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883536 | ||||||
| chr3:99883626
|
T | C | 122 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0102others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.64+65583T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883626 | ||||||
| chr3:99883632
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64+65589C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883632 | ||||||
| chr3:99883634
|
C | G | 1 | a0001c0001t0004g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64+65591C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883634 | ||||||
| chr3:99883711
|
A | G | 39 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(36): Show | 39 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.64+65668A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883711 | ||||||
| chr3:99883894
|
C | T | 1 | a0002c0002t0003g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64+65851C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883894 | ||||||
| chr3:99883901
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+65858T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99883901 | ||||||
| chr3:99884058
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+66015T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884058 | ||||||
| chr3:99884065
|
G | A | 1 | a0001c0001t0005g0177 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+66022G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884065 | ||||||
| chr3:99884386
|
G | A | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.64+66343G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884386 | ||||||
| chr3:99884628
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+66585G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884628 | ||||||
| chr3:99884669
|
G | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+66626G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884669 | ||||||
| chr3:99884795
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+66752A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884795 | ||||||
| chr3:99884817
|
T | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+66774T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884817 | ||||||
| chr3:99884853
|
C | T | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+66810C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884853 | ||||||
| chr3:99884905
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+66862A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884905 | ||||||
| chr3:99884936
|
T | A | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+66893T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99884936 | ||||||
| chr3:99885039
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64+66996A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885039 | ||||||
| chr3:99885323
|
T | C | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+67280T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885323 | ||||||
| chr3:99885341
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+67298T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885341 | ||||||
| chr3:99885378
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+67335A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885378 | ||||||
| chr3:99885695
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+67652T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885695 | ||||||
| chr3:99885713
|
T | C | 2 | a0002c0002t0003g0136a0002c0002t0003g0137 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.64+67670T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885713 | ||||||
| chr3:99885783
|
CAT | C | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | HG00423.hp2 HG02027.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+67741_64+67742d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885783 | ||||||
| chr3:99885798
|
A | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+67755A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885798 | ||||||
| chr3:99885855
|
A | G | 1 | a0002c0002t0003g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.64+67812A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99885855 | ||||||
| chr3:99886074
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64+68031A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99886074 | ||||||
| chr3:99886099
|
CTA | C | 5 | a0001c0001t0001g0198a0001c0001t0002g0093a0001c0001t0002g0094others(2): Show | 5 | HG00280.hp1 HG02735.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+68058_64+68059d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99886099 | |||||
| chr3:99886124
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0203 | 2 | HG03654.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.64+68081C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99886124 | ||||||
| chr3:99886177
|
G | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.64+68134G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99886177 | ||||||
| chr3:99886216
|
TTTATCAC others(46): Show |
T | 122 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0102others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.64+68228_64+68280d others(55): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99886216 | |||||
| chr3:99886580
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+68537C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99886580 | ||||||
| chr3:99886761
|
T | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+68718T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99886761 | ||||||
| chr3:99886826
|
C | T | 2 | a0001c0001t0001g0194a0003c0003t0001g0231 | 2 | HG00323.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.64+68783C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99886826 | ||||||
| chr3:99886969
|
C | CA | 5 | a0001c0001t0002g0145a0001c0001t0009g0009a0001c0001t0009g0010others(2): Show | 5 | HG01891.hp2 HG02738.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+68941dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99886969 | |||||
| chr3:99887128
|
G | A | 1 | a0001c0001t0005g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64+69085G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99887128 | ||||||
| chr3:99887481
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+69438C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99887481 | ||||||
| chr3:99887779
|
G | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+69736G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99887779 | ||||||
| chr3:99887969
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0004g0014 | 2 | HG01516.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.64+69926G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99887969 | ||||||
| chr3:99888223
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+70180A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99888223 | ||||||
| chr3:99888535
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+70492G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99888535 | ||||||
| chr3:99888616
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+70573C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99888616 | ||||||
| chr3:99888746
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.64+70703G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99888746 | ||||||
| chr3:99888944
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64+70901T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99888944 | ||||||
| chr3:99888998
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.64+70955A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99888998 | ||||||
| chr3:99889036
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+70993A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99889036 | ||||||
| chr3:99889196
|
G | T | 3 | a0001c0001t0002g0074a0001c0001t0006g0057a0001c0001t0006g0071 | 3 | HG02280.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+71153G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99889196 | ||||||
| chr3:99889263
|
T | C | 4 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(1): Show | 4 | HG02040.hp2 HG02129.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+71220T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99889263 | ||||||
| chr3:99889367
|
T | A | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64+71324T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99889367 | ||||||
| chr3:99889484
|
A | G | 3 | a0001c0001t0007g0029a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+71441A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99889484 | ||||||
| chr3:99889489
|
G | A | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.64+71446G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99889489 | ||||||
| chr3:99889770
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+71727A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99889770 | ||||||
| chr3:99890597
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.64+72554T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99890597 | ||||||
| chr3:99890598
|
C | G | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.64+72555C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99890598 | ||||||
| chr3:99890724
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.64+72681C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99890724 | ||||||
| chr3:99890877
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+72834A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99890877 | ||||||
| chr3:99890879
|
G | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64+72836G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99890879 | ||||||
| chr3:99890966
|
G | A | 1 | a0001c0001t0002g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.64+72923G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99890966 | ||||||
| chr3:99890993
|
C | T | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+72950C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99890993 | ||||||
| chr3:99891072
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+73029A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99891072 | ||||||
| chr3:99891115
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64+73072A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99891115 | ||||||
| chr3:99891201
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+73158C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99891201 | ||||||
| chr3:99891541
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+73498T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99891541 | ||||||
| chr3:99891570
|
G | GT | 9 | a0001c0001t0001g0031a0001c0001t0001g0070a0001c0001t0002g0013others(6): Show | 9 | HG01516.hp1 HG01975.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+73535dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99891570 | |||||
| chr3:99891582
|
T | C | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+73539T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99891582 | ||||||
| chr3:99891838
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+73795C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99891838 | ||||||
| chr3:99892314
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+74271A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99892314 | ||||||
| chr3:99892695
|
C | T | 1 | a0001c0001t0007g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64+74652C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99892695 | ||||||
| chr3:99892836
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+74793C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99892836 | ||||||
| chr3:99893014
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+74971A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893014 | ||||||
| chr3:99893162
|
C | CT | 64 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0001g0194others(61): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.64+75140dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99893162 | |||||
| chr3:99893162
|
CT | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0073a0001c0001t0005g0082others(2): Show | 5 | HG02451.hp2 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+75140delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99893162 | |||||
| chr3:99893235
|
G | T | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+75192G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893235 | ||||||
| chr3:99893256
|
C | T | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64+75213C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893256 | ||||||
| chr3:99893381
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+75338G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893381 | ||||||
| chr3:99893456
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+75413C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893456 | ||||||
| chr3:99893574
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.64+75531G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893574 | ||||||
| chr3:99893618
|
G | A | 1 | a0001c0001t0015g0230 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.64+75575G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893618 | ||||||
| chr3:99893623
|
A | G | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+75580A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893623 | ||||||
| chr3:99893833
|
G | C | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+75790G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99893833 | ||||||
| chr3:99894008
|
A | G | 4 | a0001c0001t0002g0145a0001c0001t0002g0149a0001c0001t0002g0150others(1): Show | 4 | HG00741.hp1 HG01256.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+75965A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894008 | ||||||
| chr3:99894143
|
A | G | 1 | a0001c0001t0010g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.64+76100A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894143 | ||||||
| chr3:99894215
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+76172G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894215 | ||||||
| chr3:99894335
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+76292G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894335 | ||||||
| chr3:99894445
|
G | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+76402G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894445 | ||||||
| chr3:99894486
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+76443A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894486 | ||||||
| chr3:99894677
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64+76634C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894677 | ||||||
| chr3:99894678
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+76635G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894678 | ||||||
| chr3:99894819
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64+76776T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894819 | ||||||
| chr3:99894884
|
C | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+76841C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894884 | ||||||
| chr3:99894951
|
T | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+76908T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99894951 | ||||||
| chr3:99895080
|
G | GCCAT | 13 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0183others(10): Show | 13 | HG01978.hp1 HG02148.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+77040_64+77043d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99895080 | |||||
| chr3:99895349
|
A | G | 1 | a0001c0001t0004g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64+77306A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99895349 | ||||||
| chr3:99895377
|
C | CT | 7 | a0001c0001t0001g0070a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG01934.hp2 HG01978.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+77352dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99895377 | |||||
| chr3:99895377
|
CT | C | 9 | a0001c0001t0001g0224a0001c0001t0002g0054a0001c0001t0002g0104others(6): Show | 9 | HG02809.hp2 HG02895.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+77352delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99895377 | |||||
| chr3:99895633
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+77590A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99895633 | ||||||
| chr3:99895714
|
C | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+77671C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99895714 | ||||||
| chr3:99895782
|
A | G | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(12): Show | 15 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+77739A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99895782 | ||||||
| chr3:99895924
|
A | G | 1 | a0001c0001t0010g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.64+77881A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99895924 | ||||||
| chr3:99895992
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+77949G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99895992 | ||||||
| chr3:99896419
|
T | G | 11 | a0001c0001t0001g0069a0001c0001t0002g0062a0001c0001t0002g0063others(8): Show | 11 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+78376T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896419 | ||||||
| chr3:99896427
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.64+78384A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896427 | ||||||
| chr3:99896600
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+78557A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896600 | ||||||
| chr3:99896641
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.64+78598A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896641 | ||||||
| chr3:99896748
|
A | G | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.64+78705A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896748 | ||||||
| chr3:99896772
|
G | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+78729G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896772 | ||||||
| chr3:99896889
|
G | A | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+78846G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896889 | ||||||
| chr3:99896914
|
C | T | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+78871C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99896914 | ||||||
| chr3:99897129
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+79086T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99897129 | ||||||
| chr3:99897369
|
CA | C | 6 | a0001c0001t0002g0095a0001c0001t0002g0098a0001c0001t0002g0099others(3): Show | 6 | HG00423.hp2 HG02027.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+79339delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99897369 | |||||
| chr3:99897617
|
G | A | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+79574G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99897617 | ||||||
| chr3:99897843
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+79800A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99897843 | ||||||
| chr3:99898037
|
T | C | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+79994T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99898037 | ||||||
| chr3:99898091
|
T | C | 2 | a0001c0001t0002g0097a0001c0001t0002g0103 | 2 | HG02129.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.64+80048T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99898091 | ||||||
| chr3:99898182
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+80139A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99898182 | ||||||
| chr3:99898617
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+80574C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99898617 | ||||||
| chr3:99898628
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+80585T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99898628 | ||||||
| chr3:99898764
|
T | TA | 5 | a0001c0001t0001g0031a0001c0001t0001g0204a0001c0001t0001g0229others(2): Show | 5 | HG03225.hp1 HG03225.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+80742dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99898764 | |||||
| chr3:99898764
|
TA | T | 83 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(80): Show | 83 | HG01168.hp1 HG01168.hp2 HG01257.hp1 others(80): Show |
intron_variant | MODIFIER | c.64+80742delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99898764 | |||||
| chr3:99898764
|
TAA | T | 72 | a0001c0001t0001g0132a0001c0001t0002g0065a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+80741_64+80742d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99898764 | |||||
| chr3:99898909
|
T | A | 42 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(39): Show | 42 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(39): Show |
intron_variant | MODIFIER | c.64+80866T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99898909 | ||||||
| chr3:99899025
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.64+80982C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99899025 | ||||||
| chr3:99899038
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.64+80995G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99899038 | ||||||
| chr3:99899059
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.64+81016G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99899059 | ||||||
| chr3:99899373
|
AC | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+81331delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99899373 | ||||||
| chr3:99899394
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+81351A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99899394 | ||||||
| chr3:99899557
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+81514T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99899557 | ||||||
| chr3:99899847
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64+81804G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99899847 | ||||||
| chr3:99900817
|
G | A | 1 | a0002c0002t0003g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64+82774G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99900817 | ||||||
| chr3:99900958
|
A | C | 6 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0112others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+82915A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99900958 | ||||||
| chr3:99901189
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+83146G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99901189 | ||||||
| chr3:99901217
|
G | A | 2 | a0001c0001t0002g0013a0001c0001t0004g0014 | 2 | HG01516.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.64+83174G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99901217 | ||||||
| chr3:99901233
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.64+83190G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99901233 | ||||||
| chr3:99901408
|
T | C | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+83365T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99901408 | ||||||
| chr3:99901587
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64+83544C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99901587 | ||||||
| chr3:99901683
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64+83640T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99901683 | ||||||
| chr3:99902158
|
G | A | 122 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0102others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.64+84115G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902158 | ||||||
| chr3:99902434
|
A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64+84391A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902434 | ||||||
| chr3:99902524
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.64+84481C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902524 | ||||||
| chr3:99902760
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+84717G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902760 | ||||||
| chr3:99902806
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+84763A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902806 | ||||||
| chr3:99902882
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0011others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+84839A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902882 | ||||||
| chr3:99902947
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+84904G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902947 | ||||||
| chr3:99902965
|
C | T | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.64+84922C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99902965 | ||||||
| chr3:99903128
|
T | C | 9 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+85085T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903128 | ||||||
| chr3:99903205
|
G | A | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.64+85162G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903205 | ||||||
| chr3:99903258
|
G | GT | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+85226dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99903258 | |||||
| chr3:99903274
|
C | T | 6 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0112others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+85231C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903274 | ||||||
| chr3:99903275
|
G | A | 6 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0112others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+85232G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903275 | ||||||
| chr3:99903278
|
A | G | 6 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0112others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+85235A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903278 | ||||||
| chr3:99903282
|
C | T | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64+85239C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903282 | ||||||
| chr3:99903471
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64+85428C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903471 | ||||||
| chr3:99903530
|
G | C | 22 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+85487G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903530 | ||||||
| chr3:99903673
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+85630T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903673 | ||||||
| chr3:99903760
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+85717G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903760 | ||||||
| chr3:99903882
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+85839C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903882 | ||||||
| chr3:99903890
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+85847G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903890 | ||||||
| chr3:99903897
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+85854A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903897 | ||||||
| chr3:99903940
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64+85897A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99903940 | ||||||
| chr3:99904117
|
A | G | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+86074A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99904117 | ||||||
| chr3:99904200
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64+86157A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99904200 | ||||||
| chr3:99904210
|
G | T | 1 | a0001c0001t0004g0017 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.64+86167G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99904210 | ||||||
| chr3:99904235
|
G | A | 2 | a0001c0001t0001g0194a0003c0003t0001g0231 | 2 | HG00323.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.64+86192G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99904235 | ||||||
| chr3:99904693
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.64+86650C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99904693 | ||||||
| chr3:99904900
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+86857C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99904900 | ||||||
| chr3:99904919
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+86876T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99904919 | ||||||
| chr3:99905076
|
C | T | 3 | a0001c0001t0002g0074a0001c0001t0006g0057a0001c0001t0006g0071 | 3 | HG02280.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+87033C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99905076 | ||||||
| chr3:99905724
|
T | C | 3 | a0001c0001t0007g0029a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+87681T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99905724 | ||||||
| chr3:99905831
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+87788C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99905831 | ||||||
| chr3:99905917
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64+87874G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99905917 | ||||||
| chr3:99905973
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+87930A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99905973 | ||||||
| chr3:99906087
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64+88044C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99906087 | ||||||
| chr3:99906440
|
T | A | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.64+88397T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99906440 | ||||||
| chr3:99906923
|
G | A | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+88880G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99906923 | ||||||
| chr3:99906964
|
TTTTAAGT others(14): Show |
T | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64+88942_64+88962d others(23): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99906964 | |||||
| chr3:99907171
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+89128A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99907171 | ||||||
| chr3:99907184
|
G | A | 126 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0102others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.64+89141G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99907184 | ||||||
| chr3:99907700
|
T | A | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+89657T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99907700 | ||||||
| chr3:99907787
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+89744G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99907787 | ||||||
| chr3:99907920
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.64+89877A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99907920 | ||||||
| chr3:99908128
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.64+90085A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908128 | ||||||
| chr3:99908305
|
G | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+90262G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908305 | ||||||
| chr3:99908316
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+90273A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908316 | ||||||
| chr3:99908475
|
T | C | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.64+90432T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908475 | ||||||
| chr3:99908582
|
C | T | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.64+90539C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908582 | ||||||
| chr3:99908823
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+90780G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908823 | ||||||
| chr3:99908825
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+90782A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908825 | ||||||
| chr3:99908906
|
A | G | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+90863A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99908906 | ||||||
| chr3:99909038
|
A | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+90995A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99909038 | ||||||
| chr3:99909430
|
T | A | 1 | a0002c0002t0003g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.64+91387T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99909430 | ||||||
| chr3:99909508
|
A | G | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | HG01934.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.64+91465A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99909508 | ||||||
| chr3:99909563
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.64+91520G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99909563 | ||||||
| chr3:99909830
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.64+91787T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99909830 | ||||||
| chr3:99909937
|
GTCATCTG others(841): Show |
G | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+91896_64+92743d others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99909937 | |||||
| chr3:99910248
|
C | T | 1 | a0001c0001t0004g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64+92205C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99910248 | ||||||
| chr3:99910395
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+92352A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99910395 | ||||||
| chr3:99910787
|
G | T | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+92744G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99910787 | ||||||
| chr3:99911089
|
G | A | 8 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(5): Show | 8 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+93046G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99911089 | ||||||
| chr3:99911440
|
C | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+93397C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99911440 | ||||||
| chr3:99911568
|
C | G | 1 | a0001c0001t0002g0100 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.64+93525C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99911568 | ||||||
| chr3:99911683
|
G | C | 85 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0049others(82): Show | 86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.64+93640G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99911683 | ||||||
| chr3:99911703
|
A | G | 4 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0104others(1): Show | 4 | HG00280.hp1 HG02735.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+93660A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99911703 | ||||||
| chr3:99912130
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64+94087C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99912130 | ||||||
| chr3:99912172
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+94129G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99912172 | ||||||
| chr3:99912545
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+94502A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99912545 | ||||||
| chr3:99913092
|
C | CA | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+95050dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99913092 | |||||
| chr3:99913093
|
A | T | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64+95050A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99913093 | ||||||
| chr3:99913280
|
A | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+95237A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99913280 | ||||||
| chr3:99913349
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+95306C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99913349 | ||||||
| chr3:99913415
|
T | C | 18 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0011others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+95372T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99913415 | ||||||
| chr3:99913564
|
T | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.64+95521T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99913564 | ||||||
| chr3:99913731
|
G | A | 5 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0211others(2): Show | 5 | HG02071.hp1 HG02080.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+95688G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99913731 | ||||||
| chr3:99914282
|
G | C | 2 | a0001c0001t0002g0099a0001c0001t0002g0105 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.64+96239G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99914282 | ||||||
| chr3:99914411
|
T | C | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64+96368T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99914411 | ||||||
| chr3:99914646
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+96603G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99914646 | ||||||
| chr3:99914780
|
G | A | 7 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+96737G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99914780 | ||||||
| chr3:99915063
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+97020G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99915063 | ||||||
| chr3:99915527
|
C | T | 2 | a0001c0001t0006g0057a0001c0001t0006g0071 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.64+97484C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99915527 | ||||||
| chr3:99916010
|
G | A | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+97967G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916010 | ||||||
| chr3:99916074
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+98031C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916074 | ||||||
| chr3:99916349
|
T | C | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+98306T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916349 | ||||||
| chr3:99916435
|
T | TACAC | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+98393_64+98394i others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916435 | |||||
| chr3:99916437
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+98394T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916437 | ||||||
| chr3:99916437
|
T | TAC | 15 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.64+98441_64+98442d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
T | TACAC | 4 | a0001c0001t0001g0070a0001c0001t0001g0222a0001c0001t0002g0085others(1): Show | 4 | HG02615.hp2 HG02895.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+98439_64+98442d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
T | TACACACA others(1): Show |
3 | a0001c0001t0001g0220a0001c0001t0016g0195a0002c0002t0019g0012 | 3 | HG01981.hp1 HG04204.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.64+98435_64+98442d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
T | TACACACA others(5): Show |
1 | a0001c0001t0005g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+98431_64+98442d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
TAC | T | 11 | a0001c0001t0001g0174a0001c0001t0001g0190a0001c0001t0002g0013others(8): Show | 11 | HG01069.hp1 HG01516.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+98441_64+98442d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
TACAC | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0166others(20): Show | 23 | HG01168.hp1 HG01346.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+98439_64+98442d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
TACACAC | T | 7 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0073others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+98437_64+98442d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
TACACACA others(1): Show |
T | 32 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(29): Show | 32 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.64+98435_64+98442d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
TACACACA others(3): Show |
T | 55 | a0001c0001t0001g0102a0001c0001t0002g0048a0001c0001t0002g0049others(52): Show | 55 | HG00280.hp1 HG00423.hp2 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.64+98433_64+98442d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
TACACACA others(5): Show |
T | 21 | a0001c0001t0001g0132a0001c0001t0002g0086a0001c0001t0002g0096others(18): Show | 22 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.64+98431_64+98442d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916437
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64+98429_64+98442d others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99916437 | |||||
| chr3:99916612
|
A | G | 2 | a0002c0002t0003g0112a0002c0002t0003g0117 | 2 | HG01123.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.64+98569A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916612 | ||||||
| chr3:99916618
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+98575A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916618 | ||||||
| chr3:99916738
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0013g0201 | 2 | HG00140.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.64+98695G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916738 | ||||||
| chr3:99916743
|
T | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+98700T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916743 | ||||||
| chr3:99916780
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0004g0030 | 2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.64+98737C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916780 | ||||||
| chr3:99916793
|
A | G | 1 | a0002c0002t0003g0122 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.64+98750A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916793 | ||||||
| chr3:99916829
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.64+98786T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916829 | ||||||
| chr3:99916859
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+98816A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99916859 | ||||||
| chr3:99917167
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+99124C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99917167 | ||||||
| chr3:99917184
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+99141C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99917184 | ||||||
| chr3:99917508
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+99465T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99917508 | ||||||
| chr3:99917644
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+99601T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99917644 | ||||||
| chr3:99917754
|
G | A | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+99711G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99917754 | ||||||
| chr3:99917781
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+99738T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99917781 | ||||||
| chr3:99918044
|
C | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+100001C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918044 | ||||||
| chr3:99918135
|
G | A | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.64+100092G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918135 | ||||||
| chr3:99918193
|
G | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+100150G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918193 | ||||||
| chr3:99918379
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+100336A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918379 | ||||||
| chr3:99918408
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+100365G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918408 | ||||||
| chr3:99918730
|
T | C | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.64+100687T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918730 | ||||||
| chr3:99918874
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.64+100831A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918874 | ||||||
| chr3:99918892
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.64+100849A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918892 | ||||||
| chr3:99918939
|
G | A | 143 | a0001c0001t0001g0031a0001c0001t0001g0069a0001c0001t0001g0102others(140): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.64+100896G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99918939 | ||||||
| chr3:99919017
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+100974A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99919017 | ||||||
| chr3:99919423
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.64+101380A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99919423 | ||||||
| chr3:99919679
|
A | T | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.64+101636A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99919679 | ||||||
| chr3:99919968
|
C | G | 1 | a0002c0002t0003g0119 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64+101925C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99919968 | ||||||
| chr3:99919992
|
T | C | 80 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(77): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.64+101949T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99919992 | ||||||
| chr3:99920542
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+102499C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99920542 | ||||||
| chr3:99920746
|
G | T | 1 | a0002c0002t0003g0113 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.64+102703G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99920746 | ||||||
| chr3:99920895
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+102852T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99920895 | ||||||
| chr3:99921107
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+103064T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99921107 | ||||||
| chr3:99921277
|
C | T | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+103234C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99921277 | ||||||
| chr3:99921476
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+103433G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99921476 | ||||||
| chr3:99921866
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+103823A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99921866 | ||||||
| chr3:99921872
|
A | C | 18 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0011others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+103829A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99921872 | ||||||
| chr3:99922103
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+104060C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99922103 | ||||||
| chr3:99922171
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+104128T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99922171 | ||||||
| chr3:99922292
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+104249A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99922292 | ||||||
| chr3:99922376
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+104333A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99922376 | ||||||
| chr3:99922635
|
A | C | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(12): Show | 15 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+104592A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99922635 | ||||||
| chr3:99922825
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.64+104782G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99922825 | ||||||
| chr3:99922825
|
G | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0100 | 2 | HG00423.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.64+104782G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99922825 | ||||||
| chr3:99923043
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+105000C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99923043 | ||||||
| chr3:99923219
|
A | T | 4 | a0001c0001t0002g0107a0001c0001t0008g0087a0001c0001t0008g0088others(1): Show | 4 | HG02040.hp1 HG02083.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+105176A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99923219 | ||||||
| chr3:99923960
|
C | T | 22 | a0001c0001t0002g0108a0002c0002t0003g0109a0002c0002t0003g0110others(19): Show | 22 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+105917C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99923960 | ||||||
| chr3:99924022
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+105979A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99924022 | ||||||
| chr3:99924173
|
A | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+106130A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99924173 | ||||||
| chr3:99924332
|
C | T | 80 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(77): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.64+106289C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99924332 | ||||||
| chr3:99924449
|
A | G | 1 | a0001c0001t0005g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.64+106406A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99924449 | ||||||
| chr3:99924723
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+106680C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99924723 | ||||||
| chr3:99924813
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.64+106770C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99924813 | ||||||
| chr3:99924849
|
A | G | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+106806A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99924849 | ||||||
| chr3:99925015
|
T | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+106972T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99925015 | ||||||
| chr3:99925022
|
A | G | 1 | a0001c0001t0004g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.64+106979A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99925022 | ||||||
| chr3:99925579
|
TA | T | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+107544delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99925579 | |||||
| chr3:99925588
|
T | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+107545T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99925588 | ||||||
| chr3:99925652
|
G | A | 2 | a0002c0002t0003g0136a0002c0002t0003g0137 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.64+107609G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99925652 | ||||||
| chr3:99925707
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+107664G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99925707 | ||||||
| chr3:99925900
|
C | T | 1 | a0001c0001t0005g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+107857C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99925900 | ||||||
| chr3:99925935
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.64+107892A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99925935 | ||||||
| chr3:99926372
|
G | A | 72 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(69): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+108329G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926372 | ||||||
| chr3:99926404
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.64+108361T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926404 | ||||||
| chr3:99926537
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+108494A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926537 | ||||||
| chr3:99926625
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+108582T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926625 | ||||||
| chr3:99926655
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+108612G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926655 | ||||||
| chr3:99926705
|
C | T | 1 | a0001c0001t0005g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.64+108662C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926705 | ||||||
| chr3:99926797
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.64+108754G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926797 | ||||||
| chr3:99926856
|
G | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+108813G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926856 | ||||||
| chr3:99926874
|
C | G | 1 | a0001c0001t0002g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.64+108831C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926874 | ||||||
| chr3:99926890
|
T | C | 8 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(5): Show | 8 | HG02280.hp2 HG02559.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+108847T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99926890 | ||||||
| chr3:99927119
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.64+109076A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927119 | ||||||
| chr3:99927531
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+109488G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927531 | ||||||
| chr3:99927588
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.64+109545C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927588 | ||||||
| chr3:99927589
|
G | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+109546G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927589 | ||||||
| chr3:99927597
|
G | T | 1 | a0002c0002t0003g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.64+109554G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927597 | ||||||
| chr3:99927699
|
A | T | 1 | a0001c0001t0005g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+109656A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927699 | ||||||
| chr3:99927722
|
A | AT | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(12): Show | 15 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+109688dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99927722 | |||||
| chr3:99927731
|
T | A | 2 | a0001c0001t0018g0002a0002c0002t0003g0139 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.64+109688T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927731 | ||||||
| chr3:99927732
|
A | T | 3 | a0001c0001t0002g0074a0001c0001t0006g0057a0001c0001t0006g0071 | 3 | HG02280.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+109689A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927732 | ||||||
| chr3:99927924
|
C | T | 2 | a0001c0001t0002g0097a0001c0001t0002g0103 | 2 | HG02129.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.64+109881C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99927924 | ||||||
| chr3:99928022
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.64+109979A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928022 | ||||||
| chr3:99928060
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+110017G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928060 | ||||||
| chr3:99928174
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.64+110131C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928174 | ||||||
| chr3:99928277
|
G | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+110234G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928277 | ||||||
| chr3:99928552
|
G | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+110509G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928552 | ||||||
| chr3:99928565
|
A | G | 2 | a0001c0001t0004g0022a0001c0001t0004g0024 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.64+110522A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928565 | ||||||
| chr3:99928770
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+110727A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928770 | ||||||
| chr3:99928926
|
C | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0203others(1): Show | 4 | HG03654.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+110883C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928926 | ||||||
| chr3:99928929
|
C | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+110886C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928929 | ||||||
| chr3:99928994
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+110951C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99928994 | ||||||
| chr3:99929006
|
G | A | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.64+110963G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99929006 | ||||||
| chr3:99929164
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+111121A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99929164 | ||||||
| chr3:99929287
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+111244G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99929287 | ||||||
| chr3:99929513
|
A | AGT | 24 | a0001c0001t0001g0200a0001c0001t0002g0047a0001c0001t0002g0049others(21): Show | 24 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.64+111497_64+11149 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99929513 | |||||
| chr3:99929513
|
A | AGTGT | 80 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0054others(77): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.64+111495_64+11149 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99929513 | |||||
| chr3:99929513
|
A | AGTGTGT | 7 | a0001c0001t0001g0070a0001c0001t0002g0103a0001c0001t0002g0147others(4): Show | 7 | HG00738.hp2 HG00741.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+111493_64+11149 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99929513 | |||||
| chr3:99929513
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0097 | 3 | HG02129.hp1 HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64+111491_64+11149 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99929513 | |||||
| chr3:99929513
|
AGT | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0224a0001c0001t0002g0209others(1): Show | 4 | HG03017.hp1 HG03927.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+111497_64+11149 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99929513 | |||||
| chr3:99929513
|
AGTGT | A | 5 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0001t0005g0177others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+111495_64+11149 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99929513 | |||||
| chr3:99929513
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+111487_64+11149 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99929513 | |||||
| chr3:99929653
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+111610A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99929653 | ||||||
| chr3:99929702
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.64+111659C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99929702 | ||||||
| chr3:99929716
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+111673G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99929716 | ||||||
| chr3:99929748
|
G | A | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64+111705G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99929748 | ||||||
| chr3:99930162
|
T | G | 1 | a0001c0001t0002g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.64+112119T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99930162 | ||||||
| chr3:99930198
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+112155C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99930198 | ||||||
| chr3:99930542
|
T | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+112499T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99930542 | ||||||
| chr3:99930555
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64+112512A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99930555 | ||||||
| chr3:99930740
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+112697A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99930740 | ||||||
| chr3:99930806
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64+112763A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99930806 | ||||||
| chr3:99930875
|
G | A | 1 | a0001c0001t0007g0032 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+112832G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99930875 | ||||||
| chr3:99931366
|
C | CTTAAG | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+113324_64+11332 others(9): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99931366 | |||||
| chr3:99931373
|
C | T | 23 | a0001c0001t0001g0069a0001c0001t0002g0048a0001c0001t0002g0054others(20): Show | 23 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+113330C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99931373 | ||||||
| chr3:99931383
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.64+113340A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99931383 | ||||||
| chr3:99931431
|
C | G | 1 | a0001c0001t0004g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64+113388C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99931431 | ||||||
| chr3:99931472
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+113429A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99931472 | ||||||
| chr3:99931718
|
G | A | 1 | a0001c0001t0004g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.64+113675G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99931718 | ||||||
| chr3:99931990
|
A | C | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64+113947A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99931990 | ||||||
| chr3:99932248
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+114205C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99932248 | ||||||
| chr3:99932518
|
A | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+114475A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99932518 | ||||||
| chr3:99932848
|
G | A | 6 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0112others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+114805G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99932848 | ||||||
| chr3:99932862
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+114819C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99932862 | ||||||
| chr3:99933116
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.64+115073C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99933116 | ||||||
| chr3:99933180
|
C | T | 18 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0011others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+115137C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99933180 | ||||||
| chr3:99933248
|
T | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+115205T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99933248 | ||||||
| chr3:99933279
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.64+115236A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99933279 | ||||||
| chr3:99933426
|
G | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+115383G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99933426 | ||||||
| chr3:99933567
|
A | C | 1 | a0001c0001t0002g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.64+115524A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99933567 | ||||||
| chr3:99933733
|
C | G | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+115690C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99933733 | ||||||
| chr3:99934272
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+116229G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99934272 | ||||||
| chr3:99934488
|
G | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+116445G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99934488 | ||||||
| chr3:99934564
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+116521C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99934564 | ||||||
| chr3:99934656
|
T | A | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(12): Show | 15 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+116613T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99934656 | ||||||
| chr3:99935016
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+116973G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935016 | ||||||
| chr3:99935265
|
C | CA | 229 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.64+117235dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99935265 | |||||
| chr3:99935339
|
T | A | 31 | a0001c0001t0001g0069a0001c0001t0002g0048a0001c0001t0002g0049others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+117296T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935339 | ||||||
| chr3:99935350
|
G | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+117307G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935350 | ||||||
| chr3:99935383
|
C | G | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+117340C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935383 | ||||||
| chr3:99935435
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+117392C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935435 | ||||||
| chr3:99935517
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+117474G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935517 | ||||||
| chr3:99935550
|
G | T | 2 | a0001c0001t0002g0072a0001c0001t0002g0073 | 2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.64+117507G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935550 | ||||||
| chr3:99935666
|
G | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+117623G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935666 | ||||||
| chr3:99935788
|
A | G | 4 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+117745A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935788 | ||||||
| chr3:99935973
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+117930T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99935973 | ||||||
| chr3:99936369
|
C | CT | 46 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0157others(43): Show | 46 | HG00423.hp1 HG01069.hp1 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.64+118350dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936369 | |||||
| chr3:99936385
|
T | C | 2 | a0002c0002t0003g0001a0002c0002t0003g0135 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.64+118342T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99936385 | ||||||
| chr3:99936415
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | NA19009.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.64+118372G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99936415 | ||||||
| chr3:99936424
|
A | G | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64+118381A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99936424 | ||||||
| chr3:99936540
|
T | TAATTGTT others(322): Show |
1 | a0001c0001t0002g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64+118501_64+11850 others(333): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(304): Show |
2 | a0001c0001t0001g0197a0002c0002t0019g0012 | 2 | NA18973.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.64+118512_64+11851 others(315): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(308): Show |
2 | a0001c0001t0001g0069a0001c0001t0002g0077 | 2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.64+118512_64+11851 others(319): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(309): Show |
1 | a0001c0001t0002g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.64+118512_64+11851 others(320): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(309): Show |
1 | a0001c0001t0002g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64+118512_64+11851 others(320): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(317): Show |
2 | a0001c0001t0005g0084a0001c0001t0006g0057 | 2 | HG02280.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.64+118512_64+11851 others(328): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(318): Show |
2 | a0001c0001t0001g0205a0001c0001t0006g0071 | 2 | HG01192.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+118512_64+11851 others(329): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(319): Show |
4 | a0001c0001t0001g0192a0001c0001t0002g0048a0001c0001t0005g0082others(1): Show | 4 | HG02015.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+118512_64+11851 others(330): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(320): Show |
9 | a0001c0001t0002g0045a0001c0001t0002g0054a0001c0001t0002g0061others(6): Show | 9 | HG01516.hp1 HG02040.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+118512_64+11851 others(331): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(320): Show |
1 | a0001c0001t0004g0015 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.64+118512_64+11851 others(331): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(321): Show |
25 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0034others(22): Show | 25 | HG01168.hp1 HG01952.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.64+118512_64+11851 others(332): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(322): Show |
34 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0038others(31): Show | 34 | HG01168.hp2 HG01257.hp1 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+118512_64+11851 others(333): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(322): Show |
1 | a0001c0001t0001g0008 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.64+118512_64+11851 others(333): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(322): Show |
1 | a0001c0001t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64+118512_64+11851 others(333): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(323): Show |
33 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0166others(30): Show | 33 | HG00280.hp2 HG00423.hp1 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.64+118512_64+11851 others(334): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(323): Show |
1 | a0001c0001t0001g0037 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.64+118512_64+11851 others(334): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(324): Show |
21 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0001t0001g0183others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.64+118512_64+11851 others(335): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(325): Show |
5 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0193others(2): Show | 5 | HG01256.hp1 HG01261.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+118512_64+11851 others(336): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(326): Show |
2 | a0001c0001t0001g0227a0001c0001t0021g0018 | 2 | HG01071.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.64+118512_64+11851 others(337): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(327): Show |
1 | a0001c0001t0001g0196 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.64+118512_64+11851 others(338): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(328): Show |
1 | a0001c0001t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.64+118512_64+11851 others(339): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936540
|
T | TAATTTTT others(332): Show |
1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+118512_64+11851 others(343): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99936540 | |||||
| chr3:99936842
|
T | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+118799T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99936842 | ||||||
| chr3:99937083
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.64+119040G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99937083 | ||||||
| chr3:99937375
|
ATTGT | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.64+119335_64+11933 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99937375 | |||||
| chr3:99937692
|
G | A | 1 | a0002c0002t0003g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.64+119649G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99937692 | ||||||
| chr3:99937771
|
A | G | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+119728A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99937771 | ||||||
| chr3:99938000
|
A | T | 3 | a0001c0001t0002g0074a0001c0001t0006g0057a0001c0001t0006g0071 | 3 | HG02280.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+119957A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938000 | ||||||
| chr3:99938050
|
A | AGT | 32 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0095others(29): Show | 32 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.64+120031_64+12003 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938050 | |||||
| chr3:99938050
|
A | AGTGT | 6 | a0001c0001t0002g0094a0001c0001t0002g0098a0001c0001t0002g0104others(3): Show | 6 | HG00280.hp1 HG01261.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+120029_64+12003 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938050 | |||||
| chr3:99938050
|
AGT | A | 7 | a0001c0001t0001g0157a0001c0001t0001g0182a0001c0001t0001g0198others(4): Show | 7 | HG02717.hp2 HG03225.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+120031_64+12003 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938050 | |||||
| chr3:99938050
|
AGTGT | A | 2 | a0001c0001t0001g0216a0002c0002t0019g0012 | 2 | NA18980.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.64+120029_64+12003 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938050 | |||||
| chr3:99938050
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0005g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+120021_64+12003 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938050 | |||||
| chr3:99938068
|
TGTGTGTG others(1): Show |
T | 7 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0002g0078others(4): Show | 7 | HG01975.hp2 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+120027_64+12003 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938068 | |||||
| chr3:99938070
|
TGTGTGC | T | 3 | a0001c0001t0006g0057a0001c0001t0010g0055a0001c0001t0010g0056 | 3 | HG02257.hp1 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.64+120029_64+12003 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938070 | |||||
| chr3:99938072
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+120029T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938072 | ||||||
| chr3:99938072
|
TGTGC | T | 97 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0034others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.64+120031_64+12003 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938072 | |||||
| chr3:99938074
|
T | C | 5 | a0001c0001t0001g0165a0001c0001t0005g0082a0001c0001t0005g0083others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+120031T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938074 | ||||||
| chr3:99938074
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+120032_64+12003 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938074 | |||||
| chr3:99938074
|
TGC | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0039others(24): Show | 27 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.64+120047_64+12004 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938074 | |||||
| chr3:99938074
|
TGCGC | T | 3 | a0001c0001t0002g0049a0001c0001t0004g0023a0001c0001t0004g0028 | 3 | HG01168.hp1 HG02895.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.64+120045_64+12004 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938074 | |||||
| chr3:99938076
|
C | T | 58 | a0001c0001t0001g0038a0001c0001t0001g0070a0001c0001t0001g0102others(55): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.64+120033C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938076 | ||||||
| chr3:99938078
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0011g0169 | 3 | HG02809.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.64+120035C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938078 | ||||||
| chr3:99938082
|
CGCGCGCG others(3): Show |
C | 1 | a0001c0001t0015g0230 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.64+120042_64+12005 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99938082 | |||||
| chr3:99938086
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+120043C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938086 | ||||||
| chr3:99938091
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+120048G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938091 | ||||||
| chr3:99938238
|
C | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+120195C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938238 | ||||||
| chr3:99938361
|
A | G | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+120318A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938361 | ||||||
| chr3:99938698
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64+120655T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938698 | ||||||
| chr3:99938863
|
C | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+120820C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99938863 | ||||||
| chr3:99939065
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+121022A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99939065 | ||||||
| chr3:99939078
|
G | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.64+121035G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99939078 | ||||||
| chr3:99939417
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+121374T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99939417 | ||||||
| chr3:99939707
|
T | G | 1 | a0001c0001t0004g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.64+121664T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99939707 | ||||||
| chr3:99939858
|
C | G | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+121815C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99939858 | ||||||
| chr3:99940048
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0016g0195 | 2 | HG01981.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.64+122005C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99940048 | ||||||
| chr3:99940189
|
A | G | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | HG02015.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.64+122146A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99940189 | ||||||
| chr3:99940303
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.64+122260A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99940303 | ||||||
| chr3:99940674
|
G | A | 22 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+122631G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99940674 | ||||||
| chr3:99941200
|
T | C | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | HG02015.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.64+123157T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99941200 | ||||||
| chr3:99941295
|
C | T | 1 | a0002c0002t0003g0128 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.64+123252C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99941295 | ||||||
| chr3:99941502
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+123459G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99941502 | ||||||
| chr3:99941556
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+123513A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99941556 | ||||||
| chr3:99941736
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+123693A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99941736 | ||||||
| chr3:99941853
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+123810A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99941853 | ||||||
| chr3:99942157
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+124114G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99942157 | ||||||
| chr3:99942160
|
C | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+124117C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99942160 | ||||||
| chr3:99942372
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+124329G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99942372 | ||||||
| chr3:99942560
|
C | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+124517C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99942560 | ||||||
| chr3:99942777
|
C | T | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.64+124734C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99942777 | ||||||
| chr3:99942817
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+124774T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99942817 | ||||||
| chr3:99943069
|
T | C | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | HG00423.hp2 HG02027.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+125026T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99943069 | ||||||
| chr3:99943081
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+125038G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99943081 | ||||||
| chr3:99943119
|
T | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.64+125076T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99943119 | ||||||
| chr3:99943398
|
C | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+125355C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99943398 | ||||||
| chr3:99944736
|
A | G | 1 | a0001c0001t0007g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64+126693A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99944736 | ||||||
| chr3:99944742
|
A | T | 1 | a0001c0001t0006g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64+126699A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99944742 | ||||||
| chr3:99944848
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+126805G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99944848 | ||||||
| chr3:99944851
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+126808G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99944851 | ||||||
| chr3:99945278
|
C | G | 2 | a0001c0001t0002g0099a0001c0001t0002g0105 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.64+127235C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99945278 | ||||||
| chr3:99945554
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.64+127511A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99945554 | ||||||
| chr3:99945813
|
T | A | 1 | a0002c0002t0003g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64+127770T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99945813 | ||||||
| chr3:99945941
|
C | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+127898C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99945941 | ||||||
| chr3:99946314
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64+128271T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99946314 | ||||||
| chr3:99946588
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+128545C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99946588 | ||||||
| chr3:99946677
|
A | C | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+128634A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99946677 | ||||||
| chr3:99946689
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+128646G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99946689 | ||||||
| chr3:99946695
|
T | C | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64+128652T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99946695 | ||||||
| chr3:99946704
|
A | C | 1 | a0001c0001t0002g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64+128661A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99946704 | ||||||
| chr3:99947067
|
G | A | 1 | a0002c0002t0020g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.64+129024G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947067 | ||||||
| chr3:99947134
|
T | C | 1 | a0001c0001t0005g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.64+129091T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947134 | ||||||
| chr3:99947137
|
C | CA | 29 | a0001c0001t0001g0172a0001c0001t0001g0215a0001c0001t0001g0217others(26): Show | 29 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+129114dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99947137 | |||||
| chr3:99947137
|
C | CAA | 129 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(126): Show | 129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.64+129113_64+12911 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99947137 | |||||
| chr3:99947137
|
C | CAAA | 15 | a0001c0001t0001g0031a0001c0001t0001g0198a0001c0001t0001g0221others(12): Show | 15 | HG01516.hp1 HG01975.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.64+129112_64+12911 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99947137 | |||||
| chr3:99947170
|
T | G | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+129127T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947170 | ||||||
| chr3:99947187
|
G | A | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64+129144G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947187 | ||||||
| chr3:99947404
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+129361A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947404 | ||||||
| chr3:99947447
|
C | G | 11 | a0001c0001t0001g0069a0001c0001t0002g0062a0001c0001t0002g0063others(8): Show | 11 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+129404C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947447 | ||||||
| chr3:99947727
|
T | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+129684T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947727 | ||||||
| chr3:99947817
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+129774A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947817 | ||||||
| chr3:99947886
|
A | AT | 22 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+129849dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99947886 | |||||
| chr3:99947957
|
A | G | 1 | a0002c0002t0003g0125 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64+129914A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99947957 | ||||||
| chr3:99948063
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+130020A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99948063 | ||||||
| chr3:99948284
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.64+130241G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99948284 | ||||||
| chr3:99948721
|
G | A | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.64+130678G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99948721 | ||||||
| chr3:99948762
|
G | GAAGGAAA others(10): Show |
1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+130738_64+13075 others(21): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99948762 | |||||
| chr3:99948979
|
A | T | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | HG01934.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.64+130936A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99948979 | ||||||
| chr3:99949118
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+131075G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99949118 | ||||||
| chr3:99949288
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.64+131245A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99949288 | ||||||
| chr3:99949493
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.64+131450C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99949493 | ||||||
| chr3:99949511
|
A | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+131468A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99949511 | ||||||
| chr3:99949521
|
C | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+131478C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99949521 | ||||||
| chr3:99949980
|
C | A | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64+131937C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99949980 | ||||||
| chr3:99950155
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+132112G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99950155 | ||||||
| chr3:99950248
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+132205G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99950248 | ||||||
| chr3:99950442
|
G | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+132399G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99950442 | ||||||
| chr3:99950655
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+132612G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99950655 | ||||||
| chr3:99950705
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+132662C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99950705 | ||||||
| chr3:99951405
|
G | A | 3 | a0001c0001t0007g0029a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+133362G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99951405 | ||||||
| chr3:99951783
|
T | C | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64+133740T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99951783 | ||||||
| chr3:99951929
|
T | C | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+133886T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99951929 | ||||||
| chr3:99952020
|
A | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+133977A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952020 | ||||||
| chr3:99952052
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.64+134009C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952052 | ||||||
| chr3:99952139
|
G | T | 31 | a0001c0001t0001g0069a0001c0001t0002g0048a0001c0001t0002g0049others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+134096G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952139 | ||||||
| chr3:99952356
|
T | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+134313T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952356 | ||||||
| chr3:99952380
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+134337C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952380 | ||||||
| chr3:99952396
|
G | T | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+134353G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952396 | ||||||
| chr3:99952691
|
A | G | 5 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0096others(2): Show | 5 | HG02129.hp1 NA18954.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+134648A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952691 | ||||||
| chr3:99952803
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+134760G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952803 | ||||||
| chr3:99952858
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64+134815G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952858 | ||||||
| chr3:99952995
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+134952G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99952995 | ||||||
| chr3:99953004
|
G | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.64+134961G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99953004 | ||||||
| chr3:99953047
|
GA | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+135006delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99953047 | |||||
| chr3:99953430
|
T | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+135387T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99953430 | ||||||
| chr3:99953586
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.64+135543A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99953586 | ||||||
| chr3:99953685
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+135642C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99953685 | ||||||
| chr3:99953767
|
C | G | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.64+135724C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99953767 | ||||||
| chr3:99954072
|
A | T | 1 | a0002c0002t0003g0128 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.64+136029A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99954072 | ||||||
| chr3:99954337
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+136294C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99954337 | ||||||
| chr3:99954474
|
G | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+136431G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99954474 | ||||||
| chr3:99954617
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+136574G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99954617 | ||||||
| chr3:99954655
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+136612G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99954655 | ||||||
| chr3:99954803
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+136760G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99954803 | ||||||
| chr3:99954835
|
G | GA | 19 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0093others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.64+136802dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99954835 | |||||
| chr3:99954990
|
C | G | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+136947C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99954990 | ||||||
| chr3:99955021
|
A | G | 4 | a0002c0002t0003g0110a0002c0002t0003g0112a0002c0002t0003g0114others(1): Show | 4 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+136978A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99955021 | ||||||
| chr3:99955241
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+137198C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99955241 | ||||||
| chr3:99955249
|
G | A | 151 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.64+137206G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99955249 | ||||||
| chr3:99955322
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64+137279A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99955322 | ||||||
| chr3:99955392
|
G | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG03654.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.64+137349G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99955392 | ||||||
| chr3:99955594
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.64+137551G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99955594 | ||||||
| chr3:99956185
|
A | G | 8 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+138142A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956185 | ||||||
| chr3:99956216
|
C | T | 11 | a0001c0001t0001g0069a0001c0001t0002g0062a0001c0001t0002g0063others(8): Show | 11 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+138173C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956216 | ||||||
| chr3:99956273
|
C | G | 1 | a0001c0001t0002g0096 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.64+138230C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956273 | ||||||
| chr3:99956337
|
C | A | 20 | a0001c0001t0001g0069a0001c0001t0002g0054a0001c0001t0002g0058others(17): Show | 20 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.64+138294C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956337 | ||||||
| chr3:99956600
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+138557G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956600 | ||||||
| chr3:99956676
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+138633T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956676 | ||||||
| chr3:99956921
|
G | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+138878G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956921 | ||||||
| chr3:99956969
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.64+138926A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99956969 | ||||||
| chr3:99957116
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+139073A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957116 | ||||||
| chr3:99957281
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+139238G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957281 | ||||||
| chr3:99957443
|
C | CAT | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+139403_64+13940 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957443 | |||||
| chr3:99957463
|
T | G | 8 | a0001c0001t0001g0070a0001c0001t0002g0066a0001c0001t0002g0096others(5): Show | 8 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+139420T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957463 | ||||||
| chr3:99957540
|
G | A | 231 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.64+139497G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957540 | ||||||
| chr3:99957627
|
C | T | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+139584C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957627 | ||||||
| chr3:99957693
|
C | CT | 23 | a0001c0001t0001g0102a0001c0001t0002g0090a0001c0001t0002g0091others(20): Show | 24 | HG00423.hp2 HG00738.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.64+139678dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTT | 7 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0006g0004others(4): Show | 7 | HG02027.hp1 HG02109.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+139677_64+13967 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTCTTT others(8): Show |
1 | a0001c0001t0010g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64+139653_64+13965 others(19): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTCTTT others(10): Show |
1 | a0001c0001t0010g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.64+139653_64+13965 others(21): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT | 5 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0149others(2): Show | 5 | HG00738.hp2 HG01346.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+139672_64+13967 others(11): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0150a0001c0001t0002g0152a0001c0001t0002g0156others(3): Show | 6 | HG00741.hp1 HG01256.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+139670_64+13967 others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0001t0002g0048others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+139669_64+13967 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(4): Show |
19 | a0001c0001t0001g0176a0001c0001t0001g0200a0001c0001t0001g0219others(16): Show | 19 | HG00280.hp2 HG01071.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+139668_64+13967 others(15): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(5): Show |
31 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0037others(28): Show | 31 | HG00323.hp1 HG01123.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+139667_64+13967 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(6): Show |
39 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0035others(36): Show | 39 | HG00140.hp1 HG01069.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.64+139666_64+13967 others(17): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(7): Show |
22 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0070others(19): Show | 22 | HG01257.hp2 HG01258.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.64+139665_64+13967 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0205a0001c0001t0004g0017a0001c0001t0004g0019others(2): Show | 5 | HG01192.hp1 HG02129.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+139664_64+13967 others(19): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.64+139663_64+13967 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.64+139662_64+13967 others(21): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.64+139661_64+13967 others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0068a0001c0001t0004g0022 | 2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64+139660_64+13967 others(23): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0026 | 3 | HG03490.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.64+139659_64+13967 others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0202others(6): Show | 9 | HG01978.hp1 HG02148.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+139669_64+13967 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0190a0001c0001t0005g0082a0001c0001t0005g0083 | 3 | HG02074.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+139665_64+13967 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957693
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+139664_64+13967 others(19): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99957693 | |||||
| chr3:99957820
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+139777T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957820 | ||||||
| chr3:99957848
|
G | A | 9 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(6): Show | 9 | HG02027.hp2 HG02523.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+139805G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957848 | ||||||
| chr3:99957857
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+139814A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957857 | ||||||
| chr3:99957994
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+139951T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99957994 | ||||||
| chr3:99958059
|
C | CT | 11 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0002g0054others(8): Show | 11 | HG01928.hp1 HG01952.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+140027dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958059 | |||||
| chr3:99958149
|
C | T | 12 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(9): Show | 12 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+140106C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99958149 | ||||||
| chr3:99958203
|
C | CATT | 21 | a0001c0001t0001g0070a0001c0001t0001g0166a0001c0001t0001g0191others(18): Show | 21 | HG00423.hp1 HG01168.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.64+140206_64+14020 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958203
|
C | CATTATT | 2 | a0001c0001t0001g0222a0001c0001t0002g0047 | 2 | HG02257.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.64+140203_64+14020 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958203
|
CATT | C | 106 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(103): Show | 106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.64+140206_64+14020 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958203
|
CATTATT | C | 27 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0165others(24): Show | 27 | HG00140.hp1 HG01192.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.64+140203_64+14020 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958203
|
CATTATTA others(2): Show |
C | 5 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0104others(2): Show | 5 | HG00280.hp1 HG02735.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+140200_64+14020 others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958203
|
CATTATTA others(5): Show |
C | 3 | a0001c0001t0001g0225a0001c0001t0010g0055a0001c0001t0010g0056 | 3 | HG02257.hp1 HG02698.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.64+140197_64+14020 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958203
|
CATTATTA others(8): Show |
C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+140194_64+14020 others(19): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958203
|
CATTATTA others(11): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64+140191_64+14020 others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99958203 | |||||
| chr3:99958286
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+140243A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99958286 | ||||||
| chr3:99958344
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+140301G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99958344 | ||||||
| chr3:99958532
|
G | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+140489G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99958532 | ||||||
| chr3:99958539
|
A | T | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.64+140496A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99958539 | ||||||
| chr3:99958543
|
G | A | 2 | a0002c0002t0003g0136a0002c0002t0003g0137 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.64+140500G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99958543 | ||||||
| chr3:99959646
|
C | A | 103 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(100): Show | 103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.64+141603C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99959646 | ||||||
| chr3:99959646
|
C | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+141603C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99959646 | ||||||
| chr3:99959867
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+141824C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99959867 | ||||||
| chr3:99959991
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+141948G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99959991 | ||||||
| chr3:99960099
|
C | T | 15 | a0001c0001t0002g0013a0001c0001t0004g0011a0001c0001t0004g0014others(12): Show | 15 | HG01516.hp1 HG01975.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+142056C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960099 | ||||||
| chr3:99960336
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+142293A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960336 | ||||||
| chr3:99960345
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.64+142302G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960345 | ||||||
| chr3:99960617
|
G | A | 48 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0186others(45): Show | 48 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.64+142574G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960617 | ||||||
| chr3:99960643
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.64+142600C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960643 | ||||||
| chr3:99960740
|
T | G | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+142697T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960740 | ||||||
| chr3:99960846
|
C | T | 231 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.64+142803C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960846 | ||||||
| chr3:99960910
|
A | G | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.64+142867A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99960910 | ||||||
| chr3:99961242
|
A | G | 174 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.64+143199A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961242 | ||||||
| chr3:99961247
|
T | A | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+143204T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961247 | ||||||
| chr3:99961249
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+143206A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961249 | ||||||
| chr3:99961530
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+143487A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961530 | ||||||
| chr3:99961532
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+143489C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961532 | ||||||
| chr3:99961558
|
C | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+143515C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961558 | ||||||
| chr3:99961615
|
T | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64+143572T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961615 | ||||||
| chr3:99961666
|
G | A | 1 | a0002c0002t0003g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.64+143623G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961666 | ||||||
| chr3:99961711
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.64+143668T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99961711 | ||||||
| chr3:99961909
|
AG | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+143869delG | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99961909 | |||||
| chr3:99962011
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+143968T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962011 | ||||||
| chr3:99962030
|
G | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+143987G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962030 | ||||||
| chr3:99962063
|
A | G | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+144020A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962063 | ||||||
| chr3:99962167
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.64+144124A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962167 | ||||||
| chr3:99962253
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0012g0036 | 3 | HG01346.hp1 HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.64+144210A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962253 | ||||||
| chr3:99962306
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+144263T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962306 | ||||||
| chr3:99962544
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0011others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+144501G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962544 | ||||||
| chr3:99962600
|
T | C | 6 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0001g0213others(3): Show | 6 | HG01978.hp1 HG02148.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+144557T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99962600 | ||||||
| chr3:99963037
|
G | A | 2 | a0001c0001t0006g0057a0001c0001t0006g0071 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.64+144994G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963037 | ||||||
| chr3:99963384
|
T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0204 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.64+145341T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963384 | ||||||
| chr3:99963589
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+145546G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963589 | ||||||
| chr3:99963610
|
A | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0204 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.64+145567A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963610 | ||||||
| chr3:99963661
|
G | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64+145618G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963661 | ||||||
| chr3:99963716
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.64+145673G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963716 | ||||||
| chr3:99963848
|
T | C | 160 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(157): Show | 160 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.64+145805T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963848 | ||||||
| chr3:99963956
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64+145913G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99963956 | ||||||
| chr3:99964353
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+146310G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99964353 | ||||||
| chr3:99964354
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+146311G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99964354 | ||||||
| chr3:99964357
|
T | C | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+146314T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99964357 | ||||||
| chr3:99964358
|
T | C | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+146315T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99964358 | ||||||
| chr3:99964390
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.64+146347T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99964390 | ||||||
| chr3:99964744
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+146701G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99964744 | ||||||
| chr3:99964809
|
C | G | 12 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0130others(9): Show | 13 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+146766C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99964809 | ||||||
| chr3:99965041
|
T | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+146998T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99965041 | ||||||
| chr3:99965329
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+147286G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99965329 | ||||||
| chr3:99965422
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | HG02015.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.64+147379G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99965422 | ||||||
| chr3:99965528
|
ATTTG | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+147495_64+14749 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99965528 | |||||
| chr3:99965947
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.64+147904T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99965947 | ||||||
| chr3:99965964
|
T | C | 53 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0183others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.64+147921T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99965964 | ||||||
| chr3:99966072
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+148029A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99966072 | ||||||
| chr3:99966341
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+148298T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99966341 | ||||||
| chr3:99966614
|
G | A | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(12): Show | 15 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+148571G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99966614 | ||||||
| chr3:99966638
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+148595C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99966638 | ||||||
| chr3:99966842
|
T | A | 196 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.64+148799T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99966842 | ||||||
| chr3:99966886
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+148843C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99966886 | ||||||
| chr3:99967134
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.64+149091T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99967134 | ||||||
| chr3:99967147
|
G | T | 110 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.64+149104G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99967147 | ||||||
| chr3:99967383
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+149340G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99967383 | ||||||
| chr3:99967387
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+149344A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99967387 | ||||||
| chr3:99967612
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64+149569C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99967612 | ||||||
| chr3:99967821
|
A | G | 152 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.64+149778A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99967821 | ||||||
| chr3:99967931
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64+149888T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99967931 | ||||||
| chr3:99968216
|
G | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+150173G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99968216 | ||||||
| chr3:99968428
|
G | GA | 2 | a0001c0001t0001g0037a0001c0001t0004g0017 | 2 | HG02129.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.64+150385_64+15038 others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99968428 | ||||||
| chr3:99968429
|
G | A | 170 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0031others(167): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.64+150386G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99968429 | ||||||
| chr3:99968682
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.64+150639C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99968682 | ||||||
| chr3:99968817
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.64+150774G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99968817 | ||||||
| chr3:99968886
|
A | G | 160 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(157): Show | 160 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.64+150843A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99968886 | ||||||
| chr3:99968968
|
G | GA | 228 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(225): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.64+150934dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99968968 | |||||
| chr3:99969058
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+151015A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99969058 | ||||||
| chr3:99969122
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.64+151079G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99969122 | ||||||
| chr3:99969453
|
T | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+151410T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99969453 | ||||||
| chr3:99969505
|
G | A | 3 | a0001c0001t0002g0048a0001c0001t0002g0072a0001c0001t0002g0073 | 3 | HG02451.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.64+151462G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99969505 | ||||||
| chr3:99969559
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0199 | 2 | HG00323.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.64+151516G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99969559 | ||||||
| chr3:99969747
|
G | A | 2 | a0002c0002t0003g0130a0002c0002t0003g0138 | 2 | HG00741.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.64+151704G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99969747 | ||||||
| chr3:99970132
|
C | T | 89 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.64+152089C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99970132 | ||||||
| chr3:99970133
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+152090G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99970133 | ||||||
| chr3:99970357
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+152314G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99970357 | ||||||
| chr3:99971065
|
T | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0069a0001c0001t0001g0186others(10): Show | 13 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+153022T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971065 | ||||||
| chr3:99971075
|
C | T | 1 | a0002c0002t0003g0128 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.64+153032C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971075 | ||||||
| chr3:99971076
|
G | T | 6 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(3): Show | 6 | HG02109.hp1 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+153033G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971076 | ||||||
| chr3:99971103
|
C | A | 12 | a0001c0001t0001g0069a0001c0001t0001g0189a0001c0001t0002g0062others(9): Show | 12 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+153060C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971103 | ||||||
| chr3:99971104
|
A | G | 12 | a0001c0001t0001g0069a0001c0001t0001g0189a0001c0001t0002g0062others(9): Show | 12 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.64+153061A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971104 | ||||||
| chr3:99971108
|
C | T | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64+153065C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971108 | ||||||
| chr3:99971112
|
C | T | 1 | a0001c0001t0012g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.64+153069C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971112 | ||||||
| chr3:99971120
|
T | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+153077T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971120 | ||||||
| chr3:99971153
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0205others(1): Show | 4 | HG01192.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+153110T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971153 | ||||||
| chr3:99971154
|
G | A | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64+153111G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971154 | ||||||
| chr3:99971269
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0002g0152 | 2 | HG01069.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.64+153226C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971269 | ||||||
| chr3:99971270
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+153227G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971270 | ||||||
| chr3:99971333
|
C | CA | 138 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(135): Show | 138 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.64+153306dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99971333 | |||||
| chr3:99971487
|
T | C | 89 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.64+153444T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971487 | ||||||
| chr3:99971595
|
G | A | 30 | a0001c0001t0001g0069a0001c0001t0002g0048a0001c0001t0002g0049others(27): Show | 30 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.64+153552G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971595 | ||||||
| chr3:99971682
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.64+153639A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971682 | ||||||
| chr3:99971778
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+153735C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971778 | ||||||
| chr3:99971837
|
C | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+153794C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99971837 | ||||||
| chr3:99972109
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64+154066G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972109 | ||||||
| chr3:99972126
|
C | T | 12 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0130others(9): Show | 13 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+154083C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972126 | ||||||
| chr3:99972432
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64+154389G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972432 | ||||||
| chr3:99972541
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64+154498G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972541 | ||||||
| chr3:99972579
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+154536C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972579 | ||||||
| chr3:99972678
|
C | T | 149 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(146): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.64+154635C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972678 | ||||||
| chr3:99972832
|
T | C | 15 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(12): Show | 15 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.64+154789T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972832 | ||||||
| chr3:99972850
|
C | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.64+154807C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99972850 | ||||||
| chr3:99973027
|
C | T | 1 | a0001c0001t0012g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.64+154984C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99973027 | ||||||
| chr3:99973070
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+155027C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99973070 | ||||||
| chr3:99973082
|
T | G | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.64+155039T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99973082 | ||||||
| chr3:99973272
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | NA18969.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.64+155229C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99973272 | ||||||
| chr3:99973414
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+155371A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99973414 | ||||||
| chr3:99973417
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+155374C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99973417 | ||||||
| chr3:99973939
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+155896G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99973939 | ||||||
| chr3:99974141
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+156098A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99974141 | ||||||
| chr3:99974155
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0199 | 2 | HG00323.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.64+156112A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99974155 | ||||||
| chr3:99974448
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64+156405G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99974448 | ||||||
| chr3:99974548
|
A | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+156505A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99974548 | ||||||
| chr3:99974736
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+156693A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99974736 | ||||||
| chr3:99975373
|
G | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.64+157330G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99975373 | ||||||
| chr3:99975446
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+157403G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99975446 | ||||||
| chr3:99975517
|
G | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+157474G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99975517 | ||||||
| chr3:99975585
|
C | CA | 6 | a0001c0001t0001g0031a0001c0001t0001g0171a0001c0001t0001g0221others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+157556dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99975585 | |||||
| chr3:99975919
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64+157876C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99975919 | ||||||
| chr3:99976128
|
G | T | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.64+158085G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976128 | ||||||
| chr3:99976295
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.64+158252G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976295 | ||||||
| chr3:99976382
|
A | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+158339A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976382 | ||||||
| chr3:99976409
|
A | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+158366A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976409 | ||||||
| chr3:99976606
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+158563A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976606 | ||||||
| chr3:99976647
|
T | A | 51 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(48): Show | 51 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(48): Show |
intron_variant | MODIFIER | c.64+158604T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976647 | ||||||
| chr3:99976678
|
T | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+158635T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976678 | ||||||
| chr3:99976705
|
A | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+158662A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976705 | ||||||
| chr3:99976706
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+158663T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99976706 | ||||||
| chr3:99977377
|
C | A | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+159334C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99977377 | ||||||
| chr3:99977426
|
G | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0077 | 2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.64+159383G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99977426 | ||||||
| chr3:99977430
|
G | C | 2 | a0001c0001t0001g0210a0001c0001t0002g0209 | 2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.64+159387G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99977430 | ||||||
| chr3:99977625
|
A | G | 31 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(28): Show | 31 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+159582A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99977625 | ||||||
| chr3:99977782
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+159739T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99977782 | ||||||
| chr3:99977837
|
A | G | 1 | a0001c0001t0005g0177 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+159794A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99977837 | ||||||
| chr3:99978063
|
A | G | 1 | a0001c0001t0004g0015 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.64+160020A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99978063 | ||||||
| chr3:99978066
|
G | C | 18 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0011others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+160023G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99978066 | ||||||
| chr3:99978557
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0002g0041others(23): Show | 26 | HG01168.hp1 HG01516.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.64+160514A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99978557 | ||||||
| chr3:99978608
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+160565G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99978608 | ||||||
| chr3:99978627
|
G | T | 1 | a0002c0002t0003g0125 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64+160584G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99978627 | ||||||
| chr3:99979013
|
A | AGT | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+160973_64+16097 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99979013 | |||||
| chr3:99979171
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64+161128A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99979171 | ||||||
| chr3:99979382
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0018g0002 | 3 | HG01891.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+161339A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99979382 | ||||||
| chr3:99979498
|
C | T | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+161455C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99979498 | ||||||
| chr3:99979753
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+161710G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99979753 | ||||||
| chr3:99979918
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+161875G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99979918 | ||||||
| chr3:99980026
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+161983G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99980026 | ||||||
| chr3:99980111
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.64+162068C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99980111 | ||||||
| chr3:99980122
|
G | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+162079G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99980122 | ||||||
| chr3:99980127
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64+162084A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99980127 | ||||||
| chr3:99980760
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+162717A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99980760 | ||||||
| chr3:99980949
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.64+162906A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99980949 | ||||||
| chr3:99981033
|
G | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+162990G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981033 | ||||||
| chr3:99981112
|
C | T | 1 | a0002c0002t0003g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+163069C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981112 | ||||||
| chr3:99981267
|
T | C | 3 | a0001c0001t0007g0029a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+163224T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981267 | ||||||
| chr3:99981272
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+163229G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981272 | ||||||
| chr3:99981358
|
C | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.64+163315C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981358 | ||||||
| chr3:99981635
|
A | G | 2 | a0001c0001t0002g0097a0001c0001t0002g0103 | 2 | HG02129.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.64+163592A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981635 | ||||||
| chr3:99981704
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+163661A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981704 | ||||||
| chr3:99981739
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01168.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.64+163696G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99981739 | ||||||
| chr3:99982189
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+164146T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982189 | ||||||
| chr3:99982290
|
G | A | 164 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(161): Show | 164 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.64+164247G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982290 | ||||||
| chr3:99982327
|
C | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+164284C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982327 | ||||||
| chr3:99982401
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64+164358G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982401 | ||||||
| chr3:99982486
|
A | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+164443A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982486 | ||||||
| chr3:99982614
|
G | A | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-164359G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982614 | ||||||
| chr3:99982661
|
T | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-164312T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982661 | ||||||
| chr3:99982688
|
T | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-164285T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982688 | ||||||
| chr3:99982753
|
T | G | 1 | a0001c0001t0002g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.65-164220T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982753 | ||||||
| chr3:99982971
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-164002G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99982971 | ||||||
| chr3:99983025
|
TATGAGGG others(19): Show |
T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-163945_65-16392 others(30): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983025 | |||||
| chr3:99983308
|
C | A | 1 | a0002c0002t0003g0122 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.65-163665C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983308 | ||||||
| chr3:99983375
|
AAAAT | A | 15 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0204others(12): Show | 15 | HG01069.hp1 HG01071.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-163584_65-16358 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983375 | |||||
| chr3:99983385
|
A | AAT | 3 | a0001c0001t0001g0171a0001c0001t0001g0175a0001c0001t0001g0197 | 3 | HG02109.hp2 HG03516.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.65-163586_65-16358 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983385 | |||||
| chr3:99983385
|
AATAAAT | A | 65 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0031others(62): Show | 65 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.65-163584_65-16357 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983385 | |||||
| chr3:99983385
|
AATAAATA others(1): Show |
A | 7 | a0001c0001t0001g0021a0001c0001t0002g0013a0001c0001t0004g0022others(4): Show | 7 | HG01975.hp2 HG02622.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-163584_65-16357 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983385 | |||||
| chr3:99983385
|
AATAAATA others(3): Show |
A | 2 | a0001c0001t0001g0191a0001c0001t0001g0196 | 2 | HG00423.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.65-163584_65-16357 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983385 | |||||
| chr3:99983387
|
TAA | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0170a0001c0001t0001g0181others(3): Show | 6 | HG01891.hp1 HG02293.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-163584_65-16358 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983387 | |||||
| chr3:99983389
|
A | AAT | 3 | a0001c0001t0005g0143a0002c0002t0003g0125a0002c0002t0003g0141 | 3 | HG02717.hp1 HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.65-163555_65-16355 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
A | AATATGTA others(3): Show |
1 | a0001c0001t0002g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.65-163580_65-16357 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
A | AATATGTA others(5): Show |
2 | a0001c0001t0002g0073a0001c0001t0002g0080 | 2 | HG02451.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.65-163580_65-16357 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
A | AATATGTA others(7): Show |
3 | a0001c0001t0002g0061a0001c0001t0002g0078a0001c0001t0002g0150 | 3 | HG00741.hp1 NA18980.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.65-163580_65-16357 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
A | AATATGTA others(9): Show |
6 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0145others(3): Show | 6 | HG01256.hp2 HG01346.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-163580_65-16357 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
A | AATATGTA others(11): Show |
4 | a0001c0001t0002g0063a0001c0001t0002g0147a0001c0001t0002g0149others(1): Show | 4 | HG00738.hp2 HG01978.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163580_65-16357 others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
A | AATATGTA others(13): Show |
3 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0153 | 3 | HG01261.hp1 HG01934.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.65-163580_65-16357 others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
A | T | 13 | a0001c0001t0001g0163a0001c0001t0001g0167a0001c0001t0001g0168others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-163584A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983389 | ||||||
| chr3:99983389
|
AAT | A | 36 | a0001c0001t0001g0069a0001c0001t0001g0132a0001c0001t0002g0067others(33): Show | 37 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.65-163555_65-16355 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983389
|
AATAT | A | 16 | a0001c0001t0001g0102a0001c0001t0002g0092a0001c0001t0002g0093others(13): Show | 16 | HG00280.hp1 HG00423.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-163557_65-16355 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983389 | |||||
| chr3:99983392
|
A | ATG | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0054others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-163580_65-16357 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983392 | |||||
| chr3:99983393
|
T | A | 11 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-163580T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983393 | ||||||
| chr3:99983394
|
A | G | 10 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(7): Show | 10 | HG01433.hp1 HG01981.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-163579A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983394 | ||||||
| chr3:99983396
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0002g0067a0001c0001t0002g0068others(1): Show | 4 | HG04184.hp2 HG04199.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163577A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983396 | ||||||
| chr3:99983397
|
T | A | 6 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(3): Show | 6 | HG02809.hp2 HG02895.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-163576T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983397 | ||||||
| chr3:99983401
|
T | A | 4 | a0001c0001t0005g0084a0001c0001t0009g0009a0001c0001t0009g0010others(1): Show | 4 | HG02809.hp2 HG02895.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163572T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983401 | ||||||
| chr3:99983412
|
ATATATAT others(27): Show |
A | 2 | a0001c0001t0001g0163a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.65-163553_65-16352 others(38): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983412 | |||||
| chr3:99983414
|
ATATATGT others(7): Show |
A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-163555_65-16354 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983414 | |||||
| chr3:99983416
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-163557A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983416 | ||||||
| chr3:99983416
|
ATATGTAT others(23): Show |
A | 2 | a0001c0001t0001g0165a0001c0001t0004g0164 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.65-163553_65-16352 others(34): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983416 | |||||
| chr3:99983418
|
A | G | 4 | a0001c0001t0001g0069a0001c0001t0002g0067a0001c0001t0002g0068others(1): Show | 4 | HG04184.hp2 HG04199.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163555A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983418 | ||||||
| chr3:99983418
|
ATG | A | 3 | a0001c0001t0002g0044a0001c0001t0002g0060a0001c0001t0006g0057 | 3 | HG02027.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.65-163553_65-16355 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983418 | |||||
| chr3:99983420
|
G | A | 46 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(43): Show | 46 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(43): Show |
intron_variant | MODIFIER | c.65-163553G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983420 | ||||||
| chr3:99983422
|
A | G | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065others(1): Show | 4 | HG01934.hp2 HG01978.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-163551A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983422 | ||||||
| chr3:99983424
|
G | A | 25 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(22): Show | 25 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.65-163549G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983424 | ||||||
| chr3:99983426
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-163547A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983426 | ||||||
| chr3:99983426
|
ATG | A | 4 | a0001c0001t0001g0069a0001c0001t0002g0067a0001c0001t0002g0068others(1): Show | 4 | HG04184.hp2 HG04199.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163545_65-16354 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983426 | |||||
| chr3:99983428
|
G | A | 22 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0044others(19): Show | 22 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-163545G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983428 | ||||||
| chr3:99983428
|
G | GTA | 23 | a0001c0001t0002g0058a0001c0001t0002g0061a0001c0001t0002g0063others(20): Show | 23 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.65-163543_65-16354 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983428 | |||||
| chr3:99983430
|
ATGTATAT others(9): Show |
A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-163541_65-16352 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983430 | |||||
| chr3:99983431
|
T | C | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.65-163542T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983431 | ||||||
| chr3:99983432
|
G | A | 19 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0046others(16): Show | 19 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-163541G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983432 | ||||||
| chr3:99983432
|
GTA | G | 3 | a0001c0001t0002g0074a0001c0001t0005g0082a0001c0001t0006g0003 | 3 | HG03139.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.65-163533_65-16353 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983432 | |||||
| chr3:99983432
|
GTATATAT others(37): Show |
G | 1 | a0001c0001t0007g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.65-163531_65-16348 others(48): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983432 | |||||
| chr3:99983434
|
A | G | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-163539A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983434 | ||||||
| chr3:99983434
|
ATATATAT others(1): Show |
A | 2 | a0001c0001t0002g0043a0001c0001t0002g0045 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.65-163535_65-16352 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983434 | |||||
| chr3:99983436
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-163537A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983436 | ||||||
| chr3:99983438
|
A | G | 9 | a0001c0001t0002g0074a0001c0001t0005g0082a0001c0001t0005g0084others(6): Show | 9 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-163535A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983438 | ||||||
| chr3:99983440
|
A | G | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.65-163533A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983440 | ||||||
| chr3:99983440
|
ATGTATG | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-163531_65-16352 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983440 | |||||
| chr3:99983442
|
G | A | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.65-163531G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983442 | ||||||
| chr3:99983446
|
G | A | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-163527G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983446 | ||||||
| chr3:99983446
|
GTATATAT others(15): Show |
G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-163513_65-16349 others(26): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983446 | |||||
| chr3:99983446
|
GTATATAT others(33): Show |
G | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.65-163513_65-16347 others(44): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983446 | |||||
| chr3:99983446
|
GTATATAT others(35): Show |
G | 55 | a0001c0001t0001g0171a0001c0001t0001g0183a0001c0001t0001g0185others(52): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.65-163513_65-16347 others(46): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983446 | |||||
| chr3:99983446
|
GTATATAT others(37): Show |
G | 48 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 48 | HG01069.hp1 HG01168.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.65-163513_65-16347 others(48): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983446 | |||||
| chr3:99983448
|
A | G | 1 | a0002c0002t0003g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.65-163525A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983448 | ||||||
| chr3:99983449
|
T | C | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-163524T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983449 | ||||||
| chr3:99983450
|
A | ATG | 12 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0046others(9): Show | 12 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-163522_65-16352 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983450 | |||||
| chr3:99983450
|
A | G | 2 | a0001c0001t0005g0084a0001c0001t0006g0057 | 2 | HG02280.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.65-163523A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983450 | ||||||
| chr3:99983452
|
A | G | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-163521A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983452 | ||||||
| chr3:99983454
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-163519A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983454 | ||||||
| chr3:99983456
|
A | ATATATGT others(1): Show |
2 | a0001c0001t0002g0152a0001c0001t0002g0154 | 2 | HG01346.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.65-163514_65-16351 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983456 | |||||
| chr3:99983456
|
A | G | 9 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0002g0074others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-163517A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983456 | ||||||
| chr3:99983456
|
ATATGTG | A | 2 | a0002c0002t0003g0128a0002c0002t0003g0129 | 2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.65-163515_65-16351 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983456 | |||||
| chr3:99983458
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.65-163515A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983458 | ||||||
| chr3:99983458
|
ATG | A | 6 | a0001c0001t0002g0108a0001c0001t0002g0140a0002c0002t0003g0109others(3): Show | 6 | HG01123.hp2 HG02055.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-163509_65-16350 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983458 | |||||
| chr3:99983458
|
ATGTGTG | A | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-163513_65-16350 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983458 | |||||
| chr3:99983460
|
G | A | 33 | a0001c0001t0001g0069a0001c0001t0001g0163a0001c0001t0001g0165others(30): Show | 33 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.65-163513G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983460 | ||||||
| chr3:99983460
|
GTGTGTAT others(9): Show |
G | 1 | a0001c0001t0002g0093 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.65-163511_65-16349 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983460 | |||||
| chr3:99983460
|
GTGTGTAT others(15): Show |
G | 14 | a0001c0001t0001g0102a0001c0001t0002g0094a0001c0001t0002g0095others(11): Show | 14 | HG00280.hp1 HG00423.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-163511_65-16349 others(26): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983460 | |||||
| chr3:99983460
|
GTGTGTAT others(17): Show |
G | 4 | a0001c0001t0002g0092a0001c0001t0002g0097a0001c0001t0002g0103others(1): Show | 4 | HG02129.hp1 HG03041.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163511_65-16348 others(28): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983460 | |||||
| chr3:99983460
|
GTGTGTAT others(19): Show |
G | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0005g0084 | 3 | HG02015.hp2 HG02071.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.65-163511_65-16348 others(30): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983460 | |||||
| chr3:99983460
|
GTGTGTAT others(23): Show |
G | 1 | a0001c0001t0005g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.65-163511_65-16348 others(34): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983460 | |||||
| chr3:99983462
|
G | A | 25 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0002g0041others(22): Show | 25 | HG01257.hp1 HG01258.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.65-163511G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983462 | ||||||
| chr3:99983462
|
G | GTA | 7 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(4): Show | 7 | HG00741.hp2 HG02895.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-163510_65-16350 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983462 | |||||
| chr3:99983462
|
G | GTATATAT others(21): Show |
1 | a0002c0002t0003g0114 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.65-163510_65-16350 others(32): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983462 | |||||
| chr3:99983462
|
GTGTA | G | 6 | a0001c0001t0002g0067a0002c0002t0003g0001a0002c0002t0003g0113others(3): Show | 7 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-163509_65-16350 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983462 | |||||
| chr3:99983462
|
GTGTATA | G | 5 | a0001c0001t0002g0068a0002c0002t0003g0118a0002c0002t0003g0125others(2): Show | 5 | HG02293.hp2 HG03927.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-163509_65-16350 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983462 | |||||
| chr3:99983462
|
GTGTATAT others(3): Show |
G | 1 | a0002c0002t0003g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.65-163509_65-16350 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983462 | |||||
| chr3:99983462
|
GTGTATAT others(19): Show |
G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-163509_65-16348 others(30): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983462 | |||||
| chr3:99983464
|
G | A | 23 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(20): Show | 23 | HG00323.hp2 HG00741.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.65-163509G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983464 | ||||||
| chr3:99983464
|
G | GTATGTGT others(3): Show |
1 | a0001c0001t0002g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.65-163506_65-16350 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983464 | |||||
| chr3:99983464
|
GTA | G | 4 | a0001c0001t0002g0078a0001c0001t0002g0081a0001c0001t0002g0156others(1): Show | 4 | HG01256.hp2 HG03492.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163465_65-16346 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983464 | |||||
| chr3:99983464
|
GTATA | G | 2 | a0001c0001t0001g0132a0001c0001t0002g0080 | 2 | HG01433.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.65-163467_65-16346 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983464 | |||||
| chr3:99983464
|
GTATATA | G | 2 | a0002c0002t0003g0121a0002c0002t0003g0124 | 2 | NA18964.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.65-163469_65-16346 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983464 | |||||
| chr3:99983464
|
GTATATAT others(1): Show |
G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-163471_65-16346 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983464 | |||||
| chr3:99983466
|
A | ATG | 5 | a0001c0001t0001g0069a0001c0001t0002g0058a0001c0001t0002g0077others(2): Show | 5 | HG02738.hp2 HG03139.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-163506_65-16350 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983466 | |||||
| chr3:99983466
|
A | ATGTG | 6 | a0001c0001t0002g0061a0001c0001t0002g0066a0001c0001t0002g0146others(3): Show | 6 | HG00741.hp1 HG01261.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-163506_65-16350 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983466 | |||||
| chr3:99983466
|
A | ATGTGTG | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | HG01934.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.65-163506_65-16350 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983466 | |||||
| chr3:99983466
|
A | G | 12 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(9): Show | 12 | HG01943.hp1 HG02109.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-163507A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983466 | ||||||
| chr3:99983468
|
A | G | 14 | a0001c0001t0001g0069a0001c0001t0001g0163a0001c0001t0001g0165others(11): Show | 14 | HG01891.hp2 HG02559.hp1 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-163505A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983468 | ||||||
| chr3:99983470
|
A | G | 11 | a0001c0001t0001g0069a0001c0001t0002g0067a0001c0001t0002g0072others(8): Show | 11 | HG01256.hp2 HG02280.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-163503A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983470 | ||||||
| chr3:99983472
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0054a0001c0001t0002g0059 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.65-163494_65-16349 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983472 | |||||
| chr3:99983472
|
A | G | 13 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0002g0067others(10): Show | 13 | HG01256.hp2 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-163501A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983472 | ||||||
| chr3:99983474
|
A | ATATATGT others(7): Show |
1 | a0001c0001t0002g0060 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.65-163494_65-16349 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983474 | |||||
| chr3:99983474
|
A | ATGTGTG | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-163498_65-16349 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983474 | |||||
| chr3:99983474
|
A | G | 4 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0080others(1): Show | 4 | HG03139.hp2 HG04184.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-163499A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983474 | ||||||
| chr3:99983476
|
A | ATATGTGT others(5): Show |
1 | a0001c0001t0002g0079 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.65-163494_65-16349 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983476 | |||||
| chr3:99983476
|
A | ATATGTGT others(7): Show |
3 | a0001c0001t0002g0062a0001c0001t0002g0075a0001c0001t0002g0076 | 3 | HG01257.hp1 HG01258.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.65-163494_65-16349 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983476 | |||||
| chr3:99983476
|
A | G | 16 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0002g0043others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-163497A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983476 | ||||||
| chr3:99983478
|
A | ATGTG | 5 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0046others(2): Show | 5 | HG01952.hp1 HG02257.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-163494_65-16349 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983478 | |||||
| chr3:99983478
|
A | G | 11 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(8): Show | 11 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-163495A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983478 | ||||||
| chr3:99983480
|
A | G | 4 | a0001c0001t0002g0074a0001c0001t0006g0003a0001c0001t0010g0055others(1): Show | 4 | HG02257.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-163493A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983480 | ||||||
| chr3:99983482
|
A | G | 9 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG01952.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-163491A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983482 | ||||||
| chr3:99983484
|
A | G | 10 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(7): Show | 10 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-163489A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983484 | ||||||
| chr3:99983486
|
A | G | 7 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0002g0073others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-163487A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983486 | ||||||
| chr3:99983488
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-163485A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983488 | ||||||
| chr3:99983490
|
A | G | 59 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0001g0183others(56): Show | 59 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.65-163483A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983490 | ||||||
| chr3:99983492
|
A | G | 9 | a0001c0001t0001g0031a0001c0001t0001g0212a0001c0001t0002g0013others(6): Show | 9 | HG01516.hp1 HG01975.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-163481A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983492 | ||||||
| chr3:99983494
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-163479A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983494 | ||||||
| chr3:99983495
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-163478T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983495 | ||||||
| chr3:99983496
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.65-163477A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983496 | ||||||
| chr3:99983500
|
A | ATGTGTAT others(3): Show |
1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-163472_65-16347 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983500 | |||||
| chr3:99983506
|
A | G | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.65-163467A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983506 | ||||||
| chr3:99983510
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0018g0002 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.65-163463G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983510 | ||||||
| chr3:99983512
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-163461A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983512 | ||||||
| chr3:99983544
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-163429G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983544 | ||||||
| chr3:99983564
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.65-163409C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983564 | ||||||
| chr3:99983613
|
C | T | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-163360C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983613 | ||||||
| chr3:99983615
|
G | A | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.65-163358G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983615 | ||||||
| chr3:99983689
|
CA | C | 6 | a0001c0001t0002g0066a0001c0001t0006g0003a0001c0001t0006g0004others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-163270delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99983689 | |||||
| chr3:99983770
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-163203A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983770 | ||||||
| chr3:99983795
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-163178G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983795 | ||||||
| chr3:99983888
|
C | G | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-163085C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99983888 | ||||||
| chr3:99984048
|
A | ATGTGTGT others(11): Show |
6 | a0001c0001t0001g0211a0001c0001t0002g0053a0001c0001t0002g0060others(3): Show | 6 | HG02027.hp2 HG02738.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-162922_65-16292 others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984048 | |||||
| chr3:99984048
|
A | ATGTGTGT others(13): Show |
34 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0165others(31): Show | 34 | HG01168.hp1 HG01192.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.65-162922_65-16292 others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984048 | |||||
| chr3:99984048
|
A | ATGTGTGT others(15): Show |
96 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(93): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.65-162922_65-16292 others(26): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984048 | |||||
| chr3:99984048
|
A | ATGTGTGT others(17): Show |
18 | a0001c0001t0001g0069a0001c0001t0001g0158a0001c0001t0001g0160others(15): Show | 18 | HG01257.hp1 HG01258.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-162922_65-16292 others(28): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984048 | |||||
| chr3:99984048
|
A | ATGTGTGT others(19): Show |
7 | a0001c0001t0001g0170a0001c0001t0002g0065a0001c0001t0002g0067others(4): Show | 7 | HG01934.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-162922_65-16292 others(30): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984048 | |||||
| chr3:99984048
|
A | ATGTGTGT others(25): Show |
1 | a0001c0001t0001g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65-162922_65-16292 others(36): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984048 | |||||
| chr3:99984052
|
A | ATGTGTGT others(9): Show |
3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-162914_65-16291 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984052 | |||||
| chr3:99984052
|
A | ATGTGTGT others(11): Show |
6 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-162914_65-16291 others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984052 | |||||
| chr3:99984052
|
A | G | 164 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(161): Show | 164 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.65-162921A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99984052 | ||||||
| chr3:99984060
|
T | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-162913T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99984060 | ||||||
| chr3:99984062
|
G | GTGTGTGT others(13): Show |
2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-162896_65-16289 others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99984062 | |||||
| chr3:99984156
|
T | A | 1 | a0001c0001t0005g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-162817T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99984156 | ||||||
| chr3:99984342
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.65-162631A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99984342 | ||||||
| chr3:99984414
|
T | A | 42 | a0001c0001t0001g0069a0001c0001t0002g0041a0001c0001t0002g0042others(39): Show | 42 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.65-162559T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99984414 | ||||||
| chr3:99984573
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-162400A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99984573 | ||||||
| chr3:99984690
|
G | C | 1 | a0001c0001t0012g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-162283G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99984690 | ||||||
| chr3:99985071
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.65-161902G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985071 | ||||||
| chr3:99985131
|
G | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-161842G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985131 | ||||||
| chr3:99985169
|
C | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-161804C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985169 | ||||||
| chr3:99985269
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.65-161704C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985269 | ||||||
| chr3:99985594
|
C | CT | 13 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(10): Show | 13 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-161367dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99985594 | |||||
| chr3:99985809
|
G | A | 1 | a0001c0001t0007g0032 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-161164G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985809 | ||||||
| chr3:99985844
|
C | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-161129C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985844 | ||||||
| chr3:99985868
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-161105C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985868 | ||||||
| chr3:99985883
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.65-161090C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985883 | ||||||
| chr3:99985909
|
TCTGTTGG others(17): Show |
T | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-161063_65-16104 others(28): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985909 | ||||||
| chr3:99985934
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-161039A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985934 | ||||||
| chr3:99985963
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-161010A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99985963 | ||||||
| chr3:99986017
|
T | C | 171 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(168): Show | 171 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.65-160956T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986017 | ||||||
| chr3:99986054
|
A | G | 1 | a0001c0001t0004g0017 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.65-160919A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986054 | ||||||
| chr3:99986170
|
C | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-160803C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986170 | ||||||
| chr3:99986267
|
A | G | 171 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(168): Show | 171 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.65-160706A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986267 | ||||||
| chr3:99986435
|
T | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0148 | 2 | HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.65-160538T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986435 | ||||||
| chr3:99986506
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-160467C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986506 | ||||||
| chr3:99986592
|
A | G | 1 | a0001c0001t0004g0019 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.65-160381A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986592 | ||||||
| chr3:99986856
|
A | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-160117A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99986856 | ||||||
| chr3:99987154
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-159819C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987154 | ||||||
| chr3:99987238
|
A | G | 9 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(6): Show | 9 | HG02027.hp2 HG02523.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-159735A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987238 | ||||||
| chr3:99987362
|
C | G | 1 | a0001c0001t0005g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.65-159611C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987362 | ||||||
| chr3:99987366
|
T | TA | 6 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0001g0213others(3): Show | 6 | HG01978.hp1 HG02148.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-159602dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99987366 | |||||
| chr3:99987385
|
G | A | 13 | a0001c0001t0001g0198a0001c0001t0002g0145a0001c0001t0002g0146others(10): Show | 13 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-159588G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987385 | ||||||
| chr3:99987421
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-159552C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987421 | ||||||
| chr3:99987454
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-159519G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987454 | ||||||
| chr3:99987465
|
G | A | 1 | a0001c0001t0005g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.65-159508G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987465 | ||||||
| chr3:99987468
|
G | T | 2 | a0002c0002t0003g0001a0002c0002t0003g0135 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.65-159505G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987468 | ||||||
| chr3:99987528
|
C | CA | 8 | a0001c0001t0001g0183a0001c0001t0001g0189a0001c0001t0001g0204others(5): Show | 8 | HG02559.hp2 HG02895.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-159427dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99987528 | |||||
| chr3:99987528
|
C | CAA | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-159428_65-15942 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99987528 | |||||
| chr3:99987639
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.65-159334A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987639 | ||||||
| chr3:99987677
|
C | A | 1 | a0001c0001t0004g0022 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.65-159296C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987677 | ||||||
| chr3:99987896
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-159077A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987896 | ||||||
| chr3:99987971
|
G | C | 1 | a0001c0001t0010g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.65-159002G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987971 | ||||||
| chr3:99987981
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-158992A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99987981 | ||||||
| chr3:99988026
|
G | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.65-158947G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988026 | ||||||
| chr3:99988059
|
A | C | 2 | a0001c0001t0002g0095a0001c0001t0002g0101 | 2 | NA18612.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.65-158914A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988059 | ||||||
| chr3:99988280
|
G | A | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.65-158693G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988280 | ||||||
| chr3:99988339
|
T | TA | 33 | a0001c0001t0001g0031a0001c0001t0001g0102a0001c0001t0001g0163others(30): Show | 33 | HG01891.hp1 HG01975.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.65-158634_65-15863 others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988339 | ||||||
| chr3:99988340
|
C | A | 195 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(192): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.65-158633C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988340 | ||||||
| chr3:99988341
|
C | A | 33 | a0001c0001t0001g0031a0001c0001t0001g0102a0001c0001t0001g0163others(30): Show | 33 | HG01891.hp1 HG01975.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.65-158632C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988341 | ||||||
| chr3:99988341
|
CA | C | 54 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0192others(51): Show | 54 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.65-158610delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99988341 | |||||
| chr3:99988343
|
A | C | 2 | a0001c0001t0002g0047a0001c0001t0002g0066 | 2 | HG02257.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.65-158630A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988343 | ||||||
| chr3:99988345
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-158628A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988345 | ||||||
| chr3:99988402
|
A | G | 167 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(164): Show | 167 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.65-158571A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988402 | ||||||
| chr3:99988460
|
C | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-158513C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988460 | ||||||
| chr3:99988511
|
C | CA | 33 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0002g0049others(30): Show | 33 | HG01168.hp1 HG01516.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.65-158443dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99988511 | |||||
| chr3:99988511
|
C | CAA | 43 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0041others(40): Show | 43 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(40): Show |
intron_variant | MODIFIER | c.65-158444_65-15844 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99988511 | |||||
| chr3:99988527
|
A | AG | 85 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(82): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.65-158446_65-15844 others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988527 | ||||||
| chr3:99988527
|
A | G | 6 | a0001c0001t0001g0179a0001c0001t0006g0003a0001c0001t0006g0004others(3): Show | 6 | HG02109.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-158446A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988527 | ||||||
| chr3:99988542
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.65-158431A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988542 | ||||||
| chr3:99988717
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-158256C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99988717 | ||||||
| chr3:99989049
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-157924C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989049 | ||||||
| chr3:99989179
|
A | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-157794A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989179 | ||||||
| chr3:99989664
|
CTA | C | 137 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(134): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.65-157289_65-15728 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99989664 | |||||
| chr3:99989668
|
A | C | 2 | a0001c0001t0002g0061a0001c0001t0002g0078 | 2 | NA18980.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.65-157305A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989668 | ||||||
| chr3:99989679
|
TA | T | 4 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0053others(1): Show | 4 | HG02486.hp1 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-157293delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989679 | ||||||
| chr3:99989680
|
A | T | 1 | a0001c0001t0002g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.65-157293A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989680 | ||||||
| chr3:99989681
|
TA | T | 9 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(6): Show | 9 | HG01952.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-157291delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989681 | ||||||
| chr3:99989681
|
TATA | T | 17 | a0001c0001t0001g0039a0001c0001t0001g0070a0001c0001t0001g0158others(14): Show | 17 | HG01168.hp2 HG01192.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-157291_65-15728 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989681 | ||||||
| chr3:99989682
|
A | T | 17 | a0001c0001t0001g0020a0001c0001t0001g0102a0001c0001t0001g0132others(14): Show | 18 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-157291A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989682 | ||||||
| chr3:99989683
|
TA | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0212 | 2 | HG02071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.65-157289delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989683 | ||||||
| chr3:99989684
|
A | T | 193 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(190): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.65-157289A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989684 | ||||||
| chr3:99989686
|
T | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0103 | 2 | HG02129.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.65-157287T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989686 | ||||||
| chr3:99989692
|
T | C | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-157281T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989692 | ||||||
| chr3:99989693
|
C | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-157280C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989693 | ||||||
| chr3:99989863
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.65-157110G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989863 | ||||||
| chr3:99989915
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-157058T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99989915 | ||||||
| chr3:99990100
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-156873A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99990100 | ||||||
| chr3:99990144
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-156829C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99990144 | ||||||
| chr3:99990201
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65-156772C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99990201 | ||||||
| chr3:99990230
|
AGAG | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01168.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.65-156739_65-15673 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99990230 | |||||
| chr3:99990306
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-156667A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99990306 | ||||||
| chr3:99990671
|
GCCT | G | 3 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0135 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-156298_65-15629 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99990671 | |||||
| chr3:99990733
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.65-156240C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99990733 | ||||||
| chr3:99990888
|
A | G | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-156085A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99990888 | ||||||
| chr3:99991029
|
G | C | 1 | a0001c0001t0007g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.65-155944G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99991029 | ||||||
| chr3:99991608
|
T | C | 186 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.65-155365T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99991608 | ||||||
| chr3:99991719
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-155254C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99991719 | ||||||
| chr3:99991834
|
A | ATG | 3 | a0001c0001t0001g0227a0001c0001t0018g0002a0002c0002t0003g0125 | 3 | HG01071.hp2 HG01891.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.65-155138_65-15513 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99991834 | |||||
| chr3:99991836
|
A | ATG | 186 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.65-155117_65-15511 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99991836 | |||||
| chr3:99991836
|
A | ATGTG | 11 | a0001c0001t0001g0166a0001c0001t0001g0211a0001c0001t0002g0097others(8): Show | 11 | HG01934.hp1 HG02109.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-155119_65-15511 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99991836 | |||||
| chr3:99991836
|
A | G | 13 | a0001c0001t0001g0227a0001c0001t0002g0049a0001c0001t0002g0050others(10): Show | 13 | HG01071.hp2 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-155137A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99991836 | ||||||
| chr3:99991838
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-155135G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99991838 | ||||||
| chr3:99991951
|
T | TATATATG others(15): Show |
1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-155020_65-15499 others(26): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99991951 | |||||
| chr3:99991951
|
T | TGTATATA others(5): Show |
3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-155022_65-15502 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99991951 | ||||||
| chr3:99991975
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-154998C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99991975 | ||||||
| chr3:99992014
|
A | G | 3 | a0001c0001t0002g0041a0001c0001t0005g0082a0001c0001t0005g0083 | 3 | HG01952.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-154959A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99992014 | ||||||
| chr3:99992107
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0175 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.65-154866G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99992107 | ||||||
| chr3:99992701
|
G | A | 109 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.65-154272G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99992701 | ||||||
| chr3:99992756
|
T | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-154217T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99992756 | ||||||
| chr3:99992843
|
G | A | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-154130G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99992843 | ||||||
| chr3:99992972
|
G | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-154001G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99992972 | ||||||
| chr3:99993060
|
G | A | 180 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.65-153913G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993060 | ||||||
| chr3:99993087
|
G | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-153886G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993087 | ||||||
| chr3:99993327
|
T | G | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.65-153646T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993327 | ||||||
| chr3:99993452
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.65-153521A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993452 | ||||||
| chr3:99993482
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-153491C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993482 | ||||||
| chr3:99993688
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.65-153285G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993688 | ||||||
| chr3:99993790
|
G | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-153183G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993790 | ||||||
| chr3:99993943
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.65-153030G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99993943 | ||||||
| chr3:99994362
|
A | C | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.65-152611A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99994362 | ||||||
| chr3:99994490
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.65-152483A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99994490 | ||||||
| chr3:99994533
|
T | C | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-152440T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99994533 | ||||||
| chr3:99994819
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-152154A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99994819 | ||||||
| chr3:99994829
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-152144A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99994829 | ||||||
| chr3:99994898
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0077 | 2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.65-152075C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99994898 | ||||||
| chr3:99995028
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.65-151945A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995028 | ||||||
| chr3:99995087
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-151886G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995087 | ||||||
| chr3:99995102
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.65-151871A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995102 | ||||||
| chr3:99995244
|
A | T | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-151729A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995244 | ||||||
| chr3:99995415
|
G | T | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-151558G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995415 | ||||||
| chr3:99995531
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-151442A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995531 | ||||||
| chr3:99995614
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG03654.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.65-151359C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995614 | ||||||
| chr3:99995677
|
C | G | 1 | a0001c0001t0004g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.65-151296C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995677 | ||||||
| chr3:99995716
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-151257G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995716 | ||||||
| chr3:99995737
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-151236C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995737 | ||||||
| chr3:99995981
|
G | A | 1 | a0001c0001t0012g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-150992G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99995981 | ||||||
| chr3:99996011
|
T | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-150962T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99996011 | ||||||
| chr3:99996246
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-150727G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99996246 | ||||||
| chr3:99996439
|
T | C | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65-150534T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99996439 | ||||||
| chr3:99996454
|
G | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-150519G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99996454 | ||||||
| chr3:99996578
|
G | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-150395G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99996578 | ||||||
| chr3:99996721
|
G | GAAACTCC others(6): Show |
1 | a0002c0002t0003g0122 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.65-150249_65-15023 others(17): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99996721 | |||||
| chr3:99996876
|
TG | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-150093delG | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 99996876 | |||||
| chr3:99996894
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-150079A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99996894 | ||||||
| chr3:99996957
|
T | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0217 | 2 | NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.65-150016T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99996957 | ||||||
| chr3:99997032
|
G | A | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.65-149941G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99997032 | ||||||
| chr3:99997137
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.65-149836A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99997137 | ||||||
| chr3:99997515
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-149458G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99997515 | ||||||
| chr3:99997784
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-149189G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99997784 | ||||||
| chr3:99997846
|
C | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-149127C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99997846 | ||||||
| chr3:99997943
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-149030G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99997943 | ||||||
| chr3:99997956
|
G | A | 189 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(186): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.65-149017G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99997956 | ||||||
| chr3:99998072
|
C | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-148901C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998072 | ||||||
| chr3:99998664
|
G | A | 2 | a0001c0001t0004g0025a0001c0001t0004g0026 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.65-148309G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998664 | ||||||
| chr3:99998674
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.65-148299C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998674 | ||||||
| chr3:99998794
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-148179C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998794 | ||||||
| chr3:99998816
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0024a0001c0001t0004g0025others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-148157G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998816 | ||||||
| chr3:99998860
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-148113C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998860 | ||||||
| chr3:99998869
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-148104A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998869 | ||||||
| chr3:99998877
|
TAAACTC | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-148095_65-14809 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99998877 | ||||||
| chr3:99999015
|
C | T | 1 | a0001c0001t0004g0019 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.65-147958C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99999015 | ||||||
| chr3:99999016
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-147957G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99999016 | ||||||
| chr3:99999087
|
T | G | 1 | a0001c0001t0001g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.65-147886T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99999087 | ||||||
| chr3:99999194
|
C | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-147779C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99999194 | ||||||
| chr3:99999247
|
T | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-147726T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99999247 | ||||||
| chr3:99999620
|
A | G | 1 | a0001c0001t0007g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.65-147353A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 99999620 | ||||||
| chr3:100000405
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-146568G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100000405 | ||||||
| chr3:100000467
|
A | C | 1 | a0002c0002t0003g0122 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.65-146506A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100000467 | ||||||
| chr3:100000676
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.65-146297T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100000676 | ||||||
| chr3:100000869
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-146104A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100000869 | ||||||
| chr3:100001017
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-145956A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001017 | ||||||
| chr3:100001134
|
GATTTAAA | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-145838_65-14583 others(11): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001134 | ||||||
| chr3:100001185
|
C | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-145788C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001185 | ||||||
| chr3:100001260
|
G | T | 2 | a0001c0001t0002g0085a0001c0001t0004g0019 | 2 | NA18959.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.65-145713G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001260 | ||||||
| chr3:100001316
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-145657G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001316 | ||||||
| chr3:100001330
|
G | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-145643G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001330 | ||||||
| chr3:100001341
|
G | A | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.65-145632G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001341 | ||||||
| chr3:100001720
|
A | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.65-145253A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001720 | ||||||
| chr3:100001876
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-145097T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001876 | ||||||
| chr3:100001892
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.65-145081G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100001892 | ||||||
| chr3:100002037
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-144936G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100002037 | ||||||
| chr3:100002080
|
G | A | 2 | a0001c0001t0018g0002a0002c0002t0003g0184 | 2 | HG01891.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.65-144893G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100002080 | ||||||
| chr3:100002089
|
G | A | 1 | a0002c0002t0003g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.65-144884G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100002089 | ||||||
| chr3:100002136
|
T | C | 2 | a0001c0001t0002g0095a0001c0001t0002g0101 | 2 | NA18612.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.65-144837T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100002136 | ||||||
| chr3:100002380
|
A | C | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-144593A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100002380 | ||||||
| chr3:100002924
|
T | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-144049T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100002924 | ||||||
| chr3:100003080
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.65-143893A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003080 | ||||||
| chr3:100003180
|
T | C | 1 | a0001c0001t0002g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.65-143793T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003180 | ||||||
| chr3:100003242
|
A | T | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65-143731A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003242 | ||||||
| chr3:100003289
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.65-143684C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003289 | ||||||
| chr3:100003412
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-143561A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003412 | ||||||
| chr3:100003430
|
T | A | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.65-143543T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003430 | ||||||
| chr3:100003552
|
A | C | 117 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.65-143421A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003552 | ||||||
| chr3:100003585
|
C | T | 2 | a0002c0002t0003g0001a0002c0002t0003g0135 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.65-143388C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003585 | ||||||
| chr3:100003720
|
G | C | 113 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.65-143253G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003720 | ||||||
| chr3:100003923
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-143050C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100003923 | ||||||
| chr3:100004044
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.65-142929C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100004044 | ||||||
| chr3:100004350
|
G | T | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-142623G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100004350 | ||||||
| chr3:100004425
|
C | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-142548C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100004425 | ||||||
| chr3:100004477
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-142496C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100004477 | ||||||
| chr3:100004736
|
G | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-142237G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100004736 | ||||||
| chr3:100004840
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-142133G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100004840 | ||||||
| chr3:100004891
|
C | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-142082C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100004891 | ||||||
| chr3:100005058
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.65-141915C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005058 | ||||||
| chr3:100005078
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-141895A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005078 | ||||||
| chr3:100005524
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-141449C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005524 | ||||||
| chr3:100005558
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-141415C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005558 | ||||||
| chr3:100005649
|
T | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-141324T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005649 | ||||||
| chr3:100005668
|
C | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-141305C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005668 | ||||||
| chr3:100005833
|
A | T | 1 | a0002c0002t0003g0125 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.65-141140A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005833 | ||||||
| chr3:100005868
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-141105T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005868 | ||||||
| chr3:100005947
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-141026C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005947 | ||||||
| chr3:100005948
|
G | A | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-141025G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100005948 | ||||||
| chr3:100006009
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.65-140964G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006009 | ||||||
| chr3:100006029
|
G | A | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-140944G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006029 | ||||||
| chr3:100006247
|
A | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-140726A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006247 | ||||||
| chr3:100006266
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.65-140707T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006266 | ||||||
| chr3:100006437
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-140536A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006437 | ||||||
| chr3:100006655
|
C | CA | 18 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-140303dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100006655 | |||||
| chr3:100006727
|
A | G | 1 | a0002c0002t0003g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-140246A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006727 | ||||||
| chr3:100006785
|
A | G | 110 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.65-140188A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006785 | ||||||
| chr3:100006980
|
A | C | 1 | a0002c0002t0003g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-139993A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100006980 | ||||||
| chr3:100007019
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.65-139954C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007019 | ||||||
| chr3:100007094
|
C | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-139879C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007094 | ||||||
| chr3:100007509
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-139464G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007509 | ||||||
| chr3:100007542
|
T | C | 1 | a0002c0002t0003g0127 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.65-139431T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007542 | ||||||
| chr3:100007628
|
AT | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-139341delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100007628 | |||||
| chr3:100007683
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-139290G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007683 | ||||||
| chr3:100007688
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-139285T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007688 | ||||||
| chr3:100007787
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-139186T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007787 | ||||||
| chr3:100007802
|
T | C | 188 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(185): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.65-139171T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007802 | ||||||
| chr3:100007853
|
A | G | 1 | a0001c0001t0002g0061 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.65-139120A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100007853 | ||||||
| chr3:100008416
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-138557G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100008416 | ||||||
| chr3:100008586
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-138387T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100008586 | ||||||
| chr3:100008717
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-138256G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100008717 | ||||||
| chr3:100008764
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.65-138209A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100008764 | ||||||
| chr3:100008903
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-138070G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100008903 | ||||||
| chr3:100008992
|
C | T | 181 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(178): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.65-137981C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100008992 | ||||||
| chr3:100009167
|
C | T | 4 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0203others(1): Show | 4 | HG03654.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-137806C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100009167 | ||||||
| chr3:100009273
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.65-137700A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100009273 | ||||||
| chr3:100009308
|
T | G | 1 | a0001c0001t0001g0206 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.65-137665T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100009308 | ||||||
| chr3:100009508
|
GA | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG00280.hp2 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-137462delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100009508 | |||||
| chr3:100009659
|
G | C | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-137314G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100009659 | ||||||
| chr3:100009847
|
G | A | 174 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.65-137126G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100009847 | ||||||
| chr3:100010040
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.65-136933A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100010040 | ||||||
| chr3:100010190
|
T | A | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.65-136783T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100010190 | ||||||
| chr3:100010247
|
C | T | 64 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(61): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.65-136726C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100010247 | ||||||
| chr3:100010267
|
A | C | 1 | a0001c0001t0012g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-136706A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100010267 | ||||||
| chr3:100010286
|
C | T | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-136687C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100010286 | ||||||
| chr3:100010288
|
T | C | 88 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.65-136685T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100010288 | ||||||
| chr3:100010612
|
C | CT | 59 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.65-136348dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100010612 | |||||
| chr3:100010721
|
TCTC | T | 35 | a0001c0001t0001g0132a0001c0001t0002g0108a0001c0001t0002g0140others(32): Show | 36 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.65-136249_65-13624 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100010721 | |||||
| chr3:100010739
|
T | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-136234T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100010739 | ||||||
| chr3:100010778
|
A | AT | 173 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.65-136174dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100010778 | |||||
| chr3:100010778
|
A | ATT | 18 | a0001c0001t0001g0132a0001c0001t0001g0167a0001c0001t0001g0220others(15): Show | 19 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-136175_65-13617 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100010778 | |||||
| chr3:100011132
|
G | A | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-135841G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100011132 | ||||||
| chr3:100011292
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-135681C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100011292 | ||||||
| chr3:100011441
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.65-135532G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100011441 | ||||||
| chr3:100011539
|
T | C | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.65-135434T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100011539 | ||||||
| chr3:100011647
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.65-135326C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100011647 | ||||||
| chr3:100011949
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-135024A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100011949 | ||||||
| chr3:100012218
|
T | G | 8 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(5): Show | 8 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-134755T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012218 | ||||||
| chr3:100012220
|
A | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-134753A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012220 | ||||||
| chr3:100012254
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-134719G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012254 | ||||||
| chr3:100012486
|
A | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.65-134487A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012486 | ||||||
| chr3:100012566
|
G | C | 1 | a0002c0002t0003g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.65-134407G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012566 | ||||||
| chr3:100012676
|
G | C | 1 | a0001c0001t0007g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.65-134297G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012676 | ||||||
| chr3:100012761
|
C | CT | 61 | a0001c0001t0001g0102a0001c0001t0001g0183a0001c0001t0001g0211others(58): Show | 62 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.65-134194dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100012761 | |||||
| chr3:100012761
|
CT | C | 8 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0005g0082others(5): Show | 8 | HG00323.hp1 HG01261.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-134194delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100012761 | |||||
| chr3:100012779
|
T | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0220a0001c0001t0004g0164 | 3 | HG02809.hp1 HG03225.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.65-134194T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012779 | ||||||
| chr3:100012784
|
T | G | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-134189T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012784 | ||||||
| chr3:100012971
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.65-134002A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100012971 | ||||||
| chr3:100013214
|
G | GTGT | 53 | a0001c0001t0001g0021a0001c0001t0001g0037a0001c0001t0001g0069others(50): Show | 53 | HG00280.hp1 HG01071.hp2 HG01256.hp1 others(50): Show |
intron_variant | MODIFIER | c.65-133715_65-13371 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100013214 | |||||
| chr3:100013214
|
G | GTGTTGT | 31 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0038others(28): Show | 31 | HG00280.hp2 HG01168.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.65-133718_65-13371 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100013214 | |||||
| chr3:100013214
|
G | GTGTTGTT others(2): Show |
8 | a0001c0001t0001g0161a0001c0001t0002g0044a0001c0001t0002g0045others(5): Show | 8 | HG02132.hp2 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-133721_65-13371 others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100013214 | |||||
| chr3:100013214
|
G | GTGTTGTT others(5): Show |
2 | a0001c0001t0001g0157a0002c0002t0003g0138 | 2 | HG00741.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.65-133724_65-13371 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100013214 | |||||
| chr3:100013214
|
GTGT | G | 19 | a0001c0001t0001g0173a0001c0001t0001g0194a0001c0001t0001g0196others(16): Show | 19 | HG00323.hp1 HG01168.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.65-133715_65-13371 others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100013214 | |||||
| chr3:100013214
|
GTGTTGT | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0002c0002t0003g0125 | 3 | HG04228.hp1 NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.65-133718_65-13371 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100013214 | |||||
| chr3:100013339
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-133634G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100013339 | ||||||
| chr3:100013679
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.65-133294C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100013679 | ||||||
| chr3:100013720
|
A | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-133253A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100013720 | ||||||
| chr3:100013848
|
A | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-133125A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100013848 | ||||||
| chr3:100014194
|
G | GTA | 2 | a0001c0001t0002g0074a0001c0001t0002g0146 | 2 | HG01981.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.65-132769_65-13276 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100014194 | |||||
| chr3:100014200
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-132773A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014200 | ||||||
| chr3:100014252
|
C | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-132721C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014252 | ||||||
| chr3:100014280
|
A | AAT | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-132693_65-13269 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014280 | ||||||
| chr3:100014332
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.65-132641A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014332 | ||||||
| chr3:100014436
|
C | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-132537C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014436 | ||||||
| chr3:100014562
|
G | T | 2 | a0001c0001t0006g0057a0001c0001t0006g0071 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.65-132411G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014562 | ||||||
| chr3:100014743
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-132230T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014743 | ||||||
| chr3:100014807
|
A | AT | 10 | a0001c0001t0001g0070a0001c0001t0001g0163a0001c0001t0002g0140others(7): Show | 10 | HG02055.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-132150dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100014807 | |||||
| chr3:100014807
|
AT | A | 48 | a0001c0001t0001g0102a0001c0001t0001g0162a0001c0001t0002g0086others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.65-132150delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100014807 | |||||
| chr3:100014894
|
TC | T | 2 | a0001c0001t0009g0009a0001c0001t0009g0040 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.65-132078delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014894 | ||||||
| chr3:100014895
|
C | CT | 16 | a0001c0001t0001g0069a0001c0001t0001g0175a0001c0001t0001g0186others(13): Show | 16 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-132055dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100014895 | |||||
| chr3:100014895
|
C | CTT | 8 | a0001c0001t0002g0063a0001c0001t0006g0003a0001c0001t0006g0004others(5): Show | 8 | HG01891.hp2 HG01978.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-132056_65-13205 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100014895 | |||||
| chr3:100014895
|
C | T | 1 | a0001c0001t0009g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65-132078C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014895 | ||||||
| chr3:100014895
|
CT | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(16): Show | 19 | HG01069.hp1 HG01257.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-132055delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100014895 | |||||
| chr3:100014898
|
T | TC | 55 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(52): Show | 56 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.65-132075_65-13207 others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014898 | ||||||
| chr3:100014899
|
T | C | 2 | a0001c0001t0005g0144a0002c0002t0003g0118 | 2 | HG02293.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.65-132074T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100014899 | ||||||
| chr3:100015080
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-131893G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015080 | ||||||
| chr3:100015081
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-131892A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015081 | ||||||
| chr3:100015157
|
T | C | 223 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(220): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.65-131816T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015157 | ||||||
| chr3:100015182
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-131791C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015182 | ||||||
| chr3:100015385
|
G | A | 1 | a0002c0002t0003g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.65-131588G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015385 | ||||||
| chr3:100015709
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-131264G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015709 | ||||||
| chr3:100015745
|
C | T | 181 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(178): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.65-131228C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015745 | ||||||
| chr3:100015846
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-131127A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100015846 | ||||||
| chr3:100016184
|
C | T | 1 | a0002c0002t0003g0119 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65-130789C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016184 | ||||||
| chr3:100016235
|
C | T | 2 | a0001c0001t0002g0013a0001c0001t0004g0014 | 2 | HG01516.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.65-130738C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016235 | ||||||
| chr3:100016261
|
C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0204a0001c0001t0014g0223 | 3 | HG03831.hp1 NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.65-130712C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016261 | ||||||
| chr3:100016291
|
C | T | 11 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0111others(8): Show | 11 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-130682C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016291 | ||||||
| chr3:100016307
|
C | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.65-130666C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016307 | ||||||
| chr3:100016723
|
C | T | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | HG02015.hp2 HG02071.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.65-130250C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016723 | ||||||
| chr3:100016906
|
A | T | 4 | a0001c0001t0001g0069a0001c0001t0002g0067a0001c0001t0002g0068others(1): Show | 4 | HG04184.hp2 HG04199.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-130067A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016906 | ||||||
| chr3:100016994
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-129979A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100016994 | ||||||
| chr3:100017133
|
T | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-129840T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100017133 | ||||||
| chr3:100017550
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-129423T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100017550 | ||||||
| chr3:100017687
|
G | A | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-129286G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100017687 | ||||||
| chr3:100017694
|
C | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-129279C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100017694 | ||||||
| chr3:100017869
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.65-129104A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100017869 | ||||||
| chr3:100017917
|
T | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0160 | 2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.65-129056T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100017917 | ||||||
| chr3:100018187
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.65-128786G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100018187 | ||||||
| chr3:100018633
|
A | G | 1 | a0002c0002t0003g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.65-128340A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100018633 | ||||||
| chr3:100018680
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-128293A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100018680 | ||||||
| chr3:100018735
|
CA | C | 202 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(199): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.65-128221delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100018735 | |||||
| chr3:100018782
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-128191T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100018782 | ||||||
| chr3:100018878
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.65-128095A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100018878 | ||||||
| chr3:100018927
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-128046A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100018927 | ||||||
| chr3:100019051
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.65-127922G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019051 | ||||||
| chr3:100019140
|
T | C | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.65-127833T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019140 | ||||||
| chr3:100019353
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-127620G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019353 | ||||||
| chr3:100019353
|
G | T | 4 | a0001c0001t0002g0107a0001c0001t0008g0087a0001c0001t0008g0088others(1): Show | 4 | HG02040.hp1 HG02083.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-127620G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019353 | ||||||
| chr3:100019375
|
T | A | 35 | a0001c0001t0001g0132a0001c0001t0002g0108a0001c0001t0002g0140others(32): Show | 36 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.65-127598T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019375 | ||||||
| chr3:100019386
|
G | A | 35 | a0001c0001t0001g0132a0001c0001t0002g0108a0001c0001t0002g0140others(32): Show | 36 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.65-127587G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019386 | ||||||
| chr3:100019554
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-127419C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019554 | ||||||
| chr3:100019555
|
G | A | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-127418G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019555 | ||||||
| chr3:100019587
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.65-127386C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019587 | ||||||
| chr3:100019649
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-127324G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019649 | ||||||
| chr3:100019728
|
C | T | 4 | a0001c0001t0002g0107a0001c0001t0008g0087a0001c0001t0008g0088others(1): Show | 4 | HG02040.hp1 HG02083.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-127245C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019728 | ||||||
| chr3:100019936
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.65-127037G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019936 | ||||||
| chr3:100019984
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-126989T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100019984 | ||||||
| chr3:100020243
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-126730T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100020243 | ||||||
| chr3:100020581
|
A | C | 3 | a0001c0001t0002g0074a0001c0001t0006g0057a0001c0001t0006g0071 | 3 | HG02280.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.65-126392A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100020581 | ||||||
| chr3:100020642
|
T | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-126331T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100020642 | ||||||
| chr3:100020760
|
C | CT | 85 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0034others(82): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.65-126188dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100020760 | |||||
| chr3:100020760
|
C | CTT | 20 | a0001c0001t0001g0031a0001c0001t0001g0157a0001c0001t0001g0163others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.65-126189_65-12618 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100020760 | |||||
| chr3:100020760
|
CT | C | 65 | a0001c0001t0001g0102a0001c0001t0002g0013a0001c0001t0002g0054others(62): Show | 66 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-126188delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100020760 | |||||
| chr3:100021016
|
T | C | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-125957T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021016 | ||||||
| chr3:100021045
|
G | A | 3 | a0001c0001t0018g0002a0002c0002t0003g0134a0002c0002t0017g0131 | 3 | HG01891.hp2 HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-125928G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021045 | ||||||
| chr3:100021144
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-125829A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021144 | ||||||
| chr3:100021262
|
C | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-125711C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021262 | ||||||
| chr3:100021455
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-125518C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021455 | ||||||
| chr3:100021541
|
A | C | 3 | a0001c0001t0008g0087a0001c0001t0008g0088a0001c0001t0008g0089 | 3 | HG02083.hp2 NA19065.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.65-125432A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021541 | ||||||
| chr3:100021550
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-125423G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021550 | ||||||
| chr3:100021882
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-125091C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021882 | ||||||
| chr3:100021915
|
T | TTG | 6 | a0001c0001t0004g0011a0001c0001t0004g0024a0001c0001t0004g0025others(3): Show | 6 | HG02257.hp1 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-125013_65-12501 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021915
|
T | TTGTG | 7 | a0001c0001t0002g0053a0001c0001t0004g0015a0001c0001t0004g0016others(4): Show | 7 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-125015_65-12501 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021915
|
TTGTGTG | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0211a0001c0001t0005g0082 | 3 | HG02080.hp2 HG03471.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.65-125017_65-12501 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021915
|
TTGTGTGT others(1): Show |
T | 10 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0193others(7): Show | 10 | HG01515.hp1 HG02071.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-125019_65-12501 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021915
|
TTGTGTGT others(3): Show |
T | 47 | a0001c0001t0001g0070a0001c0001t0001g0163a0001c0001t0001g0165others(44): Show | 47 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.65-125021_65-12501 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021915
|
TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0194a0001c0001t0001g0225 | 2 | HG00323.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.65-125023_65-12501 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021915
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.65-125025_65-12501 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021915
|
TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.65-125027_65-12501 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021915 | |||||
| chr3:100021925
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.65-125048G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021925 | ||||||
| chr3:100021934
|
TGTGTGTG others(23): Show |
T | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-125037_65-12500 others(34): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021934 | |||||
| chr3:100021950
|
TGTGTGTG others(7): Show |
T | 3 | a0001c0001t0001g0183a0001c0001t0001g0204a0001c0001t0001g0221 | 3 | NA18972.hp1 NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.65-125021_65-12500 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021950 | |||||
| chr3:100021950
|
TGTGTGTG others(15): Show |
T | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-125021_65-12500 others(26): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021950 | |||||
| chr3:100021952
|
TGTGTGTG others(3): Show |
T | 3 | a0001c0001t0001g0176a0001c0001t0001g0216a0001c0001t0001g0229 | 3 | HG02976.hp2 HG04184.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.65-125019_65-12501 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021952 | |||||
| chr3:100021952
|
TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-125019_65-12500 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021952 | |||||
| chr3:100021952
|
TGTGTGTG others(13): Show |
T | 14 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(11): Show | 14 | HG00280.hp1 HG01123.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-125019_65-12500 others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021952 | |||||
| chr3:100021954
|
TGTGTGTG others(3): Show |
T | 16 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0034others(13): Show | 16 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-125017_65-12500 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021954 | |||||
| chr3:100021954
|
TGTGTGTG others(11): Show |
T | 29 | a0001c0001t0001g0132a0001c0001t0002g0140a0002c0002t0003g0001others(26): Show | 30 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.65-125017_65-12500 others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021954 | |||||
| chr3:100021954
|
TGTGTGTG others(13): Show |
T | 7 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(4): Show | 7 | HG00423.hp2 HG02027.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-125017_65-12499 others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021954 | |||||
| chr3:100021956
|
T | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.65-125017T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021956 | ||||||
| chr3:100021956
|
TGTGTGA | T | 2 | a0001c0001t0001g0174a0001c0001t0005g0083 | 2 | HG01069.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.65-125015_65-12501 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021956 | |||||
| chr3:100021956
|
TGTGTGAG others(5): Show |
T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-125015_65-12500 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021956 | |||||
| chr3:100021956
|
TGTGTGAG others(9): Show |
T | 1 | a0002c0002t0003g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.65-125015_65-12500 others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021956 | |||||
| chr3:100021956
|
TGTGTGAG others(11): Show |
T | 3 | a0001c0001t0002g0095a0001c0001t0002g0101a0002c0002t0003g0139 | 3 | NA18612.hp2 NA18963.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.65-125015_65-12499 others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021956 | |||||
| chr3:100021958
|
T | A | 6 | a0001c0001t0001g0186a0001c0001t0001g0211a0001c0001t0002g0072others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-125015T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021958 | ||||||
| chr3:100021958
|
T | TGAGA | 5 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0066others(2): Show | 5 | HG01891.hp2 HG02602.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-125014_65-12501 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021958 | |||||
| chr3:100021958
|
TGTGAGAG others(5): Show |
T | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-125013_65-12500 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021958 | |||||
| chr3:100021958
|
TGTGAGAG others(7): Show |
T | 2 | a0001c0001t0005g0144a0002c0002t0003g0137 | 2 | HG00140.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.65-125013_65-12500 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021958 | |||||
| chr3:100021960
|
T | A | 23 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0196others(20): Show | 23 | HG01257.hp1 HG01258.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-125013T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021960 | ||||||
| chr3:100021960
|
T | TGA | 2 | a0001c0001t0002g0063a0001c0001t0002g0150 | 2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.65-124980_65-12497 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGAGA | 4 | a0001c0001t0002g0145a0001c0001t0002g0147a0001c0001t0002g0149others(1): Show | 4 | HG00738.hp2 HG01515.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-124982_65-12497 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGAGAGA | 6 | a0001c0001t0002g0048a0001c0001t0002g0054a0001c0001t0002g0058others(3): Show | 6 | HG01256.hp2 NA18942.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-124984_65-12497 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGAGAGAG others(1): Show |
3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-124986_65-12497 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGTGA | 2 | a0001c0001t0002g0050a0001c0001t0002g0052 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.65-125012_65-12501 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGTGAGAG others(1): Show |
3 | a0001c0001t0002g0060a0001c0001t0002g0079a0001c0001t0002g0080 | 3 | HG02027.hp2 HG02523.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.65-125012_65-12501 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGTGTGAG others(1): Show |
5 | a0001c0001t0001g0069a0001c0001t0002g0151a0001c0001t0002g0152others(2): Show | 5 | HG01261.hp1 HG01346.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-125012_65-12501 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0002g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.65-125012_65-12501 others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0002g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-125012_65-12501 others(28): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
TGA | T | 2 | a0001c0001t0006g0004a0002c0002t0019g0012 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.65-124980_65-12497 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
TGAGA | T | 3 | a0001c0001t0006g0005a0001c0001t0006g0006a0001c0001t0006g0007 | 3 | HG02630.hp1 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.65-124982_65-12497 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
TGAGAGA | T | 4 | a0001c0001t0002g0042a0001c0001t0002g0074a0001c0001t0007g0029others(1): Show | 4 | HG02622.hp2 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-124984_65-12497 others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
TGAGAGAG others(1): Show |
T | 7 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG01975.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-124986_65-12497 others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
TGAGAGAG others(3): Show |
T | 4 | a0001c0001t0001g0031a0001c0001t0002g0045a0001c0001t0004g0030others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-124988_65-12497 others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
TGAGAGAG others(5): Show |
T | 1 | a0002c0002t0003g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.65-124990_65-12497 others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021960
|
TGAGAGAG others(7): Show |
T | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-124992_65-12497 others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100021960 | |||||
| chr3:100021962
|
A | T | 11 | a0001c0001t0004g0011a0001c0001t0004g0014a0001c0001t0004g0015others(8): Show | 11 | HG01168.hp1 HG01516.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-125011A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021962 | ||||||
| chr3:100021964
|
A | T | 2 | a0001c0001t0004g0014a0001c0001t0006g0004 | 2 | HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.65-125009A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021964 | ||||||
| chr3:100021966
|
A | T | 1 | a0001c0001t0004g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.65-125007A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021966 | ||||||
| chr3:100021968
|
A | T | 5 | a0001c0001t0002g0042a0001c0001t0002g0074a0001c0001t0004g0014others(2): Show | 5 | HG01516.hp1 HG02622.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-125005A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021968 | ||||||
| chr3:100021970
|
A | T | 12 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0042others(9): Show | 12 | HG01516.hp1 HG01952.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-125003A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021970 | ||||||
| chr3:100021972
|
A | T | 16 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0002g0041others(13): Show | 16 | HG01516.hp1 HG01952.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-125001A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021972 | ||||||
| chr3:100021974
|
A | T | 15 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0002g0041others(12): Show | 15 | HG01516.hp1 HG01952.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-124999A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021974 | ||||||
| chr3:100021993
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0175 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.65-124980G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100021993 | ||||||
| chr3:100022188
|
T | C | 187 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(184): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.65-124785T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100022188 | ||||||
| chr3:100022399
|
C | T | 1 | a0001c0001t0007g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.65-124574C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100022399 | ||||||
| chr3:100022578
|
G | A | 1 | a0002c0002t0003g0119 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65-124395G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100022578 | ||||||
| chr3:100023202
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-123771A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023202 | ||||||
| chr3:100023435
|
C | T | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-123538C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023435 | ||||||
| chr3:100023556
|
G | A | 5 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0003g0124others(2): Show | 5 | NA18943.hp2 NA18959.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-123417G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023556 | ||||||
| chr3:100023578
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-123395A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023578 | ||||||
| chr3:100023689
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-123284T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023689 | ||||||
| chr3:100023702
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.65-123271A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023702 | ||||||
| chr3:100023718
|
C | T | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65-123255C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023718 | ||||||
| chr3:100023741
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-123232G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023741 | ||||||
| chr3:100023768
|
G | A | 3 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0065 | 3 | HG01934.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.65-123205G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023768 | ||||||
| chr3:100023784
|
G | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-123189G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023784 | ||||||
| chr3:100023960
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0149a0001c0001t0002g0150 | 3 | HG00741.hp1 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.65-123013G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100023960 | ||||||
| chr3:100024175
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-122798C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100024175 | ||||||
| chr3:100024617
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-122356C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100024617 | ||||||
| chr3:100024891
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-122082A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100024891 | ||||||
| chr3:100025077
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.65-121896A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025077 | ||||||
| chr3:100025113
|
C | G | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.65-121860C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025113 | ||||||
| chr3:100025272
|
C | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-121701C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025272 | ||||||
| chr3:100025533
|
A | G | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-121440A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025533 | ||||||
| chr3:100025540
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-121433T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025540 | ||||||
| chr3:100025724
|
AT | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-121245delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100025724 | |||||
| chr3:100025790
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-121183G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025790 | ||||||
| chr3:100025816
|
T | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-121157T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025816 | ||||||
| chr3:100025920
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.65-121053C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100025920 | ||||||
| chr3:100026434
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.65-120539C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100026434 | ||||||
| chr3:100026540
|
G | T | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-120433G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100026540 | ||||||
| chr3:100026763
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-120210C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100026763 | ||||||
| chr3:100026770
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-120203A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100026770 | ||||||
| chr3:100026859
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-120114G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100026859 | ||||||
| chr3:100027037
|
G | T | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.65-119936G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027037 | ||||||
| chr3:100027113
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-119860C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027113 | ||||||
| chr3:100027135
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.65-119838G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027135 | ||||||
| chr3:100027191
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-119782A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027191 | ||||||
| chr3:100027254
|
G | A | 219 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.65-119719G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027254 | ||||||
| chr3:100027340
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-119633A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027340 | ||||||
| chr3:100027422
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-119551G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027422 | ||||||
| chr3:100027434
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.65-119539T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027434 | ||||||
| chr3:100027581
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.65-119392C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027581 | ||||||
| chr3:100027953
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.65-119020A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100027953 | ||||||
| chr3:100028314
|
T | C | 219 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.65-118659T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100028314 | ||||||
| chr3:100028415
|
G | C | 1 | a0002c0002t0003g0115 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.65-118558G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100028415 | ||||||
| chr3:100028416
|
G | T | 1 | a0002c0002t0003g0115 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.65-118557G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100028416 | ||||||
| chr3:100028540
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-118433A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100028540 | ||||||
| chr3:100028601
|
C | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.65-118372C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100028601 | ||||||
| chr3:100028705
|
A | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0205 | 3 | HG01192.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.65-118268A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100028705 | ||||||
| chr3:100028971
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-118002G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100028971 | ||||||
| chr3:100029034
|
A | T | 5 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(2): Show | 5 | HG01952.hp1 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-117939A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029034 | ||||||
| chr3:100029067
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-117906A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029067 | ||||||
| chr3:100029323
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0204 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.65-117650A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029323 | ||||||
| chr3:100029423
|
CTAAA | C | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-117547_65-11754 others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100029423 | |||||
| chr3:100029448
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.65-117525G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029448 | ||||||
| chr3:100029511
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.65-117462C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029511 | ||||||
| chr3:100029704
|
T | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-117269T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029704 | ||||||
| chr3:100029761
|
G | A | 22 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-117212G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029761 | ||||||
| chr3:100029846
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.65-117127A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029846 | ||||||
| chr3:100029925
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-117048G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100029925 | ||||||
| chr3:100030101
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.65-116872C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100030101 | ||||||
| chr3:100030106
|
A | G | 219 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.65-116867A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100030106 | ||||||
| chr3:100030124
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.65-116849A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100030124 | ||||||
| chr3:100030146
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-116827A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100030146 | ||||||
| chr3:100030415
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.65-116558A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100030415 | ||||||
| chr3:100030673
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-116300A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100030673 | ||||||
| chr3:100030727
|
T | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-116246T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100030727 | ||||||
| chr3:100031343
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-115630T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031343 | ||||||
| chr3:100031378
|
C | G | 7 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-115595C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031378 | ||||||
| chr3:100031428
|
T | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-115545T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031428 | ||||||
| chr3:100031461
|
A | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-115512A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031461 | ||||||
| chr3:100031702
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.65-115271G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031702 | ||||||
| chr3:100031751
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.65-115222T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031751 | ||||||
| chr3:100031948
|
C | T | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.65-115025C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031948 | ||||||
| chr3:100031964
|
T | TTATGTAT others(12): Show |
2 | a0001c0001t0002g0085a0001c0001t0004g0019 | 2 | NA18959.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.65-115002_65-11500 others(23): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100031964 | |||||
| chr3:100031972
|
T | A | 2 | a0001c0001t0002g0085a0001c0001t0004g0019 | 2 | NA18959.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.65-115001T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100031972 | ||||||
| chr3:100031994
|
C | CTAATTTT others(18): Show |
2 | a0001c0001t0002g0085a0001c0001t0004g0019 | 2 | NA18959.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.65-114963_65-11496 others(29): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100031994 | |||||
| chr3:100032011
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0004g0164 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.65-114962C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032011 | ||||||
| chr3:100032080
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-114893C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032080 | ||||||
| chr3:100032251
|
G | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-114722G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032251 | ||||||
| chr3:100032395
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-114578T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032395 | ||||||
| chr3:100032549
|
C | G | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.65-114424C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032549 | ||||||
| chr3:100032592
|
G | A | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.65-114381G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032592 | ||||||
| chr3:100032623
|
A | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-114350A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032623 | ||||||
| chr3:100032636
|
C | T | 116 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.65-114337C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100032636 | ||||||
| chr3:100033152
|
G | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-113821G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100033152 | ||||||
| chr3:100033224
|
G | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-113749G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100033224 | ||||||
| chr3:100033633
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-113340G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100033633 | ||||||
| chr3:100034236
|
A | T | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.65-112737A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100034236 | ||||||
| chr3:100034316
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-112657A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100034316 | ||||||
| chr3:100034383
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0002g0013a0001c0001t0004g0014others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-112590G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100034383 | ||||||
| chr3:100034456
|
CT | C | 4 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-112512delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100034456 | |||||
| chr3:100034511
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.65-112462G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100034511 | ||||||
| chr3:100034664
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-112309C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100034664 | ||||||
| chr3:100035147
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.65-111826A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035147 | ||||||
| chr3:100035274
|
G | T | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-111699G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035274 | ||||||
| chr3:100035278
|
T | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-111695T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035278 | ||||||
| chr3:100035330
|
A | G | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.65-111643A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035330 | ||||||
| chr3:100035461
|
C | T | 35 | a0001c0001t0001g0132a0001c0001t0002g0108a0001c0001t0002g0140others(32): Show | 36 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.65-111512C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035461 | ||||||
| chr3:100035492
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0037 | 2 | HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.65-111481C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035492 | ||||||
| chr3:100035602
|
A | G | 219 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.65-111371A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035602 | ||||||
| chr3:100035654
|
A | G | 35 | a0001c0001t0001g0132a0001c0001t0002g0108a0001c0001t0002g0140others(32): Show | 36 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.65-111319A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035654 | ||||||
| chr3:100035790
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.65-111183C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035790 | ||||||
| chr3:100035797
|
T | C | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.65-111176T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035797 | ||||||
| chr3:100035888
|
T | G | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-111085T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100035888 | ||||||
| chr3:100036042
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.65-110931T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100036042 | ||||||
| chr3:100036257
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.65-110716C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100036257 | ||||||
| chr3:100036451
|
G | A | 2 | a0001c0001t0002g0054a0002c0002t0003g0119 | 2 | HG03688.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.65-110522G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100036451 | ||||||
| chr3:100036795
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-110178A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100036795 | ||||||
| chr3:100036877
|
C | G | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-110096C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100036877 | ||||||
| chr3:100037110
|
G | T | 10 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0111others(7): Show | 10 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-109863G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037110 | ||||||
| chr3:100037130
|
ATAAAATG others(56): Show |
A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-109842_65-10978 others(67): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037130 | ||||||
| chr3:100037167
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-109806T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037167 | ||||||
| chr3:100037201
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.65-109772G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037201 | ||||||
| chr3:100037351
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.65-109622T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037351 | ||||||
| chr3:100037451
|
G | GAC | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-109507_65-10950 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100037451 | |||||
| chr3:100037452
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.65-109521A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037452 | ||||||
| chr3:100037468
|
G | A | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-109505G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037468 | ||||||
| chr3:100037470
|
A | ACG | 6 | a0002c0002t0003g0121a0002c0002t0003g0122a0002c0002t0003g0123others(3): Show | 6 | NA18943.hp2 NA18959.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-109502_65-10950 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100037470 | |||||
| chr3:100037470
|
A | G | 51 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(48): Show | 52 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-109503A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037470 | ||||||
| chr3:100037603
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.65-109370T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037603 | ||||||
| chr3:100037734
|
G | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0203others(1): Show | 4 | HG03654.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-109239G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037734 | ||||||
| chr3:100037934
|
C | T | 18 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-109039C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037934 | ||||||
| chr3:100037939
|
C | CT | 32 | a0001c0001t0001g0069a0001c0001t0001g0183a0001c0001t0001g0185others(29): Show | 32 | HG00140.hp2 HG01257.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.65-109017dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100037939 | |||||
| chr3:100037956
|
T | G | 1 | a0001c0001t0002g0152 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.65-109017T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037956 | ||||||
| chr3:100037957
|
G | T | 173 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.65-109016G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037957 | ||||||
| chr3:100037958
|
G | T | 166 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.65-109015G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037958 | ||||||
| chr3:100037959
|
G | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-109014G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037959 | ||||||
| chr3:100037960
|
G | A | 2 | a0001c0001t0014g0223a0002c0002t0003g0111 | 2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.65-109013G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037960 | ||||||
| chr3:100037961
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-109012G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037961 | ||||||
| chr3:100037963
|
G | A | 3 | a0001c0001t0007g0029a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-109010G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037963 | ||||||
| chr3:100037964
|
GA | G | 9 | a0001c0001t0001g0188a0001c0001t0002g0050a0001c0001t0002g0051others(6): Show | 9 | HG01256.hp1 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-109008delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037964 | ||||||
| chr3:100037965
|
A | C | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-109008A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037965 | ||||||
| chr3:100037965
|
A | G | 179 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(176): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.65-109008A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037965 | ||||||
| chr3:100037968
|
G | A | 178 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(175): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.65-109005G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100037968 | ||||||
| chr3:100038252
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-108721G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038252 | ||||||
| chr3:100038295
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-108678A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038295 | ||||||
| chr3:100038369
|
T | C | 4 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-108604T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038369 | ||||||
| chr3:100038464
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-108509G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038464 | ||||||
| chr3:100038552
|
G | C | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-108421G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038552 | ||||||
| chr3:100038583
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.65-108390G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038583 | ||||||
| chr3:100038691
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-108282A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038691 | ||||||
| chr3:100038857
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-108116G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038857 | ||||||
| chr3:100038928
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-108045G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038928 | ||||||
| chr3:100038948
|
G | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-108025G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100038948 | ||||||
| chr3:100039009
|
G | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-107964G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039009 | ||||||
| chr3:100039063
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.65-107910C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039063 | ||||||
| chr3:100039185
|
A | T | 116 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.65-107788A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039185 | ||||||
| chr3:100039437
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-107536G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039437 | ||||||
| chr3:100039621
|
T | C | 196 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.65-107352T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039621 | ||||||
| chr3:100039734
|
C | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-107239C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039734 | ||||||
| chr3:100039756
|
CT | C | 5 | a0001c0001t0001g0069a0001c0001t0001g0188a0001c0001t0002g0067others(2): Show | 5 | HG01256.hp1 HG04184.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-107202delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100039756 | |||||
| chr3:100039785
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-107188G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039785 | ||||||
| chr3:100039809
|
A | G | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-107164A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039809 | ||||||
| chr3:100039840
|
A | G | 177 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(174): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.65-107133A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039840 | ||||||
| chr3:100039855
|
A | G | 1 | a0002c0002t0003g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.65-107118A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039855 | ||||||
| chr3:100039879
|
G | A | 1 | a0001c0001t0002g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.65-107094G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039879 | ||||||
| chr3:100039898
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.65-107075C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039898 | ||||||
| chr3:100039903
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-107070G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039903 | ||||||
| chr3:100039943
|
T | C | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-107030T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039943 | ||||||
| chr3:100039992
|
A | T | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.65-106981A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100039992 | ||||||
| chr3:100040130
|
A | T | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-106843A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100040130 | ||||||
| chr3:100040389
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-106584A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100040389 | ||||||
| chr3:100040576
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-106397A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100040576 | ||||||
| chr3:100040629
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-106344C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100040629 | ||||||
| chr3:100040894
|
A | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-106079A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100040894 | ||||||
| chr3:100040972
|
A | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-106001A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100040972 | ||||||
| chr3:100041119
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0002g0209 | 2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.65-105854A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100041119 | ||||||
| chr3:100041222
|
C | A | 1 | a0001c0001t0002g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.65-105751C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100041222 | ||||||
| chr3:100041292
|
G | GAA | 3 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG03654.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.65-105678_65-10567 others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100041292 | |||||
| chr3:100041595
|
AT | A | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.65-105377delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100041595 | ||||||
| chr3:100042020
|
A | G | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-104953A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100042020 | ||||||
| chr3:100042439
|
T | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-104534T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100042439 | ||||||
| chr3:100042458
|
G | A | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.65-104515G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100042458 | ||||||
| chr3:100042610
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.65-104363T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100042610 | ||||||
| chr3:100042889
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.65-104084G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100042889 | ||||||
| chr3:100042899
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-104074A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100042899 | ||||||
| chr3:100042943
|
A | G | 2 | a0002c0002t0003g0136a0002c0002t0003g0137 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.65-104030A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100042943 | ||||||
| chr3:100043064
|
A | G | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-103909A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100043064 | ||||||
| chr3:100043424
|
C | T | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-103549C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100043424 | ||||||
| chr3:100043429
|
A | G | 1 | a0001c0001t0002g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.65-103544A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100043429 | ||||||
| chr3:100043600
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.65-103373T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100043600 | ||||||
| chr3:100043683
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-103290A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100043683 | ||||||
| chr3:100043714
|
T | G | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-103259T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100043714 | ||||||
| chr3:100043777
|
TC | T | 4 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052others(1): Show | 4 | HG02559.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-103194delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100043777 | |||||
| chr3:100043996
|
C | T | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-102977C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100043996 | ||||||
| chr3:100044237
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.65-102736G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100044237 | ||||||
| chr3:100044366
|
A | C | 1 | a0001c0001t0007g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.65-102607A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100044366 | ||||||
| chr3:100044367
|
C | T | 1 | a0001c0001t0007g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.65-102606C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100044367 | ||||||
| chr3:100044374
|
G | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-102599G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100044374 | ||||||
| chr3:100044979
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-101994A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100044979 | ||||||
| chr3:100045147
|
G | A | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-101826G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100045147 | ||||||
| chr3:100045186
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-101787G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100045186 | ||||||
| chr3:100045250
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-101723G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100045250 | ||||||
| chr3:100045414
|
A | C | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.65-101559A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100045414 | ||||||
| chr3:100045481
|
A | AT | 7 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-101482dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100045481 | |||||
| chr3:100045731
|
G | A | 2 | a0001c0001t0004g0025a0001c0001t0004g0026 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.65-101242G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100045731 | ||||||
| chr3:100045910
|
G | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-101063G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100045910 | ||||||
| chr3:100045934
|
C | T | 2 | a0001c0001t0006g0057a0001c0001t0006g0071 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.65-101039C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100045934 | ||||||
| chr3:100046180
|
A | G | 1 | a0001c0001t0002g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.65-100793A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100046180 | ||||||
| chr3:100046182
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-100791T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100046182 | ||||||
| chr3:100046344
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-100629A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100046344 | ||||||
| chr3:100046785
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.65-100188G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100046785 | ||||||
| chr3:100046970
|
A | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-100003A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100046970 | ||||||
| chr3:100047219
|
G | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-99754G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100047219 | ||||||
| chr3:100047534
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-99439C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100047534 | ||||||
| chr3:100047623
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-99350A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100047623 | ||||||
| chr3:100047630
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.65-99343G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100047630 | ||||||
| chr3:100047647
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-99326G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100047647 | ||||||
| chr3:100047958
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-99015C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100047958 | ||||||
| chr3:100048252
|
A | G | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-98721A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048252 | ||||||
| chr3:100048371
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-98602A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048371 | ||||||
| chr3:100048447
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.65-98526G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048447 | ||||||
| chr3:100048565
|
G | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-98408G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048565 | ||||||
| chr3:100048697
|
G | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-98276G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048697 | ||||||
| chr3:100048709
|
A | C | 117 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.65-98264A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048709 | ||||||
| chr3:100048796
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-98177G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048796 | ||||||
| chr3:100048798
|
C | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-98175C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048798 | ||||||
| chr3:100048894
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0002g0077 | 2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.65-98079C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100048894 | ||||||
| chr3:100049003
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.65-97970T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100049003 | ||||||
| chr3:100049550
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-97423G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100049550 | ||||||
| chr3:100049939
|
C | G | 4 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(1): Show | 4 | HG02040.hp2 HG02129.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-97034C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100049939 | ||||||
| chr3:100050244
|
C | G | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-96729C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050244 | ||||||
| chr3:100050493
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-96480G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050493 | ||||||
| chr3:100050498
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-96475A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050498 | ||||||
| chr3:100050534
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-96439T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050534 | ||||||
| chr3:100050587
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.65-96386A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050587 | ||||||
| chr3:100050625
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.65-96348A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050625 | ||||||
| chr3:100050746
|
T | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-96227T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050746 | ||||||
| chr3:100050967
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-96006C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050967 | ||||||
| chr3:100050990
|
T | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-95983T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100050990 | ||||||
| chr3:100051302
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.65-95671G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100051302 | ||||||
| chr3:100051324
|
A | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-95649A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100051324 | ||||||
| chr3:100051463
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-95510G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100051463 | ||||||
| chr3:100051663
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-95310A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100051663 | ||||||
| chr3:100051744
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-95229C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100051744 | ||||||
| chr3:100051806
|
A | G | 2 | a0002c0002t0003g0136a0002c0002t0003g0137 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.65-95167A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100051806 | ||||||
| chr3:100051852
|
A | G | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-95121A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100051852 | ||||||
| chr3:100052025
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.65-94948A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052025 | ||||||
| chr3:100052375
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.65-94598A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052375 | ||||||
| chr3:100052404
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0024a0001c0001t0004g0025others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-94569G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052404 | ||||||
| chr3:100052430
|
G | A | 4 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-94543G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052430 | ||||||
| chr3:100052506
|
G | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-94467G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052506 | ||||||
| chr3:100052694
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-94279G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052694 | ||||||
| chr3:100052695
|
A | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-94278A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052695 | ||||||
| chr3:100052855
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01168.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.65-94118G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052855 | ||||||
| chr3:100052965
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.65-94008C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100052965 | ||||||
| chr3:100053116
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-93857A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100053116 | ||||||
| chr3:100053172
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-93801A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100053172 | ||||||
| chr3:100053551
|
A | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-93422A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100053551 | ||||||
| chr3:100053571
|
C | G | 182 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(179): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.65-93402C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100053571 | ||||||
| chr3:100054353
|
C | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-92620C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100054353 | ||||||
| chr3:100054490
|
T | TTGTTA | 39 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0165others(36): Show | 39 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.65-92434_65-92430d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100054490 | |||||
| chr3:100054490
|
T | TTGTTATG others(3): Show |
8 | a0001c0001t0001g0173a0001c0001t0001g0181a0001c0001t0002g0147others(5): Show | 8 | HG00738.hp2 HG01256.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-92439_65-92430d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100054490 | |||||
| chr3:100054490
|
T | TTGTTATG others(8): Show |
3 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0002g0155 | 3 | HG01515.hp2 HG01978.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.65-92444_65-92430d others(17): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100054490 | |||||
| chr3:100054490
|
TTGTTA | T | 119 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.65-92434_65-92430d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100054490 | |||||
| chr3:100054490
|
TTGTTATG others(3): Show |
T | 14 | a0001c0001t0001g0069a0001c0001t0001g0160a0001c0001t0001g0174others(11): Show | 14 | HG01069.hp1 HG01516.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-92439_65-92430d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100054490 | |||||
| chr3:100054536
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.65-92437T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100054536 | ||||||
| chr3:100054844
|
G | C | 1 | a0002c0002t0020g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.65-92129G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100054844 | ||||||
| chr3:100054885
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-92088A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100054885 | ||||||
| chr3:100055072
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-91901T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100055072 | ||||||
| chr3:100055210
|
A | G | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.65-91763A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100055210 | ||||||
| chr3:100055292
|
C | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-91681C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100055292 | ||||||
| chr3:100055864
|
T | C | 4 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(1): Show | 4 | HG02040.hp2 HG02129.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-91109T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100055864 | ||||||
| chr3:100055876
|
T | G | 69 | a0001c0001t0001g0031a0001c0001t0001g0163a0001c0001t0001g0165others(66): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-91097T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100055876 | ||||||
| chr3:100055969
|
T | A | 1 | a0001c0001t0004g0017 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.65-91004T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100055969 | ||||||
| chr3:100055993
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-90980G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100055993 | ||||||
| chr3:100056282
|
A | G | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.65-90691A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056282 | ||||||
| chr3:100056621
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.65-90352T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056621 | ||||||
| chr3:100056701
|
T | TA | 34 | a0001c0001t0001g0132a0001c0001t0002g0108a0001c0001t0002g0140others(31): Show | 35 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.65-90259dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100056701 | |||||
| chr3:100056723
|
G | A | 19 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0093others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.65-90250G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056723 | ||||||
| chr3:100056727
|
C | A | 1 | a0001c0001t0005g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-90246C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056727 | ||||||
| chr3:100056727
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.65-90246C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056727 | ||||||
| chr3:100056776
|
G | A | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043 | 3 | HG01952.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65-90197G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056776 | ||||||
| chr3:100056780
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-90193G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056780 | ||||||
| chr3:100056850
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-90123A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056850 | ||||||
| chr3:100056877
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.65-90096G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056877 | ||||||
| chr3:100056894
|
C | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-90079C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056894 | ||||||
| chr3:100056993
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.65-89980G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100056993 | ||||||
| chr3:100057014
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-89959G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057014 | ||||||
| chr3:100057102
|
G | C | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-89871G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057102 | ||||||
| chr3:100057223
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.65-89750G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057223 | ||||||
| chr3:100057301
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-89672C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057301 | ||||||
| chr3:100057428
|
A | C | 1 | a0001c0001t0002g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.65-89545A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057428 | ||||||
| chr3:100057601
|
G | A | 18 | a0001c0001t0002g0013a0001c0001t0004g0011a0001c0001t0004g0014others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-89372G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057601 | ||||||
| chr3:100057792
|
A | C | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.65-89181A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057792 | ||||||
| chr3:100057968
|
A | T | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.65-89005A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057968 | ||||||
| chr3:100057990
|
C | G | 1 | a0002c0002t0003g0113 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.65-88983C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100057990 | ||||||
| chr3:100058186
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-88787G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058186 | ||||||
| chr3:100058304
|
A | T | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-88669A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058304 | ||||||
| chr3:100058334
|
TA | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-88638delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058334 | ||||||
| chr3:100058336
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-88637C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058336 | ||||||
| chr3:100058432
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-88541A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058432 | ||||||
| chr3:100058616
|
C | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-88357C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058616 | ||||||
| chr3:100058645
|
A | G | 3 | a0001c0001t0007g0029a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-88328A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058645 | ||||||
| chr3:100058745
|
G | A | 1 | a0002c0002t0003g0184 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.65-88228G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100058745 | ||||||
| chr3:100059003
|
A | C | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.65-87970A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100059003 | ||||||
| chr3:100059394
|
C | G | 7 | a0001c0001t0002g0013a0001c0001t0004g0014a0001c0001t0004g0030others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-87579C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100059394 | ||||||
| chr3:100059568
|
A | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-87405A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100059568 | ||||||
| chr3:100059648
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-87325G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100059648 | ||||||
| chr3:100059811
|
T | C | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-87162T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100059811 | ||||||
| chr3:100060077
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-86896A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060077 | ||||||
| chr3:100060097
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-86876C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060097 | ||||||
| chr3:100060130
|
G | T | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.65-86843G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060130 | ||||||
| chr3:100060191
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.65-86782A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060191 | ||||||
| chr3:100060226
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.65-86747A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060226 | ||||||
| chr3:100060420
|
A | G | 112 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.65-86553A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060420 | ||||||
| chr3:100060493
|
C | T | 1 | a0001c0001t0002g0080 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.65-86480C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060493 | ||||||
| chr3:100060580
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-86393C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060580 | ||||||
| chr3:100060640
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-86333A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060640 | ||||||
| chr3:100060706
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-86267C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060706 | ||||||
| chr3:100060814
|
C | T | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-86159C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060814 | ||||||
| chr3:100060981
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-85992G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100060981 | ||||||
| chr3:100061139
|
TA | T | 5 | a0001c0001t0001g0188a0001c0001t0002g0075a0001c0001t0002g0209others(2): Show | 5 | HG01256.hp1 HG01257.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-85820delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100061139 | |||||
| chr3:100061140
|
A | T | 99 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(96): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.65-85833A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061140 | ||||||
| chr3:100061141
|
A | T | 3 | a0001c0001t0002g0209a0001c0001t0005g0084a0001c0001t0007g0032 | 3 | HG01975.hp2 HG02895.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.65-85832A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061141 | ||||||
| chr3:100061158
|
A | T | 1 | a0001c0001t0002g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.65-85815A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061158 | ||||||
| chr3:100061338
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-85635G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061338 | ||||||
| chr3:100061549
|
A | C | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-85424A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061549 | ||||||
| chr3:100061706
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-85267A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061706 | ||||||
| chr3:100061789
|
C | T | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.65-85184C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061789 | ||||||
| chr3:100061830
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-85143G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100061830 | ||||||
| chr3:100062093
|
C | CT | 10 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0221others(7): Show | 10 | HG00323.hp1 HG01261.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-84844dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
C | CTT | 7 | a0001c0001t0001g0069a0001c0001t0001g0190a0001c0001t0001g0217others(4): Show | 7 | HG01346.hp2 HG02074.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-84845_65-84844d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
C | CTTT | 10 | a0001c0001t0002g0013a0001c0001t0002g0046a0001c0001t0002g0067others(7): Show | 10 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-84846_65-84844d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0004g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.65-84853_65-84844d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0004g0011a0001c0001t0004g0023 | 2 | HG01168.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.65-84855_65-84844d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CT | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0070a0001c0001t0001g0160others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.65-84844delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTT | C | 37 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(34): Show | 37 | HG00423.hp1 HG01123.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.65-84845_65-84844d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTT | C | 22 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0031others(19): Show | 22 | HG01069.hp1 HG01257.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-84846_65-84844d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0026 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.65-84853_65-84844d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0151a0001c0001t0004g0025 | 2 | HG03490.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.65-84854_65-84844d others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-84855_65-84844d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTTTTTT others(9): Show |
C | 9 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(6): Show | 9 | HG02027.hp2 HG02523.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-84859_65-84844d others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTTTTTT others(10): Show |
C | 14 | a0001c0001t0001g0132a0001c0001t0018g0002a0002c0002t0003g0001others(11): Show | 15 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-84860_65-84844d others(19): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTTTTTT others(11): Show |
C | 22 | a0001c0001t0002g0108a0001c0001t0002g0140a0002c0002t0003g0115others(19): Show | 22 | HG00140.hp2 HG00741.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-84861_65-84844d others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062093
|
CTTTTTTT others(12): Show |
C | 25 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(22): Show | 25 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.65-84862_65-84844d others(21): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100062093 | |||||
| chr3:100062100
|
T | C | 1 | a0001c0001t0015g0230 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.65-84873T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062100 | ||||||
| chr3:100062108
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-84865T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062108 | ||||||
| chr3:100062113
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-84860T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062113 | ||||||
| chr3:100062156
|
G | A | 2 | a0002c0002t0003g0128a0002c0002t0003g0129 | 2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.65-84817G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062156 | ||||||
| chr3:100062185
|
C | A | 1 | a0001c0001t0010g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.65-84788C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062185 | ||||||
| chr3:100062358
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG03654.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.65-84615G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062358 | ||||||
| chr3:100062390
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-84583T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062390 | ||||||
| chr3:100062407
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-84566G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062407 | ||||||
| chr3:100062409
|
T | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-84564T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062409 | ||||||
| chr3:100062563
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-84410T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062563 | ||||||
| chr3:100062680
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-84293C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062680 | ||||||
| chr3:100062786
|
C | G | 1 | a0001c0001t0002g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.65-84187C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062786 | ||||||
| chr3:100062816
|
C | G | 1 | a0002c0002t0003g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-84157C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062816 | ||||||
| chr3:100062826
|
C | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-84147C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062826 | ||||||
| chr3:100062961
|
G | A | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-84012G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100062961 | ||||||
| chr3:100063026
|
G | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.65-83947G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063026 | ||||||
| chr3:100063296
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-83677A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063296 | ||||||
| chr3:100063357
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-83616G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063357 | ||||||
| chr3:100063383
|
T | G | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-83590T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063383 | ||||||
| chr3:100063420
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-83553A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063420 | ||||||
| chr3:100063731
|
GA | G | 60 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.65-83235delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100063731 | |||||
| chr3:100063898
|
A | C | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.65-83075A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063898 | ||||||
| chr3:100063950
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-83023G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063950 | ||||||
| chr3:100063978
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.65-82995G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063978 | ||||||
| chr3:100063988
|
A | C | 1 | a0002c0002t0003g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.65-82985A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100063988 | ||||||
| chr3:100064354
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-82619C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100064354 | ||||||
| chr3:100064811
|
A | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-82162A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100064811 | ||||||
| chr3:100065076
|
T | C | 22 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(19): Show | 22 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-81897T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065076 | ||||||
| chr3:100065165
|
A | C | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-81808A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065165 | ||||||
| chr3:100065230
|
A | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-81743A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065230 | ||||||
| chr3:100065561
|
C | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-81412C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065561 | ||||||
| chr3:100065591
|
C | A | 1 | a0001c0001t0002g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.65-81382C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065591 | ||||||
| chr3:100065672
|
G | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-81301G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065672 | ||||||
| chr3:100065683
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-81290A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065683 | ||||||
| chr3:100065684
|
CTTGAT | C | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.65-81285_65-81281d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100065684 | |||||
| chr3:100065833
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-81140C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100065833 | ||||||
| chr3:100066271
|
A | G | 1 | a0002c0002t0003g0123 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.65-80702A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100066271 | ||||||
| chr3:100066343
|
T | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-80630T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100066343 | ||||||
| chr3:100066362
|
G | C | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-80611G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100066362 | ||||||
| chr3:100066383
|
G | A | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-80590G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100066383 | ||||||
| chr3:100066506
|
AGGCTTTG others(299): Show |
A | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-80453_65-80148d others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100066506 | |||||
| chr3:100066517
|
C | CT | 8 | a0001c0001t0002g0067a0001c0001t0002g0145a0001c0001t0002g0146others(5): Show | 8 | HG00741.hp1 HG01981.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-80424dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100066517 | |||||
| chr3:100066517
|
CT | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0069others(57): Show | 60 | HG00423.hp1 HG01168.hp1 HG01257.hp1 others(57): Show |
intron_variant | MODIFIER | c.65-80424delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100066517 | |||||
| chr3:100066517
|
CTT | C | 58 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0034others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.65-80425_65-80424d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100066517 | |||||
| chr3:100066886
|
T | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-80087T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100066886 | ||||||
| chr3:100067050
|
G | A | 10 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0111others(7): Show | 10 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-79923G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067050 | ||||||
| chr3:100067104
|
G | A | 1 | a0002c0002t0003g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.65-79869G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067104 | ||||||
| chr3:100067109
|
A | G | 1 | a0001c0001t0004g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.65-79864A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067109 | ||||||
| chr3:100067166
|
C | CGTTT | 62 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(59): Show | 63 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.65-79778_65-79775d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100067166 | |||||
| chr3:100067166
|
C | CGTTTGTT others(1): Show |
22 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0034others(19): Show | 22 | HG01516.hp1 HG01928.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-79782_65-79775d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100067166 | |||||
| chr3:100067166
|
CGTTT | C | 7 | a0001c0001t0001g0180a0001c0001t0001g0190a0001c0001t0006g0003others(4): Show | 7 | HG02074.hp1 HG02109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-79778_65-79775d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100067166 | |||||
| chr3:100067166
|
CGTTTGTT others(5): Show |
C | 2 | a0002c0002t0003g0130a0002c0002t0003g0138 | 2 | HG00741.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.65-79786_65-79775d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100067166 | |||||
| chr3:100067286
|
G | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-79687G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067286 | ||||||
| chr3:100067324
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.65-79649A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067324 | ||||||
| chr3:100067445
|
A | G | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-79528A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067445 | ||||||
| chr3:100067548
|
T | G | 2 | a0001c0001t0006g0057a0001c0001t0006g0071 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.65-79425T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067548 | ||||||
| chr3:100067605
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-79368G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100067605 | ||||||
| chr3:100068167
|
T | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-78806T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100068167 | ||||||
| chr3:100068186
|
A | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-78787A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100068186 | ||||||
| chr3:100068350
|
C | CTG | 6 | a0001c0001t0002g0078a0001c0001t0002g0080a0001c0001t0002g0081others(3): Show | 6 | HG02280.hp2 HG03139.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-78591_65-78590d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100068350 | |||||
| chr3:100068350
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-78599_65-78590d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100068350 | |||||
| chr3:100068350
|
CTG | C | 77 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0001g0179others(74): Show | 78 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.65-78591_65-78590d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100068350 | |||||
| chr3:100068350
|
CTGTG | C | 92 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0031others(89): Show | 92 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.65-78593_65-78590d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100068350 | |||||
| chr3:100068350
|
CTGTGTG | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0194a0001c0001t0001g0199others(1): Show | 4 | HG00323.hp1 HG01261.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-78595_65-78590d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100068350 | |||||
| chr3:100068654
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.65-78319G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100068654 | ||||||
| chr3:100068697
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-78276G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100068697 | ||||||
| chr3:100068811
|
A | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-78162A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100068811 | ||||||
| chr3:100069138
|
G | A | 174 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(171): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.65-77835G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069138 | ||||||
| chr3:100069187
|
G | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG00280.hp2 HG01071.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-77786G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069187 | ||||||
| chr3:100069229
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-77744A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069229 | ||||||
| chr3:100069448
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-77525G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069448 | ||||||
| chr3:100069551
|
A | G | 1 | a0001c0001t0004g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.65-77422A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069551 | ||||||
| chr3:100069609
|
A | G | 4 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(1): Show | 4 | HG02040.hp2 HG02129.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-77364A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069609 | ||||||
| chr3:100069619
|
C | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-77354C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069619 | ||||||
| chr3:100069944
|
A | G | 1 | a0002c0002t0003g0118 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.65-77029A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069944 | ||||||
| chr3:100069976
|
T | C | 1 | a0002c0002t0003g0118 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.65-76997T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100069976 | ||||||
| chr3:100070020
|
T | TA | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-76947dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100070020 | |||||
| chr3:100070102
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-76871C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070102 | ||||||
| chr3:100070118
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-76855G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070118 | ||||||
| chr3:100070187
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-76786C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070187 | ||||||
| chr3:100070438
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-76535A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070438 | ||||||
| chr3:100070439
|
TA | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.65-76533delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070439 | ||||||
| chr3:100070613
|
G | A | 1 | a0002c0002t0003g0109 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.65-76360G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070613 | ||||||
| chr3:100070618
|
G | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-76355G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070618 | ||||||
| chr3:100070692
|
C | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.65-76281C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070692 | ||||||
| chr3:100070693
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-76280G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070693 | ||||||
| chr3:100070703
|
C | T | 1 | a0002c0002t0003g0125 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.65-76270C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070703 | ||||||
| chr3:100070922
|
C | T | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-76051C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100070922 | ||||||
| chr3:100071090
|
C | CT | 66 | a0001c0001t0001g0132a0001c0001t0001g0198a0001c0001t0001g0213others(63): Show | 67 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.65-75862dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100071090 | |||||
| chr3:100071090
|
C | CTT | 95 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0031others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.65-75863_65-75862d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100071090 | |||||
| chr3:100071090
|
C | CTTT | 32 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0035others(29): Show | 32 | HG00140.hp1 HG01168.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.65-75864_65-75862d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100071090 | |||||
| chr3:100071164
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-75809A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100071164 | ||||||
| chr3:100071240
|
C | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-75733C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100071240 | ||||||
| chr3:100071359
|
A | G | 1 | a0001c0001t0005g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-75614A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100071359 | ||||||
| chr3:100071488
|
A | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-75485A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100071488 | ||||||
| chr3:100071723
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.65-75250C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100071723 | ||||||
| chr3:100071900
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-75073G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100071900 | ||||||
| chr3:100071905
|
T | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-75068T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100071905 | ||||||
| chr3:100072407
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-74566G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100072407 | ||||||
| chr3:100072562
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.65-74411C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100072562 | ||||||
| chr3:100072668
|
A | G | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.65-74305A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100072668 | ||||||
| chr3:100072681
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-74292T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100072681 | ||||||
| chr3:100072706
|
C | G | 189 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(186): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.65-74267C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100072706 | ||||||
| chr3:100072900
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.65-74073C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100072900 | ||||||
| chr3:100073143
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.65-73830G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100073143 | ||||||
| chr3:100073194
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-73779T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100073194 | ||||||
| chr3:100073271
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-73702C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100073271 | ||||||
| chr3:100073430
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-73543T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100073430 | ||||||
| chr3:100073431
|
A | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-73542A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100073431 | ||||||
| chr3:100073571
|
AAG | A | 6 | a0002c0002t0003g0121a0002c0002t0003g0122a0002c0002t0003g0123others(3): Show | 6 | NA18943.hp2 NA18959.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-73397_65-73396d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100073571 | |||||
| chr3:100073983
|
TCCTTC | T | 3 | a0001c0001t0002g0074a0001c0001t0006g0057a0001c0001t0006g0071 | 3 | HG02280.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.65-72985_65-72981d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100073983 | |||||
| chr3:100074033
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-72940C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100074033 | ||||||
| chr3:100074408
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.65-72565T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100074408 | ||||||
| chr3:100074675
|
A | AT | 18 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(15): Show | 18 | HG00741.hp1 HG01258.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-72262dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATT | 9 | a0001c0001t0001g0069a0001c0001t0002g0047a0001c0001t0002g0054others(6): Show | 9 | HG01256.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-72263_65-72262d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTT | 6 | a0001c0001t0002g0067a0001c0001t0002g0077a0001c0001t0002g0147others(3): Show | 6 | HG00738.hp2 HG02080.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-72264_65-72262d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTT | 6 | a0001c0001t0001g0031a0001c0001t0001g0165a0001c0001t0001g0176others(3): Show | 6 | HG02809.hp1 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-72267_65-72262d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT | 7 | a0001c0001t0001g0037a0001c0001t0001g0162a0001c0001t0001g0170others(4): Show | 7 | HG02602.hp2 HG03195.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-72268_65-72262d others(9): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(1): Show |
24 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0158others(21): Show | 24 | HG00280.hp2 HG00323.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-72269_65-72262d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(2): Show |
23 | a0001c0001t0001g0020a0001c0001t0001g0160a0001c0001t0001g0167others(20): Show | 23 | HG00140.hp1 HG00423.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-72270_65-72262d others(11): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(3): Show |
15 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0181others(12): Show | 15 | HG01515.hp1 HG01891.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-72271_65-72262d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(4): Show |
12 | a0001c0001t0001g0185a0001c0001t0001g0204a0001c0001t0001g0214others(9): Show | 12 | HG01168.hp1 HG01978.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-72272_65-72262d others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0203a0001c0001t0001g0207a0001c0001t0004g0019others(1): Show | 4 | HG01975.hp2 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-72273_65-72262d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0157a0001c0001t0007g0033 | 2 | NA18522.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.65-72274_65-72262d others(15): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0222a0001c0001t0004g0030a0001c0001t0010g0055 | 3 | HG02486.hp2 HG02970.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.65-72275_65-72262d others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0004g0014a0001c0001t0010g0056 | 2 | HG01516.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.65-72276_65-72262d others(17): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-72283_65-72262d others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0038a0001c0001t0002g0094a0001c0001t0002g0103others(3): Show | 6 | HG01257.hp2 HG02055.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-72271_65-72262d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
ATTTTTTT others(4): Show |
A | 18 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0102others(15): Show | 18 | HG00280.hp1 HG00423.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-72272_65-72262d others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
ATTTTTTT others(5): Show |
A | 36 | a0001c0001t0001g0132a0001c0001t0001g0219a0001c0001t0002g0090others(33): Show | 37 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.65-72273_65-72262d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
ATTTTTTT others(6): Show |
A | 1 | a0002c0002t0003g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.65-72274_65-72262d others(15): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.65-72277_65-72262d others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074675
|
ATTTTTTT others(12): Show |
A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-72280_65-72262d others(21): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100074675 | |||||
| chr3:100074717
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-72256G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100074717 | ||||||
| chr3:100074720
|
G | A | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-72253G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100074720 | ||||||
| chr3:100074913
|
C | T | 49 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0186others(46): Show | 49 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.65-72060C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100074913 | ||||||
| chr3:100074990
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-71983G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100074990 | ||||||
| chr3:100075060
|
TA | T | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-71912delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075060 | ||||||
| chr3:100075068
|
T | A | 1 | a0001c0001t0002g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.65-71905T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075068 | ||||||
| chr3:100075359
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-71614C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075359 | ||||||
| chr3:100075370
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.65-71603A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075370 | ||||||
| chr3:100075681
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-71292G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075681 | ||||||
| chr3:100075769
|
T | C | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-71204T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075769 | ||||||
| chr3:100075886
|
G | T | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-71087G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075886 | ||||||
| chr3:100075901
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0165 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.65-71072G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075901 | ||||||
| chr3:100075910
|
G | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-71063G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075910 | ||||||
| chr3:100075998
|
G | A | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-70975G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100075998 | ||||||
| chr3:100076144
|
T | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-70829T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076144 | ||||||
| chr3:100076150
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.65-70823G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076150 | ||||||
| chr3:100076150
|
G | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-70823G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076150 | ||||||
| chr3:100076154
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-70819A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076154 | ||||||
| chr3:100076207
|
T | A | 1 | a0002c0002t0003g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.65-70766T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076207 | ||||||
| chr3:100076397
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-70576G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076397 | ||||||
| chr3:100076581
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.65-70392C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076581 | ||||||
| chr3:100076590
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-70383G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076590 | ||||||
| chr3:100076663
|
A | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-70310A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076663 | ||||||
| chr3:100076807
|
G | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-70166G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076807 | ||||||
| chr3:100076817
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-70156G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100076817 | ||||||
| chr3:100077002
|
C | T | 1 | a0002c0002t0003g0127 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.65-69971C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100077002 | ||||||
| chr3:100077024
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-69949G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100077024 | ||||||
| chr3:100077231
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.65-69742A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100077231 | ||||||
| chr3:100077331
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-69642C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100077331 | ||||||
| chr3:100077565
|
A | T | 1 | a0002c0002t0003g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-69408A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100077565 | ||||||
| chr3:100077782
|
T | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-69191T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100077782 | ||||||
| chr3:100078061
|
T | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-68912T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078061 | ||||||
| chr3:100078063
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-68910G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078063 | ||||||
| chr3:100078078
|
TA | T | 12 | a0001c0001t0001g0165a0001c0001t0001g0210a0001c0001t0002g0049others(9): Show | 12 | HG00280.hp1 HG01123.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-68883delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100078078 | |||||
| chr3:100078169
|
C | G | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-68804C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078169 | ||||||
| chr3:100078551
|
A | G | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043 | 3 | HG01952.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.65-68422A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078551 | ||||||
| chr3:100078594
|
GA | G | 23 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0093others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.65-68369delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100078594 | |||||
| chr3:100078602
|
A | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-68371A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078602 | ||||||
| chr3:100078617
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-68356G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078617 | ||||||
| chr3:100078625
|
G | A | 1 | a0001c0001t0008g0087 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.65-68348G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078625 | ||||||
| chr3:100078743
|
T | C | 26 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(23): Show | 26 | HG01168.hp1 HG01516.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-68230T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078743 | ||||||
| chr3:100078798
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-68175G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078798 | ||||||
| chr3:100078912
|
T | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-68061T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078912 | ||||||
| chr3:100078970
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-68003A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100078970 | ||||||
| chr3:100080255
|
T | C | 2 | a0002c0002t0003g0001a0002c0002t0003g0135 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.65-66718T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100080255 | ||||||
| chr3:100080323
|
GA | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-66641delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100080323 | |||||
| chr3:100080345
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-66628A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100080345 | ||||||
| chr3:100080397
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.65-66576C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100080397 | ||||||
| chr3:100080442
|
AT | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-66527delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100080442 | |||||
| chr3:100080550
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.65-66423T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100080550 | ||||||
| chr3:100080705
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-66268G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100080705 | ||||||
| chr3:100081175
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-65798C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100081175 | ||||||
| chr3:100081231
|
G | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-65742G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100081231 | ||||||
| chr3:100081302
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-65671G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100081302 | ||||||
| chr3:100081618
|
A | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-65355A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100081618 | ||||||
| chr3:100081838
|
G | GTA | 2 | a0001c0001t0006g0057a0001c0001t0006g0071 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.65-65134_65-65133d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100081838 | |||||
| chr3:100081958
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-65015G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100081958 | ||||||
| chr3:100081972
|
G | A | 8 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-65001G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100081972 | ||||||
| chr3:100082033
|
T | C | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.65-64940T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082033 | ||||||
| chr3:100082185
|
G | C | 8 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-64788G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082185 | ||||||
| chr3:100082254
|
A | G | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65-64719A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082254 | ||||||
| chr3:100082382
|
G | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-64591G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082382 | ||||||
| chr3:100082784
|
A | C | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-64189A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082784 | ||||||
| chr3:100082803
|
T | C | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-64170T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082803 | ||||||
| chr3:100082806
|
T | G | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-64167T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082806 | ||||||
| chr3:100082812
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0165 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.65-64161A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082812 | ||||||
| chr3:100082898
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-64075A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082898 | ||||||
| chr3:100082925
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-64048G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100082925 | ||||||
| chr3:100083402
|
C | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-63571C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100083402 | ||||||
| chr3:100083492
|
C | T | 1 | a0002c0002t0003g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.65-63481C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100083492 | ||||||
| chr3:100083618
|
T | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-63355T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100083618 | ||||||
| chr3:100083800
|
TCTGGG | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0037 | 2 | HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.65-63170_65-63166d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100083800 | |||||
| chr3:100084296
|
C | T | 1 | a0002c0002t0003g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.65-62677C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100084296 | ||||||
| chr3:100084529
|
A | C | 1 | a0001c0001t0004g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-62444A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100084529 | ||||||
| chr3:100084743
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-62230G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100084743 | ||||||
| chr3:100085233
|
G | C | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.65-61740G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100085233 | ||||||
| chr3:100085642
|
C | T | 2 | a0002c0002t0003g0136a0002c0002t0003g0137 | 2 | HG00140.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.65-61331C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100085642 | ||||||
| chr3:100086180
|
A | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-60793A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086180 | ||||||
| chr3:100086214
|
T | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-60759T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086214 | ||||||
| chr3:100086231
|
G | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-60742G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086231 | ||||||
| chr3:100086260
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-60713C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086260 | ||||||
| chr3:100086291
|
G | T | 4 | a0001c0001t0004g0022a0001c0001t0004g0024a0001c0001t0004g0025others(1): Show | 4 | HG03490.hp2 HG03492.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-60682G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086291 | ||||||
| chr3:100086421
|
GA | G | 8 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(5): Show | 8 | HG01891.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-60544delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100086421 | |||||
| chr3:100086470
|
G | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-60503G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086470 | ||||||
| chr3:100086811
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.65-60162G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086811 | ||||||
| chr3:100086817
|
C | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-60156C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086817 | ||||||
| chr3:100086874
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-60099A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086874 | ||||||
| chr3:100086883
|
C | T | 7 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-60090C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100086883 | ||||||
| chr3:100087260
|
T | G | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.65-59713T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087260 | ||||||
| chr3:100087426
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-59547C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087426 | ||||||
| chr3:100087630
|
C | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-59343C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087630 | ||||||
| chr3:100087631
|
T | C | 1 | a0002c0002t0003g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.65-59342T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087631 | ||||||
| chr3:100087643
|
A | G | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-59330A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087643 | ||||||
| chr3:100087652
|
G | A | 175 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(172): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.65-59321G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087652 | ||||||
| chr3:100087801
|
A | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-59172A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087801 | ||||||
| chr3:100087832
|
C | CT | 10 | a0001c0001t0001g0211a0001c0001t0002g0047a0001c0001t0002g0049others(7): Show | 10 | HG01516.hp1 HG01981.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-59119dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100087832 | |||||
| chr3:100087832
|
CT | C | 65 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(62): Show | 66 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-59119delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100087832 | |||||
| chr3:100087934
|
A | G | 229 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(226): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.65-59039A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100087934 | ||||||
| chr3:100088105
|
A | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-58868A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100088105 | ||||||
| chr3:100088322
|
G | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-58651G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100088322 | ||||||
| chr3:100088328
|
C | T | 1 | a0002c0002t0003g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.65-58645C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100088328 | ||||||
| chr3:100088379
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-58594A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100088379 | ||||||
| chr3:100088514
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-58459G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100088514 | ||||||
| chr3:100088727
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-58246T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100088727 | ||||||
| chr3:100088891
|
G | A | 69 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-58082G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100088891 | ||||||
| chr3:100089309
|
C | CTAA | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-57662_65-57661i others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100089309 | |||||
| chr3:100089456
|
T | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-57517T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089456 | ||||||
| chr3:100089494
|
A | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-57479A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089494 | ||||||
| chr3:100089557
|
C | CA | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-57415dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100089557 | |||||
| chr3:100089559
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-57414G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089559 | ||||||
| chr3:100089601
|
G | A | 105 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.65-57372G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089601 | ||||||
| chr3:100089714
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-57259A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089714 | ||||||
| chr3:100089717
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.65-57256A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089717 | ||||||
| chr3:100089885
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-57088C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089885 | ||||||
| chr3:100089960
|
A | T | 69 | a0001c0001t0001g0031a0001c0001t0001g0163a0001c0001t0001g0165others(66): Show | 69 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-57013A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100089960 | ||||||
| chr3:100090085
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-56888T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100090085 | ||||||
| chr3:100090214
|
T | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-56759T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100090214 | ||||||
| chr3:100090281
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-56692G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100090281 | ||||||
| chr3:100090528
|
C | G | 196 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.65-56445C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100090528 | ||||||
| chr3:100090564
|
C | T | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-56409C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100090564 | ||||||
| chr3:100090582
|
C | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-56391C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100090582 | ||||||
| chr3:100090994
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-55979C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100090994 | ||||||
| chr3:100091082
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-55891G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091082 | ||||||
| chr3:100091111
|
C | T | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-55862C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091111 | ||||||
| chr3:100091126
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.65-55847A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091126 | ||||||
| chr3:100091129
|
C | CAAAAACT others(305): Show |
3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-55833_65-55832i others(314): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100091129 | |||||
| chr3:100091141
|
T | C | 25 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(22): Show | 25 | HG01168.hp1 HG01516.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.65-55832T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091141 | ||||||
| chr3:100091145
|
C | T | 25 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(22): Show | 25 | HG01168.hp1 HG01516.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.65-55828C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091145 | ||||||
| chr3:100091146
|
A | G | 25 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(22): Show | 25 | HG01168.hp1 HG01516.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.65-55827A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091146 | ||||||
| chr3:100091174
|
A | C | 1 | a0002c0002t0017g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.65-55799A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091174 | ||||||
| chr3:100091212
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-55761A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091212 | ||||||
| chr3:100091241
|
C | T | 2 | a0001c0001t0002g0095a0001c0001t0002g0101 | 2 | NA18612.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.65-55732C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091241 | ||||||
| chr3:100091284
|
C | CA | 6 | a0001c0001t0001g0157a0001c0001t0001g0190a0001c0001t0001g0199others(3): Show | 6 | HG01261.hp2 HG01952.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-55671dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100091284 | |||||
| chr3:100091284
|
CA | C | 8 | a0001c0001t0001g0207a0001c0001t0001g0222a0001c0001t0002g0073others(5): Show | 8 | HG02451.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-55671delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100091284 | |||||
| chr3:100091284
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-55681_65-55671d others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100091284 | |||||
| chr3:100091296
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-55677A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091296 | ||||||
| chr3:100091324
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-55649A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091324 | ||||||
| chr3:100091338
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-55635T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091338 | ||||||
| chr3:100091565
|
A | G | 219 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(216): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.65-55408A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091565 | ||||||
| chr3:100091771
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.65-55202A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091771 | ||||||
| chr3:100091813
|
G | T | 1 | a0001c0001t0002g0041 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-55160G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091813 | ||||||
| chr3:100091928
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-55045G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100091928 | ||||||
| chr3:100092414
|
G | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-54559G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100092414 | ||||||
| chr3:100092419
|
G | A | 1 | a0002c0002t0003g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.65-54554G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100092419 | ||||||
| chr3:100092464
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.65-54509G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100092464 | ||||||
| chr3:100092595
|
T | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-54378T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100092595 | ||||||
| chr3:100092709
|
T | C | 59 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0001g0183others(56): Show | 60 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.65-54264T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100092709 | ||||||
| chr3:100093219
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.65-53754G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100093219 | ||||||
| chr3:100093526
|
C | T | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-53447C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100093526 | ||||||
| chr3:100093527
|
G | A | 1 | a0002c0002t0003g0139 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-53446G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100093527 | ||||||
| chr3:100093576
|
G | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.65-53397G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100093576 | ||||||
| chr3:100094374
|
C | G | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-52599C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100094374 | ||||||
| chr3:100094449
|
T | C | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.65-52524T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100094449 | ||||||
| chr3:100094566
|
A | G | 1 | a0001c0001t0002g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.65-52407A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100094566 | ||||||
| chr3:100094674
|
C | CT | 24 | a0001c0001t0001g0202a0001c0001t0001g0213a0001c0001t0001g0214others(21): Show | 24 | HG00741.hp1 HG01257.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-52270dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100094674 | |||||
| chr3:100094674
|
CT | C | 76 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0034others(73): Show | 76 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.65-52270delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100094674 | |||||
| chr3:100094674
|
CTT | C | 40 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0001g0181others(37): Show | 40 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.65-52271_65-52270d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100094674 | |||||
| chr3:100094674
|
CTTTTTTT others(3): Show |
C | 25 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(22): Show | 25 | HG01168.hp1 HG01516.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.65-52279_65-52270d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100094674 | |||||
| chr3:100094674
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0015 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.65-52280_65-52270d others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100094674 | |||||
| chr3:100094778
|
G | A | 35 | a0001c0001t0001g0132a0001c0001t0002g0108a0001c0001t0002g0140others(32): Show | 36 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.65-52195G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100094778 | ||||||
| chr3:100094851
|
T | G | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.65-52122T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100094851 | ||||||
| chr3:100094870
|
A | G | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-52103A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100094870 | ||||||
| chr3:100094887
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-52086A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100094887 | ||||||
| chr3:100095140
|
T | TA | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-51827dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100095140 | |||||
| chr3:100095198
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-51775T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100095198 | ||||||
| chr3:100095246
|
C | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-51727C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100095246 | ||||||
| chr3:100095872
|
C | T | 7 | a0001c0001t0004g0014a0001c0001t0004g0019a0001c0001t0004g0030others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-51101C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100095872 | ||||||
| chr3:100096386
|
T | C | 18 | a0001c0001t0004g0011a0001c0001t0004g0014a0001c0001t0004g0015others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-50587T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100096386 | ||||||
| chr3:100097246
|
A | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0085 | 2 | NA18959.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.65-49727A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100097246 | ||||||
| chr3:100097511
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-49462A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100097511 | ||||||
| chr3:100097685
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-49288G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100097685 | ||||||
| chr3:100097742
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-49231C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100097742 | ||||||
| chr3:100097861
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.65-49112C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100097861 | ||||||
| chr3:100097882
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.65-49091T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100097882 | ||||||
| chr3:100097952
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.65-49021C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100097952 | ||||||
| chr3:100098058
|
G | A | 1 | a0002c0002t0003g0138 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-48915G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100098058 | ||||||
| chr3:100098167
|
C | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-48806C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100098167 | ||||||
| chr3:100098536
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-48437A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100098536 | ||||||
| chr3:100098711
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-48262A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100098711 | ||||||
| chr3:100098969
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-48004A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100098969 | ||||||
| chr3:100098998
|
G | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-47975G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100098998 | ||||||
| chr3:100099240
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.65-47733C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100099240 | ||||||
| chr3:100099252
|
G | A | 49 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0048others(46): Show | 49 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(46): Show |
intron_variant | MODIFIER | c.65-47721G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100099252 | ||||||
| chr3:100099378
|
C | G | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-47595C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100099378 | ||||||
| chr3:100099525
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.65-47448C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100099525 | ||||||
| chr3:100099784
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-47189G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100099784 | ||||||
| chr3:100099919
|
T | A | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.65-47054T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100099919 | ||||||
| chr3:100100201
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.65-46772G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100100201 | ||||||
| chr3:100100553
|
A | G | 2 | a0001c0001t0006g0057a0001c0001t0006g0071 | 2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.65-46420A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100100553 | ||||||
| chr3:100100774
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.65-46199C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100100774 | ||||||
| chr3:100100808
|
T | G | 14 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(11): Show | 14 | HG01516.hp1 HG01952.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-46165T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100100808 | ||||||
| chr3:100101528
|
G | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-45445G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100101528 | ||||||
| chr3:100101769
|
G | C | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-45204G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100101769 | ||||||
| chr3:100101776
|
T | C | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-45197T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100101776 | ||||||
| chr3:100101780
|
C | T | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-45193C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100101780 | ||||||
| chr3:100101882
|
G | C | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-45091G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100101882 | ||||||
| chr3:100102003
|
C | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-44970C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100102003 | ||||||
| chr3:100102125
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-44848G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100102125 | ||||||
| chr3:100102126
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-44847G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100102126 | ||||||
| chr3:100102167
|
C | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.65-44806C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100102167 | ||||||
| chr3:100102405
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.65-44568A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100102405 | ||||||
| chr3:100102465
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-44508G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100102465 | ||||||
| chr3:100102835
|
A | G | 12 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0130others(9): Show | 13 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-44138A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100102835 | ||||||
| chr3:100103244
|
C | T | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.65-43729C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103244 | ||||||
| chr3:100103291
|
C | T | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-43682C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103291 | ||||||
| chr3:100103313
|
G | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-43660G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103313 | ||||||
| chr3:100103451
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-43522C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103451 | ||||||
| chr3:100103595
|
A | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-43378A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103595 | ||||||
| chr3:100103692
|
C | T | 43 | a0001c0001t0001g0069a0001c0001t0002g0048a0001c0001t0002g0049others(40): Show | 43 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(40): Show |
intron_variant | MODIFIER | c.65-43281C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103692 | ||||||
| chr3:100103809
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-43164A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103809 | ||||||
| chr3:100103843
|
G | C | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-43130G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103843 | ||||||
| chr3:100103959
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-43014G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100103959 | ||||||
| chr3:100104098
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.65-42875C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100104098 | ||||||
| chr3:100104136
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-42837G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100104136 | ||||||
| chr3:100104406
|
A | G | 1 | a0002c0002t0003g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.65-42567A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100104406 | ||||||
| chr3:100105276
|
T | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0203others(1): Show | 4 | HG03654.hp1 HG03704.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-41697T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105276 | ||||||
| chr3:100105713
|
G | A | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.65-41260G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105713 | ||||||
| chr3:100105741
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-41232A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105741 | ||||||
| chr3:100105770
|
C | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-41203C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105770 | ||||||
| chr3:100105815
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0221 | 2 | HG00423.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.65-41158C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105815 | ||||||
| chr3:100105841
|
G | A | 57 | a0001c0001t0001g0102a0001c0001t0001g0132a0001c0001t0002g0086others(54): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.65-41132G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105841 | ||||||
| chr3:100105986
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-40987T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105986 | ||||||
| chr3:100105994
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-40979A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100105994 | ||||||
| chr3:100106453
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.65-40520G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100106453 | ||||||
| chr3:100106695
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-40278T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100106695 | ||||||
| chr3:100106773
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-40200G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100106773 | ||||||
| chr3:100106797
|
C | T | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-40176C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100106797 | ||||||
| chr3:100106804
|
C | T | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-40169C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100106804 | ||||||
| chr3:100106858
|
T | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-40115T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100106858 | ||||||
| chr3:100107237
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-39736T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100107237 | ||||||
| chr3:100107247
|
T | A | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-39726T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100107247 | ||||||
| chr3:100107488
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-39485G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100107488 | ||||||
| chr3:100107536
|
A | G | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-39437A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100107536 | ||||||
| chr3:100107550
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-39423C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100107550 | ||||||
| chr3:100107657
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.65-39316T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100107657 | ||||||
| chr3:100107848
|
T | C | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-39125T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100107848 | ||||||
| chr3:100107877
|
T | TA | 24 | a0001c0001t0001g0102a0001c0001t0001g0194a0001c0001t0001g0199others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.65-39078dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100107877 | |||||
| chr3:100107877
|
TA | T | 62 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0188others(59): Show | 62 | HG00140.hp1 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.65-39078delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100107877 | |||||
| chr3:100108098
|
T | G | 126 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0102others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.65-38875T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100108098 | ||||||
| chr3:100108369
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.65-38604G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100108369 | ||||||
| chr3:100108665
|
G | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-38308G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100108665 | ||||||
| chr3:100109087
|
TA | T | 108 | a0001c0001t0001g0069a0001c0001t0001g0102a0001c0001t0001g0132others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.65-37872delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100109087 | |||||
| chr3:100109087
|
TAA | T | 9 | a0001c0001t0002g0068a0001c0001t0006g0003a0001c0001t0006g0004others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-37873_65-37872d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100109087 | |||||
| chr3:100109144
|
C | T | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.65-37829C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109144 | ||||||
| chr3:100109161
|
G | T | 8 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-37812G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109161 | ||||||
| chr3:100109228
|
A | T | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-37745A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109228 | ||||||
| chr3:100109296
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.65-37677G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109296 | ||||||
| chr3:100109379
|
A | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-37594A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109379 | ||||||
| chr3:100109557
|
A | C | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-37416A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109557 | ||||||
| chr3:100109627
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.65-37346A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109627 | ||||||
| chr3:100109903
|
A | AC | 36 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0037others(33): Show | 36 | HG00423.hp1 HG01192.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.65-37058dupC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100109903 | |||||
| chr3:100109903
|
AC | A | 91 | a0001c0001t0001g0031a0001c0001t0001g0102a0001c0001t0001g0163others(88): Show | 92 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.65-37058delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100109903 | |||||
| chr3:100109911
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.65-37062C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109911 | ||||||
| chr3:100109912
|
C | G | 1 | a0001c0001t0004g0019 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.65-37061C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109912 | ||||||
| chr3:100109928
|
C | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0212a0001c0001t0001g0217 | 3 | HG02071.hp1 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.65-37045C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100109928 | ||||||
| chr3:100110072
|
AC | A | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-36897delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100110072 | |||||
| chr3:100110149
|
C | T | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.65-36824C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110149 | ||||||
| chr3:100110476
|
C | A | 34 | a0001c0001t0001g0102a0001c0001t0002g0086a0001c0001t0002g0090others(31): Show | 34 | HG00280.hp1 HG00423.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.65-36497C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110476 | ||||||
| chr3:100110483
|
C | G | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-36490C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110483 | ||||||
| chr3:100110500
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-36473T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110500 | ||||||
| chr3:100110577
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-36396C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110577 | ||||||
| chr3:100110663
|
A | G | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.65-36310A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110663 | ||||||
| chr3:100110708
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-36265G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110708 | ||||||
| chr3:100110787
|
T | C | 1 | a0002c0002t0003g0125 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.65-36186T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110787 | ||||||
| chr3:100110819
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-36154C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110819 | ||||||
| chr3:100110851
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-36122G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110851 | ||||||
| chr3:100110940
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.65-36033G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100110940 | ||||||
| chr3:100111067
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.65-35906G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111067 | ||||||
| chr3:100111335
|
C | G | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-35638C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111335 | ||||||
| chr3:100111368
|
G | A | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-35605G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111368 | ||||||
| chr3:100111433
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-35540A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111433 | ||||||
| chr3:100111566
|
A | C | 1 | a0002c0002t0003g0128 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.65-35407A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111566 | ||||||
| chr3:100111668
|
C | A | 2 | a0001c0001t0001g0220a0001c0001t0016g0195 | 2 | HG01981.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.65-35305C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111668 | ||||||
| chr3:100111777
|
C | T | 9 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(6): Show | 9 | HG02027.hp2 HG02523.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-35196C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111777 | ||||||
| chr3:100111801
|
C | T | 1 | a0001c0001t0002g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.65-35172C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111801 | ||||||
| chr3:100111838
|
G | A | 24 | a0001c0001t0001g0102a0001c0001t0002g0013a0001c0001t0002g0085others(21): Show | 24 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.65-35135G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111838 | ||||||
| chr3:100111928
|
A | G | 28 | a0001c0001t0001g0102a0001c0001t0002g0013a0001c0001t0002g0073others(25): Show | 28 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.65-35045A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100111928 | ||||||
| chr3:100112087
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-34886C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100112087 | ||||||
| chr3:100112123
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-34850A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100112123 | ||||||
| chr3:100112192
|
A | G | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-34781A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100112192 | ||||||
| chr3:100112723
|
AGAG | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-34249_65-34247d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100112723 | ||||||
| chr3:100112955
|
A | C | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-34018A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100112955 | ||||||
| chr3:100113149
|
C | T | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-33824C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100113149 | ||||||
| chr3:100113623
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.65-33350G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100113623 | ||||||
| chr3:100113756
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-33217A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100113756 | ||||||
| chr3:100113823
|
A | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-33150A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100113823 | ||||||
| chr3:100113949
|
C | A | 31 | a0001c0001t0001g0102a0001c0001t0002g0013a0001c0001t0002g0073others(28): Show | 31 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.65-33024C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100113949 | ||||||
| chr3:100114065
|
G | A | 18 | a0001c0001t0004g0011a0001c0001t0004g0014a0001c0001t0004g0015others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-32908G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114065 | ||||||
| chr3:100114065
|
G | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-32908G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114065 | ||||||
| chr3:100114066
|
TGCAGG | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-32906_65-32902d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114066 | ||||||
| chr3:100114095
|
T | G | 1 | a0001c0001t0001g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.65-32878T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114095 | ||||||
| chr3:100114491
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0002g0049others(4): Show | 7 | HG01928.hp1 HG01952.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-32482C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114491 | ||||||
| chr3:100114599
|
C | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-32374C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114599 | ||||||
| chr3:100114672
|
C | G | 1 | a0001c0001t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.65-32301C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114672 | ||||||
| chr3:100114861
|
C | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-32112C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114861 | ||||||
| chr3:100114879
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-32094C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114879 | ||||||
| chr3:100114883
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.65-32090A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100114883 | ||||||
| chr3:100115231
|
G | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-31742G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100115231 | ||||||
| chr3:100115512
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-31461A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100115512 | ||||||
| chr3:100115551
|
TTCTCTTT others(33): Show |
T | 1 | a0001c0001t0005g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.65-31416_65-31377d others(42): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115551 | |||||
| chr3:100115557
|
TTCTCTCT others(29): Show |
T | 1 | a0001c0001t0005g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.65-31398_65-31363d others(38): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115557 | |||||
| chr3:100115557
|
TTCTCTCT others(31): Show |
T | 1 | a0001c0001t0008g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.65-31398_65-31361d others(40): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115557 | |||||
| chr3:100115557
|
TTCTCTCT others(33): Show |
T | 28 | a0001c0001t0001g0102a0001c0001t0002g0013a0001c0001t0002g0073others(25): Show | 28 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.65-31398_65-31359d others(42): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115557 | |||||
| chr3:100115560
|
T | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-31413T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100115560 | ||||||
| chr3:100115574
|
T | C | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.65-31399T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100115574 | ||||||
| chr3:100115575
|
G | GTC | 16 | a0001c0001t0001g0037a0001c0001t0001g0175a0001c0001t0001g0181others(13): Show | 16 | HG00280.hp2 HG01071.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-31346_65-31345d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
G | GTCTC | 12 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0035others(9): Show | 12 | HG01346.hp1 HG01515.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-31348_65-31345d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
G | GTCTCTC | 2 | a0001c0001t0001g0197a0001c0001t0005g0178 | 2 | HG02280.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.65-31350_65-31345d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
G | GTCTCTCT others(1): Show |
2 | a0001c0001t0001g0196a0001c0001t0001g0214 | 2 | HG01978.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.65-31352_65-31345d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
G | GTCTCTCT others(3): Show |
1 | a0001c0001t0001g0185 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.65-31354_65-31345d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTC | G | 16 | a0001c0001t0001g0161a0001c0001t0001g0170a0001c0001t0001g0172others(13): Show | 16 | HG00738.hp2 HG01123.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-31346_65-31345d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTC | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0039others(11): Show | 14 | HG01168.hp2 HG01261.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.65-31348_65-31345d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTC | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0174a0001c0001t0001g0190others(5): Show | 8 | HG00140.hp1 HG01069.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-31350_65-31345d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(1): Show |
G | 6 | a0001c0001t0002g0044a0001c0001t0002g0046a0001c0001t0004g0015others(3): Show | 6 | HG02040.hp2 HG02486.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-31352_65-31345d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(3): Show |
G | 10 | a0001c0001t0001g0163a0001c0001t0001g0194a0001c0001t0002g0041others(7): Show | 10 | HG00323.hp1 HG01952.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-31354_65-31345d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(5): Show |
G | 7 | a0001c0001t0004g0011a0001c0001t0004g0023a0001c0001t0004g0028others(4): Show | 7 | HG01168.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-31356_65-31345d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(7): Show |
G | 3 | a0001c0001t0004g0164a0001c0001t0007g0032a0001c0001t0007g0033 | 3 | HG01975.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-31358_65-31345d others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(11): Show |
G | 3 | a0001c0001t0002g0072a0002c0002t0003g0001a0002c0002t0003g0135 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-31362_65-31345d others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(13): Show |
G | 11 | a0001c0001t0001g0132a0001c0001t0002g0049a0001c0001t0002g0050others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-31364_65-31345d others(22): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(15): Show |
G | 59 | a0001c0001t0001g0069a0001c0001t0002g0054a0001c0001t0002g0058others(56): Show | 59 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.65-31366_65-31345d others(24): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(17): Show |
G | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-31368_65-31345d others(26): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(19): Show |
G | 3 | a0001c0001t0002g0048a0001c0001t0002g0146a0001c0001t0002g0148 | 3 | HG01433.hp1 HG01981.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.65-31370_65-31345d others(28): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(21): Show |
G | 7 | a0001c0001t0002g0074a0001c0001t0006g0004a0001c0001t0006g0005others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-31372_65-31345d others(30): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115575
|
GTCTCTCT others(25): Show |
G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-31376_65-31345d others(34): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100115575 | |||||
| chr3:100115625
|
C | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-31348C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100115625 | ||||||
| chr3:100115643
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.65-31330T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100115643 | ||||||
| chr3:100116410
|
T | C | 122 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0102others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.65-30563T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100116410 | ||||||
| chr3:100116654
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.65-30319A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100116654 | ||||||
| chr3:100116994
|
T | C | 2 | a0001c0001t0004g0022a0001c0001t0004g0024 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.65-29979T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100116994 | ||||||
| chr3:100117071
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-29902G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117071 | ||||||
| chr3:100117386
|
C | T | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-29587C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117386 | ||||||
| chr3:100117445
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.65-29528A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117445 | ||||||
| chr3:100117461
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-29512G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117461 | ||||||
| chr3:100117557
|
A | T | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-29416A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117557 | ||||||
| chr3:100117560
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.65-29413A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117560 | ||||||
| chr3:100117656
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.65-29317G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117656 | ||||||
| chr3:100117681
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.65-29292A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117681 | ||||||
| chr3:100117825
|
G | GTA | 24 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0039others(21): Show | 24 | HG00423.hp2 HG01168.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-29121_65-29120d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117825 | |||||
| chr3:100117825
|
G | GTATA | 4 | a0001c0001t0001g0159a0001c0001t0001g0222a0001c0001t0001g0224others(1): Show | 4 | HG02523.hp2 HG03927.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-29123_65-29120d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117825 | |||||
| chr3:100117825
|
G | GTATATA | 2 | a0001c0001t0001g0171a0001c0001t0002g0094 | 2 | HG03516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.65-29125_65-29120d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117825 | |||||
| chr3:100117827
|
A | ATGTATG | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-29145_65-29144i others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117827 | |||||
| chr3:100117829
|
A | G | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.65-29144A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117829 | ||||||
| chr3:100117831
|
A | G | 2 | a0001c0001t0009g0009a0001c0001t0009g0010 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-29142A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117831 | ||||||
| chr3:100117833
|
A | G | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.65-29140A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117833 | ||||||
| chr3:100117837
|
A | G | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.65-29136A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117837 | ||||||
| chr3:100117838
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.65-29119_65-29104d others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117838 | |||||
| chr3:100117840
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0002g0105 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.65-29119_65-29106d others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117840 | |||||
| chr3:100117844
|
T | TATATATA others(1): Show |
2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.65-29122_65-29121i others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117844 | |||||
| chr3:100117844
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.65-29119_65-29110d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117844 | |||||
| chr3:100117848
|
T | TATAC | 15 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(12): Show | 15 | HG01168.hp1 HG01952.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-29122_65-29121i others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117848 | |||||
| chr3:100117848
|
TATATAC | T | 4 | a0001c0001t0002g0085a0001c0001t0005g0082a0001c0001t0005g0144others(1): Show | 4 | HG03041.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-29119_65-29114d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117848 | |||||
| chr3:100117850
|
T | TAC | 2 | a0001c0001t0002g0046a0001c0001t0004g0019 | 2 | HG03540.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.65-29122_65-29121i others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117850 | |||||
| chr3:100117852
|
T | C | 13 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(10): Show | 13 | HG01516.hp1 HG01975.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-29121T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117852 | ||||||
| chr3:100117852
|
T | TATAC | 4 | a0001c0001t0001g0170a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG02273.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-29120_65-29119i others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117852 | |||||
| chr3:100117852
|
TAC | T | 11 | a0001c0001t0002g0073a0001c0001t0002g0091a0001c0001t0002g0097others(8): Show | 11 | HG01346.hp2 HG01515.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-29119_65-29118d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117852 | |||||
| chr3:100117854
|
C | CAT | 6 | a0001c0001t0001g0037a0001c0001t0001g0186a0001c0001t0001g0189others(3): Show | 6 | HG01515.hp1 HG02080.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-29095_65-29094d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117854 | |||||
| chr3:100117854
|
C | CATATATA others(27): Show |
1 | a0001c0001t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.65-29094_65-29093i others(36): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117854 | |||||
| chr3:100117854
|
C | T | 67 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0170others(64): Show | 67 | HG00280.hp1 HG00423.hp2 HG01168.hp1 others(64): Show |
intron_variant | MODIFIER | c.65-29119C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117854 | ||||||
| chr3:100117854
|
CAT | C | 31 | a0001c0001t0001g0132a0001c0001t0002g0140a0001c0001t0006g0071others(28): Show | 32 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.65-29095_65-29094d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117854 | |||||
| chr3:100117854
|
CATAT | C | 24 | a0001c0001t0001g0069a0001c0001t0002g0053a0001c0001t0002g0054others(21): Show | 24 | HG00741.hp1 HG01261.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-29097_65-29094d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117854 | |||||
| chr3:100117854
|
CATATAT | C | 7 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(4): Show | 7 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-29099_65-29094d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117854 | |||||
| chr3:100117856
|
T | C | 5 | a0001c0001t0002g0156a0002c0002t0003g0123a0002c0002t0003g0127others(2): Show | 5 | HG01256.hp2 HG01943.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-29117T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117856 | ||||||
| chr3:100117858
|
T | C | 40 | a0001c0001t0001g0132a0001c0001t0002g0064a0001c0001t0002g0075others(37): Show | 41 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.65-29115T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117858 | ||||||
| chr3:100117858
|
T | TAC | 6 | a0001c0001t0001g0070a0001c0001t0002g0062a0001c0001t0002g0063others(3): Show | 6 | HG01978.hp2 HG02602.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-29114_65-29113i others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117858 | |||||
| chr3:100117860
|
T | C | 35 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0053others(32): Show | 35 | HG00741.hp1 HG01257.hp1 HG01258.hp1 others(32): Show |
intron_variant | MODIFIER | c.65-29113T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117860 | ||||||
| chr3:100117878
|
T | C | 89 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0132others(86): Show | 90 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.65-29095T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100117878 | ||||||
| chr3:100117878
|
T | TATATAC | 2 | a0001c0001t0006g0005a0001c0001t0006g0007 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.65-29094_65-29093i others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117878 | |||||
| chr3:100117878
|
T | TATATATA others(23): Show |
1 | a0001c0001t0002g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.65-29094_65-29093i others(32): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117878 | |||||
| chr3:100117878
|
T | TATATATA others(7): Show |
1 | a0001c0001t0006g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.65-29094_65-29093i others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117878 | |||||
| chr3:100117878
|
T | TATATATA others(25): Show |
2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-29094_65-29093i others(34): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100117878 | |||||
| chr3:100118116
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-28857G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100118116 | ||||||
| chr3:100118202
|
C | G | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.65-28771C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100118202 | ||||||
| chr3:100118272
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-28701G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100118272 | ||||||
| chr3:100118993
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-27980G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100118993 | ||||||
| chr3:100119047
|
G | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-27926G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100119047 | ||||||
| chr3:100119132
|
T | C | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-27841T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100119132 | ||||||
| chr3:100119238
|
CTATT | C | 6 | a0001c0001t0002g0095a0001c0001t0002g0098a0001c0001t0002g0099others(3): Show | 6 | HG00423.hp2 HG02027.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-27729_65-27726d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100119238 | |||||
| chr3:100119392
|
A | T | 1 | a0001c0001t0002g0208 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.65-27581A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100119392 | ||||||
| chr3:100119481
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-27492T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100119481 | ||||||
| chr3:100120262
|
G | A | 35 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0002g0140others(32): Show | 36 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.65-26711G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120262 | ||||||
| chr3:100120265
|
C | G | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-26708C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120265 | ||||||
| chr3:100120308
|
G | T | 2 | a0001c0001t0002g0146a0001c0001t0002g0148 | 2 | HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.65-26665G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120308 | ||||||
| chr3:100120335
|
G | A | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-26638G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120335 | ||||||
| chr3:100120428
|
A | G | 4 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-26545A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120428 | ||||||
| chr3:100120507
|
C | T | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-26466C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120507 | ||||||
| chr3:100120843
|
TAAG | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0100 | 2 | HG00423.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.65-26126_65-26124d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100120843 | |||||
| chr3:100120887
|
G | A | 9 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-26086G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120887 | ||||||
| chr3:100120938
|
G | A | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-26035G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100120938 | ||||||
| chr3:100121156
|
A | G | 1 | a0001c0001t0002g0062 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.65-25817A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121156 | ||||||
| chr3:100121265
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.65-25708C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121265 | ||||||
| chr3:100121290
|
G | A | 5 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-25683G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121290 | ||||||
| chr3:100121292
|
CCG | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-25680_65-25679d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121292 | ||||||
| chr3:100121422
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-25551A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121422 | ||||||
| chr3:100121570
|
T | C | 10 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(7): Show | 10 | HG02027.hp2 HG02523.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-25403T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121570 | ||||||
| chr3:100121602
|
T | C | 127 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0002g0013others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.65-25371T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121602 | ||||||
| chr3:100121848
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.65-25125G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100121848 | ||||||
| chr3:100122118
|
G | A | 5 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040others(2): Show | 5 | HG02257.hp1 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-24855G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122118 | ||||||
| chr3:100122135
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.65-24838G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122135 | ||||||
| chr3:100122192
|
G | A | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-24781G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122192 | ||||||
| chr3:100122208
|
A | C | 1 | a0002c0002t0020g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.65-24765A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122208 | ||||||
| chr3:100122447
|
T | C | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-24526T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122447 | ||||||
| chr3:100122454
|
C | G | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-24519C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122454 | ||||||
| chr3:100122528
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.65-24445A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122528 | ||||||
| chr3:100122819
|
A | G | 5 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(2): Show | 5 | HG02257.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-24154A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122819 | ||||||
| chr3:100122905
|
T | G | 27 | a0001c0001t0002g0013a0001c0001t0002g0073a0001c0001t0002g0074others(24): Show | 27 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.65-24068T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122905 | ||||||
| chr3:100122977
|
A | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-23996A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100122977 | ||||||
| chr3:100123047
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.65-23926T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123047 | ||||||
| chr3:100123262
|
C | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-23711C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123262 | ||||||
| chr3:100123263
|
G | A | 1 | a0001c0001t0002g0151 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.65-23710G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123263 | ||||||
| chr3:100123296
|
C | T | 79 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0049others(76): Show | 80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.65-23677C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123296 | ||||||
| chr3:100123609
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-23364G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123609 | ||||||
| chr3:100123611
|
G | T | 1 | a0001c0001t0002g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.65-23362G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123611 | ||||||
| chr3:100123625
|
C | A | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-23348C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123625 | ||||||
| chr3:100123718
|
C | G | 29 | a0001c0001t0002g0013a0001c0001t0002g0073a0001c0001t0002g0085others(26): Show | 29 | HG00280.hp1 HG00423.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.65-23255C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123718 | ||||||
| chr3:100123775
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.65-23198C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123775 | ||||||
| chr3:100123814
|
C | A | 1 | a0001c0001t0002g0086 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.65-23159C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123814 | ||||||
| chr3:100123954
|
T | G | 29 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(26): Show | 29 | HG01168.hp1 HG01516.hp1 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-23019T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100123954 | ||||||
| chr3:100124120
|
G | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-22853G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100124120 | ||||||
| chr3:100124412
|
T | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-22561T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100124412 | ||||||
| chr3:100124608
|
T | C | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.65-22365T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100124608 | ||||||
| chr3:100124736
|
C | A | 1 | a0001c0001t0007g0032 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.65-22237C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100124736 | ||||||
| chr3:100124902
|
C | CCT | 129 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0002g0013others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.65-22071_65-22070i others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100124902 | ||||||
| chr3:100125232
|
C | A | 1 | a0001c0001t0004g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.65-21741C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100125232 | ||||||
| chr3:100125233
|
G | A | 1 | a0001c0001t0004g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-21740G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100125233 | ||||||
| chr3:100125383
|
G | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0209 | 3 | HG01257.hp1 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.65-21590G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100125383 | ||||||
| chr3:100125449
|
G | A | 128 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0002g0013others(125): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.65-21524G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100125449 | ||||||
| chr3:100125867
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0204 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.65-21106C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100125867 | ||||||
| chr3:100126142
|
A | G | 1 | a0001c0001t0005g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.65-20831A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126142 | ||||||
| chr3:100126550
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.65-20423G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126550 | ||||||
| chr3:100126605
|
T | A | 25 | a0001c0001t0002g0013a0001c0001t0002g0073a0001c0001t0002g0074others(22): Show | 25 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.65-20368T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126605 | ||||||
| chr3:100126608
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-20365T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126608 | ||||||
| chr3:100126659
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.65-20314A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126659 | ||||||
| chr3:100126825
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.65-20148C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126825 | ||||||
| chr3:100126826
|
G | A | 1 | a0002c0002t0003g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.65-20147G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126826 | ||||||
| chr3:100126946
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.65-20027C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126946 | ||||||
| chr3:100126953
|
T | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-20020T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100126953 | ||||||
| chr3:100127027
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-19946G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100127027 | ||||||
| chr3:100127116
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-19857C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100127116 | ||||||
| chr3:100127402
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-19571G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100127402 | ||||||
| chr3:100127503
|
G | T | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-19470G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100127503 | ||||||
| chr3:100127807
|
C | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-19166C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100127807 | ||||||
| chr3:100127958
|
T | C | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG00280.hp2 HG01071.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.65-19015T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100127958 | ||||||
| chr3:100128192
|
C | A | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.65-18781C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100128192 | ||||||
| chr3:100128301
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-18672A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100128301 | ||||||
| chr3:100128731
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.65-18242G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100128731 | ||||||
| chr3:100128833
|
T | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-18140T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100128833 | ||||||
| chr3:100129085
|
AC | A | 3 | a0001c0001t0001g0132a0002c0002t0003g0001a0002c0002t0003g0135 | 4 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-17883delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100129085 | |||||
| chr3:100129258
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-17715A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100129258 | ||||||
| chr3:100129496
|
T | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-17477T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100129496 | ||||||
| chr3:100129728
|
C | G | 2 | a0001c0001t0004g0025a0001c0001t0004g0026 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.65-17245C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100129728 | ||||||
| chr3:100129840
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-17133C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100129840 | ||||||
| chr3:100129977
|
T | C | 1 | a0001c0001t0005g0177 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-16996T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100129977 | ||||||
| chr3:100129982
|
A | G | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.65-16991A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100129982 | ||||||
| chr3:100130198
|
A | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-16775A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130198 | ||||||
| chr3:100130213
|
A | G | 8 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(5): Show | 8 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-16760A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130213 | ||||||
| chr3:100130362
|
G | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-16611G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130362 | ||||||
| chr3:100130540
|
A | C | 12 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-16433A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130540 | ||||||
| chr3:100130565
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.65-16408C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130565 | ||||||
| chr3:100130691
|
T | C | 6 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(3): Show | 6 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-16282T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130691 | ||||||
| chr3:100130784
|
T | G | 1 | a0001c0001t0002g0149 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.65-16189T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130784 | ||||||
| chr3:100130874
|
C | A | 1 | a0001c0001t0001g0206 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.65-16099C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130874 | ||||||
| chr3:100130931
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-16042G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100130931 | ||||||
| chr3:100131278
|
T | C | 7 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-15695T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100131278 | ||||||
| chr3:100131290
|
T | A | 32 | a0001c0001t0002g0013a0001c0001t0002g0073a0001c0001t0002g0074others(29): Show | 32 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-15683T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100131290 | ||||||
| chr3:100131290
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-15683T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100131290 | ||||||
| chr3:100131368
|
C | T | 37 | a0001c0001t0001g0132a0001c0001t0009g0009a0001c0001t0009g0010others(34): Show | 38 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.65-15605C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100131368 | ||||||
| chr3:100131777
|
C | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-15196C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100131777 | ||||||
| chr3:100132085
|
T | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-14888T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100132085 | ||||||
| chr3:100132226
|
AC | A | 147 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0041others(144): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.65-14742delC | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100132226 | |||||
| chr3:100132676
|
G | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-14297G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100132676 | ||||||
| chr3:100132802
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-14171G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100132802 | ||||||
| chr3:100132818
|
C | CA | 22 | a0001c0001t0001g0166a0001c0001t0001g0170a0001c0001t0001g0191others(19): Show | 22 | HG00423.hp1 HG01928.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-14133dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100132818 | |||||
| chr3:100132818
|
CAAAAAAA | C | 7 | a0001c0001t0002g0152a0001c0001t0005g0082a0001c0001t0005g0083others(4): Show | 7 | HG01891.hp2 HG02080.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-14139_65-14133d others(9): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100132818 | |||||
| chr3:100133185
|
G | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-13788G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100133185 | ||||||
| chr3:100133461
|
G | GT | 9 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-13503dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100133461 | |||||
| chr3:100133461
|
G | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-13512G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100133461 | ||||||
| chr3:100133946
|
C | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-13027C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100133946 | ||||||
| chr3:100134002
|
A | G | 1 | a0003c0003t0001g0231 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.65-12971A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100134002 | ||||||
| chr3:100134141
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-12832G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100134141 | ||||||
| chr3:100134254
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-12719A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100134254 | ||||||
| chr3:100134570
|
A | C | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.65-12403A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100134570 | ||||||
| chr3:100134824
|
T | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-12149T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100134824 | ||||||
| chr3:100135326
|
A | G | 10 | a0002c0002t0003g0109a0002c0002t0003g0110a0002c0002t0003g0111others(7): Show | 10 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-11647A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100135326 | ||||||
| chr3:100135342
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.65-11631G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100135342 | ||||||
| chr3:100135437
|
CAT | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-11535_65-11534d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100135437 | ||||||
| chr3:100135438
|
A | ATG | 33 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0039others(30): Show | 33 | HG00140.hp1 HG01123.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.65-11483_65-11482d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
A | ATGTG | 10 | a0001c0001t0001g0102a0001c0001t0001g0186a0001c0001t0001g0196others(7): Show | 10 | HG01515.hp1 HG01891.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-11485_65-11482d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
A | ATGTGTG | 4 | a0001c0001t0001g0197a0001c0001t0001g0221a0001c0001t0005g0082others(1): Show | 4 | HG03041.hp1 HG03471.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-11487_65-11482d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATG | A | 20 | a0001c0001t0001g0031a0001c0001t0001g0157a0001c0001t0001g0165others(17): Show | 20 | HG00741.hp1 HG01192.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.65-11483_65-11482d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTG | A | 16 | a0001c0001t0001g0070a0001c0001t0001g0158a0001c0001t0001g0160others(13): Show | 16 | HG00741.hp2 HG01928.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-11485_65-11482d others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTGTG | A | 51 | a0001c0001t0001g0069a0001c0001t0001g0132a0001c0001t0001g0161others(48): Show | 52 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.65-11487_65-11482d others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTGTGT others(1): Show |
A | 9 | a0001c0001t0001g0166a0001c0001t0002g0047a0001c0001t0002g0054others(6): Show | 9 | HG01261.hp1 HG01516.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-11489_65-11482d others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTGTGT others(3): Show |
A | 26 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0002g0067others(23): Show | 26 | HG00323.hp1 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-11491_65-11482d others(12): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTGTGT others(5): Show |
A | 13 | a0001c0001t0002g0013a0001c0001t0002g0085a0001c0001t0002g0090others(10): Show | 13 | HG00280.hp1 HG01975.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-11493_65-11482d others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0002g0074a0001c0001t0002g0092a0001c0001t0004g0016 | 3 | HG02040.hp2 NA19030.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.65-11495_65-11482d others(16): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTGTGT others(9): Show |
A | 1 | a0002c0002t0003g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.65-11497_65-11482d others(18): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135438
|
ATGTGTGT others(11): Show |
A | 4 | a0001c0001t0001g0191a0001c0001t0005g0142a0001c0001t0005g0143others(1): Show | 4 | HG00423.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-11499_65-11482d others(20): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135438 | |||||
| chr3:100135486
|
GTGTGT | G | 3 | a0001c0001t0002g0140a0002c0002t0003g0134a0002c0002t0003g0135 | 3 | HG00738.hp1 HG02055.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.65-11485_65-11481d others(7): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135486 | |||||
| chr3:100135490
|
GT | G | 3 | a0001c0001t0004g0027a0001c0001t0014g0223a0002c0002t0003g0184 | 3 | HG03017.hp1 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.65-11480delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135490 | |||||
| chr3:100135491
|
T | TGTG | 2 | a0001c0001t0001g0203a0001c0001t0012g0036 | 2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.65-11482_65-11481i others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100135491 | ||||||
| chr3:100135493
|
T | G | 1 | a0001c0001t0004g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-11480T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100135493 | ||||||
| chr3:100135660
|
T | TTAAAAAT others(320): Show |
1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-11304_65-11303i others(329): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135660 | |||||
| chr3:100135661
|
T | TAAAAATA others(320): Show |
2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.65-11304_65-11303i others(329): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135661 | |||||
| chr3:100135661
|
T | TAAAAATA others(320): Show |
3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-11304_65-11303i others(329): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135661 | |||||
| chr3:100135661
|
T | TAAAAATA others(320): Show |
3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-11304_65-11303i others(329): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100135661 | |||||
| chr3:100135670
|
G | A | 130 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0041others(127): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.65-11303G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100135670 | ||||||
| chr3:100135762
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.65-11211C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100135762 | ||||||
| chr3:100136081
|
C | T | 3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0072 | 3 | HG02976.hp1 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.65-10892C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100136081 | ||||||
| chr3:100136284
|
G | GA | 5 | a0001c0001t0001g0176a0001c0001t0006g0004a0001c0001t0006g0005others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-10680dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100136284 | |||||
| chr3:100136374
|
G | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-10599G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100136374 | ||||||
| chr3:100136538
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0165 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.65-10435T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100136538 | ||||||
| chr3:100136686
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-10287G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100136686 | ||||||
| chr3:100136735
|
G | A | 2 | a0002c0002t0003g0128a0002c0002t0003g0129 | 2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.65-10238G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100136735 | ||||||
| chr3:100136738
|
T | A | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.65-10235T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100136738 | ||||||
| chr3:100137023
|
G | A | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-9950G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100137023 | ||||||
| chr3:100137332
|
A | G | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0221 | 3 | HG00423.hp1 HG02015.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.65-9641A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100137332 | ||||||
| chr3:100137401
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-9572A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100137401 | ||||||
| chr3:100137414
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-9559A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100137414 | ||||||
| chr3:100137564
|
C | CT | 5 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-9393dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100137564 | |||||
| chr3:100137708
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.65-9265G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100137708 | ||||||
| chr3:100137818
|
G | A | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.65-9155G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100137818 | ||||||
| chr3:100137858
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-9115A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100137858 | ||||||
| chr3:100138106
|
C | T | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.65-8867C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138106 | ||||||
| chr3:100138199
|
G | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0221 | 3 | HG00423.hp1 HG02015.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.65-8774G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138199 | ||||||
| chr3:100138404
|
C | A | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-8569C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138404 | ||||||
| chr3:100138425
|
A | G | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-8548A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138425 | ||||||
| chr3:100138492
|
A | G | 1 | a0001c0001t0016g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.65-8481A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138492 | ||||||
| chr3:100138597
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.65-8376A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138597 | ||||||
| chr3:100138831
|
C | G | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.65-8142C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138831 | ||||||
| chr3:100138893
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.65-8080G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138893 | ||||||
| chr3:100138969
|
G | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-8004G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100138969 | ||||||
| chr3:100139140
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-7833A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139140 | ||||||
| chr3:100139278
|
C | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-7695C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139278 | ||||||
| chr3:100139396
|
A | T | 18 | a0001c0001t0002g0086a0001c0001t0002g0093a0001c0001t0002g0094others(15): Show | 18 | HG00280.hp1 HG00423.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.65-7577A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139396 | ||||||
| chr3:100139529
|
A | ATG | 24 | a0001c0001t0001g0163a0001c0001t0001g0170a0001c0001t0001g0174others(21): Show | 24 | HG01069.hp1 HG01168.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.65-7408_65-7407dup others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139529
|
A | ATGTG | 8 | a0001c0001t0001g0166a0001c0001t0001g0191a0001c0001t0004g0014others(5): Show | 8 | HG00423.hp1 HG01516.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-7410_65-7407dup others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139529
|
A | ATGTGTG | 4 | a0001c0001t0001g0070a0001c0001t0004g0030a0001c0001t0007g0032others(1): Show | 4 | HG01975.hp2 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-7412_65-7407dup others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139529
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0004g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-7416_65-7407dup others(10): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139529
|
ATG | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(47): Show | 51 | HG00323.hp2 HG00738.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.65-7408_65-7407del others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139529
|
ATGTG | A | 71 | a0001c0001t0001g0031a0001c0001t0001g0165a0001c0001t0001g0176others(68): Show | 71 | HG00140.hp2 HG00423.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.65-7410_65-7407del others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139529
|
ATGTGTG | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0132others(6): Show | 9 | HG01433.hp2 HG02148.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-7412_65-7407del others(6): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139529
|
ATGTGTGT others(1): Show |
A | 4 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0104others(1): Show | 4 | HG00280.hp1 HG02735.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-7414_65-7407del others(8): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139529 | |||||
| chr3:100139563
|
GTGTATGT others(7): Show |
G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-7406_65-7393del others(14): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139563 | |||||
| chr3:100139603
|
ATG | A | 131 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0041others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.65-7360_65-7359del others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139603 | |||||
| chr3:100139611
|
GTGTA | G | 11 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-7360_65-7357del others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139611 | |||||
| chr3:100139613
|
G | A | 4 | a0001c0001t0002g0052a0001c0001t0002g0066a0001c0001t0002g0086others(1): Show | 4 | HG02040.hp2 HG02559.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-7360G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139613 | ||||||
| chr3:100139613
|
G | GTA | 2 | a0001c0001t0001g0183a0001c0001t0001g0204 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.65-7343_65-7342dup others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139613 | |||||
| chr3:100139630
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-7343T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139630 | ||||||
| chr3:100139685
|
T | G | 1 | a0001c0001t0002g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.65-7288T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139685 | ||||||
| chr3:100139751
|
C | T | 1 | a0001c0001t0009g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65-7222C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139751 | ||||||
| chr3:100139797
|
CA | C | 121 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0048others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.65-7160delA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100139797 | |||||
| chr3:100139885
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0037a0001c0001t0001g0038others(2): Show | 5 | HG01168.hp2 HG01257.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-7088T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139885 | ||||||
| chr3:100139913
|
A | G | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.65-7060A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100139913 | ||||||
| chr3:100140156
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-6817A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100140156 | ||||||
| chr3:100140240
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.65-6733C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100140240 | ||||||
| chr3:100140360
|
C | G | 3 | a0001c0001t0009g0009a0001c0001t0009g0010a0001c0001t0009g0040 | 3 | HG02809.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-6613C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100140360 | ||||||
| chr3:100140369
|
G | A | 1 | a0002c0002t0003g0119 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65-6604G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100140369 | ||||||
| chr3:100140456
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-6517A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100140456 | ||||||
| chr3:100140980
|
C | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-5993C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100140980 | ||||||
| chr3:100141028
|
T | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0165 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.65-5945T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141028 | ||||||
| chr3:100141087
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.65-5886A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141087 | ||||||
| chr3:100141120
|
C | A | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.65-5853C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141120 | ||||||
| chr3:100141187
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-5786C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141187 | ||||||
| chr3:100141334
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-5639A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141334 | ||||||
| chr3:100141386
|
A | T | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.65-5587A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141386 | ||||||
| chr3:100141531
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-5442G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141531 | ||||||
| chr3:100141557
|
G | A | 124 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0002g0013others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.65-5416G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141557 | ||||||
| chr3:100141891
|
C | G | 45 | a0001c0001t0001g0162a0001c0001t0002g0041a0001c0001t0002g0042others(42): Show | 45 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(42): Show |
intron_variant | MODIFIER | c.65-5082C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141891 | ||||||
| chr3:100141967
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.65-5006C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100141967 | ||||||
| chr3:100142256
|
A | G | 1 | a0002c0002t0003g0123 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.65-4717A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100142256 | ||||||
| chr3:100142428
|
T | C | 2 | a0002c0002t0003g0128a0002c0002t0003g0129 | 2 | HG01943.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.65-4545T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100142428 | ||||||
| chr3:100142967
|
T | C | 1 | a0002c0002t0003g0111 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.65-4006T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100142967 | ||||||
| chr3:100142978
|
G | A | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.65-3995G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100142978 | ||||||
| chr3:100143045
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-3928A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143045 | ||||||
| chr3:100143223
|
G | C | 1 | a0002c0002t0003g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.65-3750G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143223 | ||||||
| chr3:100143308
|
G | A | 9 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-3665G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143308 | ||||||
| chr3:100143423
|
C | T | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.65-3550C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143423 | ||||||
| chr3:100143508
|
A | G | 1 | a0002c0002t0003g0121 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.65-3465A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143508 | ||||||
| chr3:100143563
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0002g0085a0001c0001t0004g0014 | 3 | HG01257.hp2 HG01516.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.65-3410A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143563 | ||||||
| chr3:100143707
|
T | C | 123 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0048others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.65-3266T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143707 | ||||||
| chr3:100143708
|
G | A | 1 | a0002c0002t0003g0126 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.65-3265G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143708 | ||||||
| chr3:100143851
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.65-3122C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143851 | ||||||
| chr3:100143894
|
A | G | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-3079A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100143894 | ||||||
| chr3:100144339
|
T | C | 124 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0002g0013others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.65-2634T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100144339 | ||||||
| chr3:100144587
|
C | A | 1 | a0001c0001t0005g0177 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-2386C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100144587 | ||||||
| chr3:100145340
|
C | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-1633C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100145340 | ||||||
| chr3:100145341
|
G | A | 1 | a0002c0002t0003g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.65-1632G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100145341 | ||||||
| chr3:100145427
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.65-1546G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100145427 | ||||||
| chr3:100145447
|
C | CA | 36 | a0001c0001t0002g0013a0001c0001t0002g0049a0001c0001t0002g0050others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.65-1514dupA | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 100145447 | |||||
| chr3:100145466
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.65-1507A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100145466 | ||||||
| chr3:100145559
|
C | T | 1 | a0001c0001t0004g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.65-1414C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100145559 | ||||||
| chr3:100145593
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.65-1380T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100145593 | ||||||
| chr3:100146158
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-815G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100146158 | ||||||
| chr3:100146159
|
C | T | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.65-814C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100146159 | ||||||
| chr3:100146380
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.65-593C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100146380 | ||||||
| chr3:100146402
|
G | A | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-571G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100146402 | ||||||
| chr3:100146665
|
A | T | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.65-308A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100146665 | ||||||
| chr3:100146677
|
T | A | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-296T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100146677 | ||||||
| chr3:100146930
|
A | G | 1 | a0002c0002t0003g0118 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.65-43A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 1/9 | chr3 | 100146930 | ||||||
| chr3:100147265
|
C | CT | 7 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0193others(4): Show | 7 | HG01258.hp2 HG01891.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+227dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100147265 | |||||
| chr3:100147265
|
CT | C | 123 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0041others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.153+227delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100147265 | |||||
| chr3:100147265
|
CTT | C | 8 | a0001c0001t0002g0050a0001c0001t0002g0101a0001c0001t0002g0155others(5): Show | 8 | HG01515.hp2 HG01516.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+226_153+227del others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100147265 | |||||
| chr3:100147421
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.153+360C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100147421 | ||||||
| chr3:100147912
|
T | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG02523.hp1 NA18969.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.153+851T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100147912 | ||||||
| chr3:100147928
|
A | G | 2 | a0001c0001t0004g0022a0001c0001t0004g0024 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.153+867A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100147928 | ||||||
| chr3:100148021
|
C | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+960C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100148021 | ||||||
| chr3:100148105
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+1044G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100148105 | ||||||
| chr3:100148238
|
C | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+1177C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100148238 | ||||||
| chr3:100148367
|
G | A | 131 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0041others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.153+1306G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100148367 | ||||||
| chr3:100148556
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.153+1495G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100148556 | ||||||
| chr3:100149003
|
A | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+1942A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149003 | ||||||
| chr3:100149049
|
A | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+1988A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149049 | ||||||
| chr3:100149097
|
T | A | 1 | a0001c0001t0013g0201 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.153+2036T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149097 | ||||||
| chr3:100149235
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG03654.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.153+2174A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149235 | ||||||
| chr3:100149260
|
A | T | 118 | a0001c0001t0001g0132a0001c0001t0002g0013a0001c0001t0002g0041others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.153+2199A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149260 | ||||||
| chr3:100149363
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153+2302T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149363 | ||||||
| chr3:100149413
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182 | 3 | HG01891.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.153+2352G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149413 | ||||||
| chr3:100149745
|
G | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+2684G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149745 | ||||||
| chr3:100149795
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.153+2734G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149795 | ||||||
| chr3:100149872
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.153+2811G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100149872 | ||||||
| chr3:100150479
|
A | C | 9 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+3418A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100150479 | ||||||
| chr3:100150547
|
G | A | 1 | a0001c0001t0010g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.153+3486G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100150547 | ||||||
| chr3:100150554
|
A | G | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.153+3493A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100150554 | ||||||
| chr3:100150558
|
C | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+3497C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100150558 | ||||||
| chr3:100150558
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.153+3497C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100150558 | ||||||
| chr3:100151164
|
G | C | 1 | a0001c0001t0002g0079 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.153+4103G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151164 | ||||||
| chr3:100151184
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.153+4123T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151184 | ||||||
| chr3:100151454
|
C | T | 12 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+4393C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151454 | ||||||
| chr3:100151455
|
G | A | 118 | a0001c0001t0001g0070a0001c0001t0002g0013a0001c0001t0002g0041others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.153+4394G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151455 | ||||||
| chr3:100151532
|
G | A | 1 | a0001c0001t0011g0169 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.153+4471G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151532 | ||||||
| chr3:100151693
|
C | T | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+4632C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151693 | ||||||
| chr3:100151701
|
C | G | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+4640C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151701 | ||||||
| chr3:100151701
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153+4640C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151701 | ||||||
| chr3:100151893
|
A | G | 2 | a0001c0001t0005g0082a0001c0001t0005g0083 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.153+4832A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100151893 | ||||||
| chr3:100152192
|
T | C | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0205 | 3 | HG01192.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.153+5131T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100152192 | ||||||
| chr3:100152203
|
CT | C | 5 | a0001c0001t0001g0190a0001c0001t0004g0025a0001c0001t0009g0009others(2): Show | 5 | HG02074.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+5156delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100152203 | |||||
| chr3:100152763
|
T | A | 1 | a0002c0002t0003g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.153+5702T>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100152763 | ||||||
| chr3:100153200
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.153+6139G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100153200 | ||||||
| chr3:100153241
|
A | AT | 4 | a0001c0001t0002g0086a0001c0001t0002g0096a0001c0001t0002g0097others(1): Show | 4 | HG02129.hp1 NA18954.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+6186dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100153241 | |||||
| chr3:100153596
|
CTCT | C | 18 | a0001c0001t0004g0011a0001c0001t0004g0014a0001c0001t0004g0015others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.153+6543_153+6545d others(5): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100153596 | |||||
| chr3:100153838
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-6572_154-6562d others(13): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100153838 | |||||
| chr3:100153912
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.154-6518G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100153912 | ||||||
| chr3:100154001
|
C | T | 18 | a0001c0001t0004g0011a0001c0001t0004g0014a0001c0001t0004g0015others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.154-6429C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100154001 | ||||||
| chr3:100154153
|
A | G | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.154-6277A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100154153 | ||||||
| chr3:100154322
|
G | T | 1 | a0002c0002t0003g0141 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.154-6108G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100154322 | ||||||
| chr3:100154473
|
C | T | 129 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0042others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.154-5957C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100154473 | ||||||
| chr3:100154679
|
A | T | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.154-5751A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100154679 | ||||||
| chr3:100154787
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.154-5643A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100154787 | ||||||
| chr3:100154969
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.154-5461C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100154969 | ||||||
| chr3:100155264
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0043 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.154-5166G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100155264 | ||||||
| chr3:100155367
|
G | T | 3 | a0001c0001t0002g0093a0001c0001t0002g0104a0001c0001t0002g0106 | 3 | HG00280.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.154-5063G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100155367 | ||||||
| chr3:100155646
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.154-4784T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100155646 | ||||||
| chr3:100155871
|
TCTTTTTT others(6): Show |
T | 1 | a0001c0001t0002g0153 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.154-4554_154-4542d others(15): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100155871 | |||||
| chr3:100156032
|
G | C | 1 | a0001c0001t0005g0177 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.154-4398G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156032 | ||||||
| chr3:100156097
|
A | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.154-4333A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156097 | ||||||
| chr3:100156299
|
C | CT | 108 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0001g0158others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.154-4104dupT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100156299 | |||||
| chr3:100156299
|
C | CTT | 24 | a0001c0001t0001g0168a0001c0001t0002g0042a0001c0001t0002g0044others(21): Show | 24 | HG00423.hp2 HG00741.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-4105_154-4104d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 100156299 | |||||
| chr3:100156309
|
T | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0207 | 3 | HG03654.hp1 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.154-4121T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156309 | ||||||
| chr3:100156453
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.154-3977C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156453 | ||||||
| chr3:100156454
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154-3976G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156454 | ||||||
| chr3:100156542
|
C | T | 1 | a0001c0001t0008g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.154-3888C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156542 | ||||||
| chr3:100156543
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.154-3887G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156543 | ||||||
| chr3:100156678
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.154-3752C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156678 | ||||||
| chr3:100156709
|
G | A | 7 | a0001c0001t0004g0014a0001c0001t0004g0019a0001c0001t0004g0030others(4): Show | 7 | HG01516.hp1 HG01975.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-3721G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156709 | ||||||
| chr3:100156736
|
C | G | 1 | a0002c0002t0003g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.154-3694C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156736 | ||||||
| chr3:100156858
|
A | G | 12 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-3572A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156858 | ||||||
| chr3:100156891
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.154-3539A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100156891 | ||||||
| chr3:100157155
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154-3275C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157155 | ||||||
| chr3:100157167
|
C | G | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.154-3263C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157167 | ||||||
| chr3:100157286
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154-3144T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157286 | ||||||
| chr3:100157499
|
T | C | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.154-2931T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157499 | ||||||
| chr3:100157544
|
A | G | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.154-2886A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157544 | ||||||
| chr3:100157645
|
G | A | 18 | a0001c0001t0004g0011a0001c0001t0004g0014a0001c0001t0004g0015others(15): Show | 18 | HG01168.hp1 HG01516.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.154-2785G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157645 | ||||||
| chr3:100157678
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.154-2752C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157678 | ||||||
| chr3:100157717
|
A | G | 4 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-2713A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100157717 | ||||||
| chr3:100158022
|
C | G | 1 | a0001c0001t0002g0013 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.154-2408C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100158022 | ||||||
| chr3:100158136
|
T | C | 1 | a0001c0001t0009g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.154-2294T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100158136 | ||||||
| chr3:100158247
|
C | T | 44 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(41): Show | 44 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(41): Show |
intron_variant | MODIFIER | c.154-2183C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100158247 | ||||||
| chr3:100158351
|
T | C | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.154-2079T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100158351 | ||||||
| chr3:100158711
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.154-1719T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100158711 | ||||||
| chr3:100158820
|
T | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-1610T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100158820 | ||||||
| chr3:100158997
|
G | A | 2 | a0002c0002t0003g0001a0002c0002t0003g0135 | 3 | HG00738.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154-1433G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100158997 | ||||||
| chr3:100159188
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.154-1242C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100159188 | ||||||
| chr3:100159272
|
C | G | 33 | a0002c0002t0003g0001a0002c0002t0003g0109a0002c0002t0003g0110others(30): Show | 34 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.154-1158C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100159272 | ||||||
| chr3:100159755
|
G | A | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.154-675G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100159755 | ||||||
| chr3:100159976
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-454A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100159976 | ||||||
| chr3:100159980
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154-450T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 2/9 | chr3 | 100159980 | ||||||
| chr3:100161267
|
C | A | 1 | a0001c0001t0004g0022 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.225+766C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 3/9 | chr3 | 100161267 | ||||||
| chr3:100161286
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225+785A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 3/9 | chr3 | 100161286 | ||||||
| chr3:100161675
|
T | TAC | 12 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.226-627_226-626dup others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 100161675 | |||||
| chr3:100161725
|
T | C | 118 | a0001c0001t0001g0070a0001c0001t0002g0013a0001c0001t0002g0041others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.226-578T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 3/9 | chr3 | 100161725 | ||||||
| chr3:100161839
|
C | T | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.226-464C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 3/9 | chr3 | 100161839 | ||||||
| chr3:100162040
|
T | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226-263T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 3/9 | chr3 | 100162040 | ||||||
| chr3:100162082
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.226-221G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 3/9 | chr3 | 100162082 | ||||||
| chr3:100162530
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.355+98G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100162530 | ||||||
| chr3:100162723
|
C | T | 11 | a0001c0001t0004g0011a0001c0001t0004g0015a0001c0001t0004g0016others(8): Show | 11 | HG01168.hp1 HG02040.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.355+291C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100162723 | ||||||
| chr3:100162744
|
C | T | 1 | a0001c0001t0004g0014 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.355+312C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100162744 | ||||||
| chr3:100162745
|
G | T | 2 | a0001c0001t0004g0025a0001c0001t0004g0026 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.355+313G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100162745 | ||||||
| chr3:100162847
|
C | T | 1 | a0001c0001t0005g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.355+415C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100162847 | ||||||
| chr3:100163306
|
T | C | 9 | a0001c0001t0002g0054a0001c0001t0002g0058a0001c0001t0002g0059others(6): Show | 9 | HG02027.hp2 HG02523.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.355+874T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100163306 | ||||||
| chr3:100163405
|
T | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.355+973T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100163405 | ||||||
| chr3:100163531
|
A | T | 1 | a0002c0002t0017g0131 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.355+1099A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100163531 | ||||||
| chr3:100163905
|
AT | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0028 | 2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.355+1475delT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 100163905 | |||||
| chr3:100164026
|
C | T | 1 | a0002c0002t0003g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.355+1594C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100164026 | ||||||
| chr3:100164171
|
T | C | 25 | a0001c0001t0002g0013a0001c0001t0002g0073a0001c0001t0002g0074others(22): Show | 25 | HG00280.hp1 HG00423.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.355+1739T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100164171 | ||||||
| chr3:100164370
|
G | A | 1 | a0001c0001t0002g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.355+1938G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100164370 | ||||||
| chr3:100164686
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.356-1649A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100164686 | ||||||
| chr3:100164754
|
A | G | 44 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(41): Show | 44 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(41): Show |
intron_variant | MODIFIER | c.356-1581A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100164754 | ||||||
| chr3:100164961
|
C | A | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.356-1374C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100164961 | ||||||
| chr3:100165086
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.356-1249G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100165086 | ||||||
| chr3:100165235
|
A | T | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.356-1100A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100165235 | ||||||
| chr3:100165431
|
A | AAT | 3 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084 | 3 | HG02895.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.356-893_356-892dup others(2): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 100165431 | |||||
| chr3:100165665
|
C | T | 33 | a0002c0002t0003g0001a0002c0002t0003g0109a0002c0002t0003g0110others(30): Show | 34 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.356-670C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100165665 | ||||||
| chr3:100166047
|
T | C | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.356-288T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100166047 | ||||||
| chr3:100166235
|
T | C | 1 | a0001c0001t0002g0209 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.356-100T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 4/9 | chr3 | 100166235 | ||||||
| chr3:100166572
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.415+178G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/9 | chr3 | 100166572 | ||||||
| chr3:100166625
|
T | C | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.415+231T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/9 | chr3 | 100166625 | ||||||
| chr3:100166792
|
C | G | 5 | a0001c0001t0006g0004a0001c0001t0006g0005a0001c0001t0006g0006others(2): Show | 5 | HG02109.hp1 HG02630.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+398C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/9 | chr3 | 100166792 | ||||||
| chr3:100166967
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.415+573C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/9 | chr3 | 100166967 | ||||||
| chr3:100166981
|
C | A | 37 | a0001c0001t0001g0070a0001c0001t0009g0009a0001c0001t0009g0010others(34): Show | 38 | HG00140.hp2 HG00323.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.415+587C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/9 | chr3 | 100166981 | ||||||
| chr3:100167030
|
G | A | 1 | a0001c0001t0009g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.415+636G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/9 | chr3 | 100167030 | ||||||
| chr3:100167444
|
A | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-294A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 5/9 | chr3 | 100167444 | ||||||
| chr3:100168463
|
G | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.518+623G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168463 | ||||||
| chr3:100168499
|
G | A | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0043others(4): Show | 7 | HG01952.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.518+659G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168499 | ||||||
| chr3:100168579
|
T | C | 7 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.518+739T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168579 | ||||||
| chr3:100168743
|
T | G | 2 | a0002c0002t0003g0133a0002c0002t0003g0184 | 2 | HG02698.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.518+903T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168743 | ||||||
| chr3:100168789
|
A | G | 5 | a0002c0002t0003g0122a0002c0002t0003g0123a0002c0002t0003g0124others(2): Show | 5 | NA18943.hp2 NA18959.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.518+949A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168789 | ||||||
| chr3:100168841
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.518+1001T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168841 | ||||||
| chr3:100168863
|
T | TTA | 117 | a0001c0001t0001g0070a0001c0001t0001g0193a0001c0001t0001g0200others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.518+1040_518+1041d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 100168863 | |||||
| chr3:100168863
|
TTA | T | 3 | a0001c0001t0002g0152a0001c0001t0010g0055a0001c0001t0010g0056 | 3 | HG02080.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.518+1040_518+1041d others(4): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 100168863 | |||||
| chr3:100168879
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.518+1039A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168879 | ||||||
| chr3:100168894
|
T | C | 7 | a0001c0001t0006g0003a0001c0001t0006g0004a0001c0001t0006g0005others(4): Show | 7 | HG02109.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.518+1054T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100168894 | ||||||
| chr3:100169399
|
G | T | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.518+1559G>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100169399 | ||||||
| chr3:100169410
|
A | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.518+1570A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100169410 | ||||||
| chr3:100169816
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.518+1976A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100169816 | ||||||
| chr3:100169946
|
A | G | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-1893A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100169946 | ||||||
| chr3:100170267
|
T | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519-1572T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100170267 | ||||||
| chr3:100170339
|
G | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519-1500G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100170339 | ||||||
| chr3:100170422
|
G | A | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.519-1417G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100170422 | ||||||
| chr3:100170557
|
G | C | 5 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051others(2): Show | 5 | HG02559.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-1282G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100170557 | ||||||
| chr3:100170580
|
A | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519-1259A>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100170580 | ||||||
| chr3:100170581
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.519-1258A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100170581 | ||||||
| chr3:100170675
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.519-1164A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100170675 | ||||||
| chr3:100171272
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.519-567T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100171272 | ||||||
| chr3:100171403
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0165 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.519-436C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100171403 | ||||||
| chr3:100171433
|
C | G | 5 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.519-406C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100171433 | ||||||
| chr3:100171480
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519-359A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100171480 | ||||||
| chr3:100171740
|
C | T | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.519-99C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100171740 | ||||||
| chr3:100171800
|
G | C | 1 | a0002c0002t0003g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.519-39G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 6/9 | chr3 | 100171800 | ||||||
| chr3:100171939
|
G | A | 2 | a0002c0002t0003g0134a0002c0002t0017g0131 | 2 | HG03490.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.579+40G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 7/9 | chr3 | 100171939 | ||||||
| chr3:100171973
|
A | T | 1 | a0001c0001t0014g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.579+74A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 7/9 | chr3 | 100171973 | ||||||
| chr3:100172203
|
T | G | 1 | a0001c0001t0002g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.580-113T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 7/9 | chr3 | 100172203 | ||||||
| chr3:100172295
|
TTC | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.580-17_580-16delCT | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 100172295 | |||||
| chr3:100172945
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.667+542C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100172945 | ||||||
| chr3:100173069
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.667+666C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100173069 | ||||||
| chr3:100173255
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.667+852C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100173255 | ||||||
| chr3:100173341
|
T | G | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.667+938T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100173341 | ||||||
| chr3:100173346
|
C | A | 117 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0042others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.667+943C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100173346 | ||||||
| chr3:100173444
|
G | A | 11 | a0001c0001t0005g0082a0001c0001t0005g0084a0001c0001t0005g0142others(8): Show | 11 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.667+1041G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100173444 | ||||||
| chr3:100173660
|
T | C | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | HG02015.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.667+1257T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100173660 | ||||||
| chr3:100173981
|
C | T | 117 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0042others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.667+1578C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100173981 | ||||||
| chr3:100174098
|
A | G | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.667+1695A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174098 | ||||||
| chr3:100174121
|
A | T | 9 | a0001c0001t0005g0082a0001c0001t0005g0083a0001c0001t0005g0084others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.667+1718A>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174121 | ||||||
| chr3:100174140
|
G | C | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.667+1737G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174140 | ||||||
| chr3:100174267
|
C | T | 81 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0042others(78): Show | 81 | HG00280.hp1 HG00423.hp2 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.667+1864C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174267 | ||||||
| chr3:100174369
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.668-1958C>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174369 | ||||||
| chr3:100174578
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.668-1749A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174578 | ||||||
| chr3:100174587
|
T | C | 1 | a0001c0001t0021g0018 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.668-1740T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174587 | ||||||
| chr3:100174629
|
AAGAGAAT others(6): Show |
A | 1 | a0002c0002t0003g0128 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.668-1695_668-1683d others(15): Show |
CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 100174629 | |||||
| chr3:100174669
|
A | G | 1 | a0002c0002t0003g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.668-1658A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174669 | ||||||
| chr3:100174698
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.668-1629G>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174698 | ||||||
| chr3:100174933
|
T | G | 1 | a0001c0001t0002g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.668-1394T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100174933 | ||||||
| chr3:100175035
|
T | G | 1 | a0001c0001t0006g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.668-1292T>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100175035 | ||||||
| chr3:100175179
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.668-1148A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100175179 | ||||||
| chr3:100175190
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.668-1137A>G | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100175190 | ||||||
| chr3:100175295
|
G | A | 1 | a0001c0001t0006g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.668-1032G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100175295 | ||||||
| chr3:100175500
|
C | A | 11 | a0001c0001t0001g0163a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.668-827C>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100175500 | ||||||
| chr3:100176231
|
T | C | 1 | a0001c0001t0018g0002 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.668-96T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100176231 | ||||||
| chr3:100176312
|
T | C | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.668-15T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 8/9 | chr3 | 100176312 | ||||||
| chr3:100176439
|
T | C | 3 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144 | 3 | HG02647.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.756+24T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 9/9 | chr3 | 100176439 | ||||||
| chr3:100176954
|
T | C | 1 | a0001c0001t0005g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.756+539T>C | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 9/9 | chr3 | 100176954 | ||||||
| chr3:100177030
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.756+615G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 9/9 | chr3 | 100177030 | ||||||
| chr3:100177091
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.756+676G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 9/9 | chr3 | 100177091 | ||||||
| chr3:100177093
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.756+678C>T | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 9/9 | chr3 | 100177093 | ||||||
| chr3:100178076
|
G | A | 1 | a0002c0002t0019g0012 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.757-229G>A | CMSS1 | ENSG00000184220.12 | transcript | ENST00000421999.8 | protein_coding | 9/9 | chr3 | 100178076 |