Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4087 |
|---|---|
| ensemblid | ENSG00000175387.16 |
| hgncid | 6768 |
| symbol | SMAD2 |
| name | SMAD family member 2 |
| refseq_nuc | NM_005901.6 |
| refseq_prot | NP_005892.1 |
| ensembl_nuc | ENST00000262160.11 |
| ensembl_prot | ENSP00000262160.6 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 47808957 |
| end | 47930659 |
| strand | - |
| ver | v1.2 |
| region | chr18:47808957-47930659 |
| region5000 | chr18:47803957-47935659 |
| regionname0 | SMAD2_chr18_47808957_47930659 |
| regionname5000 | SMAD2_chr18_47803957_47935659 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 467 | 310 | 76 | 60 | 136 | 10 | 26 | 104 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1404 | 302 | 69 | 60 | 136 | 10 | 25 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| c0002 | 0/0 | 1404 | 8 | 7 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| 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 | 33229 | 10 | 1 | 0 | 8 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0002 | 0/0 | 33223 | 7 | 0 | 2 | 4 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0003 | 0/0 | 33216 | 4 | 0 | 1 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0004 | 0/0 | 33217 | 4 | 0 | 1 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0005 | 0/0 | 33227 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0006 | 0/0 | 33232 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0007 | 0/0 | 33223 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0008 | 0/0 | 33224 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0009 | 0/0 | 33221 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0010 | 0/0 | 33217 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0011 | 0/0 | 33222 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0012 | 0/0 | 33230 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0013 | 0/0 | 33229 | 2 | 0 | 1 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0014 | 0/0 | 33229 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0015 | 0/0 | 33231 | 2 | 0 | 1 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0016 | 0/0 | 33233 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0017 | 0/0 | 33233 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0018 | 0/0 | 33237 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0019 | 0/0 | 33236 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0020 | 0/0 | 33233 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0021 | 0/0 | 33223 | 2 | 1 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0022 | 0/0 | 33223 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0023 | 0/0 | 33223 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0024 | 0/0 | 33235 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0025 | 0/0 | 33245 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0026 | 0/0 | 33211 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0027 | 0/0 | 33217 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0028 | 0/0 | 33218 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0029 | 0/0 | 33217 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0030 | 0/0 | 33217 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0031 | 0/0 | 33194 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0032 | 0/0 | 33228 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0033 | 0/0 | 32772 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0034 | 0/0 | 33229 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0035 | 0/0 | 33237 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0036 | 0/0 | 33242 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0037 | 0/0 | 33240 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0038 | 0/0 | 33242 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0039 | 0/0 | 33241 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0040 | 0/0 | 33242 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0041 | 0/0 | 33243 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0042 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0043 | 0/0 | 33231 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0044 | 0/0 | 33230 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0045 | 0/0 | 33231 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0046 | 0/0 | 33239 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0047 | 0/0 | 33223 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0048 | 0/0 | 33232 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0049 | 0/0 | 33235 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0050 | 0/0 | 33232 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0051 | 0/0 | 33229 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0052 | 0/0 | 33229 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0053 | 0/0 | 33230 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0054 | 0/0 | 33231 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0055 | 0/0 | 33232 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0056 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0057 | 0/0 | 33232 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0058 | 0/0 | 33232 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0059 | 0/0 | 33231 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0060 | 0/0 | 33221 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0061 | 0/0 | 33228 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0062 | 0/0 | 33229 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0063 | 0/0 | 33220 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0064 | 0/0 | 33226 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0065 | 0/0 | 33241 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0066 | 0/0 | 33229 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0067 | 0/0 | 33229 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0068 | 0/0 | 33219 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0069 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0070 | 0/0 | 33229 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0071 | 0/0 | 33219 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0072 | 0/0 | 33231 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0073 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0074 | 0/0 | 33228 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0075 | 0/0 | 33229 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0076 | 0/0 | 33229 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0077 | 0/0 | 33228 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0078 | 0/0 | 33229 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0079 | 0/0 | 33232 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0080 | 0/0 | 33232 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0081 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0082 | 0/0 | 33231 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0083 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0084 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0085 | 0/0 | 33232 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0086 | 0/0 | 33230 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0087 | 0/0 | 33233 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0088 | 0/0 | 33232 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0089 | 0/0 | 33233 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0090 | 0/0 | 33232 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0091 | 0/0 | 33233 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0092 | 0/0 | 33232 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0093 | 0/0 | 33233 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0094 | 0/0 | 33233 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0095 | 0/0 | 33232 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0096 | 0/0 | 33234 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0097 | 0/0 | 33237 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0098 | 0/0 | 33236 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0099 | 0/0 | 33236 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0100 | 0/0 | 33234 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0101 | 0/0 | 33239 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0102 | 0/0 | 33238 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0103 | 0/0 | 33235 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0104 | 0/0 | 33233 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0105 | 0/0 | 33233 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0106 | 0/0 | 33233 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0107 | 0/0 | 33236 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0108 | 0/0 | 33235 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0109 | 0/0 | 33233 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0110 | 0/0 | 33232 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0111 | 0/0 | 33235 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0112 | 0/0 | 33233 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0113 | 0/0 | 33235 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0114 | 0/0 | 33221 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0115 | 0/0 | 33235 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0116 | 0/0 | 33231 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0117 | 0/0 | 33232 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0118 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0119 | 0/0 | 33234 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0120 | 0/0 | 33229 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0121 | 0/0 | 33230 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0122 | 0/0 | 33230 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0123 | 0/0 | 33230 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0124 | 0/0 | 33231 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0125 | 0/0 | 33230 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0126 | 0/0 | 33231 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0127 | 0/0 | 33232 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0128 | 0/0 | 33236 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0129 | 0/0 | 33233 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0130 | 0/0 | 33230 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0131 | 0/0 | 33234 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0132 | 0/0 | 33233 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0133 | 0/0 | 33238 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0134 | 0/0 | 33224 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0135 | 0/0 | 33208 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0136 | 0/0 | 33217 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0137 | 0/0 | 33221 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0138 | 0/0 | 33224 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0139 | 0/0 | 33224 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0140 | 0/0 | 33224 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0141 | 0/0 | 33223 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0142 | 0/0 | 33223 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0143 | 0/0 | 33225 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0144 | 0/0 | 33223 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0145 | 0/0 | 33225 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0146 | 0/0 | 33230 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0147 | 0/0 | 33233 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0148 | 0/0 | 33225 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0149 | 0/0 | 33225 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0150 | 0/0 | 33227 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0151 | 0/0 | 33227 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0152 | 0/0 | 33232 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0153 | 0/0 | 33223 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0154 | 0/0 | 33223 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0155 | 0/0 | 33223 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0156 | 0/0 | 33224 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0157 | 0/0 | 33224 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0158 | 0/0 | 33227 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0159 | 0/0 | 33226 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0160 | 0/0 | 33228 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0161 | 0/0 | 33232 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0162 | 0/0 | 33234 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0163 | 0/0 | 33225 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0164 | 0/0 | 33226 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0165 | 0/0 | 33224 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0166 | 0/0 | 33226 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0167 | 0/0 | 33227 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0168 | 0/0 | 33228 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0169 | 0/0 | 33224 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0170 | 0/0 | 33212 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0171 | 0/0 | 33194 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0172 | 0/0 | 33195 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0173 | 0/0 | 33227 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0174 | 0/0 | 33232 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0175 | 0/0 | 33231 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0176 | 0/0 | 33236 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0177 | 0/0 | 33234 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0178 | 0/0 | 33225 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0179 | 0/0 | 33221 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0180 | 0/0 | 33234 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0181 | 0/1 | 33231 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0182 | 0/0 | 33234 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0183 | 0/0 | 33227 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0184 | 0/0 | 33229 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0185 | 0/0 | 33229 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0186 | 0/0 | 33247 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0187 | 0/0 | 33226 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0188 | 0/0 | 33236 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0189 | 0/0 | 33244 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0190 | 0/0 | 33246 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0191 | 0/0 | 33223 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0192 | 0/0 | 33225 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0193 | 0/0 | 33230 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0194 | 0/0 | 33225 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0195 | 0/0 | 33226 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0196 | 0/0 | 33234 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0197 | 0/0 | 33233 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0198 | 0/0 | 33219 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0199 | 1/0 | 33223 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0200 | 0/0 | 33227 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0201 | 0/0 | 33226 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0202 | 0/0 | 33220 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0203 | 0/0 | 33219 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0204 | 0/0 | 33220 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0205 | 0/0 | 33215 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0206 | 0/0 | 33218 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0207 | 0/0 | 33217 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0208 | 0/0 | 33216 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0209 | 0/0 | 33217 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0210 | 0/0 | 33220 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0211 | 0/0 | 33207 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0212 | 0/0 | 33216 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0213 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0214 | 0/0 | 33215 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0215 | 0/0 | 33215 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0216 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0217 | 0/0 | 33211 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0218 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0219 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0220 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0221 | 0/0 | 33216 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0222 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0223 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0224 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0225 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0226 | 0/0 | 33216 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0227 | 0/0 | 33217 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0228 | 0/0 | 33207 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0229 | 0/0 | 33220 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0230 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0231 | 0/0 | 33222 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0232 | 0/0 | 33220 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0233 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0234 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0235 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0236 | 0/0 | 33217 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0237 | 0/0 | 33218 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0238 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0239 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0240 | 0/0 | 33222 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0241 | 0/0 | 33218 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0242 | 0/0 | 33219 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0243 | 0/0 | 33219 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0244 | 0/0 | 33228 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0245 | 0/0 | 33219 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0246 | 0/0 | 33220 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0247 | 0/0 | 33268 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0248 | 0/0 | 33266 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0249 | 0/0 | 33268 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0250 | 0/0 | 33274 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0251 | 0/0 | 33279 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0252 | 0/0 | 33253 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0253 | 0/0 | 33256 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0254 | 0/0 | 33260 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0255 | 0/0 | 33229 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0256 | 0/0 | 33235 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| t0257 | 0/0 | 33230 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| 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 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1404 | 302 | 69 | 60 | 136 | 10 | 25 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002 | 0/0 | 1404 | 8 | 7 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 34632 | 10 | 1 | 0 | 8 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0002 | 0/0 | 34626 | 7 | 0 | 2 | 4 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0003 | 0/0 | 34619 | 4 | 0 | 1 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0004 | 0/0 | 34620 | 4 | 0 | 1 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0005 | 0/0 | 34630 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0006 | 0/0 | 34635 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0007 | 0/0 | 34626 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0008 | 0/0 | 34627 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0009 | 0/0 | 34624 | 3 | 0 | 3 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0010 | 0/0 | 34620 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0011 | 0/0 | 34625 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0012 | 0/0 | 34633 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0013 | 0/0 | 34632 | 2 | 0 | 1 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0014 | 0/0 | 34632 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0015 | 0/0 | 34634 | 2 | 0 | 1 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0016 | 0/0 | 34636 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0017 | 0/0 | 34636 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0018 | 0/0 | 34640 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0019 | 0/0 | 34639 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0020 | 0/0 | 34636 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0021 | 0/0 | 34626 | 2 | 1 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0022 | 0/0 | 34626 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0023 | 0/0 | 34626 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0024 | 0/0 | 34638 | 2 | 0 | 1 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0025 | 0/0 | 34648 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0026 | 0/0 | 34614 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0027 | 0/0 | 34620 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0028 | 0/0 | 34621 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0029 | 0/0 | 34620 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0030 | 0/0 | 34620 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0031 | 0/0 | 34597 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0032 | 0/0 | 34631 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0033 | 0/0 | 34175 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0034 | 0/0 | 34632 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0035 | 0/0 | 34640 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0036 | 0/0 | 34645 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0037 | 0/0 | 34643 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0038 | 0/0 | 34645 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0039 | 0/0 | 34644 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0040 | 0/0 | 34645 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0041 | 0/0 | 34646 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0042 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0043 | 0/0 | 34634 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0044 | 0/0 | 34633 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0045 | 0/0 | 34634 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0046 | 0/0 | 34642 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0047 | 0/0 | 34626 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0048 | 0/0 | 34635 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0049 | 0/0 | 34638 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0050 | 0/0 | 34635 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0051 | 0/0 | 34632 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0052 | 0/0 | 34632 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0053 | 0/0 | 34633 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0054 | 0/0 | 34634 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0055 | 0/0 | 34635 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0056 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0057 | 0/0 | 34635 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0058 | 0/0 | 34635 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0059 | 0/0 | 34634 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0060 | 0/0 | 34624 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0061 | 0/0 | 34631 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0062 | 0/0 | 34632 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0063 | 0/0 | 34623 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0064 | 0/0 | 34629 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0065 | 0/0 | 34644 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0066 | 0/0 | 34632 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0067 | 0/0 | 34632 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0068 | 0/0 | 34622 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0069 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0070 | 0/0 | 34632 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0071 | 0/0 | 34622 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0072 | 0/0 | 34634 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0073 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0074 | 0/0 | 34631 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0075 | 0/0 | 34632 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0076 | 0/0 | 34632 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0077 | 0/0 | 34631 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0078 | 0/0 | 34632 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0079 | 0/0 | 34635 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0080 | 0/0 | 34635 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0081 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0082 | 0/0 | 34634 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0083 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0084 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0085 | 0/0 | 34635 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0086 | 0/0 | 34633 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0087 | 0/0 | 34636 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0088 | 0/0 | 34635 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0089 | 0/0 | 34636 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0090 | 0/0 | 34635 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0091 | 0/0 | 34636 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0092 | 0/0 | 34635 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0093 | 0/0 | 34636 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0094 | 0/0 | 34636 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0095 | 0/0 | 34635 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0096 | 0/0 | 34637 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0097 | 0/0 | 34640 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0098 | 0/0 | 34639 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0099 | 0/0 | 34639 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0100 | 0/0 | 34637 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0101 | 0/0 | 34642 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0102 | 0/0 | 34641 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0103 | 0/0 | 34638 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0104 | 0/0 | 34636 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0105 | 0/0 | 34636 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0106 | 0/0 | 34636 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0107 | 0/0 | 34639 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0108 | 0/0 | 34638 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0109 | 0/0 | 34636 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0110 | 0/0 | 34635 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0111 | 0/0 | 34638 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0112 | 0/0 | 34636 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0113 | 0/0 | 34638 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0114 | 0/0 | 34624 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0115 | 0/0 | 34638 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0116 | 0/0 | 34634 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0117 | 0/0 | 34635 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0118 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0119 | 0/0 | 34637 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0120 | 0/0 | 34632 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0121 | 0/0 | 34633 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0122 | 0/0 | 34633 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0123 | 0/0 | 34633 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0124 | 0/0 | 34634 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0125 | 0/0 | 34633 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0126 | 0/0 | 34634 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0127 | 0/0 | 34635 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0128 | 0/0 | 34639 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0129 | 0/0 | 34636 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0130 | 0/0 | 34633 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0131 | 0/0 | 34637 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0132 | 0/0 | 34636 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0133 | 0/0 | 34641 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0134 | 0/0 | 34627 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0135 | 0/0 | 34611 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0136 | 0/0 | 34620 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0137 | 0/0 | 34624 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0138 | 0/0 | 34627 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0139 | 0/0 | 34627 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0140 | 0/0 | 34627 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0141 | 0/0 | 34626 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0142 | 0/0 | 34626 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0143 | 0/0 | 34628 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0144 | 0/0 | 34626 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0145 | 0/0 | 34628 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0146 | 0/0 | 34633 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0147 | 0/0 | 34636 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0148 | 0/0 | 34628 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0149 | 0/0 | 34628 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0150 | 0/0 | 34630 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0151 | 0/0 | 34630 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0152 | 0/0 | 34635 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0153 | 0/0 | 34626 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0154 | 0/0 | 34626 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0155 | 0/0 | 34626 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0156 | 0/0 | 34627 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0157 | 0/0 | 34627 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0158 | 0/0 | 34630 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0159 | 0/0 | 34629 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0160 | 0/0 | 34631 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0161 | 0/0 | 34635 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0162 | 0/0 | 34637 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0163 | 0/0 | 34628 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0164 | 0/0 | 34629 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0165 | 0/0 | 34627 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0166 | 0/0 | 34629 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0167 | 0/0 | 34630 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0168 | 0/0 | 34631 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0169 | 0/0 | 34627 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0170 | 0/0 | 34615 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0171 | 0/0 | 34597 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0172 | 0/0 | 34598 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0173 | 0/0 | 34630 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0174 | 0/0 | 34635 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0175 | 0/0 | 34634 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0176 | 0/0 | 34639 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0177 | 0/0 | 34637 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0178 | 0/0 | 34628 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0179 | 0/0 | 34624 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0180 | 0/0 | 34637 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0181 | 0/1 | 34634 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0182 | 0/0 | 34637 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0183 | 0/0 | 34630 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0184 | 0/0 | 34632 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0185 | 0/0 | 34632 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0186 | 0/0 | 34650 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0187 | 0/0 | 34629 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0188 | 0/0 | 34639 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0189 | 0/0 | 34647 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0190 | 0/0 | 34649 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0191 | 0/0 | 34626 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0192 | 0/0 | 34628 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0193 | 0/0 | 34633 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0194 | 0/0 | 34628 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0195 | 0/0 | 34629 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0196 | 0/0 | 34637 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0197 | 0/0 | 34636 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0198 | 0/0 | 34622 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0199 | 1/0 | 34626 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0200 | 0/0 | 34630 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0201 | 0/0 | 34629 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0202 | 0/0 | 34623 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0203 | 0/0 | 34622 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0204 | 0/0 | 34623 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0205 | 0/0 | 34618 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0206 | 0/0 | 34621 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0207 | 0/0 | 34620 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0208 | 0/0 | 34619 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0209 | 0/0 | 34620 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0210 | 0/0 | 34623 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0211 | 0/0 | 34610 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0212 | 0/0 | 34619 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0213 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0214 | 0/0 | 34618 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0215 | 0/0 | 34618 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0216 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0217 | 0/0 | 34614 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0218 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0219 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0220 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0221 | 0/0 | 34619 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0222 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0223 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0224 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0225 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0226 | 0/0 | 34619 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0227 | 0/0 | 34620 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0228 | 0/0 | 34610 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0229 | 0/0 | 34623 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0230 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0231 | 0/0 | 34625 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0232 | 0/0 | 34623 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0233 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0234 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0235 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0236 | 0/0 | 34620 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0237 | 0/0 | 34621 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0238 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0239 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0240 | 0/0 | 34625 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0241 | 0/0 | 34621 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0242 | 0/0 | 34622 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0243 | 0/0 | 34622 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0244 | 0/0 | 34631 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0245 | 0/0 | 34622 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0246 | 0/0 | 34623 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0255 | 0/0 | 34632 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0256 | 0/0 | 34638 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0001t0257 | 0/0 | 34633 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0247 | 0/0 | 34671 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0248 | 0/0 | 34669 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0249 | 0/0 | 34671 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0250 | 0/0 | 34677 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0251 | 0/0 | 34682 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0252 | 0/0 | 34656 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0253 | 0/0 | 34659 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| a0001c0002t0254 | 0/0 | 34663 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | copy fasta | chr18 | 47803957 | 47935659 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0012g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0012g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0013g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0013g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0014g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0015g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0015g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0016g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0016g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0017g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0017g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0018g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0019g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0019g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0020g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0021g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0021g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0022g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0023g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0023g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0024g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0024g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0025g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0025g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0026g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0026g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0027g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0027g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0028g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0028g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0029g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0029g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0030g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0030g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0031g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0032g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0033g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0034g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0035g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0036g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0037g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0038g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0039g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0040g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0041g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0042g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0043g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0044g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0045g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0046g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0047g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0048g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0049g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0050g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0051g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0052g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0053g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0054g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0055g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0056g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0057g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0058g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0059g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0060g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0061g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0062g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0063g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0064g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0065g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0066g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0067g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0068g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0069g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0070g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0071g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0072g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0073g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0074g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0075g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0076g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0077g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0078g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0079g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0080g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0081g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0082g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0083g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0084g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0085g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0086g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0087g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0088g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0089g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0090g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0091g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0092g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0093g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0094g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0095g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0096g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0097g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0098g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0099g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0100g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0101g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0102g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0103g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0104g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0105g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0106g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0107g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0108g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0109g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0110g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0111g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0112g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0113g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0114g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0115g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0116g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0117g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0118g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0119g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0120g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0121g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0122g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0123g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0124g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0125g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0126g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0127g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0128g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0129g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0130g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0131g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0132g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0133g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0134g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0135g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0136g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0137g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0138g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0139g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0140g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0141g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0142g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0143g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0144g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0145g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0146g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0147g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0148g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0149g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0150g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0151g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0152g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0153g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0154g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0155g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0156g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0157g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0158g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0159g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0160g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0161g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0162g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0163g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0164g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0165g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0166g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0167g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0168g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0169g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0170g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0171g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0172g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0173g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0174g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0175g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0176g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0177g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0178g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0179g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0180g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0181g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0182g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0183g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0184g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0185g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0186g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0187g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0188g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0189g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0190g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0191g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0192g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0193g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0194g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0195g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0196g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0197g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0198g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0199g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0200g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0201g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0202g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0203g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0204g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0205g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0206g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0207g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0208g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0209g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0210g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0211g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0212g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0213g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0214g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0215g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0216g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0217g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0218g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0219g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0220g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0221g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0222g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0223g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0224g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0225g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0226g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0227g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0228g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0229g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0230g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0231g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0232g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0233g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0234g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0235g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0236g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0237g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0238g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0239g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0240g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0241g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0242g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0243g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0244g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0245g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0246g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0255g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0256g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0001t0257g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0247g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0248g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0249g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0250g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0251g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0252g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0253g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| a0001c0002t0254g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0024 | g0069 | EUR | GBR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00099 | hp2 | a0001 | c0001 | t0117 | g0281 | EUR | GBR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00140 | hp1 | a0001 | c0001 | t0092 | g0284 | EUR | GBR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00140 | hp2 | a0001 | c0001 | t0163 | g0105 | EUR | GBR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00323 | hp1 | a0001 | c0001 | t0152 | g0078 | EUR | FIN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00323 | hp2 | a0001 | c0001 | t0044 | g0256 | EUR | FIN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00423 | hp1 | a0001 | c0001 | t0127 | g0271 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00423 | hp2 | a0001 | c0001 | t0018 | g0207 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00438 | hp1 | a0001 | c0001 | t0116 | g0245 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00438 | hp2 | a0001 | c0001 | t0200 | g0175 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00544 | hp1 | a0001 | c0001 | t0223 | g0155 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00558 | hp1 | a0001 | c0001 | t0157 | g0048 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00558 | hp2 | a0001 | c0001 | t0087 | g0214 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00609 | hp1 | a0001 | c0001 | t0232 | g0129 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00609 | hp2 | a0001 | c0001 | t0023 | g0092 | EAS | CHS | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00642 | hp1 | a0001 | c0001 | t0093 | g0235 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00642 | hp2 | a0001 | c0001 | t0086 | g0116 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00735 | hp1 | a0001 | c0001 | t0136 | g0100 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00735 | hp2 | a0001 | c0001 | t0130 | g0244 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00741 | hp1 | a0001 | c0001 | t0160 | g0086 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG00741 | hp2 | a0001 | c0001 | t0015 | g0218 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01069 | hp2 | a0001 | c0001 | t0067 | g0280 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01071 | hp1 | a0001 | c0001 | t0177 | g0036 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0102 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01074 | hp2 | a0001 | c0001 | t0075 | g0288 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01081 | hp1 | a0001 | c0001 | t0014 | g0276 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0097 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01106 | hp1 | a0001 | c0001 | t0082 | g0296 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01106 | hp2 | a0001 | c0001 | t0146 | g0037 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01109 | hp1 | a0001 | c0001 | t0231 | g0147 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01109 | hp2 | a0001 | c0001 | t0036 | g0030 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01168 | hp1 | a0001 | c0001 | t0179 | g0070 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01168 | hp2 | a0001 | c0001 | t0012 | g0239 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01169 | hp1 | a0001 | c0001 | t0012 | g0243 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01169 | hp2 | a0001 | c0001 | t0161 | g0103 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0237 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01243 | hp2 | a0001 | c0001 | t0147 | g0093 | AMR | PUR | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01256 | hp1 | a0001 | c0001 | t0210 | g0294 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01256 | hp2 | a0001 | c0001 | t0077 | g0253 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01257 | hp2 | a0001 | c0001 | t0054 | g0274 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01258 | hp1 | a0001 | c0001 | t0204 | g0295 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01258 | hp2 | a0001 | c0001 | t0055 | g0275 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01261 | hp1 | a0001 | c0001 | t0024 | g0077 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01261 | hp2 | a0001 | c0001 | t0242 | g0160 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01358 | hp1 | a0001 | c0001 | t0237 | g0143 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01358 | hp2 | a0001 | c0001 | t0188 | g0075 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01361 | hp1 | a0001 | c0001 | t0060 | g0238 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01361 | hp2 | a0001 | c0001 | t0178 | g0106 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01496 | hp1 | a0001 | c0001 | t0203 | g0233 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01496 | hp2 | a0001 | c0001 | t0156 | g0104 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01884 | hp1 | a0001 | c0001 | t0173 | g0033 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01884 | hp2 | a0001 | c0001 | t0149 | g0042 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01891 | hp1 | a0001 | c0001 | t0189 | g0018 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01891 | hp2 | a0001 | c0002 | t0254 | g0016 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01928 | hp1 | a0001 | c0001 | t0229 | g0136 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01928 | hp2 | a0001 | c0001 | t0192 | g0308 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01943 | hp1 | a0001 | c0001 | t0028 | g0138 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01943 | hp2 | a0001 | c0001 | t0135 | g0045 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01975 | hp1 | a0001 | c0001 | t0191 | g0082 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0101 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01978 | hp1 | a0001 | c0001 | t0071 | g0273 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0084 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01981 | hp1 | a0001 | c0001 | t0162 | g0040 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01981 | hp2 | a0001 | c0001 | t0013 | g0177 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01993 | hp1 | a0001 | c0001 | t0202 | g0220 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01993 | hp2 | a0001 | c0001 | t0080 | g0287 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02015 | hp1 | a0001 | c0001 | t0042 | g0254 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02015 | hp2 | a0001 | c0001 | t0219 | g0139 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02040 | hp1 | a0001 | c0001 | t0072 | g0259 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02040 | hp2 | a0001 | c0001 | t0019 | g0183 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02055 | hp1 | a0001 | c0001 | t0244 | g0122 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02055 | hp2 | a0001 | c0001 | t0245 | g0007 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02056 | hp1 | a0001 | c0001 | t0198 | g0080 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02056 | hp2 | a0001 | c0001 | t0228 | g0158 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02071 | hp1 | a0001 | c0001 | t0011 | g0230 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02071 | hp2 | a0001 | c0001 | t0230 | g0153 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02074 | hp1 | a0001 | c0001 | t0073 | g0293 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02074 | hp2 | a0001 | c0001 | t0165 | g0047 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02129 | hp1 | a0001 | c0001 | t0011 | g0223 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02129 | hp2 | a0001 | c0001 | t0142 | g0050 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02132 | hp1 | a0001 | c0001 | t0224 | g0141 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02132 | hp2 | a0001 | c0001 | t0081 | g0291 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02135 | hp1 | a0001 | c0001 | t0028 | g0164 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02135 | hp2 | a0001 | c0001 | t0047 | g0222 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02145 | hp1 | a0001 | c0002 | t0252 | g0017 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02145 | hp2 | a0001 | c0001 | t0140 | g0098 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0083 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02148 | hp2 | a0001 | c0001 | t0240 | g0163 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CDX | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CDX | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02165 | hp1 | a0001 | c0001 | t0017 | g0265 | EAS | CDX | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02258 | hp1 | a0001 | c0001 | t0166 | g0043 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02258 | hp2 | a0001 | c0001 | t0132 | g0211 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02273 | hp1 | a0001 | c0001 | t0053 | g0085 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02273 | hp2 | a0001 | c0001 | t0034 | g0258 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02280 | hp1 | a0001 | c0001 | t0168 | g0107 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02293 | hp1 | a0001 | c0001 | t0016 | g0209 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02300 | hp1 | a0001 | c0001 | t0227 | g0166 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0081 | AMR | PEL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02451 | hp1 | a0001 | c0001 | t0025 | g0019 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02451 | hp2 | a0001 | c0001 | t0032 | g0003 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02523 | hp2 | a0001 | c0001 | t0008 | g0061 | EAS | KHV | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02572 | hp1 | a0001 | c0002 | t0248 | g0303 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02572 | hp2 | a0001 | c0001 | t0184 | g0035 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02602 | hp1 | a0001 | c0001 | t0015 | g0216 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02602 | hp2 | a0001 | c0001 | t0065 | g0197 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02615 | hp1 | a0001 | c0001 | t0095 | g0176 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02615 | hp2 | a0001 | c0001 | t0104 | g0215 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02622 | hp1 | a0001 | c0001 | t0041 | g0034 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02622 | hp2 | a0001 | c0001 | t0190 | g0021 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02630 | hp1 | a0001 | c0001 | t0174 | g0094 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02630 | hp2 | a0001 | c0001 | t0187 | g0108 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02647 | hp1 | a0001 | c0001 | t0172 | g0074 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02647 | hp2 | a0001 | c0001 | t0020 | g0191 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02717 | hp1 | a0001 | c0001 | t0243 | g0011 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02717 | hp2 | a0001 | c0001 | t0148 | g0109 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02895 | hp1 | a0001 | c0001 | t0020 | g0192 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02895 | hp2 | a0001 | c0001 | t0255 | g0096 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02896 | hp1 | a0001 | c0001 | t0026 | g0111 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02896 | hp2 | a0001 | c0001 | t0205 | g0120 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02897 | hp1 | a0001 | c0001 | t0026 | g0110 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02897 | hp2 | a0001 | c0001 | t0129 | g0190 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02922 | hp1 | a0001 | c0001 | t0143 | g0013 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0219 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02965 | hp1 | a0001 | c0001 | t0171 | g0039 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02965 | hp2 | a0001 | c0001 | t0109 | g0226 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02976 | hp1 | a0001 | c0001 | t0207 | g0118 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02976 | hp2 | a0001 | c0001 | t0151 | g0072 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03041 | hp1 | a0001 | c0001 | t0035 | g0028 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03041 | hp2 | a0001 | c0001 | t0175 | g0307 | AFR | GWD | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03130 | hp1 | a0001 | c0001 | t0037 | g0026 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03130 | hp2 | a0001 | c0001 | t0110 | g0231 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03139 | hp1 | a0001 | c0002 | t0250 | g0304 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03139 | hp2 | a0001 | c0001 | t0185 | g0025 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03195 | hp1 | a0001 | c0001 | t0040 | g0029 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03195 | hp2 | a0001 | c0001 | t0197 | g0005 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03209 | hp1 | a0001 | c0001 | t0186 | g0024 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03209 | hp2 | a0001 | c0001 | t0209 | g0121 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03225 | hp1 | a0001 | c0001 | t0183 | g0023 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03225 | hp2 | a0001 | c0001 | t0208 | g0119 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03239 | hp1 | a0001 | c0001 | t0064 | g0285 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03239 | hp2 | a0001 | c0001 | t0045 | g0250 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03453 | hp1 | a0001 | c0001 | t0176 | g0022 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03453 | hp2 | a0001 | c0001 | t0206 | g0117 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03486 | hp1 | a0001 | c0001 | t0106 | g0225 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03486 | hp2 | a0001 | c0001 | t0039 | g0027 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03490 | hp1 | a0001 | c0001 | t0061 | g0268 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03490 | hp2 | a0001 | c0001 | t0021 | g0057 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03491 | hp1 | a0001 | c0001 | t0125 | g0283 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03491 | hp2 | a0001 | c0001 | t0137 | g0099 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03516 | hp1 | a0001 | c0001 | t0159 | g0065 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03516 | hp2 | a0001 | c0002 | t0251 | g0305 | AFR | ESN | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03579 | hp1 | a0001 | c0001 | t0167 | g0012 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03579 | hp2 | a0001 | c0001 | t0180 | g0067 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03688 | hp1 | a0001 | c0001 | t0123 | g0252 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03688 | hp2 | a0001 | c0001 | t0126 | g0279 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03704 | hp1 | a0001 | c0001 | t0141 | g0060 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03834 | hp1 | a0001 | c0001 | t0088 | g0232 | SAS | BEB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03834 | hp2 | a0001 | c0001 | t0256 | g0073 | SAS | BEB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03927 | hp1 | a0001 | c0002 | t0247 | g0014 | SAS | BEB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03927 | hp2 | a0001 | c0001 | t0120 | g0189 | SAS | BEB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03942 | hp1 | a0001 | c0001 | t0085 | g0241 | SAS | BEB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03942 | hp2 | a0001 | c0001 | t0246 | g0126 | SAS | BEB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG04115 | hp1 | a0001 | c0001 | t0103 | g0227 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG04115 | hp2 | a0001 | c0001 | t0215 | g0144 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG04199 | hp1 | a0001 | c0001 | t0119 | g0297 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG04228 | hp1 | a0001 | c0001 | t0031 | g0002 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG04228 | hp2 | a0001 | c0001 | t0013 | g0286 | SAS | STU | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18522 | hp1 | a0001 | c0001 | t0193 | g0032 | AFR | YRI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18522 | hp2 | a0001 | c0001 | t0038 | g0031 | AFR | YRI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18906 | hp1 | a0001 | c0002 | t0249 | g0306 | AFR | YRI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18906 | hp2 | a0001 | c0001 | t0050 | g0213 | AFR | YRI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18942 | hp1 | a0001 | c0001 | t0027 | g0132 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18942 | hp2 | a0001 | c0001 | t0112 | g0179 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18943 | hp1 | a0001 | c0001 | t0238 | g0165 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18943 | hp2 | a0001 | c0001 | t0124 | g0201 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18944 | hp1 | a0001 | c0001 | t0049 | g0186 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18944 | hp2 | a0001 | c0001 | t0058 | g0240 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18945 | hp1 | a0001 | c0001 | t0033 | g0262 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18945 | hp2 | a0001 | c0001 | t0216 | g0157 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18949 | hp1 | a0001 | c0001 | t0084 | g0270 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18949 | hp2 | a0001 | c0001 | t0194 | g0010 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18950 | hp1 | a0001 | c0001 | t0090 | g0248 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18950 | hp2 | a0001 | c0001 | t0062 | g0234 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18952 | hp1 | a0001 | c0001 | t0154 | g0091 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18952 | hp2 | a0001 | c0001 | t0030 | g0134 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18954 | hp1 | a0001 | c0001 | t0213 | g0128 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18954 | hp2 | a0001 | c0001 | t0113 | g0184 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18959 | hp1 | a0001 | c0001 | t0098 | g0181 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18959 | hp2 | a0001 | c0001 | t0170 | g0087 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0145 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18960 | hp2 | a0001 | c0001 | t0094 | g0004 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18962 | hp1 | a0001 | c0001 | t0096 | g0229 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18962 | hp2 | a0001 | c0001 | t0030 | g0135 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18968 | hp1 | a0001 | c0001 | t0241 | g0137 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18968 | hp2 | a0001 | c0001 | t0019 | g0187 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18969 | hp1 | a0001 | c0001 | t0222 | g0169 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18969 | hp2 | a0001 | c0001 | t0102 | g0193 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18971 | hp1 | a0001 | c0001 | t0153 | g0054 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18972 | hp1 | a0001 | c0001 | t0164 | g0009 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18972 | hp2 | a0001 | c0001 | t0018 | g0204 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18973 | hp1 | a0001 | c0001 | t0016 | g0112 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18973 | hp2 | a0001 | c0001 | t0059 | g0264 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18974 | hp2 | a0001 | c0001 | t0236 | g0159 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18979 | hp1 | a0001 | c0001 | t0239 | g0142 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18979 | hp2 | a0001 | c0001 | t0121 | g0292 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18980 | hp1 | a0001 | c0001 | t0169 | g0089 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18981 | hp2 | a0001 | c0001 | t0074 | g0200 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18983 | hp1 | a0001 | c0001 | t0027 | g0148 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18983 | hp2 | a0001 | c0001 | t0022 | g0001 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18984 | hp2 | a0001 | c0001 | t0212 | g0167 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18986 | hp1 | a0001 | c0001 | t0234 | g0172 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18986 | hp2 | a0001 | c0001 | t0068 | g0261 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18988 | hp1 | a0001 | c0001 | t0017 | g0208 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18988 | hp2 | a0001 | c0001 | t0220 | g0151 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18989 | hp2 | a0001 | c0001 | t0029 | g0133 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18990 | hp1 | a0001 | c0001 | t0134 | g0041 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18990 | hp2 | a0001 | c0001 | t0066 | g0199 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18994 | hp2 | a0001 | c0001 | t0128 | g0114 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18997 | hp1 | a0001 | c0001 | t0070 | g0202 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18997 | hp2 | a0001 | c0001 | t0139 | g0051 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18999 | hp1 | a0001 | c0001 | t0114 | g0180 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18999 | hp2 | a0001 | c0001 | t0155 | g0090 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19002 | hp1 | a0001 | c0001 | t0235 | g0173 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19002 | hp2 | a0001 | c0001 | t0048 | g0182 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19003 | hp1 | a0001 | c0001 | t0226 | g0154 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19003 | hp2 | a0001 | c0001 | t0083 | g0178 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19004 | hp1 | a0001 | c0001 | t0052 | g0277 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0124 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19005 | hp1 | a0001 | c0001 | t0111 | g0205 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19005 | hp2 | a0001 | c0001 | t0233 | g0168 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19007 | hp1 | a0001 | c0001 | t0225 | g0152 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19007 | hp2 | a0001 | c0001 | t0115 | g0188 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19009 | hp1 | a0001 | c0001 | t0218 | g0171 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19011 | hp1 | a0001 | c0001 | t0144 | g0053 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19011 | hp2 | a0001 | c0001 | t0097 | g0185 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0224 | AFR | LWK | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19043 | hp2 | a0001 | c0001 | t0150 | g0066 | AFR | LWK | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19056 | hp1 | a0001 | c0001 | t0214 | g0123 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19057 | hp1 | a0001 | c0001 | t0069 | g0298 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0162 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19058 | hp1 | a0001 | c0001 | t0063 | g0249 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19058 | hp2 | a0001 | c0001 | t0221 | g0127 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19060 | hp1 | a0001 | c0001 | t0138 | g0038 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19060 | hp2 | a0001 | c0001 | t0118 | g0203 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19062 | hp2 | a0001 | c0001 | t0057 | g0246 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19064 | hp1 | a0001 | c0001 | t0089 | g0228 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19064 | hp2 | a0001 | c0001 | t0145 | g0068 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19065 | hp2 | a0001 | c0001 | t0078 | g0272 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19066 | hp1 | a0001 | c0001 | t0051 | g0290 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19066 | hp2 | a0001 | c0001 | t0022 | g0001 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19068 | hp2 | a0001 | c0001 | t0029 | g0161 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19070 | hp1 | a0001 | c0001 | t0046 | g0196 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19079 | hp1 | a0001 | c0001 | t0043 | g0255 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19079 | hp2 | a0001 | c0001 | t0201 | g0174 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19080 | hp2 | a0001 | c0001 | t0099 | g0221 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19088 | hp1 | a0001 | c0001 | t0056 | g0242 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19088 | hp2 | a0001 | c0001 | t0023 | g0088 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19091 | hp2 | a0001 | c0001 | t0079 | g0247 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19240 | hp1 | a0001 | c0001 | t0133 | g0095 | AFR | YRI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA19240 | hp2 | a0001 | c0001 | t0107 | g0236 | AFR | YRI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20752 | hp1 | a0001 | c0001 | t0100 | g0299 | EUR | TSI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20752 | hp2 | a0001 | c0001 | t0091 | g0210 | EUR | TSI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20805 | hp1 | a0001 | c0001 | t0014 | g0115 | EUR | TSI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20805 | hp2 | a0001 | c0001 | t0195 | g0044 | EUR | TSI | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20905 | hp1 | a0001 | c0001 | t0217 | g0131 | SAS | GIH | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20905 | hp2 | a0001 | c0001 | t0122 | g0251 | SAS | GIH | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01123 | hp1 | a0001 | c0001 | t0076 | g0289 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG01123 | hp2 | a0001 | c0001 | t0182 | g0071 | AMR | CLM | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02486 | hp1 | a0001 | c0002 | t0253 | g0015 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02486 | hp2 | a0001 | c0001 | t0131 | g0212 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02559 | hp1 | a0001 | c0001 | t0196 | g0006 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0020 | AFR | ACB | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03471 | hp1 | a0001 | c0001 | t0105 | g0302 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG03471 | hp2 | a0001 | c0001 | t0108 | g0217 | AFR | MSL | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG06807 | hp1 | a0001 | c0001 | t0021 | g0056 | AFR | USA | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| HG06807 | hp2 | a0001 | c0001 | t0211 | g0008 | AFR | USA | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18955 | hp1 | a0001 | c0001 | t0101 | g0194 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20300 | hp1 | a0001 | c0001 | t0158 | g0064 | AFR | USA | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| NA20300 | hp2 | a0001 | c0001 | t0257 | g0309 | AFR | USA | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0181 | g0076 | REF | REF | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0199 | g0079 | REF | REF | SMAD2_chr18_47803957_47935659 | SMAD2 | chr18 | 47803957 | 47935659 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47848644
|
C | T | 1 | a0001c0002 | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
synonymous_variant | LOW | c.828G>A | p.Ser276Ser | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/11 | 1180/34626 | 828/1404 | 276/467 | chr18 | 47848644 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47809076
|
C | T | 3 | a0001c0001t0062a0001c0001t0063a0001c0001t0121 | 3 | NA18950.hp2 NA18979.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*32751G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 32751 | chr18 | 47809076 | |||||
| chr18:47809214
|
C | T | 2 | a0001c0001t0150a0001c0001t0180 | 2 | HG03579.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*32613G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 32613 | chr18 | 47809214 | |||||
| chr18:47809234
|
G | C | 3 | a0001c0001t0067a0001c0001t0075a0001c0001t0076 | 3 | HG01069.hp2 HG01074.hp2 HG01123.hp1 |
3_prime_UTR_variant | MODIFIER | c.*32593C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 32593 | chr18 | 47809234 | |||||
| chr18:47809255
|
G | C | 1 | a0001c0002t0248 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32572C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 32572 | chr18 | 47809255 | |||||
| chr18:47809356
|
G | A | 58 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(55): Show | 71 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*32471C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 32471 | chr18 | 47809356 | |||||
| chr18:47809704
|
T | A | 1 | a0001c0001t0141 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32123A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 32123 | chr18 | 47809704 | |||||
| chr18:47809723
|
C | T | 1 | a0001c0001t0084 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32104G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 32104 | chr18 | 47809723 | |||||
| chr18:47809874
|
T | C | 1 | a0001c0001t0053 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31953A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 31953 | chr18 | 47809874 | |||||
| chr18:47810114
|
G | A | 60 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(57): Show | 76 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*31713C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 31713 | chr18 | 47810114 | |||||
| chr18:47810170
|
C | G | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*31657G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 31657 | chr18 | 47810170 | |||||
| chr18:47810226
|
C | T | 8 | a0001c0001t0205a0001c0001t0206a0001c0001t0207others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*31601G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 31601 | chr18 | 47810226 | |||||
| chr18:47810825
|
C | T | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31002G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 31002 | chr18 | 47810825 | |||||
| chr18:47810859
|
T | C | 2 | a0001c0001t0146a0001c0001t0147 | 2 | HG01106.hp2 HG01243.hp2 |
3_prime_UTR_variant | MODIFIER | c.*30968A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30968 | chr18 | 47810859 | |||||
| chr18:47810893
|
G | A | 1 | a0001c0001t0139 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30934C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30934 | chr18 | 47810893 | |||||
| chr18:47810930
|
C | T | 2 | a0001c0001t0222a0001c0001t0255 | 2 | HG02895.hp2 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*30897G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30897 | chr18 | 47810930 | |||||
| chr18:47810937
|
G | T | 153 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(150): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*30890C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30890 | chr18 | 47810937 | |||||
| chr18:47810997
|
C | A | 1 | a0001c0001t0221 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30830G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30830 | chr18 | 47810997 | |||||
| chr18:47811072
|
A | C | 1 | a0001c0001t0022 | 2 | NA18983.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*30755T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30755 | chr18 | 47811072 | |||||
| chr18:47811196
|
G | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*30631C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30631 | chr18 | 47811196 | |||||
| chr18:47811469
|
C | CA | 113 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(110): Show | 137 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*30357dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30357 | chr18 | 47811469 | |||||
| chr18:47811469
|
C | CAA | 11 | a0001c0001t0057a0001c0001t0061a0001c0001t0105others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*30356_*30357dupTT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30357 | chr18 | 47811469 | |||||
| chr18:47811485
|
A | G | 1 | a0001c0001t0211 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30342T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30342 | chr18 | 47811485 | |||||
| chr18:47811577
|
A | C | 1 | a0001c0001t0068 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30250T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 30250 | chr18 | 47811577 | |||||
| chr18:47811883
|
G | A | 1 | a0001c0001t0087 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29944C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 29944 | chr18 | 47811883 | |||||
| chr18:47812193
|
G | A | 1 | a0001c0001t0032 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29634C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 29634 | chr18 | 47812193 | |||||
| chr18:47812497
|
T | C | 1 | a0001c0001t0109 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*29330A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 29330 | chr18 | 47812497 | |||||
| chr18:47812663
|
T | A | 3 | a0001c0001t0065a0001c0001t0200a0001c0001t0201 | 3 | HG00438.hp2 HG02602.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29164A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 29164 | chr18 | 47812663 | |||||
| chr18:47812927
|
G | A | 3 | a0001c0001t0053a0001c0001t0054a0001c0001t0055 | 3 | HG01257.hp2 HG01258.hp2 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*28900C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28900 | chr18 | 47812927 | |||||
| chr18:47813152
|
G | T | 3 | a0001c0001t0183a0001c0001t0184a0001c0001t0185 | 3 | HG02572.hp2 HG03139.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*28675C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28675 | chr18 | 47813152 | |||||
| chr18:47813205
|
G | C | 1 | a0001c0001t0160 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28622C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28622 | chr18 | 47813205 | |||||
| chr18:47813404
|
A | AT | 14 | a0001c0001t0024a0001c0001t0036a0001c0001t0065others(11): Show | 15 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*28422dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28422 | chr18 | 47813404 | |||||
| chr18:47813404
|
AT | A | 150 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(147): Show | 186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*28422delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28422 | chr18 | 47813404 | |||||
| chr18:47813404
|
ATTT | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*28420_*28422delAA others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28420 | chr18 | 47813404 | |||||
| chr18:47813431
|
G | A | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28396C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28396 | chr18 | 47813431 | |||||
| chr18:47813467
|
C | T | 9 | a0001c0001t0026a0001c0001t0205a0001c0001t0206others(6): Show | 10 | HG02055.hp2 HG02717.hp1 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*28360G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28360 | chr18 | 47813467 | |||||
| chr18:47813620
|
C | A | 1 | a0001c0001t0243 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28207G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28207 | chr18 | 47813620 | |||||
| chr18:47813647
|
C | G | 1 | a0001c0001t0184 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28180G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28180 | chr18 | 47813647 | |||||
| chr18:47813711
|
A | AATTTTTT others(7): Show |
1 | a0001c0001t0099 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28115_*28116insAA others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(2): Show |
42 | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(39): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*28107_*28115dupAA others(7): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(3): Show |
50 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(47): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*28106_*28115dupAA others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(4): Show |
40 | a0001c0001t0016a0001c0001t0017a0001c0001t0018others(37): Show | 45 | HG00423.hp2 HG00558.hp2 HG01106.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*28105_*28115dupAA others(9): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(5): Show |
12 | a0001c0001t0058a0001c0001t0089a0001c0001t0100others(9): Show | 12 | HG00609.hp1 HG01109.hp1 HG01496.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*28104_*28115dupAA others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(6): Show |
4 | a0001c0001t0111a0001c0001t0112a0001c0001t0115others(1): Show | 4 | NA18942.hp2 NA18994.hp2 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*28103_*28115dupAA others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(7): Show |
5 | a0001c0001t0019a0001c0001t0048a0001c0001t0049others(2): Show | 6 | HG02040.hp2 NA18944.hp1 NA18954.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*28102_*28115dupAA others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0097 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28101_*28115dupAA others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0065a0001c0001t0201 | 2 | HG02602.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*28100_*28115dupAA others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0200 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*28099_*28115dupAA others(15): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
AT | A | 71 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(68): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*28115delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28115 | chr18 | 47813711 | |||||
| chr18:47813711
|
ATT | A | 15 | a0001c0001t0032a0001c0001t0035a0001c0001t0037others(12): Show | 15 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*28114_*28115delAA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 28114 | chr18 | 47813711 | |||||
| chr18:47813861
|
C | T | 1 | a0001c0001t0229 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27966G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27966 | chr18 | 47813861 | |||||
| chr18:47813882
|
T | C | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*27945A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27945 | chr18 | 47813882 | |||||
| chr18:47814160
|
G | T | 3 | a0001c0001t0065a0001c0001t0200a0001c0001t0201 | 3 | HG00438.hp2 HG02602.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*27667C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27667 | chr18 | 47814160 | |||||
| chr18:47814196
|
T | C | 2 | a0001c0001t0104a0001c0001t0105 | 2 | HG02615.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*27631A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27631 | chr18 | 47814196 | |||||
| chr18:47814293
|
A | G | 3 | a0001c0001t0025a0001c0001t0189a0001c0001t0190 | 4 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*27534T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27534 | chr18 | 47814293 | |||||
| chr18:47814424
|
A | G | 1 | a0001c0001t0012 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*27403T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27403 | chr18 | 47814424 | |||||
| chr18:47814490
|
G | A | 1 | a0001c0001t0021 | 2 | HG03490.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*27337C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27337 | chr18 | 47814490 | |||||
| chr18:47814568
|
T | C | 1 | a0001c0001t0110 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27259A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 27259 | chr18 | 47814568 | |||||
| chr18:47814877
|
C | G | 176 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(173): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*26950G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 26950 | chr18 | 47814877 | |||||
| chr18:47815196
|
T | C | 4 | a0001c0001t0056a0001c0001t0057a0001c0001t0058others(1): Show | 4 | NA18944.hp2 NA18973.hp2 NA19062.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*26631A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 26631 | chr18 | 47815196 | |||||
| chr18:47815327
|
T | C | 1 | a0001c0001t0233 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26500A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 26500 | chr18 | 47815327 | |||||
| chr18:47816251
|
T | G | 7 | a0001c0001t0007a0001c0001t0136a0001c0001t0137others(4): Show | 9 | HG00140.hp2 HG00735.hp1 HG01074.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*25576A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25576 | chr18 | 47816251 | |||||
| chr18:47816302
|
T | C | 1 | a0001c0001t0211 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25525A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25525 | chr18 | 47816302 | |||||
| chr18:47816368
|
C | T | 1 | a0001c0001t0229 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25459G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25459 | chr18 | 47816368 | |||||
| chr18:47816496
|
C | T | 2 | a0001c0001t0022a0001c0001t0023 | 4 | HG00609.hp2 NA18983.hp2 NA19066.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*25331G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25331 | chr18 | 47816496 | |||||
| chr18:47816497
|
G | A | 1 | a0001c0001t0076 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25330C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25330 | chr18 | 47816497 | |||||
| chr18:47816657
|
A | G | 1 | a0001c0001t0229 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25170T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25170 | chr18 | 47816657 | |||||
| chr18:47816754
|
T | C | 1 | a0001c0001t0165 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25073A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25073 | chr18 | 47816754 | |||||
| chr18:47816764
|
C | CT | 118 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(115): Show | 141 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*25062dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25062 | chr18 | 47816764 | |||||
| chr18:47816787
|
G | A | 1 | a0001c0001t0141 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25040C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25040 | chr18 | 47816787 | |||||
| chr18:47816788
|
T | G | 176 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(173): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*25039A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 25039 | chr18 | 47816788 | |||||
| chr18:47816845
|
C | A | 1 | a0001c0001t0119 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24982G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24982 | chr18 | 47816845 | |||||
| chr18:47817081
|
A | G | 177 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(174): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*24746T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24746 | chr18 | 47817081 | |||||
| chr18:47817137
|
C | T | 40 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(37): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*24690G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24690 | chr18 | 47817137 | |||||
| chr18:47817213
|
A | T | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*24614T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24614 | chr18 | 47817213 | |||||
| chr18:47817265
|
C | T | 1 | a0001c0001t0205 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24562G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24562 | chr18 | 47817265 | |||||
| chr18:47817332
|
T | A | 2 | a0001c0001t0013a0001c0001t0064 | 3 | HG01981.hp2 HG03239.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*24495A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24495 | chr18 | 47817332 | |||||
| chr18:47817440
|
T | A | 1 | a0001c0001t0070 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24387A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24387 | chr18 | 47817440 | |||||
| chr18:47817520
|
T | G | 1 | a0001c0001t0194 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24307A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24307 | chr18 | 47817520 | |||||
| chr18:47817561
|
A | G | 9 | a0001c0001t0035a0001c0001t0036a0001c0001t0037others(6): Show | 9 | HG01109.hp2 HG02622.hp1 HG03041.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*24266T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24266 | chr18 | 47817561 | |||||
| chr18:47817740
|
T | A | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24087A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 24087 | chr18 | 47817740 | |||||
| chr18:47818196
|
G | A | 1 | a0001c0001t0149 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*23631C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 23631 | chr18 | 47818196 | |||||
| chr18:47818419
|
G | A | 6 | a0001c0001t0014a0001c0001t0069a0001c0001t0077others(3): Show | 7 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*23408C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 23408 | chr18 | 47818419 | |||||
| chr18:47818842
|
A | G | 1 | a0001c0001t0150 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22985T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22985 | chr18 | 47818842 | |||||
| chr18:47818935
|
G | A | 3 | a0001c0001t0032a0001c0001t0173a0001c0001t0193 | 3 | HG01884.hp1 HG02451.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*22892C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22892 | chr18 | 47818935 | |||||
| chr18:47819022
|
T | G | 44 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(41): Show | 56 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*22805A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22805 | chr18 | 47819022 | |||||
| chr18:47819031
|
G | A | 2 | a0001c0001t0136a0001c0001t0137 | 2 | HG00735.hp1 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*22796C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22796 | chr18 | 47819031 | |||||
| chr18:47819125
|
G | A | 177 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(174): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*22702C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22702 | chr18 | 47819125 | |||||
| chr18:47819228
|
C | CA | 3 | a0001c0002t0252a0001c0002t0253a0001c0002t0254 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*22598dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22598 | chr18 | 47819228 | |||||
| chr18:47819591
|
G | A | 1 | a0001c0001t0078 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22236C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22236 | chr18 | 47819591 | |||||
| chr18:47819624
|
G | A | 1 | a0001c0001t0142 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22203C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22203 | chr18 | 47819624 | |||||
| chr18:47819656
|
C | T | 64 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(61): Show | 78 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*22171G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22171 | chr18 | 47819656 | |||||
| chr18:47819659
|
G | A | 1 | a0001c0001t0155 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22168C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22168 | chr18 | 47819659 | |||||
| chr18:47819669
|
G | A | 3 | a0001c0001t0065a0001c0001t0200a0001c0001t0201 | 3 | HG00438.hp2 HG02602.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*22158C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22158 | chr18 | 47819669 | |||||
| chr18:47819728
|
G | A | 1 | a0001c0001t0115 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22099C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22099 | chr18 | 47819728 | |||||
| chr18:47819783
|
G | A | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22044C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22044 | chr18 | 47819783 | |||||
| chr18:47819795
|
C | CA | 36 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(33): Show | 47 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*22031dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22031 | chr18 | 47819795 | |||||
| chr18:47819795
|
C | CAA | 21 | a0001c0001t0029a0001c0001t0054a0001c0001t0061others(18): Show | 22 | HG00544.hp1 HG01257.hp2 HG01891.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*22030_*22031dupTT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22031 | chr18 | 47819795 | |||||
| chr18:47819795
|
C | CAAA | 98 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(95): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*22029_*22031dupTT others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22031 | chr18 | 47819795 | |||||
| chr18:47819795
|
C | CAAAA | 10 | a0001c0001t0018a0001c0001t0057a0001c0001t0060others(7): Show | 11 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*22028_*22031dupTT others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22031 | chr18 | 47819795 | |||||
| chr18:47819795
|
CA | C | 58 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(55): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*22031delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22031 | chr18 | 47819795 | |||||
| chr18:47819795
|
CAAAA | C | 9 | a0001c0001t0026a0001c0001t0205a0001c0001t0206others(6): Show | 10 | HG02055.hp2 HG02717.hp1 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*22028_*22031delTT others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 22028 | chr18 | 47819795 | |||||
| chr18:47819836
|
G | T | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21991C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21991 | chr18 | 47819836 | |||||
| chr18:47819863
|
T | C | 1 | a0001c0001t0096 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21964A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21964 | chr18 | 47819863 | |||||
| chr18:47819947
|
G | C | 3 | a0001c0001t0149a0001c0001t0158a0001c0001t0159 | 3 | HG01884.hp2 HG03516.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*21880C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21880 | chr18 | 47819947 | |||||
| chr18:47820154
|
T | C | 1 | a0001c0001t0095 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21673A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21673 | chr18 | 47820154 | |||||
| chr18:47820181
|
C | T | 1 | a0001c0001t0082 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21646G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21646 | chr18 | 47820181 | |||||
| chr18:47820304
|
A | C | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*21523T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21523 | chr18 | 47820304 | |||||
| chr18:47820346
|
A | T | 9 | a0001c0001t0026a0001c0001t0205a0001c0001t0206others(6): Show | 10 | HG02055.hp2 HG02717.hp1 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*21481T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21481 | chr18 | 47820346 | |||||
| chr18:47820514
|
A | G | 1 | a0001c0001t0218 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21313T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21313 | chr18 | 47820514 | |||||
| chr18:47820533
|
G | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*21294C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21294 | chr18 | 47820533 | |||||
| chr18:47820561
|
A | T | 170 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(167): Show | 206 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*21266T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21266 | chr18 | 47820561 | |||||
| chr18:47820609
|
T | C | 1 | a0001c0001t0179 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*21218A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21218 | chr18 | 47820609 | |||||
| chr18:47820752
|
T | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*21075A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21075 | chr18 | 47820752 | |||||
| chr18:47820776
|
A | G | 1 | a0001c0001t0194 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21051T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21051 | chr18 | 47820776 | |||||
| chr18:47820784
|
T | C | 166 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(163): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*21043A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 21043 | chr18 | 47820784 | |||||
| chr18:47820853
|
A | G | 2 | a0001c0001t0032a0001c0001t0193 | 2 | HG02451.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20974T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20974 | chr18 | 47820853 | |||||
| chr18:47820856
|
T | C | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20971A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20971 | chr18 | 47820856 | |||||
| chr18:47820857
|
T | A | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20970A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20970 | chr18 | 47820857 | |||||
| chr18:47820859
|
G | A | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20968C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20968 | chr18 | 47820859 | |||||
| chr18:47820866
|
C | T | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20961G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20961 | chr18 | 47820866 | |||||
| chr18:47820869
|
G | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*20958C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20958 | chr18 | 47820869 | |||||
| chr18:47820894
|
TATACACA others(5): Show |
T | 4 | a0001c0002t0248a0001c0002t0249a0001c0002t0250others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*20921_*20932delGT others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20921 | chr18 | 47820894 | |||||
| chr18:47820894
|
TATACACA others(7): Show |
T | 1 | a0001c0002t0247 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20919_*20932delGT others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20919 | chr18 | 47820894 | |||||
| chr18:47820894
|
TATACACA others(17): Show |
T | 3 | a0001c0002t0252a0001c0002t0253a0001c0002t0254 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20909_*20932delGT others(22): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20909 | chr18 | 47820894 | |||||
| chr18:47820896
|
T | TACAC | 9 | a0001c0001t0024a0001c0001t0152a0001c0001t0161others(6): Show | 10 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*20927_*20930dupGT others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20930 | chr18 | 47820896 | |||||
| chr18:47820896
|
T | TACACAC | 3 | a0001c0001t0176a0001c0001t0177a0001c0001t0256 | 3 | HG01071.hp1 HG03453.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20925_*20930dupGT others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20930 | chr18 | 47820896 | |||||
| chr18:47820896
|
T | TACACACA others(3): Show |
2 | a0001c0001t0035a0001c0001t0133 | 2 | HG03041.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20921_*20930dupGT others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20930 | chr18 | 47820896 | |||||
| chr18:47820896
|
T | TACACACA others(5): Show |
5 | a0001c0001t0025a0001c0001t0036a0001c0001t0037others(2): Show | 6 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*20919_*20930dupGT others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20930 | chr18 | 47820896 | |||||
| chr18:47820896
|
T | TACACACA others(7): Show |
4 | a0001c0001t0038a0001c0001t0039a0001c0001t0040others(1): Show | 4 | HG02622.hp2 HG03195.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*20917_*20930dupGT others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20930 | chr18 | 47820896 | |||||
| chr18:47820896
|
T | TACACACA others(11): Show |
1 | a0001c0001t0186 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20913_*20930dupGT others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20930 | chr18 | 47820896 | |||||
| chr18:47820896
|
TAC | T | 10 | a0001c0001t0143a0001c0001t0145a0001c0001t0148others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*20929_*20930delGT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20929 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACAC | T | 25 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(22): Show | 38 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*20927_*20930delGT others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20927 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACAC | T | 4 | a0001c0001t0009a0001c0001t0137a0001c0001t0192others(1): Show | 6 | HG01928.hp2 HG01978.hp2 HG02055.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*20925_*20930delGT others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20925 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0179a0001c0001t0196a0001c0001t0197others(1): Show | 4 | HG01168.hp1 HG02056.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*20923_*20930delGT others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20923 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(3): Show |
T | 4 | a0001c0001t0026a0001c0001t0136a0001c0001t0243others(1): Show | 5 | HG00735.hp1 HG02055.hp2 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*20921_*20930delGT others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20921 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(5): Show |
T | 9 | a0001c0001t0028a0001c0001t0065a0001c0001t0200others(6): Show | 10 | HG00438.hp2 HG01109.hp1 HG01261.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*20919_*20930delGT others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20919 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(7): Show |
T | 43 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(40): Show | 54 | HG00544.hp1 HG00609.hp1 HG01257.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*20917_*20930delGT others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20917 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0018 | 2 | HG00423.hp2 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20915_*20930delGT others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20915 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(11): Show |
T | 6 | a0001c0001t0054a0001c0001t0055a0001c0001t0080others(3): Show | 6 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*20913_*20930delGT others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20913 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(13): Show |
T | 103 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(100): Show | 125 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*20911_*20930delGT others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20911 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(17): Show |
T | 1 | a0001c0001t0211 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20907_*20930delGT others(22): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20907 | chr18 | 47820896 | |||||
| chr18:47820896
|
TACACACA others(21): Show |
T | 2 | a0001c0001t0171a0001c0001t0172 | 2 | HG02647.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20903_*20930delGT others(26): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20903 | chr18 | 47820896 | |||||
| chr18:47820943
|
A | C | 1 | a0001c0001t0167 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20884T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20884 | chr18 | 47820943 | |||||
| chr18:47821003
|
AAG | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*20822_*20823delCT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20822 | chr18 | 47821003 | |||||
| chr18:47821122
|
T | A | 1 | a0001c0001t0237 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20705A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20705 | chr18 | 47821122 | |||||
| chr18:47821185
|
T | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*20642A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20642 | chr18 | 47821185 | |||||
| chr18:47821248
|
T | C | 3 | a0001c0001t0025a0001c0001t0189a0001c0001t0190 | 4 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*20579A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20579 | chr18 | 47821248 | |||||
| chr18:47821341
|
T | G | 2 | a0001c0001t0048a0001c0001t0049 | 2 | NA18944.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20486A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20486 | chr18 | 47821341 | |||||
| chr18:47821360
|
T | C | 1 | a0001c0001t0144 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*20467A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20467 | chr18 | 47821360 | |||||
| chr18:47821418
|
C | T | 1 | a0001c0001t0216 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20409G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20409 | chr18 | 47821418 | |||||
| chr18:47821450
|
C | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*20377G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20377 | chr18 | 47821450 | |||||
| chr18:47821478
|
G | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*20349C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20349 | chr18 | 47821478 | |||||
| chr18:47821555
|
T | C | 1 | a0001c0001t0017 | 2 | HG02165.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20272A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20272 | chr18 | 47821555 | |||||
| chr18:47821568
|
C | T | 3 | a0001c0001t0065a0001c0001t0200a0001c0001t0201 | 3 | HG00438.hp2 HG02602.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20259G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20259 | chr18 | 47821568 | |||||
| chr18:47821617
|
T | C | 1 | a0001c0001t0145 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20210A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20210 | chr18 | 47821617 | |||||
| chr18:47821706
|
C | T | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(38): Show | 53 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*20121G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20121 | chr18 | 47821706 | |||||
| chr18:47821723
|
A | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*20104T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20104 | chr18 | 47821723 | |||||
| chr18:47821790
|
T | G | 1 | a0001c0001t0257 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20037A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 20037 | chr18 | 47821790 | |||||
| chr18:47821893
|
G | A | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19934C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19934 | chr18 | 47821893 | |||||
| chr18:47821998
|
C | T | 3 | a0001c0001t0032a0001c0001t0173a0001c0001t0193 | 3 | HG01884.hp1 HG02451.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19829G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19829 | chr18 | 47821998 | |||||
| chr18:47822005
|
T | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*19822A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19822 | chr18 | 47822005 | |||||
| chr18:47822050
|
A | G | 2 | a0001c0001t0122a0001c0001t0123 | 2 | HG03688.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*19777T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19777 | chr18 | 47822050 | |||||
| chr18:47822560
|
A | G | 178 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(175): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*19267T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19267 | chr18 | 47822560 | |||||
| chr18:47822621
|
A | G | 121 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(118): Show | 144 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*19206T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19206 | chr18 | 47822621 | |||||
| chr18:47822653
|
C | T | 2 | a0001c0001t0069a0001c0001t0157 | 2 | HG00558.hp1 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19174G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19174 | chr18 | 47822653 | |||||
| chr18:47822703
|
G | A | 2 | a0001c0001t0054a0001c0001t0055 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*19124C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19124 | chr18 | 47822703 | |||||
| chr18:47822731
|
A | G | 121 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(118): Show | 144 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*19096T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19096 | chr18 | 47822731 | |||||
| chr18:47822873
|
C | A | 1 | a0001c0001t0257 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18954G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18954 | chr18 | 47822873 | |||||
| chr18:47822873
|
C | G | 177 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(174): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*18954G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18954 | chr18 | 47822873 | |||||
| chr18:47823024
|
C | T | 256 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(253): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*18803G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18803 | chr18 | 47823024 | |||||
| chr18:47823187
|
G | C | 6 | a0001c0001t0015a0001c0001t0020a0001c0001t0091others(3): Show | 8 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*18640C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18640 | chr18 | 47823187 | |||||
| chr18:47823208
|
T | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*18619A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18619 | chr18 | 47823208 | |||||
| chr18:47823388
|
A | G | 44 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(41): Show | 56 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*18439T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18439 | chr18 | 47823388 | |||||
| chr18:47823417
|
G | A | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18410C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18410 | chr18 | 47823417 | |||||
| chr18:47823420
|
C | A | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18407G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18407 | chr18 | 47823420 | |||||
| chr18:47823440
|
T | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*18387A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18387 | chr18 | 47823440 | |||||
| chr18:47823471
|
C | T | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*18356G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18356 | chr18 | 47823471 | |||||
| chr18:47823730
|
A | G | 1 | a0001c0001t0211 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*18097T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18097 | chr18 | 47823730 | |||||
| chr18:47823750
|
G | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*18077C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 18077 | chr18 | 47823750 | |||||
| chr18:47823972
|
A | C | 1 | a0001c0001t0106 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17855T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17855 | chr18 | 47823972 | |||||
| chr18:47824028
|
T | C | 26 | a0001c0001t0024a0001c0001t0082a0001c0001t0133others(23): Show | 27 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*17799A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17799 | chr18 | 47824028 | |||||
| chr18:47824164
|
C | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*17663G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17663 | chr18 | 47824164 | |||||
| chr18:47824178
|
C | G | 153 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(150): Show | 191 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*17649G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17649 | chr18 | 47824178 | |||||
| chr18:47824278
|
C | T | 1 | a0001c0001t0122 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17549G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17549 | chr18 | 47824278 | |||||
| chr18:47824309
|
G | A | 1 | a0001c0001t0153 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17518C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17518 | chr18 | 47824309 | |||||
| chr18:47824581
|
C | T | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17246G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17246 | chr18 | 47824581 | |||||
| chr18:47824668
|
T | C | 3 | a0001c0001t0053a0001c0001t0054a0001c0001t0055 | 3 | HG01257.hp2 HG01258.hp2 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17159A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17159 | chr18 | 47824668 | |||||
| chr18:47824699
|
G | A | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*17128C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17128 | chr18 | 47824699 | |||||
| chr18:47824760
|
G | A | 3 | a0001c0001t0089a0001c0001t0090a0001c0001t0170 | 3 | NA18950.hp1 NA18959.hp2 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17067C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 17067 | chr18 | 47824760 | |||||
| chr18:47824976
|
C | T | 1 | a0001c0001t0205 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16851G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16851 | chr18 | 47824976 | |||||
| chr18:47824980
|
C | G | 1 | a0001c0001t0103 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16847G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16847 | chr18 | 47824980 | |||||
| chr18:47825071
|
G | A | 1 | a0001c0001t0171 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16756C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16756 | chr18 | 47825071 | |||||
| chr18:47825163
|
G | A | 3 | a0001c0001t0200a0001c0001t0201a0001c0001t0244 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16664C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16664 | chr18 | 47825163 | |||||
| chr18:47825272
|
G | C | 176 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(173): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*16555C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16555 | chr18 | 47825272 | |||||
| chr18:47825283
|
A | G | 4 | a0001c0001t0202a0001c0001t0203a0001c0001t0204others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*16544T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16544 | chr18 | 47825283 | |||||
| chr18:47825424
|
T | C | 1 | a0001c0001t0103 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16403A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16403 | chr18 | 47825424 | |||||
| chr18:47825426
|
G | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*16401C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16401 | chr18 | 47825426 | |||||
| chr18:47825569
|
T | C | 1 | a0001c0001t0065 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16258A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16258 | chr18 | 47825569 | |||||
| chr18:47825746
|
A | C | 1 | a0001c0001t0174 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16081T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16081 | chr18 | 47825746 | |||||
| chr18:47825825
|
C | A | 1 | a0001c0001t0050 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16002G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 16002 | chr18 | 47825825 | |||||
| chr18:47825957
|
T | G | 4 | a0001c0001t0022a0001c0001t0023a0001c0001t0154others(1): Show | 6 | HG00609.hp2 NA18952.hp1 NA18983.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*15870A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15870 | chr18 | 47825957 | |||||
| chr18:47826149
|
A | G | 256 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(253): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*15678T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15678 | chr18 | 47826149 | |||||
| chr18:47826382
|
T | C | 6 | a0001c0001t0006a0001c0001t0106a0001c0001t0107others(3): Show | 8 | HG01243.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*15445A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15445 | chr18 | 47826382 | |||||
| chr18:47826402
|
T | G | 1 | a0001c0001t0214 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15425A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15425 | chr18 | 47826402 | |||||
| chr18:47826564
|
C | T | 1 | a0001c0001t0243 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15263G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15263 | chr18 | 47826564 | |||||
| chr18:47826707
|
C | T | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15120G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15120 | chr18 | 47826707 | |||||
| chr18:47826791
|
A | G | 1 | a0001c0001t0175 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15036T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15036 | chr18 | 47826791 | |||||
| chr18:47826793
|
T | C | 1 | a0001c0001t0235 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15034A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 15034 | chr18 | 47826793 | |||||
| chr18:47827022
|
G | A | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14805C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14805 | chr18 | 47827022 | |||||
| chr18:47827024
|
G | A | 3 | a0001c0001t0200a0001c0001t0201a0001c0001t0244 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14803C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14803 | chr18 | 47827024 | |||||
| chr18:47827043
|
G | A | 1 | a0001c0001t0083 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14784C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14784 | chr18 | 47827043 | |||||
| chr18:47827126
|
A | G | 1 | a0001c0001t0095 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14701T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14701 | chr18 | 47827126 | |||||
| chr18:47827156
|
G | A | 1 | a0001c0001t0118 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14671C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14671 | chr18 | 47827156 | |||||
| chr18:47827343
|
G | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*14484C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14484 | chr18 | 47827343 | |||||
| chr18:47827365
|
C | T | 1 | a0001c0001t0094 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14462G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14462 | chr18 | 47827365 | |||||
| chr18:47827435
|
G | A | 1 | a0001c0001t0209 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14392C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14392 | chr18 | 47827435 | |||||
| chr18:47827513
|
G | C | 1 | a0001c0001t0058 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14314C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14314 | chr18 | 47827513 | |||||
| chr18:47827606
|
G | C | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14221C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14221 | chr18 | 47827606 | |||||
| chr18:47827678
|
C | T | 2 | a0001c0001t0200a0001c0001t0201 | 2 | HG00438.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14149G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14149 | chr18 | 47827678 | |||||
| chr18:47827692
|
G | A | 1 | a0001c0001t0040 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14135C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14135 | chr18 | 47827692 | |||||
| chr18:47827769
|
C | T | 10 | a0001c0001t0026a0001c0001t0050a0001c0001t0205others(7): Show | 11 | HG02055.hp2 HG02717.hp1 HG02896.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*14058G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14058 | chr18 | 47827769 | |||||
| chr18:47827787
|
T | C | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14040A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14040 | chr18 | 47827787 | |||||
| chr18:47827814
|
C | T | 1 | a0001c0001t0005 | 3 | NA18974.hp1 NA18980.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14013G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14013 | chr18 | 47827814 | |||||
| chr18:47827825
|
C | T | 1 | a0001c0001t0065 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14002G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 14002 | chr18 | 47827825 | |||||
| chr18:47827849
|
G | A | 1 | a0001c0001t0234 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13978C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13978 | chr18 | 47827849 | |||||
| chr18:47827896
|
C | T | 1 | a0001c0001t0134 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13931G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13931 | chr18 | 47827896 | |||||
| chr18:47828005
|
T | TCCCGGCC others(33): Show |
8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13821_*13822insCA others(38): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13821 | chr18 | 47828005 | |||||
| chr18:47828115
|
G | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13712C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13712 | chr18 | 47828115 | |||||
| chr18:47828122
|
C | T | 110 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(107): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*13705G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13705 | chr18 | 47828122 | |||||
| chr18:47828197
|
C | T | 1 | a0001c0001t0181 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13630G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13630 | chr18 | 47828197 | |||||
| chr18:47828209
|
G | A | 1 | a0001c0001t0243 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13618C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13618 | chr18 | 47828209 | |||||
| chr18:47828214
|
G | A | 5 | a0001c0001t0029a0001c0001t0030a0001c0001t0225others(2): Show | 7 | NA18952.hp2 NA18962.hp2 NA18968.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*13613C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13613 | chr18 | 47828214 | |||||
| chr18:47828245
|
T | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13582A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13582 | chr18 | 47828245 | |||||
| chr18:47828264
|
G | A | 1 | a0001c0001t0234 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13563C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13563 | chr18 | 47828264 | |||||
| chr18:47828271
|
G | T | 6 | a0001c0001t0015a0001c0001t0020a0001c0001t0091others(3): Show | 8 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13556C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13556 | chr18 | 47828271 | |||||
| chr18:47828289
|
G | A | 3 | a0001c0001t0200a0001c0001t0201a0001c0001t0244 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13538C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13538 | chr18 | 47828289 | |||||
| chr18:47828327
|
G | A | 2 | a0001c0001t0200a0001c0001t0201 | 2 | HG00438.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13500C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13500 | chr18 | 47828327 | |||||
| chr18:47828353
|
TG | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13473delC | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13473 | chr18 | 47828353 | |||||
| chr18:47828415
|
C | T | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13412G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13412 | chr18 | 47828415 | |||||
| chr18:47828418
|
C | A | 173 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(170): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*13409G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13409 | chr18 | 47828418 | |||||
| chr18:47828420
|
T | C | 174 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(171): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*13407A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13407 | chr18 | 47828420 | |||||
| chr18:47828421
|
G | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13406C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13406 | chr18 | 47828421 | |||||
| chr18:47828453
|
G | A | 1 | a0001c0001t0126 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13374C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13374 | chr18 | 47828453 | |||||
| chr18:47828471
|
G | A | 1 | a0001c0001t0235 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13356C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13356 | chr18 | 47828471 | |||||
| chr18:47828474
|
G | A | 9 | a0001c0001t0026a0001c0001t0205a0001c0001t0206others(6): Show | 10 | HG02055.hp2 HG02717.hp1 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*13353C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13353 | chr18 | 47828474 | |||||
| chr18:47828483
|
G | A | 1 | a0001c0001t0018 | 2 | HG00423.hp2 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13344C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13344 | chr18 | 47828483 | |||||
| chr18:47828558
|
CAT | C | 2 | a0001c0001t0018a0001c0001t0111 | 3 | HG00423.hp2 NA18972.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13267_*13268delAT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13267 | chr18 | 47828558 | |||||
| chr18:47828637
|
A | G | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13190T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13190 | chr18 | 47828637 | |||||
| chr18:47828826
|
C | G | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13001G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 13001 | chr18 | 47828826 | |||||
| chr18:47828856
|
T | C | 1 | a0001c0001t0084 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12971A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12971 | chr18 | 47828856 | |||||
| chr18:47828857
|
G | C | 1 | a0001c0001t0084 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12970C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12970 | chr18 | 47828857 | |||||
| chr18:47828935
|
T | TA | 38 | a0001c0001t0026a0001c0001t0035a0001c0001t0036others(35): Show | 39 | HG00558.hp1 HG00741.hp1 HG01109.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*12891dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12891 | chr18 | 47828935 | |||||
| chr18:47828935
|
T | TAA | 17 | a0001c0001t0024a0001c0001t0032a0001c0001t0087others(14): Show | 18 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*12890_*12891dupTT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12891 | chr18 | 47828935 | |||||
| chr18:47828935
|
T | TAAA | 80 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(77): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*12889_*12891dupTT others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12891 | chr18 | 47828935 | |||||
| chr18:47828935
|
T | TAAAA | 21 | a0001c0001t0006a0001c0001t0018a0001c0001t0033others(18): Show | 24 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*12888_*12891dupTT others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12891 | chr18 | 47828935 | |||||
| chr18:47828935
|
TA | T | 36 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(33): Show | 47 | HG00544.hp1 HG00609.hp1 HG01257.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*12891delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12891 | chr18 | 47828935 | |||||
| chr18:47828935
|
TAAAAA | T | 7 | a0001c0002t0248a0001c0002t0249a0001c0002t0250others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12887_*12891delTT others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12887 | chr18 | 47828935 | |||||
| chr18:47828962
|
A | T | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12865T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12865 | chr18 | 47828962 | |||||
| chr18:47829156
|
T | G | 2 | a0001c0001t0169a0001c0001t0170 | 2 | NA18959.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12671A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12671 | chr18 | 47829156 | |||||
| chr18:47829202
|
A | C | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12625T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12625 | chr18 | 47829202 | |||||
| chr18:47829288
|
C | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12539G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12539 | chr18 | 47829288 | |||||
| chr18:47829333
|
A | C | 3 | a0001c0001t0062a0001c0001t0063a0001c0001t0121 | 3 | NA18950.hp2 NA18979.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12494T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12494 | chr18 | 47829333 | |||||
| chr18:47829362
|
T | C | 5 | a0001c0001t0019a0001c0001t0112a0001c0001t0113others(2): Show | 6 | HG02040.hp2 NA18942.hp2 NA18954.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*12465A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12465 | chr18 | 47829362 | |||||
| chr18:47829378
|
T | C | 1 | a0001c0001t0031 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12449A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12449 | chr18 | 47829378 | |||||
| chr18:47829394
|
CA | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12432delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12432 | chr18 | 47829394 | |||||
| chr18:47829499
|
G | C | 163 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(160): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*12328C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12328 | chr18 | 47829499 | |||||
| chr18:47829631
|
T | TA | 249 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(246): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*12195_*12196insT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12195 | chr18 | 47829631 | |||||
| chr18:47829786
|
A | G | 2 | a0001c0002t0253a0001c0002t0254 | 2 | HG01891.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12041T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 12041 | chr18 | 47829786 | |||||
| chr18:47829955
|
C | G | 174 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(171): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*11872G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11872 | chr18 | 47829955 | |||||
| chr18:47830297
|
C | T | 1 | a0001c0001t0164 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11530G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11530 | chr18 | 47830297 | |||||
| chr18:47830372
|
T | G | 166 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(163): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*11455A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11455 | chr18 | 47830372 | |||||
| chr18:47830493
|
C | T | 1 | a0001c0001t0243 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11334G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11334 | chr18 | 47830493 | |||||
| chr18:47830576
|
C | CA | 215 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(212): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*11250dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830576
|
C | CAA | 11 | a0001c0001t0008a0001c0001t0059a0001c0001t0127others(8): Show | 13 | HG00423.hp1 HG00544.hp2 HG01109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*11249_*11250dupTT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830576
|
C | CAAAAAAA others(11): Show |
2 | a0001c0002t0247a0001c0002t0252 | 2 | HG02145.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11233_*11250dupTT others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830576
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0253 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11250_*11251insTT others(17): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830576
|
C | CAAAAAAA others(13): Show |
2 | a0001c0002t0248a0001c0002t0249 | 2 | HG02572.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11250_*11251insTT others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830576
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0254 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11250_*11251insTT others(21): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830576
|
C | CAAAAAAA others(19): Show |
1 | a0001c0002t0250 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11250_*11251insTT others(24): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830576
|
C | CAAAAAAA others(24): Show |
1 | a0001c0002t0251 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11250_*11251insTT others(29): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11250 | chr18 | 47830576 | |||||
| chr18:47830686
|
T | C | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11141A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 11141 | chr18 | 47830686 | |||||
| chr18:47830884
|
T | G | 15 | a0001c0001t0025a0001c0001t0035a0001c0001t0036others(12): Show | 16 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*10943A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10943 | chr18 | 47830884 | |||||
| chr18:47830959
|
T | TAC | 54 | a0001c0001t0006a0001c0001t0011a0001c0001t0015others(51): Show | 63 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*10866_*10867dupGT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10867 | chr18 | 47830959 | |||||
| chr18:47830959
|
TAC | T | 9 | a0001c0001t0243a0001c0002t0247a0001c0002t0248others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*10866_*10867delGT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10866 | chr18 | 47830959 | |||||
| chr18:47831200
|
G | A | 1 | a0001c0001t0232 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10627C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10627 | chr18 | 47831200 | |||||
| chr18:47831234
|
T | C | 3 | a0001c0001t0167a0001c0001t0168a0001c0001t0187 | 3 | HG02280.hp1 HG02630.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10593A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10593 | chr18 | 47831234 | |||||
| chr18:47831249
|
G | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10578C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10578 | chr18 | 47831249 | |||||
| chr18:47831659
|
ATTG | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10165_*10167delCA others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10165 | chr18 | 47831659 | |||||
| chr18:47831738
|
T | C | 163 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(160): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*10089A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10089 | chr18 | 47831738 | |||||
| chr18:47831769
|
TGAC | T | 40 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(37): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*10055_*10057delGT others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 10055 | chr18 | 47831769 | |||||
| chr18:47831856
|
A | C | 111 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(108): Show | 134 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*9971T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 9971 | chr18 | 47831856 | |||||
| chr18:47831919
|
C | CTGTG | 174 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(171): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*9907_*9908insCACA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 9907 | chr18 | 47831919 | |||||
| chr18:47831952
|
G | C | 2 | a0001c0001t0169a0001c0001t0170 | 2 | NA18959.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9875C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 9875 | chr18 | 47831952 | |||||
| chr18:47832038
|
T | C | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9789A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 9789 | chr18 | 47832038 | |||||
| chr18:47832295
|
A | G | 3 | a0001c0001t0012a0001c0001t0060a0001c0001t0116 | 4 | HG00438.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9532T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 9532 | chr18 | 47832295 | |||||
| chr18:47832296
|
T | C | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9531A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 9531 | chr18 | 47832296 | |||||
| chr18:47832853
|
G | A | 3 | a0001c0001t0053a0001c0001t0054a0001c0001t0055 | 3 | HG01257.hp2 HG01258.hp2 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8974C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8974 | chr18 | 47832853 | |||||
| chr18:47832954
|
T | TA | 4 | a0001c0001t0010a0001c0001t0233a0001c0001t0234others(1): Show | 6 | NA18960.hp1 NA18986.hp1 NA19002.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8872dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8872 | chr18 | 47832954 | |||||
| chr18:47832996
|
G | T | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8831C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8831 | chr18 | 47832996 | |||||
| chr18:47833276
|
T | C | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8551A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8551 | chr18 | 47833276 | |||||
| chr18:47833293
|
T | A | 107 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(104): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*8534A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8534 | chr18 | 47833293 | |||||
| chr18:47833432
|
C | T | 2 | a0001c0001t0200a0001c0001t0201 | 2 | HG00438.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8395G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8395 | chr18 | 47833432 | |||||
| chr18:47833579
|
C | A | 1 | a0001c0001t0190 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8248G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8248 | chr18 | 47833579 | |||||
| chr18:47833593
|
C | T | 4 | a0001c0001t0056a0001c0001t0057a0001c0001t0058others(1): Show | 4 | NA18944.hp2 NA18973.hp2 NA19062.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8234G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8234 | chr18 | 47833593 | |||||
| chr18:47833641
|
G | A | 3 | a0001c0002t0252a0001c0002t0253a0001c0002t0254 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8186C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8186 | chr18 | 47833641 | |||||
| chr18:47833675
|
T | A | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8152A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8152 | chr18 | 47833675 | |||||
| chr18:47833713
|
C | G | 3 | a0001c0001t0053a0001c0001t0054a0001c0001t0055 | 3 | HG01257.hp2 HG01258.hp2 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8114G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8114 | chr18 | 47833713 | |||||
| chr18:47833740
|
C | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8087G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8087 | chr18 | 47833740 | |||||
| chr18:47833802
|
C | T | 1 | a0001c0001t0191 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8025G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8025 | chr18 | 47833802 | |||||
| chr18:47833809
|
G | A | 1 | a0001c0001t0116 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8018C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8018 | chr18 | 47833809 | |||||
| chr18:47833823
|
G | T | 9 | a0001c0001t0026a0001c0001t0205a0001c0001t0206others(6): Show | 10 | HG02055.hp2 HG02717.hp1 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*8004C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 8004 | chr18 | 47833823 | |||||
| chr18:47833895
|
A | C | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7932T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7932 | chr18 | 47833895 | |||||
| chr18:47833915
|
G | A | 1 | a0001c0001t0043 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7912C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7912 | chr18 | 47833915 | |||||
| chr18:47834126
|
T | G | 1 | a0001c0001t0117 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7701A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7701 | chr18 | 47834126 | |||||
| chr18:47834152
|
C | T | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7675G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7675 | chr18 | 47834152 | |||||
| chr18:47834397
|
C | G | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7430G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7430 | chr18 | 47834397 | |||||
| chr18:47834455
|
A | G | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7372T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7372 | chr18 | 47834455 | |||||
| chr18:47834620
|
A | G | 163 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(160): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*7207T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7207 | chr18 | 47834620 | |||||
| chr18:47834645
|
C | CTTAT | 253 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(250): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*7181_*7182insATAA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7181 | chr18 | 47834645 | |||||
| chr18:47834746
|
A | G | 1 | a0001c0001t0237 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7081T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7081 | chr18 | 47834746 | |||||
| chr18:47834804
|
T | C | 3 | a0001c0001t0032a0001c0001t0173a0001c0001t0193 | 3 | HG01884.hp1 HG02451.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7023A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7023 | chr18 | 47834804 | |||||
| chr18:47834812
|
G | C | 1 | a0001c0001t0119 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7015C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7015 | chr18 | 47834812 | |||||
| chr18:47834820
|
T | C | 1 | a0001c0001t0120 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7007A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 7007 | chr18 | 47834820 | |||||
| chr18:47835098
|
C | T | 1 | a0001c0001t0052 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6729G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 6729 | chr18 | 47835098 | |||||
| chr18:47835272
|
A | T | 1 | a0001c0001t0202 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6555T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 6555 | chr18 | 47835272 | |||||
| chr18:47835339
|
A | C | 1 | a0001c0001t0176 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6488T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 6488 | chr18 | 47835339 | |||||
| chr18:47835452
|
G | C | 1 | a0001c0001t0174 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6375C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 6375 | chr18 | 47835452 | |||||
| chr18:47835512
|
G | A | 1 | a0001c0001t0175 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6315C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 6315 | chr18 | 47835512 | |||||
| chr18:47835742
|
C | T | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6085G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 6085 | chr18 | 47835742 | |||||
| chr18:47835823
|
T | C | 164 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(161): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*6004A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 6004 | chr18 | 47835823 | |||||
| chr18:47836094
|
T | C | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5733A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 5733 | chr18 | 47836094 | |||||
| chr18:47836350
|
C | T | 57 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(54): Show | 70 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*5477G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 5477 | chr18 | 47836350 | |||||
| chr18:47836425
|
T | C | 40 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(37): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*5402A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 5402 | chr18 | 47836425 | |||||
| chr18:47836427
|
G | T | 1 | a0001c0001t0192 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5400C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 5400 | chr18 | 47836427 | |||||
| chr18:47836429
|
A | G | 1 | a0001c0001t0051 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5398T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 5398 | chr18 | 47836429 | |||||
| chr18:47836746
|
T | TA | 4 | a0001c0001t0202a0001c0001t0203a0001c0001t0204others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5080dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 5080 | chr18 | 47836746 | |||||
| chr18:47836843
|
A | T | 106 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(103): Show | 129 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*4984T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4984 | chr18 | 47836843 | |||||
| chr18:47836918
|
A | G | 54 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(51): Show | 67 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*4909T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4909 | chr18 | 47836918 | |||||
| chr18:47837076
|
C | G | 2 | a0001c0001t0211a0001c0001t0244 | 2 | HG02055.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4751G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4751 | chr18 | 47837076 | |||||
| chr18:47837118
|
C | A | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4709G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4709 | chr18 | 47837118 | |||||
| chr18:47837229
|
A | G | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4598T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4598 | chr18 | 47837229 | |||||
| chr18:47837237
|
A | T | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4590T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4590 | chr18 | 47837237 | |||||
| chr18:47837282
|
G | A | 40 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(37): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*4545C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4545 | chr18 | 47837282 | |||||
| chr18:47837291
|
G | A | 2 | a0001c0001t0214a0001c0001t0236 | 2 | NA18974.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4536C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4536 | chr18 | 47837291 | |||||
| chr18:47837315
|
C | A | 1 | a0001c0001t0188 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4512G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4512 | chr18 | 47837315 | |||||
| chr18:47837358
|
C | T | 1 | a0001c0001t0133 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4469G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4469 | chr18 | 47837358 | |||||
| chr18:47837379
|
G | A | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4448C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4448 | chr18 | 47837379 | |||||
| chr18:47837435
|
G | A | 2 | a0001c0001t0020a0001c0001t0129 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4392C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4392 | chr18 | 47837435 | |||||
| chr18:47837549
|
G | A | 1 | a0001c0001t0242 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4278C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4278 | chr18 | 47837549 | |||||
| chr18:47837561
|
C | CA | 147 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(144): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*4265dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4265 | chr18 | 47837561 | |||||
| chr18:47837561
|
C | CAA | 23 | a0001c0001t0004a0001c0001t0025a0001c0001t0031others(20): Show | 27 | HG00423.hp1 HG00735.hp2 HG01257.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4264_*4265dupTT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4265 | chr18 | 47837561 | |||||
| chr18:47837561
|
CA | C | 15 | a0001c0001t0200a0001c0001t0201a0001c0001t0202others(12): Show | 15 | HG00438.hp2 HG01258.hp1 HG01496.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4265delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4265 | chr18 | 47837561 | |||||
| chr18:47837571
|
A | C | 2 | a0001c0001t0200a0001c0001t0201 | 2 | HG00438.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4256T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4256 | chr18 | 47837571 | |||||
| chr18:47837573
|
A | C | 3 | a0001c0001t0200a0001c0001t0201a0001c0001t0244 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4254T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4254 | chr18 | 47837573 | |||||
| chr18:47837580
|
C | A | 41 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(38): Show | 53 | HG00544.hp1 HG00609.hp1 HG00735.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4247G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 4247 | chr18 | 47837580 | |||||
| chr18:47837892
|
T | A | 1 | a0001c0001t0243 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3935A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 3935 | chr18 | 47837892 | |||||
| chr18:47837905
|
T | C | 3 | a0001c0001t0009a0001c0001t0191a0001c0001t0192 | 5 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3922A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 3922 | chr18 | 47837905 | |||||
| chr18:47838114
|
C | A | 1 | a0001c0001t0255 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3713G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 3713 | chr18 | 47838114 | |||||
| chr18:47838152
|
T | G | 2 | a0001c0001t0131a0001c0001t0132 | 2 | HG02258.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3675A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 3675 | chr18 | 47838152 | |||||
| chr18:47838534
|
A | G | 1 | a0001c0001t0026 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3293T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 3293 | chr18 | 47838534 | |||||
| chr18:47838909
|
G | T | 2 | a0001c0001t0011a0001c0001t0047 | 3 | HG02071.hp1 HG02129.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2918C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2918 | chr18 | 47838909 | |||||
| chr18:47839020
|
G | A | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2807C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2807 | chr18 | 47839020 | |||||
| chr18:47839025
|
CA | C | 174 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(171): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*2801delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2801 | chr18 | 47839025 | |||||
| chr18:47839047
|
T | C | 1 | a0001c0001t0244 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2780A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2780 | chr18 | 47839047 | |||||
| chr18:47839263
|
A | G | 1 | a0001c0001t0046 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2564T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2564 | chr18 | 47839263 | |||||
| chr18:47839317
|
G | C | 2 | a0001c0001t0200a0001c0001t0201 | 2 | HG00438.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2510C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2510 | chr18 | 47839317 | |||||
| chr18:47839637
|
G | C | 2 | a0001c0001t0032a0001c0001t0193 | 2 | HG02451.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2190C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2190 | chr18 | 47839637 | |||||
| chr18:47839642
|
T | C | 1 | a0001c0001t0194 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2185A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2185 | chr18 | 47839642 | |||||
| chr18:47839769
|
C | T | 2 | a0001c0001t0044a0001c0001t0045 | 2 | HG00323.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2058G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 2058 | chr18 | 47839769 | |||||
| chr18:47839839
|
C | T | 2 | a0001c0001t0200a0001c0001t0201 | 2 | HG00438.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1988G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 1988 | chr18 | 47839839 | |||||
| chr18:47840051
|
T | G | 1 | a0001c0001t0195 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1776A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 1776 | chr18 | 47840051 | |||||
| chr18:47840316
|
G | A | 2 | a0001c0001t0196a0001c0001t0197 | 2 | HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1511C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 1511 | chr18 | 47840316 | |||||
| chr18:47840443
|
A | T | 2 | a0001c0001t0042a0001c0001t0043 | 2 | HG02015.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1384T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 1384 | chr18 | 47840443 | |||||
| chr18:47840481
|
G | C | 1 | a0001c0001t0198 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 1346 | chr18 | 47840481 | |||||
| chr18:47840733
|
C | A | 1 | a0001c0001t0245 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1094G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 1094 | chr18 | 47840733 | |||||
| chr18:47840954
|
A | G | 7 | a0001c0001t0035a0001c0001t0036a0001c0001t0037others(4): Show | 7 | HG01109.hp2 HG02622.hp1 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*873T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 873 | chr18 | 47840954 | |||||
| chr18:47841050
|
T | C | 1 | a0001c0001t0246 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*777A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 777 | chr18 | 47841050 | |||||
| chr18:47841097
|
G | A | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*730C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 730 | chr18 | 47841097 | |||||
| chr18:47841099
|
T | A | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*728A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 728 | chr18 | 47841099 | |||||
| chr18:47841100
|
TGGAAAGG others(451): Show |
T | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269_*726del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 269 | chr18 | 47841100 | |||||
| chr18:47841113
|
A | G | 255 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(252): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*714T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 714 | chr18 | 47841113 | |||||
| chr18:47841121
|
T | G | 3 | a0001c0002t0252a0001c0002t0253a0001c0002t0254 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*706A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 706 | chr18 | 47841121 | |||||
| chr18:47841148
|
AAAAAAAA others(2): Show |
A | 56 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(53): Show | 69 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*670_*678delGTTTTT others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 670 | chr18 | 47841148 | |||||
| chr18:47841154
|
A | AAAAC | 8 | a0001c0002t0247a0001c0002t0248a0001c0002t0249others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*672_*673insGTTT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 672 | chr18 | 47841154 | |||||
| chr18:47841157
|
C | A | 9 | a0001c0001t0255a0001c0002t0247a0001c0002t0248others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*670G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 670 | chr18 | 47841157 | |||||
| chr18:47841350
|
A | T | 1 | a0001c0001t0034 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 477 | chr18 | 47841350 | |||||
| chr18:47841561
|
C | T | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 266 | chr18 | 47841561 | |||||
| chr18:47841563
|
C | A | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*264G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 264 | chr18 | 47841563 | |||||
| chr18:47841567
|
T | A | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*260A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 260 | chr18 | 47841567 | |||||
| chr18:47841571
|
T | A | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*256A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 256 | chr18 | 47841571 | |||||
| chr18:47841573
|
C | A | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 254 | chr18 | 47841573 | |||||
| chr18:47841577
|
A | T | 1 | a0001c0001t0033 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*250T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 250 | chr18 | 47841577 | |||||
| chr18:47841808
|
G | A | 1 | a0001c0001t0256 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*19C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 11/11 | 19 | chr18 | 47841808 | |||||
| chr18:47930411
|
C | G | 1 | a0001c0001t0032 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-104G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/11 | 33655 | chr18 | 47930411 | |||||
| chr18:47930462
|
G | A | 1 | a0001c0001t0257 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-155C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/11 | 33706 | chr18 | 47930462 | |||||
| chr18:47930575
|
GAGGGGAG others(18): Show |
G | 1 | a0001c0001t0031 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-293_-269delTCCCTC others(19): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/11 | 33820 | chr18 | 47930575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:47842086
|
C | T | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1281-136G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842086 | ||||||
| chr18:47842178
|
T | A | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1281-228A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842178 | ||||||
| chr18:47842216
|
G | A | 52 | a0001c0001t0006g0219a0001c0001t0006g0224a0001c0001t0006g0237others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1281-266C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842216 | ||||||
| chr18:47842268
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-318C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842268 | ||||||
| chr18:47842369
|
G | C | 1 | a0001c0001t0217g0131 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1281-419C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842369 | ||||||
| chr18:47842408
|
C | T | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1281-458G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842408 | ||||||
| chr18:47842433
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-483C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842433 | ||||||
| chr18:47842544
|
G | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.1281-594C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842544 | ||||||
| chr18:47842590
|
T | C | 5 | a0001c0001t0148g0109a0001c0001t0167g0012a0001c0001t0168g0107others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281-640A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842590 | ||||||
| chr18:47842744
|
A | C | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1281-794T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842744 | ||||||
| chr18:47842869
|
C | A | 2 | a0001c0001t0122g0251a0001c0001t0123g0252 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1281-919G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842869 | ||||||
| chr18:47842884
|
C | T | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1281-934G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842884 | ||||||
| chr18:47842906
|
T | C | 8 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(5): Show | 8 | HG01109.hp2 HG02622.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-956A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842906 | ||||||
| chr18:47842945
|
T | C | 9 | a0001c0001t0024g0069a0001c0001t0024g0077a0001c0001t0152g0078others(6): Show | 9 | HG00099.hp1 HG00323.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281-995A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47842945 | ||||||
| chr18:47843171
|
A | G | 3 | a0001c0001t0001g0266a0001c0001t0034g0258a0001c0001t0071g0273 | 3 | HG01978.hp1 HG02273.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1281-1221T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47843171 | ||||||
| chr18:47843186
|
C | G | 1 | a0001c0001t0008g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1281-1236G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47843186 | ||||||
| chr18:47843196
|
A | G | 4 | a0001c0001t0008g0061a0001c0001t0008g0062a0001c0001t0008g0063others(1): Show | 4 | HG00544.hp2 HG02523.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-1246T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47843196 | ||||||
| chr18:47843198
|
C | A | 4 | a0001c0001t0008g0061a0001c0001t0008g0062a0001c0001t0008g0063others(1): Show | 4 | HG00544.hp2 HG02523.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-1248G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47843198 | ||||||
| chr18:47843486
|
A | G | 130 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1281-1536T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47843486 | ||||||
| chr18:47843794
|
T | C | 3 | a0001c0002t0252g0017a0001c0002t0253g0015a0001c0002t0254g0016 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1280+1546A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47843794 | ||||||
| chr18:47843964
|
AC | A | 77 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(74): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1280+1375delG | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47843964 | ||||||
| chr18:47844095
|
G | T | 65 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(62): Show | 65 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1280+1245C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47844095 | ||||||
| chr18:47844307
|
T | C | 1 | a0001c0001t0103g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1280+1033A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47844307 | ||||||
| chr18:47844379
|
A | T | 1 | a0001c0001t0193g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1280+961T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47844379 | ||||||
| chr18:47844707
|
C | A | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1280+633G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47844707 | ||||||
| chr18:47844715
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0061g0268 | 2 | HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1280+625C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47844715 | ||||||
| chr18:47844821
|
G | A | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1280+519C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47844821 | ||||||
| chr18:47845039
|
T | C | 1 | a0001c0001t0082g0296 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1280+301A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47845039 | ||||||
| chr18:47845074
|
C | T | 8 | a0001c0001t0016g0112a0001c0001t0017g0208a0001c0001t0017g0265others(5): Show | 8 | HG00423.hp2 HG02165.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.1280+266G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47845074 | ||||||
| chr18:47845138
|
C | T | 133 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(130): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1280+202G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47845138 | ||||||
| chr18:47845315
|
T | C | 9 | a0001c0001t0050g0213a0001c0001t0205g0120a0001c0001t0206g0117others(6): Show | 9 | HG02055.hp2 HG02717.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280+25A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47845315 | ||||||
| chr18:47845324
|
A | G | 3 | a0001c0001t0014g0115a0001c0001t0077g0253a0001c0001t0086g0116 | 3 | HG00642.hp2 HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1280+16T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 10/10 | chr18 | 47845324 | ||||||
| chr18:47845818
|
T | C | 1 | a0001c0001t0095g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.998-18A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47845818 | ||||||
| chr18:47845858
|
T | C | 1 | a0001c0001t0232g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.998-58A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47845858 | ||||||
| chr18:47846105
|
T | C | 2 | a0001c0001t0018g0204a0001c0001t0018g0207 | 2 | HG00423.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.998-305A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47846105 | ||||||
| chr18:47846166
|
G | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.998-366C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47846166 | ||||||
| chr18:47846565
|
G | A | 8 | a0001c0001t0006g0219a0001c0001t0006g0224a0001c0001t0006g0237others(5): Show | 8 | HG01243.hp1 HG02922.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.998-765C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47846565 | ||||||
| chr18:47846635
|
T | C | 9 | a0001c0001t0003g0140a0001c0001t0027g0132a0001c0001t0027g0148others(6): Show | 9 | HG00609.hp1 NA18942.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.998-835A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47846635 | ||||||
| chr18:47846694
|
G | T | 3 | a0001c0001t0032g0003a0001c0001t0173g0033a0001c0001t0193g0032 | 3 | HG01884.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.998-894C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47846694 | ||||||
| chr18:47847142
|
A | C | 4 | a0001c0001t0149g0042a0001c0001t0158g0064a0001c0001t0159g0065others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+1333T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847142 | ||||||
| chr18:47847208
|
C | T | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.997+1267G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847208 | ||||||
| chr18:47847356
|
G | A | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.997+1119C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847356 | ||||||
| chr18:47847431
|
A | C | 198 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.997+1044T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847431 | ||||||
| chr18:47847630
|
CA | C | 127 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.997+844delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847630 | ||||||
| chr18:47847700
|
C | CA | 14 | a0001c0001t0008g0061a0001c0001t0008g0062a0001c0001t0008g0063others(11): Show | 14 | HG00438.hp2 HG00544.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.997+774dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847700 | ||||||
| chr18:47847700
|
C | CAA | 9 | a0001c0001t0004g0130a0001c0001t0205g0120a0001c0001t0206g0117others(6): Show | 9 | HG02717.hp1 HG02896.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.997+773_997+774dup others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847700 | ||||||
| chr18:47847700
|
C | CAAA | 48 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(45): Show | 48 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.997+772_997+774dup others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847700 | ||||||
| chr18:47847700
|
CAAAAAA | C | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.997+769_997+774del others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847700 | ||||||
| chr18:47847700
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0015g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.997+765_997+774del others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847700 | ||||||
| chr18:47847700
|
CAAAAAAA others(4): Show |
C | 131 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.997+764_997+774del others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847700 | ||||||
| chr18:47847700
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0016g0112 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.997+763_997+774del others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847700 | ||||||
| chr18:47847764
|
T | C | 5 | a0001c0001t0009g0081a0001c0001t0009g0083a0001c0001t0009g0084others(2): Show | 5 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.997+711A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847764 | ||||||
| chr18:47847904
|
T | C | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.997+571A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47847904 | ||||||
| chr18:47848123
|
A | AACAAG | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.997+351_997+352ins others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47848123 | ||||||
| chr18:47848125
|
C | G | 1 | a0001c0001t0125g0283 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.997+350G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47848125 | ||||||
| chr18:47848387
|
A | C | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.997+88T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47848387 | ||||||
| chr18:47848457
|
A | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.997+18T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 8/10 | chr18 | 47848457 | ||||||
| chr18:47848752
|
T | C | 1 | a0001c0001t0043g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.785-65A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47848752 | ||||||
| chr18:47848774
|
A | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.785-87T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47848774 | ||||||
| chr18:47848829
|
G | C | 1 | a0001c0001t0173g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.785-142C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47848829 | ||||||
| chr18:47848879
|
C | A | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.785-192G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47848879 | ||||||
| chr18:47848964
|
T | C | 2 | a0001c0001t0183g0023a0001c0001t0185g0025 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.785-277A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47848964 | ||||||
| chr18:47849273
|
A | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.785-586T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849273 | ||||||
| chr18:47849285
|
T | C | 1 | a0001c0001t0230g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.785-598A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849285 | ||||||
| chr18:47849346
|
A | G | 1 | a0001c0001t0177g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.785-659T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849346 | ||||||
| chr18:47849368
|
G | A | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.785-681C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849368 | ||||||
| chr18:47849414
|
G | A | 185 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.785-727C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849414 | ||||||
| chr18:47849436
|
GAAATAGG others(3): Show |
G | 1 | a0001c0001t0046g0196 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.785-759_785-750del others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849436 | ||||||
| chr18:47849483
|
GTATGTA | G | 12 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(9): Show | 12 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.785-802_785-797del others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849483 | ||||||
| chr18:47849487
|
GTA | G | 95 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(92): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.785-802_785-801del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849487 | ||||||
| chr18:47849487
|
GTATA | G | 10 | a0001c0001t0019g0183a0001c0001t0026g0110a0001c0001t0026g0111others(7): Show | 10 | HG02040.hp2 HG02055.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.785-804_785-801del others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849487 | ||||||
| chr18:47849487
|
GTATATA | G | 185 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.785-806_785-801del others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849487 | ||||||
| chr18:47849491
|
A | G | 1 | a0001c0001t0188g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.785-804T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849491 | ||||||
| chr18:47849493
|
A | T | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.785-806T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849493 | ||||||
| chr18:47849657
|
T | A | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.785-970A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849657 | ||||||
| chr18:47849740
|
G | A | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.785-1053C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849740 | ||||||
| chr18:47849750
|
G | A | 1 | a0001c0001t0022g0001 | 2 | NA18983.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.785-1063C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849750 | ||||||
| chr18:47849761
|
A | T | 71 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(68): Show | 71 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.785-1074T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849761 | ||||||
| chr18:47849785
|
T | C | 1 | a0001c0001t0002g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.785-1098A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849785 | ||||||
| chr18:47849891
|
C | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.785-1204G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849891 | ||||||
| chr18:47849974
|
T | A | 1 | a0001c0002t0247g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.785-1287A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849974 | ||||||
| chr18:47849984
|
G | C | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.784+1290C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849984 | ||||||
| chr18:47849985
|
C | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+1289G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47849985 | ||||||
| chr18:47850017
|
T | A | 1 | a0001c0001t0161g0103 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.784+1257A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850017 | ||||||
| chr18:47850052
|
C | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+1222G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850052 | ||||||
| chr18:47850114
|
G | A | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784+1160C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850114 | ||||||
| chr18:47850145
|
C | T | 1 | a0001c0001t0063g0249 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.784+1129G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850145 | ||||||
| chr18:47850171
|
C | A | 1 | a0001c0001t0044g0256 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.784+1103G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850171 | ||||||
| chr18:47850187
|
TTATATAT others(22): Show |
T | 1 | a0001c0001t0197g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784+1058_784+1086d others(31): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850187 | ||||||
| chr18:47850195
|
A | AT | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+1078_784+1079i others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850195 | ||||||
| chr18:47850216
|
A | ATATGTAT others(32): Show |
1 | a0001c0001t0180g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784+1019_784+1057d others(41): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850216 | ||||||
| chr18:47850216
|
A | ATATGTAT others(71): Show |
1 | a0001c0001t0150g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.784+1057_784+1058i others(80): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850216 | ||||||
| chr18:47850224
|
A | C | 2 | a0001c0001t0219g0139a0001c0001t0228g0158 | 2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.784+1050T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850224 | ||||||
| chr18:47850232
|
T | TTATATAT others(29): Show |
5 | a0001c0001t0092g0284a0001c0001t0202g0220a0001c0001t0203g0233others(2): Show | 5 | HG00140.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+1041_784+1042i others(38): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850232 | ||||||
| chr18:47850232
|
T | TTATATAT others(72): Show |
4 | a0001c0001t0028g0164a0001c0001t0224g0141a0001c0001t0227g0166others(1): Show | 4 | HG01261.hp2 HG02132.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+1041_784+1042i others(81): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850232 | ||||||
| chr18:47850232
|
T | TTATATAT others(25): Show |
4 | a0001c0001t0032g0003a0001c0001t0173g0033a0001c0001t0189g0018others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+1010_784+1041d others(34): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850232 | ||||||
| chr18:47850238
|
A | AGTAT | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+1035_784+1036i others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850238 | ||||||
| chr18:47850239
|
T | A | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+1035A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850239 | ||||||
| chr18:47850239
|
T | TTATA | 141 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(138): Show | 141 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.784+1031_784+1034d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850239 | ||||||
| chr18:47850239
|
T | TTATATAT others(40): Show |
38 | a0001c0001t0003g0146a0001c0001t0003g0149a0001c0001t0003g0170others(35): Show | 38 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.784+1034_784+1035i others(49): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850239 | ||||||
| chr18:47850239
|
T | TTATATAT others(83): Show |
1 | a0001c0001t0003g0140 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.784+1034_784+1035i others(92): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850239 | ||||||
| chr18:47850239
|
T | TTATATAT others(4): Show |
2 | a0001c0001t0044g0256a0001c0001t0045g0250 | 2 | HG00323.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.784+1024_784+1034d others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850239 | ||||||
| chr18:47850243
|
ATATTATA others(3): Show |
A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+1021_784+1030d others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850243 | ||||||
| chr18:47850243
|
ATATTATA others(21): Show |
A | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.784+1003_784+1030d others(30): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850243 | ||||||
| chr18:47850255
|
T | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+1019A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850255 | ||||||
| chr18:47850263
|
A | C | 1 | a0001c0001t0228g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.784+1011T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850263 | ||||||
| chr18:47850266
|
ATATAT | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+1003_784+1007d others(7): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850266 | ||||||
| chr18:47850270
|
A | T | 1 | a0001c0001t0197g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784+1004T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850270 | ||||||
| chr18:47850271
|
T | TTATATAT others(4): Show |
1 | a0001c0001t0005g0278 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.784+992_784+1002du others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850271 | ||||||
| chr18:47850275
|
A | G | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+999T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850275 | ||||||
| chr18:47850278
|
T | TTATATAT others(74): Show |
1 | a0001c0001t0228g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.784+995_784+996ins others(81): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850278 | ||||||
| chr18:47850282
|
A | ATATATAT others(32): Show |
8 | a0001c0001t0010g0124a0001c0001t0010g0145a0001c0001t0010g0162others(5): Show | 8 | HG03942.hp2 HG04115.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+991_784+992ins others(39): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850282 | ||||||
| chr18:47850291
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+983C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850291 | ||||||
| chr18:47850292
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+982A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850292 | ||||||
| chr18:47850295
|
AAT | A | 3 | a0001c0001t0205g0120a0001c0001t0208g0119a0001c0001t0209g0121 | 3 | HG02896.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.784+977_784+978del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850295 | ||||||
| chr18:47850300
|
A | G | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+974T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850300 | ||||||
| chr18:47850300
|
ATATTATG others(4): Show |
A | 1 | a0001c0001t0197g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784+963_784+973del others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850300 | ||||||
| chr18:47850301
|
TATTATGT others(318): Show |
T | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.784+648_784+972del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850301 | ||||||
| chr18:47850302
|
A | T | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+972T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850302 | ||||||
| chr18:47850303
|
T | A | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+971A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850303 | ||||||
| chr18:47850303
|
TTATGTAT others(196): Show |
T | 2 | a0001c0001t0026g0110a0001c0001t0026g0111 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.784+768_784+970del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850303 | ||||||
| chr18:47850306
|
T | TATATTAT others(30): Show |
1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784+967_784+968ins others(37): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850306 | ||||||
| chr18:47850307
|
G | A | 19 | a0001c0001t0014g0115a0001c0001t0086g0116a0001c0001t0196g0006others(16): Show | 19 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+967C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850307 | ||||||
| chr18:47850307
|
G | GTA | 45 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(42): Show | 45 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.784+965_784+966dup others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850307 | ||||||
| chr18:47850307
|
G | GTATAA | 130 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.784+966_784+967ins others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850307 | ||||||
| chr18:47850310
|
TGTTA | T | 14 | a0001c0001t0196g0006a0001c0001t0205g0120a0001c0001t0208g0119others(11): Show | 14 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.784+960_784+963del others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850310 | ||||||
| chr18:47850310
|
TGTTATAT others(393): Show |
T | 2 | a0001c0001t0206g0117a0001c0001t0207g0118 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.784+564_784+963del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850310 | ||||||
| chr18:47850311
|
G | A | 2 | a0001c0001t0030g0134a0001c0001t0102g0193 | 2 | NA18952.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.784+963C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850311 | ||||||
| chr18:47850311
|
G | T | 2 | a0001c0001t0014g0115a0001c0001t0086g0116 | 2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.784+963C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850311 | ||||||
| chr18:47850312
|
T | A | 3 | a0001c0001t0014g0115a0001c0001t0086g0116a0001c0001t0102g0193 | 3 | HG00642.hp2 NA18969.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.784+962A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850312 | ||||||
| chr18:47850313
|
T | G | 1 | a0001c0001t0030g0134 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.784+961A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850313 | ||||||
| chr18:47850314
|
A | ATATATTA others(207): Show |
2 | a0001c0001t0014g0115a0001c0001t0086g0116 | 2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.784+959_784+960ins others(214): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850314 | ||||||
| chr18:47850314
|
A | T | 2 | a0001c0001t0030g0134a0001c0001t0197g0005 | 2 | HG03195.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.784+960T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850314 | ||||||
| chr18:47850319
|
C | T | 195 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.784+955G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850319 | ||||||
| chr18:47850323
|
T | A | 2 | a0001c0001t0176g0022a0001c0001t0196g0006 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.784+951A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850323 | ||||||
| chr18:47850324
|
T | G | 1 | a0001c0001t0116g0245 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.784+950A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850324 | ||||||
| chr18:47850331
|
AAT | A | 11 | a0001c0001t0014g0276a0001c0001t0027g0132a0001c0001t0027g0148others(8): Show | 11 | HG00735.hp2 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.784+941_784+942del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850331 | ||||||
| chr18:47850336
|
ATG | A | 7 | a0001c0002t0248g0303a0001c0002t0249g0306a0001c0002t0250g0304others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+936_784+937del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850336 | ||||||
| chr18:47850337
|
TGTTA | T | 5 | a0001c0001t0205g0120a0001c0001t0208g0119a0001c0001t0209g0121others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+933_784+936del others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850337 | ||||||
| chr18:47850338
|
G | A | 7 | a0001c0001t0014g0115a0001c0001t0066g0199a0001c0001t0083g0178others(4): Show | 7 | HG00642.hp2 HG02559.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+936C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850338 | ||||||
| chr18:47850338
|
G | T | 1 | a0001c0001t0197g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784+936C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850338 | ||||||
| chr18:47850341
|
ATATATAT others(190): Show |
A | 1 | a0001c0002t0247g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.784+736_784+932del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850341 | ||||||
| chr18:47850350
|
ATACATAA others(124): Show |
A | 4 | a0001c0001t0205g0120a0001c0001t0208g0119a0001c0001t0209g0121others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+793_784+923del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850350 | ||||||
| chr18:47850353
|
C | T | 5 | a0001c0001t0014g0115a0001c0001t0066g0199a0001c0001t0083g0178others(2): Show | 5 | HG00642.hp2 HG02055.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+921G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850353 | ||||||
| chr18:47850357
|
A | T | 197 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.784+917T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850357 | ||||||
| chr18:47850361
|
G | A | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.784+913C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850361 | ||||||
| chr18:47850365
|
A | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.784+909T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850365 | ||||||
| chr18:47850370
|
ATATTATA others(126): Show |
A | 4 | a0001c0002t0248g0303a0001c0002t0249g0306a0001c0002t0250g0304others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+771_784+903del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850370 | ||||||
| chr18:47850372
|
A | T | 1 | a0001c0001t0197g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784+902T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850372 | ||||||
| chr18:47850374
|
T | TATATATA others(86): Show |
1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784+899_784+900ins others(93): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850374 | ||||||
| chr18:47850374
|
T | TATGTATT others(16): Show |
1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.784+899_784+900ins others(23): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850374 | ||||||
| chr18:47850375
|
ATATATAT others(156): Show |
A | 3 | a0001c0002t0252g0017a0001c0002t0253g0015a0001c0002t0254g0016 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.784+736_784+898del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850375 | ||||||
| chr18:47850377
|
A | ATATTATA others(120): Show |
2 | a0001c0001t0066g0199a0001c0001t0083g0178 | 2 | NA18990.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.784+896_784+897ins others(127): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850377 | ||||||
| chr18:47850377
|
A | G | 128 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.784+897T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850377 | ||||||
| chr18:47850379
|
A | G | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+895T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850379 | ||||||
| chr18:47850381
|
A | T | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+893T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850381 | ||||||
| chr18:47850382
|
T | A | 131 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.784+892A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(15): Show |
17 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(14): Show | 17 | HG00544.hp1 HG00609.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.784+891_784+892ins others(22): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(17): Show |
1 | a0001c0001t0030g0134 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.784+891_784+892ins others(24): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(122): Show |
6 | a0001c0001t0029g0133a0001c0001t0029g0161a0001c0001t0030g0135others(3): Show | 6 | NA18962.hp2 NA18968.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+891_784+892ins others(129): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(56): Show |
4 | a0001c0001t0027g0132a0001c0001t0027g0148a0001c0001t0216g0157others(1): Show | 4 | NA18942.hp1 NA18945.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+891_784+892ins others(63): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(115): Show |
2 | a0001c0001t0219g0139a0001c0001t0228g0158 | 2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.784+891_784+892ins others(122): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(122): Show |
1 | a0001c0001t0236g0159 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.784+891_784+892ins others(129): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(154): Show |
1 | a0001c0001t0217g0131 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.784+891_784+892ins others(161): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(90): Show |
2 | a0001c0001t0004g0130a0001c0001t0246g0126 | 2 | HG03942.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.784+891_784+892ins others(97): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(122): Show |
14 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(11): Show | 14 | HG01109.hp1 HG01261.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.784+891_784+892ins others(129): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(56): Show |
2 | a0001c0001t0237g0143a0001c0001t0240g0163 | 2 | HG01358.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.784+891_784+892ins others(63): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850382
|
T | TATTATAC others(90): Show |
2 | a0001c0001t0004g0156a0001c0001t0215g0144 | 2 | HG01257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.784+891_784+892ins others(97): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850382 | ||||||
| chr18:47850383
|
T | A | 1 | a0001c0001t0035g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.784+891A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850383 | ||||||
| chr18:47850384
|
ATATAATA others(5): Show |
A | 3 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0001t0245g0007 | 3 | HG00438.hp2 HG02055.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.784+878_784+889del others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850384 | ||||||
| chr18:47850386
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.784+888T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850386 | ||||||
| chr18:47850388
|
A | ATTATGTA others(181): Show |
1 | a0001c0001t0020g0191 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.784+885_784+886ins others(188): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850388 | ||||||
| chr18:47850388
|
A | ATTATGTA others(213): Show |
2 | a0001c0001t0020g0192a0001c0001t0129g0190 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.784+885_784+886ins others(220): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850388 | ||||||
| chr18:47850388
|
A | T | 35 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(32): Show | 35 | HG01109.hp1 HG01257.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.784+886T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850388 | ||||||
| chr18:47850389
|
A | T | 145 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.784+885T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850389 | ||||||
| chr18:47850395
|
A | T | 6 | a0001c0001t0020g0191a0001c0001t0020g0192a0001c0001t0035g0028others(3): Show | 6 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+879T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850395 | ||||||
| chr18:47850396
|
T | A | 7 | a0001c0001t0020g0191a0001c0001t0020g0192a0001c0001t0030g0134others(4): Show | 7 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+878A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTA | 23 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0027g0132others(20): Show | 23 | HG01109.hp2 HG01358.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.784+876_784+877dup others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(182): Show |
1 | a0001c0001t0070g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(189): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(233): Show |
1 | a0001c0001t0113g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(240): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(108): Show |
1 | a0001c0001t0110g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(115): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(74): Show |
1 | a0001c0001t0006g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(81): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(283): Show |
1 | a0001c0001t0103g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(290): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(247): Show |
1 | a0001c0001t0097g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(254): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(149): Show |
1 | a0001c0001t0089g0228 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(156): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(181): Show |
28 | a0001c0001t0001g0198a0001c0001t0001g0257a0001c0001t0001g0267others(25): Show | 28 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(188): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(213): Show |
7 | a0001c0001t0001g0206a0001c0001t0005g0260a0001c0001t0005g0282others(4): Show | 7 | HG01123.hp1 HG02165.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(220): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(245): Show |
2 | a0001c0001t0001g0195a0001c0001t0072g0259 | 2 | HG02040.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.784+877_784+878ins others(252): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(277): Show |
1 | a0001c0001t0130g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(284): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(183): Show |
1 | a0001c0001t0090g0248 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(190): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(215): Show |
5 | a0001c0001t0046g0196a0001c0001t0094g0004a0001c0001t0100g0299others(2): Show | 5 | NA18955.hp1 NA18960.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(222): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(181): Show |
1 | a0001c0001t0060g0238 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(188): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(147): Show |
1 | a0001c0001t0125g0283 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(154): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(117): Show |
3 | a0001c0001t0006g0237a0001c0001t0107g0236a0001c0001t0108g0217 | 3 | HG01243.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.784+877_784+878ins others(124): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(149): Show |
2 | a0001c0001t0080g0287a0001c0001t0105g0302 | 2 | HG01993.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.784+877_784+878ins others(156): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(185): Show |
1 | a0001c0001t0118g0203 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(192): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(185): Show |
1 | a0001c0001t0011g0223 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(192): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(217): Show |
1 | a0001c0001t0047g0222 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(224): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(181): Show |
1 | a0001c0001t0092g0284 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(188): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(115): Show |
4 | a0001c0001t0001g0266a0001c0001t0042g0254a0001c0001t0071g0273others(1): Show | 4 | HG00423.hp1 HG01978.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(122): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(147): Show |
4 | a0001c0001t0001g0301a0001c0001t0015g0216a0001c0001t0034g0258others(1): Show | 4 | HG02273.hp2 HG02602.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(154): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(147): Show |
10 | a0001c0001t0001g0269a0001c0001t0044g0256a0001c0001t0045g0250others(7): Show | 10 | HG00323.hp2 HG01106.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(154): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(179): Show |
1 | a0001c0001t0001g0263 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(186): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(179): Show |
3 | a0001c0001t0062g0234a0001c0001t0063g0249a0001c0001t0121g0292 | 3 | NA18950.hp2 NA18979.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.784+877_784+878ins others(186): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(262): Show |
1 | a0001c0001t0016g0112 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(269): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(192): Show |
1 | a0001c0001t0077g0253 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(199): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(224): Show |
4 | a0001c0001t0014g0276a0001c0001t0019g0187a0001c0001t0095g0176others(1): Show | 4 | HG01081.hp1 HG02615.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(231): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(256): Show |
5 | a0001c0001t0019g0183a0001c0001t0048g0182a0001c0001t0049g0186others(2): Show | 5 | HG02040.hp2 NA18944.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(263): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(224): Show |
1 | a0001c0001t0115g0188 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(231): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(192): Show |
1 | a0001c0001t0109g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(199): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(158): Show |
4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+877_784+878ins others(165): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(190): Show |
1 | a0001c0001t0081g0291 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(197): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(190): Show |
1 | a0001c0001t0051g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(197): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(160): Show |
2 | a0001c0001t0017g0208a0001c0001t0017g0265 | 2 | HG02165.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.784+877_784+878ins others(167): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(115): Show |
1 | a0001c0001t0096g0229 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(122): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(117): Show |
1 | a0001c0001t0006g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(124): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(183): Show |
1 | a0001c0001t0087g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(190): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(215): Show |
3 | a0001c0001t0018g0207a0001c0001t0099g0221a0001c0001t0111g0205 | 3 | HG00423.hp2 NA19005.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.784+877_784+878ins others(222): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(217): Show |
1 | a0001c0001t0018g0204 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(224): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(249): Show |
1 | a0001c0001t0088g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(256): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(217): Show |
1 | a0001c0001t0016g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(224): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(243): Show |
1 | a0001c0001t0005g0278 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(250): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(183): Show |
1 | a0001c0001t0011g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(190): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(113): Show |
3 | a0001c0001t0013g0177a0001c0001t0013g0286a0001c0001t0064g0285 | 3 | HG01981.hp2 HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.784+877_784+878ins others(120): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(113): Show |
1 | a0001c0001t0085g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(120): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0193g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.784+877_784+878ins others(34): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTATATAT others(59): Show |
1 | a0001c0001t0032g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784+877_784+878ins others(66): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850396
|
T | TTTTATAT others(4): Show |
2 | a0001c0001t0014g0115a0001c0001t0086g0116 | 2 | HG00642.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.784+877_784+878ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850396 | ||||||
| chr18:47850398
|
ATATATTA others(133): Show |
A | 2 | a0001c0001t0122g0251a0001c0001t0123g0252 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.784+736_784+875del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850398 | ||||||
| chr18:47850399
|
T | C | 3 | a0001c0001t0030g0134a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 NA18952.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.784+875A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850399 | ||||||
| chr18:47850399
|
T | TAC | 17 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(14): Show | 17 | HG00544.hp1 HG00609.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.784+874_784+875ins others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850399 | ||||||
| chr18:47850404
|
T | A | 2 | a0001c0001t0017g0208a0001c0001t0190g0021 | 2 | HG02622.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.784+870A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850404 | ||||||
| chr18:47850405
|
A | T | 1 | a0001c0001t0190g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.784+869T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850405 | ||||||
| chr18:47850407
|
G | A | 3 | a0001c0001t0043g0255a0001c0001t0106g0225a0001c0001t0190g0021 | 3 | HG02622.hp2 HG03486.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.784+867C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850407 | ||||||
| chr18:47850411
|
A | T | 2 | a0001c0001t0043g0255a0001c0001t0106g0225 | 2 | HG03486.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.784+863T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850411 | ||||||
| chr18:47850418
|
A | ATT | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG01109.hp1 HG01257.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.784+855_784+856ins others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850418 | ||||||
| chr18:47850418
|
A | T | 2 | a0001c0001t0042g0254a0001c0001t0127g0271 | 2 | HG00423.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.784+856T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850418 | ||||||
| chr18:47850419
|
T | TTATATAT others(4): Show |
1 | a0001c0001t0058g0240 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.784+854_784+855ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850419 | ||||||
| chr18:47850420
|
A | T | 190 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.784+854T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850420 | ||||||
| chr18:47850423
|
A | G | 2 | a0001c0001t0043g0255a0001c0001t0106g0225 | 2 | HG03486.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.784+851T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850423 | ||||||
| chr18:47850426
|
T | A | 1 | a0001c0001t0101g0194 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.784+848A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850426 | ||||||
| chr18:47850427
|
T | A | 7 | a0001c0001t0027g0132a0001c0001t0027g0148a0001c0001t0043g0255others(4): Show | 7 | HG01358.hp1 HG03486.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+847A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850427 | ||||||
| chr18:47850428
|
A | T | 5 | a0001c0001t0027g0132a0001c0001t0027g0148a0001c0001t0216g0157others(2): Show | 5 | HG01358.hp1 NA18942.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+846T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850428 | ||||||
| chr18:47850431
|
T | C | 9 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0176g0022others(6): Show | 9 | HG00438.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.784+843A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850431 | ||||||
| chr18:47850435
|
T | A | 5 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0189g0018others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+839A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850435 | ||||||
| chr18:47850436
|
T | A | 2 | a0001c0001t0017g0208a0001c0001t0017g0265 | 2 | HG02165.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.784+838A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850436 | ||||||
| chr18:47850439
|
G | A | 3 | a0001c0001t0043g0255a0001c0001t0106g0225a0001c0001t0176g0022 | 3 | HG03453.hp1 HG03486.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.784+835C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850439 | ||||||
| chr18:47850440
|
T | TATAATAT others(16): Show |
2 | a0001c0001t0150g0066a0001c0001t0180g0067 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.784+811_784+833dup others(23): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850440 | ||||||
| chr18:47850443
|
A | T | 3 | a0001c0001t0043g0255a0001c0001t0106g0225a0001c0001t0119g0297 | 3 | HG03486.hp1 HG04199.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.784+831T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850443 | ||||||
| chr18:47850444
|
A | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.784+830T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850444 | ||||||
| chr18:47850451
|
T | TTATATAT others(2): Show |
24 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(21): Show | 24 | HG01109.hp1 HG01257.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.784+822_784+823ins others(9): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850451 | ||||||
| chr18:47850451
|
T | TTATATAT others(36): Show |
1 | a0001c0001t0240g0163 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.784+822_784+823ins others(43): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850451 | ||||||
| chr18:47850451
|
T | TTTTATAT others(4): Show |
5 | a0001c0001t0027g0132a0001c0001t0027g0148a0001c0001t0216g0157others(2): Show | 5 | HG01358.hp1 NA18942.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+822_784+823ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850451 | ||||||
| chr18:47850451
|
TTATATAT others(107): Show |
T | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.784+709_784+822del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850451 | ||||||
| chr18:47850452
|
T | A | 1 | a0001c0001t0007g0102 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.784+822A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850452 | ||||||
| chr18:47850455
|
A | G | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+819T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850455 | ||||||
| chr18:47850458
|
T | TAACA | 5 | a0001c0001t0001g0195a0001c0001t0017g0208a0001c0001t0089g0228others(2): Show | 5 | HG00140.hp1 NA18950.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+815_784+816ins others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850458 | ||||||
| chr18:47850459
|
T | A | 3 | a0001c0001t0119g0297a0001c0001t0219g0139a0001c0001t0246g0126 | 3 | HG02015.hp2 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.784+815A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850459 | ||||||
| chr18:47850462
|
A | AATG | 6 | a0001c0001t0001g0195a0001c0001t0017g0208a0001c0001t0089g0228others(3): Show | 6 | HG00140.hp1 HG03688.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+811_784+812ins others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850462 | ||||||
| chr18:47850462
|
A | ATATAATG | 84 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0257others(81): Show | 84 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.784+811_784+812ins others(7): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850462 | ||||||
| chr18:47850462
|
A | ATATATTA others(77): Show |
12 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0028g0138others(9): Show | 12 | HG00544.hp1 HG00609.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.784+811_784+812ins others(84): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850462 | ||||||
| chr18:47850462
|
A | ATATATTA others(2): Show |
13 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0004g0130others(10): Show | 13 | HG01069.hp2 HG01978.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.784+811_784+812ins others(9): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850462 | ||||||
| chr18:47850462
|
A | ATATTATG | 10 | a0001c0001t0006g0219a0001c0001t0006g0237a0001c0001t0015g0218others(7): Show | 10 | HG00741.hp2 HG01243.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.784+811_784+812ins others(7): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850462 | ||||||
| chr18:47850462
|
A | ATATTATG others(60): Show |
3 | a0001c0001t0014g0115a0001c0001t0077g0253a0001c0001t0086g0116 | 3 | HG00642.hp2 HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.784+811_784+812ins others(67): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850462 | ||||||
| chr18:47850462
|
A | G | 36 | a0001c0001t0001g0300a0001c0001t0003g0146a0001c0001t0003g0170others(33): Show | 36 | HG01109.hp1 HG01257.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.784+812T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850462 | ||||||
| chr18:47850463
|
C | T | 188 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.784+811G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850463 | ||||||
| chr18:47850467
|
A | T | 11 | a0001c0001t0010g0124a0001c0001t0010g0145a0001c0001t0010g0162others(8): Show | 11 | HG01884.hp1 HG02015.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.784+807T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850467 | ||||||
| chr18:47850469
|
A | G | 11 | a0001c0001t0016g0112a0001c0001t0080g0287a0001c0001t0087g0214others(8): Show | 11 | HG00558.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.784+805T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850469 | ||||||
| chr18:47850471
|
A | G | 4 | a0001c0001t0173g0033a0001c0001t0219g0139a0001c0001t0246g0126others(1): Show | 4 | HG01884.hp1 HG02015.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+803T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850471 | ||||||
| chr18:47850473
|
A | G | 38 | a0001c0001t0001g0195a0001c0001t0003g0146a0001c0001t0003g0170others(35): Show | 38 | HG00140.hp1 HG00642.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.784+801T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850473 | ||||||
| chr18:47850474
|
T | A | 12 | a0001c0001t0016g0112a0001c0001t0080g0287a0001c0001t0087g0214others(9): Show | 12 | HG00558.hp2 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.784+800A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850474 | ||||||
| chr18:47850474
|
T | TAATATAT others(40): Show |
2 | a0001c0001t0219g0139a0001c0001t0246g0126 | 2 | HG02015.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.784+799_784+800ins others(47): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850474 | ||||||
| chr18:47850474
|
T | TATTATGT others(147): Show |
2 | a0001c0001t0028g0164a0001c0001t0224g0141 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.784+799_784+800ins others(154): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850474 | ||||||
| chr18:47850474
|
T | TATTATGT others(79): Show |
4 | a0001c0001t0010g0124a0001c0001t0010g0145a0001c0001t0010g0162others(1): Show | 4 | NA18960.hp1 NA19004.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+799_784+800ins others(86): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850474 | ||||||
| chr18:47850475
|
T | A | 3 | a0001c0001t0032g0003a0001c0001t0173g0033a0001c0001t0193g0032 | 3 | HG01884.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.784+799A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850475 | ||||||
| chr18:47850480
|
A | T | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+794T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850480 | ||||||
| chr18:47850481
|
T | A | 10 | a0001c0001t0010g0124a0001c0001t0010g0145a0001c0001t0010g0162others(7): Show | 10 | HG02015.hp2 HG02132.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+793A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
T | TAA | 28 | a0001c0001t0001g0195a0001c0001t0003g0140a0001c0001t0003g0149others(25): Show | 28 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.784+792_784+793ins others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
T | TATAA | 27 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(24): Show | 27 | HG01109.hp1 HG01257.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.784+792_784+793ins others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
T | TTA | 3 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0001t0255g0096 | 3 | HG00438.hp2 HG02895.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.784+791_784+792dup others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
T | TTATATAT others(62): Show |
2 | a0001c0001t0080g0287a0001c0001t0088g0232 | 2 | HG01993.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.784+792_784+793ins others(69): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
T | TTATATAT others(32): Show |
1 | a0001c0001t0087g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.784+792_784+793ins others(39): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
T | TTATATAT others(62): Show |
2 | a0001c0001t0016g0112a0001c0001t0095g0176 | 2 | HG02615.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.784+792_784+793ins others(69): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
T | TTATATAT others(27): Show |
3 | a0001c0001t0183g0023a0001c0001t0184g0035a0001c0001t0185g0025 | 3 | HG02572.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.784+792_784+793ins others(34): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850481
|
TTATATAT others(27): Show |
T | 8 | a0001c0001t0002g0113a0001c0001t0007g0101a0001c0001t0007g0102others(5): Show | 8 | HG01074.hp1 HG01884.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.784+759_784+792del others(34): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850481 | ||||||
| chr18:47850482
|
T | A | 98 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0257others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.784+792A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850482 | ||||||
| chr18:47850484
|
T | C | 98 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0257others(95): Show | 98 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.784+790A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850484 | ||||||
| chr18:47850489
|
T | A | 109 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(106): Show | 109 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.784+785A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850489 | ||||||
| chr18:47850489
|
T | TATATATA others(30): Show |
4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+784_784+785ins others(37): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850489 | ||||||
| chr18:47850490
|
A | ACATATAA others(30): Show |
1 | a0001c0001t0094g0004 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.784+783_784+784ins others(37): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850490 | ||||||
| chr18:47850492
|
G | T | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+782C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850492 | ||||||
| chr18:47850497
|
ATATATGT others(283): Show |
A | 1 | a0001c0001t0197g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784+487_784+776del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850497 | ||||||
| chr18:47850502
|
TGTTA | T | 4 | a0001c0001t0205g0120a0001c0001t0208g0119a0001c0001t0209g0121others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+768_784+771del others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850502 | ||||||
| chr18:47850503
|
G | A | 12 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0016g0209others(9): Show | 12 | HG00438.hp2 HG01978.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.784+771C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850503 | ||||||
| chr18:47850504
|
T | TTATATAT others(256): Show |
1 | a0001c0001t0001g0267 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.784+769_784+770ins others(263): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850504 | ||||||
| chr18:47850504
|
T | TTATATAT others(93): Show |
1 | a0001c0001t0071g0273 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.784+769_784+770ins others(100): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850504 | ||||||
| chr18:47850504
|
TTA | T | 102 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(99): Show | 102 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.784+768_784+769del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850504 | ||||||
| chr18:47850506
|
A | ATATATAA others(51): Show |
1 | a0001c0001t0016g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.784+767_784+768ins others(58): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850506 | ||||||
| chr18:47850506
|
A | ATATATAA others(21): Show |
2 | a0001c0001t0067g0280a0001c0001t0118g0203 | 2 | HG01069.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.784+767_784+768ins others(28): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850506 | ||||||
| chr18:47850506
|
A | ATATATAA others(23): Show |
1 | a0001c0001t0110g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.784+767_784+768ins others(30): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850506 | ||||||
| chr18:47850506
|
A | T | 4 | a0001c0001t0043g0255a0001c0001t0058g0240a0001c0001t0106g0225others(1): Show | 4 | HG03486.hp1 HG04199.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+768T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850506 | ||||||
| chr18:47850514
|
A | T | 20 | a0001c0001t0001g0267a0001c0001t0026g0110a0001c0001t0026g0111others(17): Show | 20 | HG00438.hp2 HG01978.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.784+760T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850514 | ||||||
| chr18:47850514
|
AATATATA others(70): Show |
A | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.784+683_784+759del others(77): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850514 | ||||||
| chr18:47850516
|
T | C | 3 | a0001c0001t0032g0003a0001c0001t0065g0197a0001c0001t0116g0245 | 3 | HG00438.hp1 HG02451.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.784+758A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850516 | ||||||
| chr18:47850518
|
T | C | 6 | a0001c0001t0001g0266a0001c0001t0196g0006a0001c0002t0248g0303others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+756A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850518 | ||||||
| chr18:47850523
|
T | A | 1 | a0001c0001t0001g0266 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.784+751A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850523 | ||||||
| chr18:47850536
|
TGTTA | T | 6 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(3): Show | 6 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+734_784+737del others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850536 | ||||||
| chr18:47850537
|
G | A | 26 | a0001c0001t0001g0267a0001c0001t0014g0115a0001c0001t0016g0112others(23): Show | 26 | HG00140.hp1 HG00438.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.784+737C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850537 | ||||||
| chr18:47850538
|
T | TTATATAT others(204): Show |
1 | a0001c0001t0100g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.784+735_784+736ins others(211): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(77): Show |
2 | a0001c0001t0077g0253a0001c0001t0080g0287 | 2 | HG01256.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.784+735_784+736ins others(84): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(550): Show |
1 | a0001c0001t0016g0112 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.784+735_784+736ins others(557): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(120): Show |
2 | a0001c0001t0086g0116a0001c0001t0126g0279 | 2 | HG00642.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.784+735_784+736ins others(127): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(163): Show |
1 | a0001c0001t0017g0208 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.784+735_784+736ins others(170): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(206): Show |
2 | a0001c0001t0014g0115a0001c0001t0094g0004 | 2 | NA18960.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.784+735_784+736ins others(213): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(378): Show |
1 | a0001c0001t0090g0248 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.784+735_784+736ins others(385): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(421): Show |
1 | a0001c0001t0087g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.784+735_784+736ins others(428): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(464): Show |
1 | a0001c0001t0095g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.784+735_784+736ins others(471): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
T | TTATATAT others(202): Show |
1 | a0001c0001t0089g0228 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.784+735_784+736ins others(209): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850538
|
TTA | T | 4 | a0001c0001t0001g0266a0001c0001t0071g0273a0001c0001t0106g0225others(1): Show | 4 | HG01978.hp1 HG02280.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+734_784+735del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850538 | ||||||
| chr18:47850539
|
T | A | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+735A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850539 | ||||||
| chr18:47850540
|
A | ATATATAA others(66): Show |
1 | a0001c0001t0073g0293 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.784+733_784+734ins others(73): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850540 | ||||||
| chr18:47850540
|
A | ATATATTA others(223): Show |
1 | a0001c0001t0088g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.784+733_784+734ins others(230): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850540 | ||||||
| chr18:47850540
|
A | ATATATTA others(30): Show |
1 | a0001c0001t0092g0284 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.784+733_784+734ins others(37): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850540 | ||||||
| chr18:47850540
|
A | T | 6 | a0001c0001t0043g0255a0001c0001t0058g0240a0001c0001t0119g0297others(3): Show | 6 | HG00438.hp2 HG02559.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+734T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850540 | ||||||
| chr18:47850545
|
TATAATAT others(29): Show |
T | 1 | a0001c0001t0256g0073 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.784+693_784+728del others(36): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850545 | ||||||
| chr18:47850548
|
A | AATATATA others(111): Show |
1 | a0001c0001t0001g0198 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(118): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(154): Show |
1 | a0001c0001t0046g0196 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(161): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(206): Show |
1 | a0001c0001t0082g0296 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(213): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(68): Show |
7 | a0001c0001t0001g0300a0001c0001t0070g0202a0001c0001t0074g0200others(4): Show | 7 | HG00099.hp2 HG01074.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+651_784+725dup others(75): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(240): Show |
1 | a0001c0001t0018g0204 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(247): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(199): Show |
1 | a0001c0001t0001g0206 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(206): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(111): Show |
7 | a0001c0001t0019g0187a0001c0001t0045g0250a0001c0001t0078g0272others(4): Show | 7 | HG00423.hp1 HG03239.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+725_784+726ins others(118): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(143): Show |
1 | a0001c0001t0099g0221 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(150): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(154): Show |
4 | a0001c0001t0014g0276a0001c0001t0019g0183a0001c0001t0063g0249others(1): Show | 4 | HG01081.hp1 HG02040.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+725_784+726ins others(161): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(197): Show |
1 | a0001c0001t0044g0256 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(204): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(577): Show |
2 | a0001c0001t0012g0239a0001c0001t0012g0243 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.784+725_784+726ins others(584): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(240): Show |
1 | a0001c0001t0017g0265 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(247): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(283): Show |
3 | a0001c0001t0018g0207a0001c0001t0079g0247a0001c0001t0120g0189 | 3 | HG00423.hp2 HG03927.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.784+725_784+726ins others(290): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(412): Show |
2 | a0001c0001t0011g0223a0001c0001t0047g0222 | 2 | HG02129.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.784+725_784+726ins others(419): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(455): Show |
1 | a0001c0001t0020g0191 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(462): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(541): Show |
2 | a0001c0001t0020g0192a0001c0001t0129g0190 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.784+725_784+726ins others(548): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(584): Show |
1 | a0001c0001t0060g0238 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(591): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(324): Show |
1 | a0001c0001t0132g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(331): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(322): Show |
1 | a0001c0001t0131g0212 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(329): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(315): Show |
1 | a0001c0001t0096g0229 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(322): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(186): Show |
2 | a0001c0001t0083g0178a0001c0001t0102g0193 | 2 | NA18969.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.784+725_784+726ins others(193): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(272): Show |
1 | a0001c0001t0121g0292 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(279): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(616): Show |
1 | a0001c0001t0016g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(623): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(261): Show |
1 | a0001c0001t0081g0291 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(268): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(326): Show |
1 | a0001c0001t0005g0260 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(333): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(401): Show |
1 | a0001c0001t0005g0282 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(408): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(444): Show |
1 | a0001c0001t0005g0278 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(451): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(308): Show |
1 | a0001c0001t0068g0261 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(315): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(308): Show |
1 | a0001c0001t0033g0262 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(315): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(66): Show |
1 | a0001c0001t0013g0286 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(73): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(109): Show |
2 | a0001c0001t0013g0177a0001c0001t0064g0285 | 2 | HG01981.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.784+725_784+726ins others(116): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(238): Show |
1 | a0001c0001t0066g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(245): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(107): Show |
1 | a0001c0001t0257g0309 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.784+725_784+726ins others(114): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(236): Show |
1 | a0001c0001t0051g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(243): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(236): Show |
1 | a0001c0001t0072g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(243): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | AATATATA others(109): Show |
1 | a0001c0001t0042g0254 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(116): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | ACTATATA others(369): Show |
1 | a0001c0001t0085g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.784+725_784+726ins others(376): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | ATT | 4 | a0001c0002t0248g0303a0001c0002t0249g0306a0001c0002t0250g0304others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+725_784+726ins others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
A | T | 39 | a0001c0001t0001g0267a0001c0001t0014g0115a0001c0001t0016g0112others(36): Show | 39 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.784+726T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850548
|
AATATATA others(36): Show |
A | 1 | a0001c0001t0133g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.784+683_784+725del others(43): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850548 | ||||||
| chr18:47850551
|
A | G | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.784+723T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850551 | ||||||
| chr18:47850552
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+722A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850552 | ||||||
| chr18:47850565
|
ATATATAT | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+702_784+708del others(7): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850565 | ||||||
| chr18:47850570
|
TATTATAT others(6): Show |
T | 2 | a0001c0001t0026g0110a0001c0001t0026g0111 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.784+691_784+703del others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850570 | ||||||
| chr18:47850571
|
A | G | 23 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(20): Show | 23 | HG00544.hp1 HG01109.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.784+703T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850571 | ||||||
| chr18:47850572
|
TTATATAT others(2): Show |
T | 17 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(14): Show | 17 | HG00544.hp1 HG01358.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.784+693_784+701del others(9): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850572 | ||||||
| chr18:47850579
|
T | C | 6 | a0001c0001t0008g0061a0001c0001t0008g0062a0001c0001t0008g0063others(3): Show | 6 | HG00544.hp2 HG02523.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+695A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850579 | ||||||
| chr18:47850579
|
TTA | T | 40 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(37): Show | 40 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.784+693_784+694del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850579 | ||||||
| chr18:47850580
|
T | A | 1 | a0001c0001t0028g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.784+694A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850580 | ||||||
| chr18:47850581
|
A | AATATATA others(17): Show |
1 | a0001c0001t0215g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.784+692_784+693ins others(24): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850581 | ||||||
| chr18:47850581
|
A | ATATATAT others(66): Show |
1 | a0001c0001t0001g0301 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.784+692_784+693ins others(73): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850581 | ||||||
| chr18:47850581
|
A | ATATATAT others(108): Show |
1 | a0001c0001t0058g0240 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.784+692_784+693ins others(115): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850581 | ||||||
| chr18:47850581
|
A | ATATATTA others(76): Show |
1 | a0001c0001t0106g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.784+692_784+693ins others(83): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850581 | ||||||
| chr18:47850581
|
A | T | 1 | a0001c0001t0028g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.784+693T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850581 | ||||||
| chr18:47850582
|
T | A | 1 | a0001c0001t0028g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.784+692A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850582 | ||||||
| chr18:47850582
|
T | TATATATA others(179): Show |
1 | a0001c0001t0103g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.784+691_784+692ins others(186): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850582 | ||||||
| chr18:47850583
|
A | ATATATAT others(25): Show |
11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0015g0216others(8): Show | 11 | HG00438.hp1 HG00735.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.784+659_784+690dup others(32): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850583 | ||||||
| chr18:47850583
|
A | ATATATAT others(89): Show |
1 | a0001c0001t0125g0283 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.784+690_784+691ins others(96): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850583 | ||||||
| chr18:47850587
|
A | AATGTATA others(26): Show |
1 | a0001c0001t0043g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.784+686_784+687ins others(33): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850587 | ||||||
| chr18:47850587
|
A | G | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.784+687T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850587 | ||||||
| chr18:47850590
|
T | TATATTAT others(19): Show |
1 | a0001c0001t0001g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.784+683_784+684ins others(26): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850590 | ||||||
| chr18:47850591
|
T | A | 26 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(23): Show | 26 | HG00438.hp2 HG00544.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.784+683A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850591 | ||||||
| chr18:47850593
|
T | A | 1 | a0001c0001t0111g0205 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.784+681A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850593 | ||||||
| chr18:47850595
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+679A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850595 | ||||||
| chr18:47850598
|
A | G | 3 | a0001c0001t0043g0255a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.784+676T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850598 | ||||||
| chr18:47850599
|
T | TTATGTAT others(160): Show |
1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.784+674_784+675ins others(167): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850599 | ||||||
| chr18:47850603
|
G | A | 6 | a0001c0001t0028g0138a0001c0001t0043g0255a0001c0001t0056g0242others(3): Show | 6 | HG00438.hp2 HG01943.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+671C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850603 | ||||||
| chr18:47850603
|
G | GTATAATA others(59): Show |
3 | a0001c0001t0053g0085a0001c0001t0054g0274a0001c0001t0055g0275 | 3 | HG01257.hp2 HG01258.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.784+670_784+671ins others(66): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850603 | ||||||
| chr18:47850607
|
A | T | 3 | a0001c0001t0028g0138a0001c0001t0056g0242a0001c0001t0119g0297 | 3 | HG01943.hp1 HG04199.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.784+667T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850607 | ||||||
| chr18:47850608
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0015g0218a0001c0001t0091g0210 | 2 | HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.784+665_784+666ins others(30): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850608 | ||||||
| chr18:47850609
|
T | C | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.784+665A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850609 | ||||||
| chr18:47850614
|
A | G | 3 | a0001c0001t0027g0132a0001c0001t0229g0136a0001c0001t0244g0122 | 3 | HG01928.hp1 HG02055.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.784+660T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850614 | ||||||
| chr18:47850615
|
TTATATAT others(4): Show |
T | 5 | a0001c0001t0001g0266a0001c0001t0048g0182a0001c0001t0049g0186others(2): Show | 5 | HG02280.hp2 NA18944.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+648_784+658del others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850615 | ||||||
| chr18:47850616
|
T | TATATATT others(25): Show |
1 | a0001c0001t0076g0289 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.784+657_784+658ins others(32): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850616 | ||||||
| chr18:47850617
|
A | ATATATTA others(195): Show |
1 | a0001c0001t0105g0302 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.784+656_784+657ins others(202): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850617 | ||||||
| chr18:47850618
|
T | A | 5 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(2): Show | 5 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+656A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850618 | ||||||
| chr18:47850619
|
A | G | 3 | a0001c0001t0028g0138a0001c0001t0056g0242a0001c0001t0119g0297 | 3 | HG01943.hp1 HG04199.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.784+655T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850619 | ||||||
| chr18:47850620
|
T | TATTATAT others(22): Show |
1 | a0001c0001t0001g0269 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.784+653_784+654ins others(29): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850620 | ||||||
| chr18:47850622
|
T | C | 18 | a0001c0001t0008g0061a0001c0001t0008g0062a0001c0001t0008g0063others(15): Show | 19 | HG00544.hp2 HG00609.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+652A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850622 | ||||||
| chr18:47850622
|
T | TTATATAT others(67): Show |
1 | a0001c0001t0101g0194 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.784+651_784+652ins others(74): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850622 | ||||||
| chr18:47850622
|
TTA | T | 21 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(18): Show | 21 | HG00544.hp1 HG01358.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.784+650_784+651del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850622 | ||||||
| chr18:47850623
|
T | A | 11 | a0001c0001t0028g0138a0001c0001t0056g0242a0001c0001t0119g0297others(8): Show | 11 | HG01891.hp2 HG01943.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.784+651A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850623 | ||||||
| chr18:47850623
|
T | G | 3 | a0001c0001t0043g0255a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.784+651A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850623 | ||||||
| chr18:47850624
|
A | T | 11 | a0001c0001t0043g0255a0001c0001t0200g0175a0001c0001t0201g0174others(8): Show | 11 | HG00438.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.784+650T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850624 | ||||||
| chr18:47850625
|
T | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+649A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850625 | ||||||
| chr18:47850626
|
A | ATATATTA others(12): Show |
3 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0242g0160 | 3 | HG01261.hp2 HG01496.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.784+647_784+648ins others(19): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850626 | ||||||
| chr18:47850626
|
A | ATATATTA others(14): Show |
2 | a0001c0001t0057g0246a0001c0001t0059g0264 | 2 | NA18973.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.784+647_784+648ins others(21): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850626 | ||||||
| chr18:47850626
|
A | ATATATTA others(48): Show |
1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+647_784+648ins others(55): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850626 | ||||||
| chr18:47850626
|
A | ATATATTA others(57): Show |
1 | a0001c0001t0067g0280 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.784+647_784+648ins others(64): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850626 | ||||||
| chr18:47850630
|
A | AT | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+643dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850630 | ||||||
| chr18:47850630
|
A | ATTATGTA others(163): Show |
1 | a0001c0001t0050g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.784+643_784+644ins others(170): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850630 | ||||||
| chr18:47850633
|
T | TG | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+640_784+641ins others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850633 | ||||||
| chr18:47850634
|
T | A | 4 | a0001c0001t0043g0255a0001c0001t0050g0213a0001c0001t0200g0175others(1): Show | 4 | HG00438.hp2 NA18906.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+640A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850634 | ||||||
| chr18:47850636
|
T | TA | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+637dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850636 | ||||||
| chr18:47850642
|
T | C | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+632A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850642 | ||||||
| chr18:47850643
|
T | A | 18 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0035g0028others(15): Show | 18 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.784+631A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850643 | ||||||
| chr18:47850643
|
T | TATGTATA others(36): Show |
1 | a0001c0001t0186g0024 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.784+630_784+631ins others(43): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850643 | ||||||
| chr18:47850646
|
G | A | 31 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(28): Show | 31 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.784+628C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850646 | ||||||
| chr18:47850650
|
A | T | 32 | a0001c0001t0001g0195a0001c0001t0003g0146a0001c0001t0003g0170others(29): Show | 32 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.784+624T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850650 | ||||||
| chr18:47850656
|
TATTATAT others(6): Show |
T | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.784+605_784+617del others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850656 | ||||||
| chr18:47850657
|
A | T | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+617T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850657 | ||||||
| chr18:47850658
|
TTATATAC others(4): Show |
T | 1 | a0001c0001t0243g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.784+605_784+615del others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850658 | ||||||
| chr18:47850659
|
T | A | 1 | a0001c0001t0050g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.784+615A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850659 | ||||||
| chr18:47850660
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0242g0160 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.784+613_784+614ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850660 | ||||||
| chr18:47850660
|
A | ATG | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+613_784+614ins others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850660 | ||||||
| chr18:47850664
|
AC | A | 9 | a0001c0001t0001g0195a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.784+609delG | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850664 | ||||||
| chr18:47850664
|
ACT | A | 3 | a0001c0001t0205g0120a0001c0001t0208g0119a0001c0001t0209g0121 | 3 | HG02896.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.784+608_784+609del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850664 | ||||||
| chr18:47850665
|
C | A | 31 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(28): Show | 31 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.784+609G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850665 | ||||||
| chr18:47850665
|
C | G | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+609G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850665 | ||||||
| chr18:47850665
|
C | T | 158 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0257others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.784+609G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850665 | ||||||
| chr18:47850666
|
T | A | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+608A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850666 | ||||||
| chr18:47850667
|
A | T | 3 | a0001c0001t0205g0120a0001c0001t0208g0119a0001c0001t0209g0121 | 3 | HG02896.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.784+607T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850667 | ||||||
| chr18:47850667
|
ATATATAT others(175): Show |
A | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.784+425_784+606del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850667 | ||||||
| chr18:47850668
|
T | C | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+606A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850668 | ||||||
| chr18:47850668
|
T | TA | 9 | a0001c0001t0196g0006a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.784+605dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850668 | ||||||
| chr18:47850669
|
A | AT | 31 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(28): Show | 31 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.784+604dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850669 | ||||||
| chr18:47850669
|
A | ATATATTA others(12): Show |
1 | a0001c0001t0227g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.784+604_784+605ins others(19): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850669 | ||||||
| chr18:47850669
|
A | ATATATTA others(14): Show |
1 | a0001c0001t0058g0240 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.784+604_784+605ins others(21): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850669 | ||||||
| chr18:47850669
|
A | ATATATTA others(42): Show |
1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784+604_784+605ins others(49): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850669 | ||||||
| chr18:47850673
|
A | AT | 20 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(17): Show | 20 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.784+600dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850673 | ||||||
| chr18:47850675
|
A | T | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+599T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850675 | ||||||
| chr18:47850676
|
T | C | 1 | a0001c0001t0100g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.784+598A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850676 | ||||||
| chr18:47850676
|
T | TG | 20 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(17): Show | 20 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.784+597_784+598ins others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850676 | ||||||
| chr18:47850677
|
T | A | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+597A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850677 | ||||||
| chr18:47850679
|
T | TA | 20 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(17): Show | 20 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.784+594dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850679 | ||||||
| chr18:47850684
|
A | G | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+590T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850684 | ||||||
| chr18:47850686
|
A | ATGTATAT others(135): Show |
1 | a0001c0001t0001g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.784+587_784+588ins others(142): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850686 | ||||||
| chr18:47850686
|
A | T | 206 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0257others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.784+588T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850686 | ||||||
| chr18:47850689
|
G | A | 29 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(26): Show | 29 | HG00544.hp1 HG01358.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.784+585C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850689 | ||||||
| chr18:47850693
|
A | AATATATT others(7): Show |
3 | a0001c0001t0031g0002a0001c0001t0212g0167a0001c0001t0222g0169 | 3 | HG04228.hp1 NA18969.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.784+580_784+581ins others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850693 | ||||||
| chr18:47850693
|
A | ATT | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+580_784+581ins others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850693 | ||||||
| chr18:47850693
|
A | T | 20 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(17): Show | 20 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.784+581T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850693 | ||||||
| chr18:47850693
|
AAT | A | 28 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(25): Show | 28 | HG00609.hp1 HG01109.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.784+579_784+580del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850693 | ||||||
| chr18:47850700
|
A | T | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+574T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850700 | ||||||
| chr18:47850701
|
T | TTATATAT others(77): Show |
1 | a0001c0001t0093g0235 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.784+572_784+573ins others(84): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850701 | ||||||
| chr18:47850702
|
T | A | 1 | a0001c0001t0087g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.784+572A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850702 | ||||||
| chr18:47850703
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0227g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.784+570_784+571ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850703 | ||||||
| chr18:47850703
|
A | ATG | 24 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(21): Show | 24 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.784+570_784+571ins others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850703 | ||||||
| chr18:47850705
|
A | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+569T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850705 | ||||||
| chr18:47850707
|
ACT | A | 10 | a0001c0001t0074g0200a0001c0001t0211g0008a0001c0002t0247g0014others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+565_784+566del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850707 | ||||||
| chr18:47850708
|
C | A | 25 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(22): Show | 25 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.784+566G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850708 | ||||||
| chr18:47850708
|
C | G | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+566G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850708 | ||||||
| chr18:47850708
|
C | T | 167 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.784+566G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850708 | ||||||
| chr18:47850708
|
CTA | C | 7 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(4): Show | 7 | HG01109.hp2 HG03041.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+564_784+565del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850708 | ||||||
| chr18:47850710
|
A | T | 10 | a0001c0001t0074g0200a0001c0001t0211g0008a0001c0002t0247g0014others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+564T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850710 | ||||||
| chr18:47850710
|
ATATATAT others(132): Show |
A | 3 | a0001c0001t0205g0120a0001c0001t0208g0119a0001c0001t0209g0121 | 3 | HG02896.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.784+425_784+563del | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850710 | ||||||
| chr18:47850712
|
A | AT | 24 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(21): Show | 24 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.784+561dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850712 | ||||||
| chr18:47850716
|
A | AT | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+557dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850716 | ||||||
| chr18:47850719
|
T | TG | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+554_784+555ins others(1): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850719 | ||||||
| chr18:47850720
|
T | A | 3 | a0001c0001t0006g0237a0001c0001t0119g0297a0001c0001t0244g0122 | 3 | HG01243.hp1 HG02055.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.784+554A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850720 | ||||||
| chr18:47850722
|
T | TA | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+551dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850722 | ||||||
| chr18:47850729
|
T | A | 2 | a0001c0001t0024g0069a0001c0001t0173g0033 | 2 | HG00099.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.784+545A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850729 | ||||||
| chr18:47850732
|
G | A | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+542C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850732 | ||||||
| chr18:47850736
|
A | T | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+538T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850736 | ||||||
| chr18:47850737
|
A | ATATAT | 23 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(20): Show | 23 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.784+532_784+536dup others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850737 | ||||||
| chr18:47850737
|
A | T | 2 | a0001c0001t0001g0198a0001c0001t0074g0200 | 2 | NA18981.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.784+537T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850737 | ||||||
| chr18:47850743
|
ATTATATA others(4): Show |
A | 3 | a0001c0002t0252g0017a0001c0002t0253g0015a0001c0002t0254g0016 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.784+520_784+530del others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850743 | ||||||
| chr18:47850747
|
T | C | 1 | a0001c0001t0109g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784+527A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850747 | ||||||
| chr18:47850748
|
A | G | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+526T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850748 | ||||||
| chr18:47850751
|
T | C | 6 | a0001c0001t0024g0069a0001c0001t0025g0019a0001c0001t0025g0020others(3): Show | 6 | HG00099.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+523A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850751 | ||||||
| chr18:47850751
|
T | TATTATGT others(4): Show |
23 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(20): Show | 23 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.784+522_784+523ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850751 | ||||||
| chr18:47850752
|
T | A | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+522A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850752 | ||||||
| chr18:47850753
|
A | C | 1 | a0001c0001t0175g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784+521T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850753 | ||||||
| chr18:47850753
|
ATATATAT others(89): Show |
A | 2 | a0001c0001t0206g0117a0001c0001t0207g0118 | 2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.784+425_784+520del others(96): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850753 | ||||||
| chr18:47850755
|
A | AT | 23 | a0001c0001t0003g0140a0001c0001t0003g0149a0001c0001t0010g0124others(20): Show | 23 | HG00544.hp1 HG01358.hp1 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.784+518dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850755 | ||||||
| chr18:47850755
|
A | ATAT | 30 | a0001c0001t0003g0146a0001c0001t0003g0170a0001c0001t0004g0125others(27): Show | 30 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.784+516_784+518dup others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850755 | ||||||
| chr18:47850755
|
A | ATATATTA others(42): Show |
1 | a0001c0001t0235g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.784+518_784+519ins others(49): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850755 | ||||||
| chr18:47850757
|
A | ATTATATA others(75): Show |
1 | a0001c0001t0006g0237 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784+516_784+517ins others(82): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850757 | ||||||
| chr18:47850758
|
TATATTAT others(4): Show |
T | 5 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(2): Show | 5 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+505_784+515del others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850758 | ||||||
| chr18:47850769
|
C | T | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.784+505G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850769 | ||||||
| chr18:47850769
|
CATTATGT others(25): Show |
C | 75 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(72): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.784+473_784+504del others(32): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850769 | ||||||
| chr18:47850775
|
GTATAATA others(30): Show |
G | 1 | a0001c0001t0134g0041 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.784+462_784+498del others(37): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850775 | ||||||
| chr18:47850779
|
AAT | A | 55 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(52): Show | 55 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.784+493_784+494del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850779 | ||||||
| chr18:47850787
|
T | TTATATAT others(2): Show |
4 | a0001c0001t0050g0213a0001c0001t0105g0302a0001c0001t0131g0212others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+478_784+486dup others(9): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850787 | ||||||
| chr18:47850787
|
T | TTATATAT others(4): Show |
104 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0257others(101): Show | 104 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.784+476_784+486dup others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850787 | ||||||
| chr18:47850787
|
T | TTATATAT others(131): Show |
1 | a0001c0001t0092g0284 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.784+486_784+487ins others(138): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850787 | ||||||
| chr18:47850787
|
T | TTATATAT others(174): Show |
1 | a0001c0001t0101g0194 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.784+486_784+487ins others(181): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850787 | ||||||
| chr18:47850795
|
T | A | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+479A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850795 | ||||||
| chr18:47850796
|
A | ATATATAT others(4): Show |
5 | a0001c0001t0019g0183a0001c0001t0019g0187a0001c0001t0112g0179others(2): Show | 5 | HG02040.hp2 NA18942.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+477_784+478ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850796 | ||||||
| chr18:47850796
|
ATATATAT others(46): Show |
A | 3 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0243g0011 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.784+425_784+477del others(53): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850796 | ||||||
| chr18:47850801
|
T | TATATTAT others(4): Show |
2 | a0001c0001t0024g0069a0001c0001t0175g0307 | 2 | HG00099.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.784+472_784+473ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850801 | ||||||
| chr18:47850802
|
AT | A | 14 | a0001c0001t0001g0195a0001c0001t0015g0218a0001c0001t0048g0182others(11): Show | 14 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.784+471delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850802 | ||||||
| chr18:47850806
|
TG | T | 14 | a0001c0001t0001g0195a0001c0001t0015g0218a0001c0001t0048g0182others(11): Show | 14 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.784+467delC | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850806 | ||||||
| chr18:47850807
|
G | A | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+467C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850807 | ||||||
| chr18:47850810
|
TA | T | 14 | a0001c0001t0001g0195a0001c0001t0015g0218a0001c0001t0048g0182others(11): Show | 14 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.784+463delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850810 | ||||||
| chr18:47850811
|
A | AAT | 5 | a0001c0001t0014g0276a0001c0001t0053g0085a0001c0001t0054g0274others(2): Show | 5 | HG01081.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+461_784+462dup others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850811 | ||||||
| chr18:47850812
|
A | G | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+462T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850812 | ||||||
| chr18:47850817
|
T | A | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784+457A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATAATAT others(6): Show |
1 | a0001c0001t0052g0277 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATATATA others(48): Show |
1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(55): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(5): Show |
1 | a0001c0001t0101g0194 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(4): Show |
5 | a0001c0001t0056g0242a0001c0001t0202g0220a0001c0001t0203g0233others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.784+456_784+457ins others(11): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(6): Show |
83 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0257others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.784+456_784+457ins others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(49): Show |
2 | a0001c0001t0110g0231a0001c0001t0118g0203 | 2 | HG03130.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.784+456_784+457ins others(56): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(176): Show |
1 | a0001c0001t0104g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(183): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(92): Show |
5 | a0001c0001t0001g0266a0001c0001t0006g0224a0001c0001t0017g0265others(2): Show | 5 | HG02165.hp1 HG02280.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+456_784+457ins others(99): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(135): Show |
1 | a0001c0001t0017g0208 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(142): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(178): Show |
1 | a0001c0001t0006g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(185): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(221): Show |
1 | a0001c0001t0109g0226 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(228): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(264): Show |
1 | a0001c0001t0062g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(271): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(393): Show |
1 | a0001c0001t0111g0205 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(400): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(176): Show |
1 | a0001c0001t0015g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(183): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(135): Show |
1 | a0001c0001t0113g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(142): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(178): Show |
1 | a0001c0001t0115g0188 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(185): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(178): Show |
1 | a0001c0001t0019g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(185): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(221): Show |
1 | a0001c0001t0019g0187 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(228): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(264): Show |
1 | a0001c0001t0112g0179 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.784+456_784+457ins others(271): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(221): Show |
1 | a0001c0001t0114g0180 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(228): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(6): Show |
1 | a0001c0001t0103g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.784+456_784+457ins others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850817
|
T | TATTATAT others(6): Show |
2 | a0001c0001t0050g0213a0001c0001t0105g0302 | 2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.784+456_784+457ins others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850817 | ||||||
| chr18:47850818
|
T | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+456A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850818 | ||||||
| chr18:47850819
|
A | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+455T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850819 | ||||||
| chr18:47850821
|
A | G | 15 | a0001c0001t0001g0195a0001c0001t0015g0218a0001c0001t0048g0182others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.784+453T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850821 | ||||||
| chr18:47850821
|
ATAT | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+450_784+452del others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850821 | ||||||
| chr18:47850823
|
A | T | 2 | a0001c0001t0131g0212a0001c0001t0132g0211 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.784+451T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850823 | ||||||
| chr18:47850825
|
T | A | 15 | a0001c0001t0001g0195a0001c0001t0015g0218a0001c0001t0048g0182others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.784+449A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850825 | ||||||
| chr18:47850830
|
A | ATATATTA others(54): Show |
1 | a0001c0001t0006g0237 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784+443_784+444ins others(61): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850830 | ||||||
| chr18:47850834
|
T | A | 1 | a0001c0001t0006g0237 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784+440A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850834 | ||||||
| chr18:47850835
|
ATG | A | 13 | a0001c0001t0015g0218a0001c0001t0048g0182a0001c0001t0049g0186others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.784+437_784+438del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850835 | ||||||
| chr18:47850835
|
ATGTATAT others(7): Show |
A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.784+425_784+438del others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850835 | ||||||
| chr18:47850837
|
G | A | 6 | a0001c0001t0001g0195a0001c0001t0006g0237a0001c0001t0119g0297others(3): Show | 6 | HG01243.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+437C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850837 | ||||||
| chr18:47850841
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.784+433T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850841 | ||||||
| chr18:47850842
|
T | A | 171 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.784+432A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850842 | ||||||
| chr18:47850844
|
ATATAT | A | 13 | a0001c0001t0015g0218a0001c0001t0048g0182a0001c0001t0049g0186others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.784+425_784+429del others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850844 | ||||||
| chr18:47850846
|
A | G | 4 | a0001c0001t0119g0297a0001c0001t0131g0212a0001c0001t0132g0211others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+428T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850846 | ||||||
| chr18:47850849
|
T | TAATATAT others(97): Show |
1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784+424_784+425ins others(104): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850849 | ||||||
| chr18:47850849
|
T | TATTA | 3 | a0001c0001t0042g0254a0001c0001t0043g0255a0001c0001t0127g0271 | 3 | HG00423.hp1 HG02015.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.784+424_784+425ins others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850849 | ||||||
| chr18:47850849
|
T | TTA | 48 | a0001c0001t0001g0206a0001c0001t0006g0237a0001c0001t0024g0069others(45): Show | 48 | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.784+423_784+424dup others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850849 | ||||||
| chr18:47850849
|
T | TTATATAT others(2): Show |
164 | a0001c0001t0001g0198a0001c0001t0001g0257a0001c0001t0001g0263others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.784+424_784+425ins others(9): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850849 | ||||||
| chr18:47850850
|
T | A | 3 | a0001c0001t0131g0212a0001c0001t0132g0211a0001c0001t0211g0008 | 3 | HG02258.hp2 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.784+424A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850850 | ||||||
| chr18:47850859
|
T | A | 4 | a0001c0001t0003g0140a0001c0001t0214g0123a0001c0001t0232g0129others(1): Show | 4 | HG00609.hp1 NA18970.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.784+415A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850859 | ||||||
| chr18:47850875
|
A | AATATATA others(123): Show |
1 | a0001c0001t0130g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.784+398_784+399ins others(130): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850875 | ||||||
| chr18:47850979
|
T | C | 2 | a0001c0001t0101g0194a0001c0001t0102g0193 | 2 | NA18955.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.784+295A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850979 | ||||||
| chr18:47850984
|
A | T | 6 | a0001c0001t0024g0069a0001c0001t0024g0077a0001c0001t0152g0078others(3): Show | 6 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.784+290T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 7/10 | chr18 | 47850984 | ||||||
| chr18:47851505
|
G | A | 1 | a0001c0001t0050g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.731-178C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851505 | ||||||
| chr18:47851510
|
G | C | 1 | a0001c0002t0247g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.731-183C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851510 | ||||||
| chr18:47851511
|
G | C | 98 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.731-184C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851511 | ||||||
| chr18:47851567
|
T | C | 1 | a0001c0001t0085g0241 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.731-240A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851567 | ||||||
| chr18:47851579
|
T | C | 1 | a0001c0001t0067g0280 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.731-252A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851579 | ||||||
| chr18:47851754
|
CAATT | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-431_731-428del others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851754 | ||||||
| chr18:47851782
|
C | T | 308 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.731-455G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851782 | ||||||
| chr18:47851784
|
T | C | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-457A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851784 | ||||||
| chr18:47851837
|
A | C | 6 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(3): Show | 6 | HG02717.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-510T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851837 | ||||||
| chr18:47851980
|
A | T | 1 | a0001c0001t0003g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.731-653T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47851980 | ||||||
| chr18:47852240
|
T | A | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.731-913A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852240 | ||||||
| chr18:47852268
|
T | C | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-941A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852268 | ||||||
| chr18:47852406
|
G | A | 5 | a0001c0001t0014g0115a0001c0001t0014g0276a0001c0001t0077g0253others(2): Show | 5 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-1079C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852406 | ||||||
| chr18:47852548
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.731-1221T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852548 | ||||||
| chr18:47852656
|
C | T | 1 | a0001c0001t0134g0041 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.731-1329G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852656 | ||||||
| chr18:47852670
|
A | G | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.731-1343T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852670 | ||||||
| chr18:47852675
|
G | A | 8 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(5): Show | 8 | HG01109.hp2 HG02622.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-1348C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852675 | ||||||
| chr18:47852793
|
G | A | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.731-1466C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852793 | ||||||
| chr18:47852803
|
C | T | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.731-1476G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852803 | ||||||
| chr18:47852903
|
A | G | 79 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(76): Show | 80 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.731-1576T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852903 | ||||||
| chr18:47852978
|
C | A | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.731-1651G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47852978 | ||||||
| chr18:47853174
|
A | T | 198 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.731-1847T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853174 | ||||||
| chr18:47853228
|
G | A | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1901C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853228 | ||||||
| chr18:47853242
|
ATGGCCGT others(187): Show |
A | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.731-2109_731-1916d others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853242 | ||||||
| chr18:47853456
|
G | T | 2 | a0001c0001t0136g0100a0001c0001t0137g0099 | 2 | HG00735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.731-2129C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853456 | ||||||
| chr18:47853566
|
T | G | 71 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.731-2239A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853566 | ||||||
| chr18:47853645
|
G | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.731-2318C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853645 | ||||||
| chr18:47853742
|
AAAATCTG others(12): Show |
A | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.731-2434_731-2416d others(21): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853742 | ||||||
| chr18:47853772
|
G | A | 1 | a0001c0001t0016g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.731-2445C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853772 | ||||||
| chr18:47853812
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-2485A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853812 | ||||||
| chr18:47853873
|
A | G | 2 | a0001c0001t0142g0050a0001c0001t0157g0048 | 2 | HG00558.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.731-2546T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853873 | ||||||
| chr18:47853921
|
C | T | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.731-2594G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853921 | ||||||
| chr18:47853979
|
A | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-2652T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853979 | ||||||
| chr18:47853998
|
G | A | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.731-2671C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47853998 | ||||||
| chr18:47854010
|
G | C | 1 | a0001c0001t0002g0113 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.731-2683C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854010 | ||||||
| chr18:47854078
|
T | A | 1 | a0001c0001t0015g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.731-2751A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854078 | ||||||
| chr18:47854088
|
TA | T | 118 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(115): Show | 118 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.731-2762delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854088 | ||||||
| chr18:47854088
|
TAA | T | 17 | a0001c0001t0006g0219a0001c0001t0006g0224a0001c0001t0006g0237others(14): Show | 17 | HG01243.hp1 HG02615.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.731-2763_731-2762d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854088 | ||||||
| chr18:47854165
|
C | T | 1 | a0001c0001t0130g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.731-2838G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854165 | ||||||
| chr18:47854222
|
T | C | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.731-2895A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854222 | ||||||
| chr18:47854320
|
G | A | 2 | a0001c0001t0146g0037a0001c0001t0147g0093 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.731-2993C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854320 | ||||||
| chr18:47854377
|
G | A | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.731-3050C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854377 | ||||||
| chr18:47854405
|
TCTCA | T | 6 | a0001c0001t0009g0081a0001c0001t0009g0083a0001c0001t0009g0084others(3): Show | 6 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-3082_731-3079d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854405 | ||||||
| chr18:47854640
|
GTT | G | 198 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.731-3315_731-3314d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854640 | ||||||
| chr18:47854648
|
TTA | T | 10 | a0001c0001t0016g0112a0001c0001t0016g0209a0001c0001t0017g0208others(7): Show | 10 | HG00423.hp2 HG01928.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.731-3323_731-3322d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854648 | ||||||
| chr18:47854698
|
T | G | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.731-3371A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854698 | ||||||
| chr18:47854754
|
G | A | 1 | a0001c0001t0175g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.731-3427C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854754 | ||||||
| chr18:47854852
|
C | T | 1 | a0001c0001t0175g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.731-3525G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47854852 | ||||||
| chr18:47855086
|
A | G | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-3759T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855086 | ||||||
| chr18:47855127
|
A | G | 1 | a0001c0001t0190g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.731-3800T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855127 | ||||||
| chr18:47855640
|
C | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-4313G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855640 | ||||||
| chr18:47855745
|
C | G | 73 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-4418G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855745 | ||||||
| chr18:47855783
|
G | A | 1 | a0001c0001t0257g0309 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.731-4456C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855783 | ||||||
| chr18:47855837
|
T | A | 1 | a0001c0001t0043g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.731-4510A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855837 | ||||||
| chr18:47855838
|
C | A | 1 | a0001c0001t0043g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.731-4511G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855838 | ||||||
| chr18:47855839
|
T | C | 1 | a0001c0001t0043g0255 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.731-4512A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855839 | ||||||
| chr18:47855840
|
C | T | 1 | a0001c0001t0162g0040 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.731-4513G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855840 | ||||||
| chr18:47855862
|
C | T | 1 | a0001c0001t0215g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.731-4535G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855862 | ||||||
| chr18:47855927
|
C | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-4600G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855927 | ||||||
| chr18:47855975
|
C | T | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.731-4648G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47855975 | ||||||
| chr18:47856066
|
G | C | 2 | a0001c0001t0016g0112a0001c0001t0128g0114 | 2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.731-4739C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856066 | ||||||
| chr18:47856141
|
G | T | 5 | a0001c0001t0149g0042a0001c0001t0158g0064a0001c0001t0159g0065others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-4814C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856141 | ||||||
| chr18:47856141
|
GT | G | 200 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.731-4815delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856141 | ||||||
| chr18:47856234
|
A | C | 117 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(114): Show | 117 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.731-4907T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856234 | ||||||
| chr18:47856309
|
T | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.731-4982A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856309 | ||||||
| chr18:47856435
|
T | C | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.731-5108A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856435 | ||||||
| chr18:47856613
|
C | T | 2 | a0001c0001t0146g0037a0001c0001t0147g0093 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.731-5286G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856613 | ||||||
| chr18:47856673
|
G | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-5346C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856673 | ||||||
| chr18:47856728
|
TAATGAGG others(111): Show |
T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.731-5519_731-5402d others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856728 | ||||||
| chr18:47856848
|
A | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.731-5521T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856848 | ||||||
| chr18:47856850
|
G | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.731-5523C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856850 | ||||||
| chr18:47856851
|
C | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.731-5524G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856851 | ||||||
| chr18:47856853
|
A | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.731-5526T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856853 | ||||||
| chr18:47856854
|
A | AT | 88 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.731-5528dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856854 | ||||||
| chr18:47856854
|
A | ATT | 16 | a0001c0001t0001g0257a0001c0001t0008g0063a0001c0001t0058g0240others(13): Show | 16 | HG00438.hp2 HG00735.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.731-5529_731-5528d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856854 | ||||||
| chr18:47856854
|
A | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.731-5527T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856854 | ||||||
| chr18:47856854
|
AT | A | 11 | a0001c0001t0010g0145a0001c0001t0012g0239a0001c0001t0012g0243others(8): Show | 11 | HG00438.hp1 HG01168.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-5528delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856854 | ||||||
| chr18:47856918
|
C | T | 2 | a0001c0001t0026g0110a0001c0001t0026g0111 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.731-5591G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47856918 | ||||||
| chr18:47857018
|
C | T | 1 | a0001c0001t0209g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.731-5691G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857018 | ||||||
| chr18:47857048
|
G | A | 51 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(48): Show | 51 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.731-5721C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857048 | ||||||
| chr18:47857055
|
C | T | 73 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.731-5728G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857055 | ||||||
| chr18:47857067
|
C | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.731-5740G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857067 | ||||||
| chr18:47857068
|
G | A | 3 | a0001c0002t0252g0017a0001c0002t0253g0015a0001c0002t0254g0016 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.731-5741C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857068 | ||||||
| chr18:47857100
|
G | A | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.731-5773C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857100 | ||||||
| chr18:47857103
|
C | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-5776G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857103 | ||||||
| chr18:47857104
|
G | A | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.731-5777C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857104 | ||||||
| chr18:47857316
|
A | G | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.731-5989T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857316 | ||||||
| chr18:47857325
|
T | A | 1 | a0001c0001t0125g0283 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.731-5998A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857325 | ||||||
| chr18:47857332
|
TTTC | T | 9 | a0001c0001t0007g0097a0001c0001t0007g0101a0001c0001t0007g0102others(6): Show | 9 | HG00140.hp2 HG00735.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-6008_731-6006d others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857332 | ||||||
| chr18:47857366
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-6039A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857366 | ||||||
| chr18:47857384
|
A | G | 1 | a0001c0001t0189g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.731-6057T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857384 | ||||||
| chr18:47857756
|
G | A | 2 | a0001c0001t0001g0267a0001c0001t0072g0259 | 2 | HG02040.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.731-6429C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857756 | ||||||
| chr18:47857773
|
C | A | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-6446G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857773 | ||||||
| chr18:47857774
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-6447C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857774 | ||||||
| chr18:47857894
|
T | G | 1 | a0001c0001t0114g0180 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.731-6567A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857894 | ||||||
| chr18:47857933
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.731-6606T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47857933 | ||||||
| chr18:47858093
|
A | T | 1 | a0001c0001t0009g0084 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.731-6766T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47858093 | ||||||
| chr18:47858158
|
G | GA | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-6832dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47858158 | ||||||
| chr18:47858304
|
T | C | 1 | a0001c0001t0257g0309 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.730+6755A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47858304 | ||||||
| chr18:47858343
|
A | G | 1 | a0001c0001t0215g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.730+6716T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47858343 | ||||||
| chr18:47858360
|
A | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.730+6699T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47858360 | ||||||
| chr18:47858724
|
A | G | 13 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(10): Show | 13 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.730+6335T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47858724 | ||||||
| chr18:47858787
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+6272C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47858787 | ||||||
| chr18:47859077
|
G | C | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.730+5982C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47859077 | ||||||
| chr18:47859170
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.730+5889A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47859170 | ||||||
| chr18:47859195
|
C | T | 1 | a0001c0001t0095g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.730+5864G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47859195 | ||||||
| chr18:47859656
|
T | C | 74 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.730+5403A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47859656 | ||||||
| chr18:47859763
|
T | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.730+5296A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47859763 | ||||||
| chr18:47859824
|
A | G | 1 | a0001c0001t0018g0207 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.730+5235T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47859824 | ||||||
| chr18:47859964
|
A | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.730+5095T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47859964 | ||||||
| chr18:47860024
|
T | C | 213 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(210): Show | 213 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.730+5035A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860024 | ||||||
| chr18:47860155
|
A | T | 1 | a0001c0001t0173g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.730+4904T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860155 | ||||||
| chr18:47860165
|
A | AAC | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+4892_730+4893d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860165 | ||||||
| chr18:47860224
|
T | C | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.730+4835A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860224 | ||||||
| chr18:47860236
|
T | C | 1 | a0001c0001t0133g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+4823A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860236 | ||||||
| chr18:47860364
|
T | TGGGC | 13 | a0001c0001t0008g0061a0001c0001t0008g0062a0001c0001t0008g0063others(10): Show | 14 | HG00544.hp2 HG00609.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.730+4691_730+4694d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860364 | ||||||
| chr18:47860441
|
T | A | 10 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0002t0247g0014others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.730+4618A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860441 | ||||||
| chr18:47860441
|
TA | T | 6 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(3): Show | 6 | HG01109.hp2 HG02622.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+4617delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860441 | ||||||
| chr18:47860455
|
T | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+4604A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860455 | ||||||
| chr18:47860681
|
AATAAACA others(9): Show |
A | 44 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(41): Show | 44 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.730+4362_730+4377d others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47860681 | ||||||
| chr18:47861057
|
A | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.730+4002T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861057 | ||||||
| chr18:47861084
|
A | G | 11 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+3975T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861084 | ||||||
| chr18:47861098
|
G | A | 1 | a0001c0001t0227g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.730+3961C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861098 | ||||||
| chr18:47861213
|
G | A | 200 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.730+3846C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861213 | ||||||
| chr18:47861287
|
G | C | 1 | a0001c0001t0105g0302 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.730+3772C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861287 | ||||||
| chr18:47861295
|
G | T | 4 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0189g0018others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+3764C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861295 | ||||||
| chr18:47861334
|
T | A | 11 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+3725A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861334 | ||||||
| chr18:47861444
|
G | A | 2 | a0001c0001t0080g0287a0001c0001t0092g0284 | 2 | HG00140.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.730+3615C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861444 | ||||||
| chr18:47861451
|
G | T | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.730+3608C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861451 | ||||||
| chr18:47861519
|
C | T | 11 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+3540G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861519 | ||||||
| chr18:47861592
|
A | G | 1 | a0001c0001t0082g0296 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730+3467T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861592 | ||||||
| chr18:47861628
|
A | G | 2 | a0001c0001t0032g0003a0001c0001t0193g0032 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.730+3431T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861628 | ||||||
| chr18:47861650
|
G | A | 1 | a0001c0001t0143g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.730+3409C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861650 | ||||||
| chr18:47861965
|
T | C | 11 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+3094A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47861965 | ||||||
| chr18:47862020
|
A | G | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.730+3039T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862020 | ||||||
| chr18:47862050
|
G | T | 200 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.730+3009C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862050 | ||||||
| chr18:47862250
|
C | T | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+2809G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862250 | ||||||
| chr18:47862352
|
G | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.730+2707C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862352 | ||||||
| chr18:47862657
|
T | C | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.730+2402A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862657 | ||||||
| chr18:47862716
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+2343C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862716 | ||||||
| chr18:47862740
|
G | A | 1 | a0001c0001t0174g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.730+2319C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862740 | ||||||
| chr18:47862822
|
T | C | 1 | a0001c0001t0126g0279 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.730+2237A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862822 | ||||||
| chr18:47862988
|
C | CA | 10 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0002t0247g0014others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.730+2070dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47862988 | ||||||
| chr18:47863183
|
T | C | 11 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+1876A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863183 | ||||||
| chr18:47863259
|
A | T | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.730+1800T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863259 | ||||||
| chr18:47863301
|
T | C | 3 | a0001c0001t0009g0084a0001c0001t0196g0006a0001c0001t0197g0005 | 3 | HG01978.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.730+1758A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863301 | ||||||
| chr18:47863314
|
AT | A | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.730+1744delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863314 | ||||||
| chr18:47863558
|
T | C | 1 | a0001c0002t0247g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.730+1501A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863558 | ||||||
| chr18:47863562
|
C | G | 1 | a0001c0001t0177g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.730+1497G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863562 | ||||||
| chr18:47863630
|
C | T | 1 | a0001c0001t0050g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.730+1429G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863630 | ||||||
| chr18:47863877
|
A | G | 138 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.730+1182T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863877 | ||||||
| chr18:47863936
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+1123A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47863936 | ||||||
| chr18:47864097
|
G | C | 1 | a0001c0002t0247g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.730+962C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864097 | ||||||
| chr18:47864118
|
A | G | 7 | a0001c0001t0030g0134a0001c0001t0030g0135a0001c0001t0148g0109others(4): Show | 7 | HG02280.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+941T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864118 | ||||||
| chr18:47864134
|
A | G | 1 | a0001c0001t0124g0201 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.730+925T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864134 | ||||||
| chr18:47864173
|
C | T | 1 | a0001c0001t0014g0276 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.730+886G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864173 | ||||||
| chr18:47864178
|
A | G | 4 | a0001c0001t0056g0242a0001c0001t0057g0246a0001c0001t0058g0240others(1): Show | 4 | NA18944.hp2 NA18973.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+881T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864178 | ||||||
| chr18:47864221
|
C | A | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.730+838G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864221 | ||||||
| chr18:47864232
|
G | C | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730+827C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864232 | ||||||
| chr18:47864446
|
C | T | 1 | a0001c0001t0243g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.730+613G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864446 | ||||||
| chr18:47864804
|
T | C | 1 | a0001c0001t0045g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.730+255A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864804 | ||||||
| chr18:47864875
|
A | T | 4 | a0001c0002t0248g0303a0001c0002t0249g0306a0001c0002t0250g0304others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+184T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864875 | ||||||
| chr18:47864952
|
T | C | 1 | a0001c0001t0177g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.730+107A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864952 | ||||||
| chr18:47864989
|
T | C | 1 | a0001c0001t0133g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+70A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47864989 | ||||||
| chr18:47865048
|
A | AT | 7 | a0001c0001t0036g0030a0001c0001t0037g0026a0001c0001t0038g0031others(4): Show | 7 | HG01109.hp2 HG02622.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.730+10dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47865048 | ||||||
| chr18:47865048
|
A | T | 4 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0189g0018others(1): Show | 4 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+11T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 6/10 | chr18 | 47865048 | ||||||
| chr18:47865368
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-235A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47865368 | ||||||
| chr18:47865398
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.656-265T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47865398 | ||||||
| chr18:47865564
|
A | G | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-431T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47865564 | ||||||
| chr18:47865639
|
T | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-506A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47865639 | ||||||
| chr18:47865753
|
T | C | 3 | a0001c0001t0014g0115a0001c0001t0077g0253a0001c0001t0086g0116 | 3 | HG00642.hp2 HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.656-620A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47865753 | ||||||
| chr18:47865846
|
G | A | 1 | a0001c0001t0184g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.656-713C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47865846 | ||||||
| chr18:47865979
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-846C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47865979 | ||||||
| chr18:47866029
|
G | C | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.656-896C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866029 | ||||||
| chr18:47866031
|
A | G | 3 | a0001c0001t0015g0218a0001c0001t0091g0210a0001c0001t0093g0235 | 3 | HG00642.hp1 HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.656-898T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866031 | ||||||
| chr18:47866106
|
G | T | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.656-973C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866106 | ||||||
| chr18:47866160
|
C | T | 214 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.656-1027G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866160 | ||||||
| chr18:47866256
|
C | T | 2 | a0001c0001t0169g0089a0001c0001t0170g0087 | 2 | NA18959.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.656-1123G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866256 | ||||||
| chr18:47866316
|
C | CA | 158 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0257others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.656-1184dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866316 | ||||||
| chr18:47866316
|
C | CAA | 19 | a0001c0001t0006g0219a0001c0001t0006g0224a0001c0001t0006g0237others(16): Show | 19 | HG01243.hp1 HG01978.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.656-1185_656-1184d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866316 | ||||||
| chr18:47866316
|
C | CAAAAA | 8 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(5): Show | 8 | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-1188_656-1184d others(7): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866316 | ||||||
| chr18:47866316
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-1194_656-1184d others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866316 | ||||||
| chr18:47866316
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0016g0112 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.656-1198_656-1184d others(17): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866316 | ||||||
| chr18:47866342
|
G | A | 1 | a0001c0001t0103g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.656-1209C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866342 | ||||||
| chr18:47866747
|
C | G | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+1576G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866747 | ||||||
| chr18:47866881
|
A | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.655+1442T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866881 | ||||||
| chr18:47866891
|
A | G | 211 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.655+1432T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866891 | ||||||
| chr18:47866951
|
T | C | 1 | a0001c0001t0198g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.655+1372A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47866951 | ||||||
| chr18:47867024
|
C | T | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+1299G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867024 | ||||||
| chr18:47867106
|
C | T | 1 | a0001c0001t0231g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.655+1217G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867106 | ||||||
| chr18:47867335
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+988A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867335 | ||||||
| chr18:47867352
|
T | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.655+971A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867352 | ||||||
| chr18:47867408
|
A | T | 1 | a0001c0001t0193g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+915T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867408 | ||||||
| chr18:47867481
|
A | G | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.655+842T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867481 | ||||||
| chr18:47867499
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.655+824T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867499 | ||||||
| chr18:47867605
|
C | A | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.655+718G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867605 | ||||||
| chr18:47867657
|
C | CA | 9 | a0001c0001t0001g0300a0001c0001t0019g0183a0001c0001t0019g0187others(6): Show | 9 | HG00099.hp1 HG02040.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+665dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867657 | ||||||
| chr18:47867697
|
G | C | 1 | a0001c0001t0091g0210 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.655+626C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867697 | ||||||
| chr18:47867707
|
C | T | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+616G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867707 | ||||||
| chr18:47867732
|
T | C | 1 | a0001c0001t0234g0172 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.655+591A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867732 | ||||||
| chr18:47867801
|
C | T | 1 | a0001c0001t0080g0287 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.655+522G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867801 | ||||||
| chr18:47867835
|
T | G | 211 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.655+488A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47867835 | ||||||
| chr18:47868230
|
A | T | 11 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.655+93T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47868230 | ||||||
| chr18:47868282
|
G | A | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.655+41C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47868282 | ||||||
| chr18:47868291
|
C | A | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.655+32G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 5/10 | chr18 | 47868291 | ||||||
| chr18:47868548
|
T | C | 7 | a0001c0001t0015g0216a0001c0001t0015g0218a0001c0001t0020g0191others(4): Show | 7 | HG00642.hp1 HG00741.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.521-91A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 4/10 | chr18 | 47868548 | ||||||
| chr18:47868740
|
G | C | 206 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.521-283C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 4/10 | chr18 | 47868740 | ||||||
| chr18:47868810
|
A | T | 1 | a0001c0001t0165g0047 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.521-353T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 4/10 | chr18 | 47868810 | ||||||
| chr18:47868982
|
G | A | 3 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0001t0244g0122 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.520+261C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 4/10 | chr18 | 47868982 | ||||||
| chr18:47869084
|
A | T | 5 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(2): Show | 5 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+159T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 4/10 | chr18 | 47869084 | ||||||
| chr18:47869474
|
TA | T | 187 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.327-39delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869474 | ||||||
| chr18:47869474
|
TAA | T | 20 | a0001c0001t0004g0150a0001c0001t0005g0260a0001c0001t0005g0282others(17): Show | 20 | HG01257.hp2 HG02055.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.327-40_327-39delTT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869474 | ||||||
| chr18:47869475
|
A | T | 1 | a0001c0001t0173g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.327-39T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869475 | ||||||
| chr18:47869505
|
G | A | 2 | a0001c0001t0208g0119a0001c0001t0209g0121 | 2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.327-69C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869505 | ||||||
| chr18:47869711
|
A | G | 3 | a0001c0001t0183g0023a0001c0001t0184g0035a0001c0001t0185g0025 | 3 | HG02572.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.327-275T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869711 | ||||||
| chr18:47869757
|
T | C | 7 | a0001c0001t0016g0209a0001c0001t0017g0208a0001c0001t0017g0265others(4): Show | 7 | HG00423.hp2 HG02165.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.327-321A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869757 | ||||||
| chr18:47869782
|
G | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.327-346C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869782 | ||||||
| chr18:47869788
|
C | T | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.327-352G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47869788 | ||||||
| chr18:47870098
|
A | AT | 207 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.326+376dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47870098 | ||||||
| chr18:47870260
|
A | C | 1 | a0001c0001t0133g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.326+215T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 3/10 | chr18 | 47870260 | ||||||
| chr18:47870880
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.237-316C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47870880 | ||||||
| chr18:47871186
|
T | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.237-622A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871186 | ||||||
| chr18:47871196
|
T | C | 1 | a0001c0001t0082g0296 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.237-632A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871196 | ||||||
| chr18:47871252
|
G | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.237-688C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871252 | ||||||
| chr18:47871677
|
T | TC | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-1114dupG | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871677 | ||||||
| chr18:47871819
|
A | G | 1 | a0001c0001t0186g0024 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.237-1255T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871819 | ||||||
| chr18:47871834
|
C | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.237-1270G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871834 | ||||||
| chr18:47871841
|
T | C | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-1277A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871841 | ||||||
| chr18:47871863
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.237-1299T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871863 | ||||||
| chr18:47871888
|
C | CTGAGTT | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.237-1325_237-1324i others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871888 | ||||||
| chr18:47871937
|
A | C | 1 | a0001c0001t0174g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.237-1373T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871937 | ||||||
| chr18:47871955
|
C | T | 6 | a0001c0001t0009g0081a0001c0001t0009g0083a0001c0001t0009g0084others(3): Show | 6 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-1391G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47871955 | ||||||
| chr18:47872034
|
A | C | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.237-1470T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872034 | ||||||
| chr18:47872112
|
A | G | 2 | a0001c0001t0032g0003a0001c0001t0193g0032 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.237-1548T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872112 | ||||||
| chr18:47872195
|
C | T | 1 | a0001c0001t0217g0131 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.237-1631G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872195 | ||||||
| chr18:47872709
|
G | A | 2 | a0001c0001t0026g0110a0001c0001t0026g0111 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.237-2145C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872709 | ||||||
| chr18:47872724
|
C | G | 3 | a0001c0001t0167g0012a0001c0001t0168g0107a0001c0001t0187g0108 | 3 | HG02280.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.237-2160G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872724 | ||||||
| chr18:47872798
|
C | T | 4 | a0001c0001t0010g0124a0001c0001t0010g0145a0001c0001t0010g0162others(1): Show | 4 | NA18960.hp1 NA19004.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-2234G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872798 | ||||||
| chr18:47872888
|
A | G | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-2324T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872888 | ||||||
| chr18:47872985
|
C | T | 5 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0021g0056others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-2421G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47872985 | ||||||
| chr18:47873006
|
CGT | C | 39 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(36): Show | 39 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.237-2444_237-2443d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873006 | ||||||
| chr18:47873110
|
G | A | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-2546C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873110 | ||||||
| chr18:47873228
|
G | C | 1 | a0001c0001t0041g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.237-2664C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873228 | ||||||
| chr18:47873231
|
T | C | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-2667A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873231 | ||||||
| chr18:47873236
|
T | C | 1 | a0001c0001t0084g0270 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.237-2672A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873236 | ||||||
| chr18:47873523
|
C | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-2959G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873523 | ||||||
| chr18:47873613
|
C | T | 1 | a0001c0001t0050g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.237-3049G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873613 | ||||||
| chr18:47873974
|
A | G | 1 | a0001c0001t0162g0040 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.237-3410T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873974 | ||||||
| chr18:47873989
|
AC | A | 16 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0200g0175others(13): Show | 16 | HG00438.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.237-3426delG | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47873989 | ||||||
| chr18:47874224
|
A | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.237-3660T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874224 | ||||||
| chr18:47874803
|
T | C | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-4239A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874803 | ||||||
| chr18:47874868
|
A | G | 1 | a0001c0001t0180g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.237-4304T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874868 | ||||||
| chr18:47874876
|
T | C | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.237-4312A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874876 | ||||||
| chr18:47874908
|
GAAGA | G | 3 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0001t0244g0122 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.237-4348_237-4345d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874908 | ||||||
| chr18:47874915
|
A | T | 3 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0001t0244g0122 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.237-4351T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874915 | ||||||
| chr18:47874950
|
C | T | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.237-4386G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874950 | ||||||
| chr18:47874974
|
G | A | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.237-4410C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47874974 | ||||||
| chr18:47875125
|
T | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.237-4561A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47875125 | ||||||
| chr18:47875126
|
G | A | 1 | a0001c0001t0004g0150 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.237-4562C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47875126 | ||||||
| chr18:47875205
|
A | G | 1 | a0001c0001t0051g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.237-4641T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47875205 | ||||||
| chr18:47875254
|
A | C | 1 | a0001c0001t0015g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.237-4690T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47875254 | ||||||
| chr18:47875280
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.237-4716A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47875280 | ||||||
| chr18:47875308
|
G | A | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.237-4744C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47875308 | ||||||
| chr18:47875634
|
A | G | 1 | a0001c0001t0133g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.237-5070T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47875634 | ||||||
| chr18:47876084
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-5520C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47876084 | ||||||
| chr18:47876166
|
T | A | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.237-5602A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47876166 | ||||||
| chr18:47876185
|
T | C | 6 | a0001c0001t0009g0081a0001c0001t0009g0083a0001c0001t0009g0084others(3): Show | 6 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-5621A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47876185 | ||||||
| chr18:47876407
|
G | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.237-5843C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47876407 | ||||||
| chr18:47876473
|
G | C | 8 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0002g0055others(5): Show | 8 | HG00558.hp1 HG02074.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-5909C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47876473 | ||||||
| chr18:47876777
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.237-6213T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47876777 | ||||||
| chr18:47877112
|
T | C | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.237-6548A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877112 | ||||||
| chr18:47877161
|
A | AT | 53 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(50): Show | 53 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.237-6598dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877161 | ||||||
| chr18:47877161
|
AT | A | 10 | a0001c0001t0150g0066a0001c0001t0167g0012a0001c0001t0168g0107others(7): Show | 10 | HG02280.hp1 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-6598delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877161 | ||||||
| chr18:47877238
|
CACTCAGT others(1): Show |
C | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-6682_237-6675d others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877238 | ||||||
| chr18:47877243
|
A | G | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.237-6679T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877243 | ||||||
| chr18:47877342
|
G | T | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237-6778C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877342 | ||||||
| chr18:47877476
|
T | G | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.237-6912A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877476 | ||||||
| chr18:47877706
|
A | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-7142T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877706 | ||||||
| chr18:47877755
|
ATTT | A | 29 | a0001c0001t0011g0223a0001c0001t0011g0230a0001c0001t0016g0209others(26): Show | 29 | HG00558.hp2 HG02071.hp1 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.237-7194_237-7192d others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877755 | ||||||
| chr18:47877828
|
T | C | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-7264A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47877828 | ||||||
| chr18:47878232
|
T | A | 127 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.237-7668A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47878232 | ||||||
| chr18:47878495
|
T | C | 5 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0052g0277others(2): Show | 5 | NA18949.hp1 NA18971.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-7931A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47878495 | ||||||
| chr18:47878563
|
C | G | 131 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.237-7999G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47878563 | ||||||
| chr18:47878584
|
G | A | 1 | a0001c0001t0198g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.237-8020C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47878584 | ||||||
| chr18:47878676
|
T | C | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-8112A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47878676 | ||||||
| chr18:47878693
|
T | A | 2 | a0001c0001t0089g0228a0001c0001t0090g0248 | 2 | NA18950.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.237-8129A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47878693 | ||||||
| chr18:47878964
|
G | A | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.237-8400C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47878964 | ||||||
| chr18:47879189
|
C | T | 1 | a0001c0001t0123g0252 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.237-8625G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879189 | ||||||
| chr18:47879224
|
G | A | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.237-8660C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879224 | ||||||
| chr18:47879402
|
A | C | 1 | a0001c0001t0038g0031 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.237-8838T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879402 | ||||||
| chr18:47879495
|
C | CGT | 12 | a0001c0001t0009g0083a0001c0001t0025g0019a0001c0001t0025g0020others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.237-8933_237-8932d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGT | 8 | a0001c0001t0011g0223a0001c0001t0047g0222a0001c0001t0089g0228others(5): Show | 8 | HG02055.hp2 HG02129.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-8935_237-8932d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGT | 8 | a0001c0001t0011g0230a0001c0001t0050g0213a0001c0001t0104g0215others(5): Show | 8 | HG02071.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-8937_237-8932d others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(1): Show |
26 | a0001c0001t0001g0195a0001c0001t0001g0257a0001c0001t0004g0156others(23): Show | 26 | HG00642.hp1 HG01243.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.237-8939_237-8932d others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(3): Show |
33 | a0001c0001t0015g0218a0001c0001t0016g0209a0001c0001t0019g0187others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.237-8941_237-8932d others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(5): Show |
56 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0300others(53): Show | 56 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.237-8943_237-8932d others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(7): Show |
33 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0001t0001g0269others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.237-8945_237-8932d others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(9): Show |
21 | a0001c0001t0001g0263a0001c0001t0003g0146a0001c0001t0003g0149others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.237-8947_237-8932d others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(11): Show |
5 | a0001c0001t0052g0277a0001c0001t0130g0244a0001c0001t0212g0167others(2): Show | 5 | HG00735.hp2 HG03942.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-8949_237-8932d others(20): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(13): Show |
5 | a0001c0001t0010g0162a0001c0001t0029g0133a0001c0001t0215g0144others(2): Show | 5 | HG02071.hp2 HG04115.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-8951_237-8932d others(22): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(15): Show |
2 | a0001c0001t0010g0124a0001c0001t0235g0173 | 2 | NA19002.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.237-8953_237-8932d others(24): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
C | CGTGTGTG others(19): Show |
2 | a0001c0001t0029g0161a0001c0001t0233g0168 | 2 | NA19005.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.237-8957_237-8932d others(28): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
CGT | C | 9 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(6): Show | 9 | HG01109.hp2 HG02622.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.237-8933_237-8932d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879495
|
CGTGTGT | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-8937_237-8932d others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879495 | ||||||
| chr18:47879525
|
T | G | 1 | a0001c0001t0087g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.237-8961A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879525 | ||||||
| chr18:47879590
|
C | G | 2 | a0001c0001t0026g0110a0001c0001t0026g0111 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.237-9026G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879590 | ||||||
| chr18:47879664
|
T | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.237-9100A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879664 | ||||||
| chr18:47879688
|
C | T | 1 | a0001c0001t0097g0185 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.237-9124G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879688 | ||||||
| chr18:47879856
|
T | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-9292A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879856 | ||||||
| chr18:47879871
|
T | C | 131 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.237-9307A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879871 | ||||||
| chr18:47879886
|
T | C | 1 | a0001c0001t0017g0208 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.237-9322A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47879886 | ||||||
| chr18:47880030
|
T | A | 1 | a0001c0001t0117g0281 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.237-9466A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880030 | ||||||
| chr18:47880227
|
G | A | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.237-9663C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880227 | ||||||
| chr18:47880319
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-9755C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880319 | ||||||
| chr18:47880378
|
T | C | 183 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.237-9814A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880378 | ||||||
| chr18:47880595
|
A | C | 1 | a0001c0001t0166g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.237-10031T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880595 | ||||||
| chr18:47880703
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-10139A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880703 | ||||||
| chr18:47880824
|
TG | T | 3 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0001t0244g0122 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.237-10261delC | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880824 | ||||||
| chr18:47880881
|
G | C | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.237-10317C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880881 | ||||||
| chr18:47880904
|
G | C | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237-10340C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880904 | ||||||
| chr18:47880988
|
C | T | 1 | a0001c0002t0247g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.237-10424G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47880988 | ||||||
| chr18:47881041
|
T | A | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.237-10477A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881041 | ||||||
| chr18:47881060
|
T | C | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.237-10496A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881060 | ||||||
| chr18:47881090
|
ATTCGCCT others(2): Show |
A | 194 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.237-10535_237-1052 others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881090 | ||||||
| chr18:47881128
|
C | T | 4 | a0001c0001t0048g0182a0001c0001t0049g0186a0001c0001t0097g0185others(1): Show | 4 | NA18944.hp1 NA18959.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-10564G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881128 | ||||||
| chr18:47881148
|
T | G | 3 | a0001c0001t0080g0287a0001c0001t0092g0284a0001c0001t0117g0281 | 3 | HG00099.hp2 HG00140.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.237-10584A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881148 | ||||||
| chr18:47881242
|
G | A | 1 | a0001c0001t0088g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.237-10678C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881242 | ||||||
| chr18:47881258
|
T | A | 1 | a0001c0001t0188g0075 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.237-10694A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881258 | ||||||
| chr18:47881303
|
C | G | 1 | a0001c0001t0186g0024 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.237-10739G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881303 | ||||||
| chr18:47881545
|
T | C | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237-10981A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881545 | ||||||
| chr18:47881579
|
T | C | 1 | a0001c0001t0175g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.237-11015A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881579 | ||||||
| chr18:47881629
|
T | C | 3 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096 | 3 | HG02055.hp2 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.237-11065A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881629 | ||||||
| chr18:47881743
|
A | G | 1 | a0001c0001t0216g0157 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.237-11179T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881743 | ||||||
| chr18:47881784
|
A | C | 8 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(5): Show | 8 | HG01109.hp2 HG02622.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-11220T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881784 | ||||||
| chr18:47881847
|
G | C | 1 | a0001c0001t0001g0301 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.237-11283C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881847 | ||||||
| chr18:47881904
|
G | T | 3 | a0001c0002t0252g0017a0001c0002t0253g0015a0001c0002t0254g0016 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.237-11340C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881904 | ||||||
| chr18:47881929
|
G | A | 202 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.237-11365C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47881929 | ||||||
| chr18:47882041
|
C | CT | 62 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.237-11478dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTT | 10 | a0001c0001t0009g0081a0001c0001t0009g0084a0001c0001t0023g0092others(7): Show | 10 | HG00609.hp2 HG00735.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.237-11479_237-1147 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTT | 6 | a0001c0001t0001g0266a0001c0001t0013g0177a0001c0001t0071g0273others(3): Show | 6 | HG01256.hp1 HG01496.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-11482_237-1147 others(9): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0198a0001c0001t0018g0207a0001c0001t0089g0228others(3): Show | 6 | HG00423.hp2 HG03927.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-11485_237-1147 others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0016g0209a0001c0001t0111g0205a0001c0001t0124g0201others(5): Show | 8 | HG02055.hp2 HG02293.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-11486_237-1147 others(13): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0205g0120a0001c0002t0248g0303a0001c0002t0249g0306 | 3 | HG02572.hp1 HG02896.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.237-11487_237-1147 others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0078g0272others(2): Show | 5 | HG02976.hp1 HG03453.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-11488_237-1147 others(15): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(5): Show |
10 | a0001c0001t0001g0206a0001c0001t0017g0265a0001c0001t0052g0277others(7): Show | 10 | HG01891.hp2 HG02145.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.237-11489_237-1147 others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0057g0246a0001c0001t0058g0240a0001c0001t0094g0004others(1): Show | 4 | HG03927.hp2 NA18944.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-11490_237-1147 others(17): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0056g0242a0001c0001t0122g0251 | 2 | NA19088.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.237-11491_237-1147 others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0300a0001c0001t0005g0278a0001c0001t0005g0282others(3): Show | 6 | HG02523.hp1 HG03688.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.237-11492_237-1147 others(19): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(9): Show |
8 | a0001c0001t0001g0267a0001c0001t0005g0260a0001c0001t0006g0219others(5): Show | 8 | HG00558.hp2 HG01243.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-11493_237-1147 others(20): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(10): Show |
6 | a0001c0001t0020g0191a0001c0001t0095g0176a0001c0001t0104g0215others(3): Show | 6 | HG02615.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.237-11494_237-1147 others(21): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0091g0210a0001c0001t0093g0235a0001c0001t0107g0236 | 3 | HG00642.hp1 NA19240.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.237-11495_237-1147 others(22): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0015g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.237-11496_237-1147 others(23): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0072g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.237-11497_237-1147 others(24): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(15): Show |
3 | a0001c0001t0018g0204a0001c0001t0096g0229a0001c0001t0109g0226 | 3 | HG02965.hp2 NA18962.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.237-11499_237-1147 others(26): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(16): Show |
5 | a0001c0001t0015g0218a0001c0001t0077g0253a0001c0001t0106g0225others(2): Show | 5 | HG00741.hp2 HG01256.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-11500_237-1147 others(27): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(20): Show |
5 | a0001c0001t0017g0208a0001c0001t0065g0197a0001c0001t0083g0178others(2): Show | 5 | HG00642.hp2 HG02602.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-11478_237-1147 others(31): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(21): Show |
4 | a0001c0001t0014g0115a0001c0001t0069g0298a0001c0001t0073g0293others(1): Show | 4 | HG02074.hp1 HG04115.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-11478_237-1147 others(32): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(22): Show |
2 | a0001c0001t0043g0255a0001c0001t0075g0288 | 2 | HG01074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.237-11478_237-1147 others(33): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(23): Show |
3 | a0001c0001t0014g0276a0001c0001t0081g0291a0001c0001t0125g0283 | 3 | HG01081.hp1 HG02132.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.237-11478_237-1147 others(34): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0102g0193 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.237-11478_237-1147 others(35): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.237-11478_237-1147 others(36): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(26): Show |
3 | a0001c0001t0011g0223a0001c0001t0042g0254a0001c0001t0100g0299 | 3 | HG02015.hp1 HG02129.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.237-11478_237-1147 others(37): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.237-11478_237-1147 others(38): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(28): Show |
2 | a0001c0001t0011g0230a0001c0001t0050g0213 | 2 | HG02071.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.237-11478_237-1147 others(39): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(29): Show |
3 | a0001c0001t0047g0222a0001c0001t0099g0221a0001c0001t0130g0244 | 3 | HG00735.hp2 HG02135.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.237-11478_237-1147 others(40): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(31): Show |
1 | a0001c0001t0001g0301 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.237-11478_237-1147 others(42): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(34): Show |
2 | a0001c0001t0082g0296a0001c0001t0116g0245 | 2 | HG00438.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.237-11478_237-1147 others(45): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
C | CTTTTTTT others(37): Show |
1 | a0001c0001t0051g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.237-11478_237-1147 others(48): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
CT | C | 16 | a0001c0001t0019g0183a0001c0001t0019g0187a0001c0001t0032g0003others(13): Show | 16 | HG00323.hp2 HG01884.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.237-11478delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
CTTTTTT | C | 50 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(47): Show | 50 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.237-11483_237-1147 others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882041
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0257a0001c0001t0061g0268 | 2 | HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.237-11487_237-1147 others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882041 | ||||||
| chr18:47882143
|
C | T | 2 | a0001c0001t0012g0239a0001c0001t0012g0243 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.237-11579G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882143 | ||||||
| chr18:47882166
|
A | G | 1 | a0001c0001t0041g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.237-11602T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882166 | ||||||
| chr18:47882207
|
G | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-11643C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882207 | ||||||
| chr18:47882351
|
T | A | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.237-11787A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882351 | ||||||
| chr18:47882443
|
T | C | 1 | a0001c0001t0128g0114 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.237-11879A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882443 | ||||||
| chr18:47882488
|
C | T | 2 | a0001c0001t0104g0215a0001c0001t0105g0302 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.237-11924G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882488 | ||||||
| chr18:47882531
|
C | G | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.237-11967G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882531 | ||||||
| chr18:47882698
|
A | C | 1 | a0001c0001t0087g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.237-12134T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882698 | ||||||
| chr18:47882701
|
T | C | 2 | a0001c0001t0183g0023a0001c0001t0185g0025 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.237-12137A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47882701 | ||||||
| chr18:47883024
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.237-12460C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883024 | ||||||
| chr18:47883104
|
T | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.237-12540A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883104 | ||||||
| chr18:47883198
|
T | C | 1 | a0001c0001t0257g0309 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.237-12634A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883198 | ||||||
| chr18:47883484
|
T | C | 1 | a0001c0001t0084g0270 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.237-12920A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883484 | ||||||
| chr18:47883489
|
C | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.237-12925G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883489 | ||||||
| chr18:47883558
|
C | T | 1 | a0001c0001t0095g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236+12963G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883558 | ||||||
| chr18:47883580
|
G | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+12941C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883580 | ||||||
| chr18:47883598
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+12923T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883598 | ||||||
| chr18:47883776
|
C | T | 194 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.236+12745G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883776 | ||||||
| chr18:47883901
|
C | A | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+12620G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883901 | ||||||
| chr18:47883926
|
G | A | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+12595C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47883926 | ||||||
| chr18:47884102
|
G | T | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+12419C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47884102 | ||||||
| chr18:47884126
|
T | C | 3 | a0001c0001t0167g0012a0001c0001t0168g0107a0001c0001t0187g0108 | 3 | HG02280.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.236+12395A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47884126 | ||||||
| chr18:47884183
|
T | C | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+12338A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47884183 | ||||||
| chr18:47884192
|
G | A | 202 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.236+12329C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47884192 | ||||||
| chr18:47884371
|
G | A | 131 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.236+12150C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47884371 | ||||||
| chr18:47884797
|
T | C | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.236+11724A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47884797 | ||||||
| chr18:47884850
|
C | T | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.236+11671G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47884850 | ||||||
| chr18:47885109
|
T | C | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+11412A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885109 | ||||||
| chr18:47885128
|
C | CAT | 8 | a0001c0001t0022g0001a0001c0001t0133g0095a0001c0001t0145g0068others(5): Show | 9 | HG01071.hp1 HG01106.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.236+11391_236+1139 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885128 | ||||||
| chr18:47885130
|
TATACACA others(5): Show |
T | 3 | a0001c0001t0001g0257a0001c0001t0061g0268a0001c0001t0255g0096 | 3 | HG02895.hp2 HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.236+11379_236+1139 others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885130 | ||||||
| chr18:47885130
|
TATACACA others(7): Show |
T | 2 | a0001c0001t0054g0274a0001c0001t0055g0275 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.236+11377_236+1139 others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885130 | ||||||
| chr18:47885132
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.236+11389A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TAC | T | 42 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0007g0097others(39): Show | 42 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.236+11387_236+1138 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACAC | T | 28 | a0001c0001t0002g0113a0001c0001t0003g0170a0001c0001t0004g0130others(25): Show | 28 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.236+11385_236+1138 others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACAC | T | 47 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(44): Show | 47 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.236+11383_236+1138 others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACACA others(1): Show |
T | 14 | a0001c0001t0006g0224a0001c0001t0013g0286a0001c0001t0020g0191others(11): Show | 14 | HG00642.hp1 HG02015.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.236+11381_236+1138 others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACACA others(3): Show |
T | 38 | a0001c0001t0001g0206a0001c0001t0001g0266a0001c0001t0001g0267others(35): Show | 38 | HG00140.hp1 HG00642.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.236+11379_236+1138 others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACACA others(5): Show |
T | 66 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0005g0260others(63): Show | 66 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.236+11377_236+1138 others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACACA others(7): Show |
T | 12 | a0001c0001t0027g0148a0001c0001t0173g0033a0001c0001t0194g0010others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+11375_236+1138 others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACACA others(9): Show |
T | 14 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0300others(11): Show | 14 | HG00438.hp2 HG02074.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+11373_236+1138 others(20): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0127g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.236+11367_236+1138 others(26): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885132
|
TACACACA others(17): Show |
T | 1 | a0001c0001t0015g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.236+11365_236+1138 others(28): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885132 | ||||||
| chr18:47885134
|
C | T | 15 | a0001c0001t0002g0055a0001c0001t0002g0058a0001c0001t0002g0059others(12): Show | 15 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.236+11387G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885134 | ||||||
| chr18:47885136
|
C | T | 38 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0007g0097others(35): Show | 38 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.236+11385G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885136 | ||||||
| chr18:47885138
|
C | T | 18 | a0001c0001t0002g0113a0001c0001t0009g0083a0001c0001t0024g0069others(15): Show | 18 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.236+11383G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885138 | ||||||
| chr18:47885140
|
C | T | 17 | a0001c0001t0006g0219a0001c0001t0006g0237a0001c0001t0032g0003others(14): Show | 17 | HG00558.hp2 HG01243.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.236+11381G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885140 | ||||||
| chr18:47885142
|
C | T | 8 | a0001c0001t0006g0224a0001c0001t0020g0191a0001c0001t0020g0192others(5): Show | 8 | HG00642.hp1 HG02615.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+11379G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885142 | ||||||
| chr18:47885144
|
C | T | 27 | a0001c0001t0001g0206a0001c0001t0011g0223a0001c0001t0011g0230others(24): Show | 27 | HG01168.hp1 HG02071.hp1 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.236+11377G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885144 | ||||||
| chr18:47885146
|
C | T | 17 | a0001c0001t0018g0207a0001c0001t0019g0183a0001c0001t0019g0187others(14): Show | 17 | HG00423.hp2 HG02040.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.236+11375G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885146 | ||||||
| chr18:47885148
|
C | T | 7 | a0001c0001t0173g0033a0001c0001t0194g0010a0001c0001t0243g0011others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+11373G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885148 | ||||||
| chr18:47885150
|
C | T | 3 | a0001c0001t0164g0009a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 NA18972.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.236+11371G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885150 | ||||||
| chr18:47885158
|
C | T | 1 | a0001c0001t0015g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.236+11363G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885158 | ||||||
| chr18:47885170
|
CACACACA others(7): Show |
C | 4 | a0001c0001t0062g0234a0001c0001t0063g0249a0001c0001t0079g0247others(1): Show | 4 | NA18950.hp2 NA18979.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+11337_236+1135 others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885170 | ||||||
| chr18:47885176
|
C | T | 20 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0200g0175others(17): Show | 20 | HG00438.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.236+11345G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885176 | ||||||
| chr18:47885184
|
T | C | 6 | a0001c0001t0133g0095a0001c0001t0167g0012a0001c0001t0168g0107others(3): Show | 6 | HG02280.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+11337A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885184 | ||||||
| chr18:47885188
|
C | A | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.236+11333G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885188 | ||||||
| chr18:47885197
|
C | A | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+11324G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885197 | ||||||
| chr18:47885200
|
A | T | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+11321T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885200 | ||||||
| chr18:47885217
|
C | T | 3 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0001t0244g0122 | 3 | HG00438.hp2 HG02055.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.236+11304G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885217 | ||||||
| chr18:47885369
|
T | C | 1 | a0001c0001t0096g0229 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.236+11152A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885369 | ||||||
| chr18:47885383
|
G | A | 3 | a0001c0001t0149g0042a0001c0001t0158g0064a0001c0001t0159g0065 | 3 | HG01884.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.236+11138C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885383 | ||||||
| chr18:47885388
|
G | A | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+11133C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885388 | ||||||
| chr18:47885700
|
G | A | 131 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.236+10821C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885700 | ||||||
| chr18:47885880
|
G | A | 1 | a0001c0001t0075g0288 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.236+10641C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47885880 | ||||||
| chr18:47886342
|
A | G | 1 | a0001c0001t0190g0021 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.236+10179T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886342 | ||||||
| chr18:47886561
|
A | G | 3 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0202g0220 | 3 | HG01993.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.236+9960T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886561 | ||||||
| chr18:47886562
|
T | TATCTATC others(1): Show |
9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+9951_236+9958d others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886562 | ||||||
| chr18:47886570
|
C | CATCT | 119 | a0001c0001t0001g0206a0001c0001t0002g0046a0001c0001t0002g0049others(116): Show | 120 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.236+9947_236+9950d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886570 | ||||||
| chr18:47886570
|
C | CATCTATC others(1): Show |
19 | a0001c0001t0015g0216a0001c0001t0026g0110a0001c0001t0026g0111others(16): Show | 19 | HG00642.hp1 HG01109.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.236+9943_236+9950d others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886570 | ||||||
| chr18:47886570
|
C | CATCTATC others(5): Show |
4 | a0001c0001t0002g0052a0001c0001t0003g0146a0001c0001t0021g0056others(1): Show | 4 | HG02293.hp2 HG06807.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+9939_236+9950d others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886570 | ||||||
| chr18:47886570
|
CATCT | C | 78 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0263others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.236+9947_236+9950d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886570 | ||||||
| chr18:47886570
|
CATCTATC others(1): Show |
C | 13 | a0001c0001t0043g0255a0001c0001t0087g0214a0001c0001t0148g0109others(10): Show | 13 | HG00558.hp2 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.236+9943_236+9950d others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886570 | ||||||
| chr18:47886570
|
CATCTATC others(5): Show |
C | 10 | a0001c0001t0200g0175a0001c0001t0201g0174a0001c0002t0247g0014others(7): Show | 10 | HG00438.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.236+9939_236+9950d others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886570 | ||||||
| chr18:47886570
|
CATCTATC others(9): Show |
C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+9935_236+9950d others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886570 | ||||||
| chr18:47886582
|
T | C | 1 | a0001c0001t0196g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.236+9939A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886582 | ||||||
| chr18:47886725
|
T | A | 1 | a0001c0001t0150g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.236+9796A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886725 | ||||||
| chr18:47886756
|
G | A | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+9765C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886756 | ||||||
| chr18:47886923
|
C | CA | 130 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.236+9597dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886923 | ||||||
| chr18:47886923
|
C | CAA | 12 | a0001c0001t0013g0177a0001c0001t0013g0286a0001c0001t0064g0285others(9): Show | 12 | HG01891.hp2 HG01981.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+9596_236+9597d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886923 | ||||||
| chr18:47886923
|
CA | C | 6 | a0001c0001t0032g0003a0001c0001t0134g0041a0001c0001t0170g0087others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.236+9597delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886923 | ||||||
| chr18:47886967
|
T | C | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.236+9554A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886967 | ||||||
| chr18:47886987
|
C | A | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.236+9534G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47886987 | ||||||
| chr18:47887182
|
A | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.236+9339T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47887182 | ||||||
| chr18:47887343
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0034g0258a0001c0001t0071g0273 | 3 | HG01978.hp1 HG02273.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.236+9178G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47887343 | ||||||
| chr18:47887478
|
ACT | A | 11 | a0001c0001t0211g0008a0001c0001t0245g0007a0001c0001t0255g0096others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.236+9041_236+9042d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47887478 | ||||||
| chr18:47887646
|
T | C | 2 | a0001c0001t0032g0003a0001c0001t0193g0032 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.236+8875A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47887646 | ||||||
| chr18:47887782
|
A | C | 1 | a0001c0001t0126g0279 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.236+8739T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47887782 | ||||||
| chr18:47887975
|
G | A | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.236+8546C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47887975 | ||||||
| chr18:47888199
|
A | G | 2 | a0001c0001t0219g0139a0001c0001t0228g0158 | 2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.236+8322T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47888199 | ||||||
| chr18:47888214
|
G | T | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.236+8307C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47888214 | ||||||
| chr18:47888241
|
A | T | 14 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0035g0028others(11): Show | 14 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.236+8280T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47888241 | ||||||
| chr18:47888486
|
T | A | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.236+8035A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47888486 | ||||||
| chr18:47888550
|
G | A | 191 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.236+7971C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47888550 | ||||||
| chr18:47889035
|
C | A | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.236+7486G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889035 | ||||||
| chr18:47889143
|
G | C | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+7378C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889143 | ||||||
| chr18:47889170
|
G | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+7351C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889170 | ||||||
| chr18:47889243
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+7278A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889243 | ||||||
| chr18:47889312
|
C | A | 1 | a0001c0001t0160g0086 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.236+7209G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889312 | ||||||
| chr18:47889383
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+7138A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889383 | ||||||
| chr18:47889547
|
G | A | 1 | a0001c0001t0151g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.236+6974C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889547 | ||||||
| chr18:47889598
|
C | A | 2 | a0001c0001t0012g0239a0001c0001t0012g0243 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.236+6923G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889598 | ||||||
| chr18:47889669
|
G | A | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.236+6852C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889669 | ||||||
| chr18:47889727
|
C | T | 3 | a0001c0002t0252g0017a0001c0002t0253g0015a0001c0002t0254g0016 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.236+6794G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889727 | ||||||
| chr18:47889920
|
G | C | 2 | a0001c0001t0169g0089a0001c0001t0170g0087 | 2 | NA18959.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.236+6601C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47889920 | ||||||
| chr18:47890142
|
C | A | 1 | a0001c0001t0233g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.236+6379G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890142 | ||||||
| chr18:47890190
|
C | T | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+6331G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890190 | ||||||
| chr18:47890357
|
A | G | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+6164T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890357 | ||||||
| chr18:47890432
|
C | A | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+6089G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890432 | ||||||
| chr18:47890513
|
C | G | 54 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(51): Show | 55 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.236+6008G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890513 | ||||||
| chr18:47890516
|
A | G | 1 | a0001c0001t0138g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.236+6005T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890516 | ||||||
| chr18:47890570
|
A | C | 2 | a0001c0001t0032g0003a0001c0001t0193g0032 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.236+5951T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890570 | ||||||
| chr18:47890789
|
A | G | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.236+5732T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890789 | ||||||
| chr18:47890860
|
A | G | 1 | a0001c0001t0228g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.236+5661T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890860 | ||||||
| chr18:47890935
|
G | A | 3 | a0001c0001t0183g0023a0001c0001t0184g0035a0001c0001t0185g0025 | 3 | HG02572.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.236+5586C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890935 | ||||||
| chr18:47890992
|
T | C | 183 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.236+5529A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47890992 | ||||||
| chr18:47891001
|
T | C | 1 | a0001c0001t0042g0254 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.236+5520A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891001 | ||||||
| chr18:47891138
|
C | T | 2 | a0001c0001t0015g0218a0001c0001t0091g0210 | 2 | HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.236+5383G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891138 | ||||||
| chr18:47891158
|
A | T | 9 | a0001c0001t0013g0177a0001c0001t0013g0286a0001c0001t0051g0290others(6): Show | 9 | HG01981.hp2 HG02132.hp2 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+5363T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891158 | ||||||
| chr18:47891187
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.236+5334G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891187 | ||||||
| chr18:47891422
|
T | C | 211 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.236+5099A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891422 | ||||||
| chr18:47891470
|
T | C | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+5051A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891470 | ||||||
| chr18:47891475
|
G | T | 1 | a0001c0001t0124g0201 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.236+5046C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891475 | ||||||
| chr18:47891517
|
C | CT | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.236+5003dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891517 | ||||||
| chr18:47891754
|
T | C | 1 | a0001c0001t0147g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.236+4767A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891754 | ||||||
| chr18:47891818
|
AAT | A | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+4701_236+4702d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891818 | ||||||
| chr18:47891945
|
T | G | 4 | a0001c0001t0056g0242a0001c0001t0057g0246a0001c0001t0058g0240others(1): Show | 4 | NA18944.hp2 NA18973.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+4576A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47891945 | ||||||
| chr18:47892013
|
T | C | 1 | a0001c0001t0127g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.236+4508A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892013 | ||||||
| chr18:47892195
|
G | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+4326C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892195 | ||||||
| chr18:47892198
|
A | AT | 11 | a0001c0001t0008g0061a0001c0001t0008g0062a0001c0001t0025g0020others(8): Show | 11 | HG00544.hp2 HG01071.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.236+4322dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892198 | ||||||
| chr18:47892198
|
AT | A | 201 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.236+4322delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892198 | ||||||
| chr18:47892209
|
T | C | 181 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.236+4312A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892209 | ||||||
| chr18:47892425
|
C | A | 15 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0035g0028others(12): Show | 15 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.236+4096G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892425 | ||||||
| chr18:47892586
|
A | T | 1 | a0001c0001t0084g0270 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.236+3935T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892586 | ||||||
| chr18:47892655
|
TAAA | T | 181 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.236+3863_236+3865d others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892655 | ||||||
| chr18:47892901
|
A | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.236+3620T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892901 | ||||||
| chr18:47892919
|
T | C | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+3602A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892919 | ||||||
| chr18:47892950
|
A | G | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+3571T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47892950 | ||||||
| chr18:47893050
|
T | C | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.236+3471A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893050 | ||||||
| chr18:47893091
|
G | A | 1 | a0001c0001t0063g0249 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.236+3430C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893091 | ||||||
| chr18:47893231
|
G | C | 3 | a0001c0001t0014g0115a0001c0001t0077g0253a0001c0001t0086g0116 | 3 | HG00642.hp2 HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.236+3290C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893231 | ||||||
| chr18:47893359
|
G | A | 1 | a0001c0001t0065g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.236+3162C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893359 | ||||||
| chr18:47893538
|
C | T | 1 | a0001c0001t0050g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.236+2983G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893538 | ||||||
| chr18:47893841
|
T | C | 2 | a0001c0001t0219g0139a0001c0001t0228g0158 | 2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.236+2680A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893841 | ||||||
| chr18:47893863
|
C | T | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+2658G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893863 | ||||||
| chr18:47893898
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.236+2623G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47893898 | ||||||
| chr18:47894326
|
G | A | 1 | a0001c0001t0069g0298 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.236+2195C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894326 | ||||||
| chr18:47894369
|
C | T | 2 | a0001c0001t0158g0064a0001c0001t0159g0065 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.236+2152G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894369 | ||||||
| chr18:47894475
|
C | T | 1 | a0001c0001t0177g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.236+2046G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894475 | ||||||
| chr18:47894553
|
C | G | 1 | a0001c0001t0040g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.236+1968G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894553 | ||||||
| chr18:47894554
|
A | G | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.236+1967T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894554 | ||||||
| chr18:47894607
|
G | C | 2 | a0001c0001t0016g0112a0001c0001t0128g0114 | 2 | NA18973.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.236+1914C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894607 | ||||||
| chr18:47894699
|
T | C | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.236+1822A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894699 | ||||||
| chr18:47894842
|
T | C | 306 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(303): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.236+1679A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47894842 | ||||||
| chr18:47895247
|
T | A | 195 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.236+1274A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47895247 | ||||||
| chr18:47895430
|
T | C | 1 | a0001c0001t0051g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.236+1091A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47895430 | ||||||
| chr18:47895469
|
C | T | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.236+1052G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47895469 | ||||||
| chr18:47895528
|
T | C | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.236+993A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47895528 | ||||||
| chr18:47895707
|
C | T | 1 | a0001c0001t0017g0265 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.236+814G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47895707 | ||||||
| chr18:47895728
|
C | T | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.236+793G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47895728 | ||||||
| chr18:47895809
|
C | T | 2 | a0001c0001t0014g0276a0001c0001t0077g0253 | 2 | HG01081.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.236+712G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47895809 | ||||||
| chr18:47896004
|
G | C | 2 | a0001c0001t0015g0218a0001c0001t0091g0210 | 2 | HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.236+517C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47896004 | ||||||
| chr18:47896034
|
A | G | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.236+487T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47896034 | ||||||
| chr18:47896231
|
C | A | 1 | a0001c0001t0141g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.236+290G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 2/10 | chr18 | 47896231 | ||||||
| chr18:47896956
|
T | C | 44 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(41): Show | 44 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-53-147A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47896956 | ||||||
| chr18:47897115
|
A | G | 2 | a0001c0001t0200g0175a0001c0001t0201g0174 | 2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-53-306T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897115 | ||||||
| chr18:47897249
|
C | G | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-53-440G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897249 | ||||||
| chr18:47897337
|
G | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-53-528C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897337 | ||||||
| chr18:47897386
|
CAT | C | 186 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-53-579_-53-578del others(2): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897386 | ||||||
| chr18:47897387
|
A | AT | 84 | a0001c0001t0002g0046a0001c0001t0002g0049a0001c0001t0002g0052others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-53-579dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897387 | ||||||
| chr18:47897490
|
A | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-53-681T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897490 | ||||||
| chr18:47897756
|
T | A | 1 | a0001c0001t0003g0140 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-53-947A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897756 | ||||||
| chr18:47897833
|
G | A | 124 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-53-1024C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897833 | ||||||
| chr18:47897988
|
T | C | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-53-1179A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47897988 | ||||||
| chr18:47898087
|
G | A | 1 | a0001c0002t0252g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-53-1278C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898087 | ||||||
| chr18:47898300
|
C | T | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-53-1491G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898300 | ||||||
| chr18:47898532
|
T | TC | 4 | a0001c0001t0148g0109a0001c0001t0167g0012a0001c0001t0168g0107others(1): Show | 4 | HG02280.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-1724dupG | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898532 | ||||||
| chr18:47898568
|
A | G | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-53-1759T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898568 | ||||||
| chr18:47898581
|
T | C | 2 | a0001c0001t0028g0164a0001c0001t0224g0141 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-53-1772A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898581 | ||||||
| chr18:47898631
|
T | C | 1 | a0001c0001t0105g0302 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-53-1822A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898631 | ||||||
| chr18:47898661
|
A | AT | 211 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-53-1853dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898661 | ||||||
| chr18:47898785
|
C | T | 1 | a0001c0001t0237g0143 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53-1976G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898785 | ||||||
| chr18:47898807
|
C | T | 9 | a0001c0001t0044g0256a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG00323.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-1998G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898807 | ||||||
| chr18:47898887
|
A | AT | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-53-2079dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898887 | ||||||
| chr18:47898994
|
C | A | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-53-2185G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47898994 | ||||||
| chr18:47899084
|
G | C | 2 | a0001c0001t0150g0066a0001c0001t0180g0067 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-53-2275C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899084 | ||||||
| chr18:47899107
|
C | A | 201 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-53-2298G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899107 | ||||||
| chr18:47899226
|
A | G | 3 | a0001c0001t0156g0104a0001c0001t0163g0105a0001c0001t0178g0106 | 3 | HG00140.hp2 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-53-2417T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899226 | ||||||
| chr18:47899285
|
C | A | 201 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-53-2476G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899285 | ||||||
| chr18:47899300
|
G | C | 53 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(50): Show | 53 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.-53-2491C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899300 | ||||||
| chr18:47899386
|
C | T | 1 | a0001c0001t0239g0142 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-53-2577G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899386 | ||||||
| chr18:47899399
|
GA | G | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-53-2591delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899399 | ||||||
| chr18:47899596
|
C | T | 204 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.-53-2787G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899596 | ||||||
| chr18:47899647
|
C | T | 1 | a0001c0001t0122g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-53-2838G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899647 | ||||||
| chr18:47899783
|
C | A | 1 | a0001c0001t0005g0282 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-53-2974G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899783 | ||||||
| chr18:47899921
|
T | A | 1 | a0001c0001t0139g0051 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-53-3112A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899921 | ||||||
| chr18:47899924
|
T | C | 2 | a0001c0001t0057g0246a0001c0001t0059g0264 | 2 | NA18973.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-53-3115A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47899924 | ||||||
| chr18:47900120
|
T | C | 3 | a0001c0001t0183g0023a0001c0001t0184g0035a0001c0001t0185g0025 | 3 | HG02572.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-53-3311A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900120 | ||||||
| chr18:47900232
|
C | A | 2 | a0001c0002t0253g0015a0001c0002t0254g0016 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-53-3423G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900232 | ||||||
| chr18:47900250
|
T | A | 10 | a0001c0001t0019g0183a0001c0001t0019g0187a0001c0001t0048g0182others(7): Show | 10 | HG02040.hp2 NA18942.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.-53-3441A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900250 | ||||||
| chr18:47900264
|
C | T | 196 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.-53-3455G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900264 | ||||||
| chr18:47900394
|
T | G | 129 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-53-3585A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900394 | ||||||
| chr18:47900430
|
G | A | 1 | a0001c0001t0243g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-53-3621C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900430 | ||||||
| chr18:47900511
|
T | C | 1 | a0001c0001t0110g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-53-3702A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900511 | ||||||
| chr18:47900834
|
A | C | 210 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-53-4025T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900834 | ||||||
| chr18:47900972
|
T | C | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-53-4163A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47900972 | ||||||
| chr18:47901061
|
A | G | 210 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-53-4252T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901061 | ||||||
| chr18:47901129
|
T | G | 207 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.-53-4320A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901129 | ||||||
| chr18:47901150
|
T | C | 2 | a0001c0001t0026g0110a0001c0001t0026g0111 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-53-4341A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901150 | ||||||
| chr18:47901187
|
G | A | 1 | a0001c0001t0212g0167 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-53-4378C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901187 | ||||||
| chr18:47901208
|
TA | T | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53-4400delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901208 | ||||||
| chr18:47901235
|
C | T | 1 | a0001c0001t0185g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-53-4426G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901235 | ||||||
| chr18:47901556
|
T | A | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53-4747A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901556 | ||||||
| chr18:47901575
|
T | TAC | 207 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.-53-4768_-53-4767d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901575 | ||||||
| chr18:47901685
|
G | C | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-53-4876C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901685 | ||||||
| chr18:47901706
|
T | C | 1 | a0001c0001t0046g0196 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-53-4897A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901706 | ||||||
| chr18:47901762
|
G | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-53-4953C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901762 | ||||||
| chr18:47901893
|
C | T | 1 | a0001c0001t0114g0180 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-53-5084G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901893 | ||||||
| chr18:47901898
|
G | A | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-53-5089C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47901898 | ||||||
| chr18:47902096
|
T | A | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-5287A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902096 | ||||||
| chr18:47902199
|
T | C | 5 | a0001c0001t0024g0069a0001c0001t0024g0077a0001c0001t0181g0076others(2): Show | 5 | HG00099.hp1 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53-5390A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902199 | ||||||
| chr18:47902202
|
T | C | 1 | a0001c0001t0124g0201 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-53-5393A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902202 | ||||||
| chr18:47902298
|
G | A | 1 | a0001c0001t0127g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-53-5489C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902298 | ||||||
| chr18:47902393
|
C | T | 1 | a0001c0001t0234g0172 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-53-5584G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902393 | ||||||
| chr18:47902587
|
C | A | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-53-5778G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902587 | ||||||
| chr18:47902593
|
A | C | 1 | a0001c0001t0189g0018 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-53-5784T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902593 | ||||||
| chr18:47902595
|
G | T | 1 | a0001c0001t0014g0276 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-53-5786C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902595 | ||||||
| chr18:47902606
|
G | A | 205 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.-53-5797C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902606 | ||||||
| chr18:47902621
|
A | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-5812T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902621 | ||||||
| chr18:47902624
|
C | T | 224 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(221): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.-53-5815G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902624 | ||||||
| chr18:47902878
|
T | C | 7 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0183g0023others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53-6069A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902878 | ||||||
| chr18:47902887
|
G | A | 3 | a0001c0001t0203g0233a0001c0001t0204g0295a0001c0001t0210g0294 | 3 | HG01256.hp1 HG01258.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-53-6078C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47902887 | ||||||
| chr18:47903095
|
C | T | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-6286G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903095 | ||||||
| chr18:47903098
|
A | G | 1 | a0001c0001t0018g0204 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-53-6289T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903098 | ||||||
| chr18:47903451
|
C | T | 198 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.-53-6642G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903451 | ||||||
| chr18:47903644
|
T | G | 4 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174others(1): Show | 4 | HG00438.hp2 HG02055.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-6835A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903644 | ||||||
| chr18:47903759
|
C | A | 202 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-53-6950G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903759 | ||||||
| chr18:47903871
|
C | CAG | 60 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(57): Show | 60 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.-53-7064_-53-7063d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903871 | ||||||
| chr18:47903874
|
T | A | 68 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0300others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-53-7065A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903874 | ||||||
| chr18:47903875
|
G | T | 1 | a0001c0001t0056g0242 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-53-7066C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903875 | ||||||
| chr18:47903876
|
T | G | 61 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(58): Show | 61 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-53-7067A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903876 | ||||||
| chr18:47903876
|
T | TG | 109 | a0001c0001t0001g0263a0001c0001t0001g0300a0001c0001t0002g0049others(106): Show | 109 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-53-7068dupC | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903876 | ||||||
| chr18:47903876
|
T | TGG | 55 | a0001c0001t0002g0046a0001c0001t0002g0052a0001c0001t0002g0055others(52): Show | 55 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.-53-7069_-53-7068d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903876 | ||||||
| chr18:47903877
|
G | GT | 3 | a0001c0001t0151g0072a0001c0001t0196g0006a0001c0001t0197g0005 | 3 | HG02559.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-53-7069_-53-7068i others(3): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903877 | ||||||
| chr18:47903974
|
T | C | 2 | a0001c0001t0214g0123a0001c0001t0236g0159 | 2 | NA18974.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-53-7165A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47903974 | ||||||
| chr18:47904137
|
A | C | 1 | a0001c0001t0175g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-53-7328T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904137 | ||||||
| chr18:47904143
|
A | T | 1 | a0001c0001t0012g0239 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-53-7334T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904143 | ||||||
| chr18:47904211
|
G | A | 204 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.-53-7402C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904211 | ||||||
| chr18:47904265
|
C | T | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-53-7456G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904265 | ||||||
| chr18:47904340
|
T | G | 1 | a0001c0001t0078g0272 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-53-7531A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904340 | ||||||
| chr18:47904355
|
G | C | 9 | a0001c0001t0007g0097a0001c0001t0007g0101a0001c0001t0007g0102others(6): Show | 9 | HG00140.hp2 HG00735.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-7546C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904355 | ||||||
| chr18:47904466
|
G | A | 1 | a0001c0001t0007g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-53-7657C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904466 | ||||||
| chr18:47904478
|
G | A | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-53-7669C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904478 | ||||||
| chr18:47904521
|
G | C | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-7712C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904521 | ||||||
| chr18:47904586
|
C | T | 2 | a0001c0001t0131g0212a0001c0001t0132g0211 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-53-7777G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904586 | ||||||
| chr18:47904630
|
A | T | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-53-7821T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904630 | ||||||
| chr18:47904766
|
G | A | 1 | a0001c0001t0179g0070 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-53-7957C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904766 | ||||||
| chr18:47904791
|
G | A | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.-53-7982C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904791 | ||||||
| chr18:47904825
|
C | G | 1 | a0001c0001t0032g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-53-8016G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904825 | ||||||
| chr18:47904974
|
G | A | 1 | a0001c0001t0094g0004 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-53-8165C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47904974 | ||||||
| chr18:47905025
|
T | C | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-8216A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905025 | ||||||
| chr18:47905041
|
T | C | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-53-8232A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905041 | ||||||
| chr18:47905078
|
C | T | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-8269G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905078 | ||||||
| chr18:47905285
|
T | C | 3 | a0001c0001t0227g0166a0001c0001t0238g0165a0001c0001t0242g0160 | 3 | HG01261.hp2 HG02300.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-53-8476A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905285 | ||||||
| chr18:47905410
|
C | A | 207 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.-53-8601G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905410 | ||||||
| chr18:47905486
|
A | G | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-53-8677T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905486 | ||||||
| chr18:47905712
|
C | G | 2 | a0001c0001t0044g0256a0001c0001t0045g0250 | 2 | HG00323.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-53-8903G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905712 | ||||||
| chr18:47905872
|
G | A | 4 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174others(1): Show | 4 | HG00438.hp2 HG02055.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-9063C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905872 | ||||||
| chr18:47905924
|
C | T | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-53-9115G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905924 | ||||||
| chr18:47905983
|
G | A | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-9174C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47905983 | ||||||
| chr18:47906175
|
C | T | 2 | a0001c0001t0133g0095a0001c0001t0244g0122 | 2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-53-9366G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906175 | ||||||
| chr18:47906210
|
ACTT | A | 4 | a0001c0001t0054g0274a0001c0001t0055g0275a0001c0001t0158g0064others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-9404_-53-9402d others(5): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906210 | ||||||
| chr18:47906222
|
C | T | 202 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-53-9413G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906222 | ||||||
| chr18:47906309
|
C | T | 3 | a0001c0001t0002g0046a0001c0001t0211g0008a0001c0001t0245g0007 | 3 | HG02055.hp2 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-53-9500G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906309 | ||||||
| chr18:47906316
|
C | A | 6 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(3): Show | 6 | HG01109.hp2 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53-9507G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906316 | ||||||
| chr18:47906333
|
G | T | 1 | a0001c0001t0002g0046 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-53-9524C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906333 | ||||||
| chr18:47906364
|
C | T | 1 | a0001c0001t0075g0288 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-53-9555G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906364 | ||||||
| chr18:47906528
|
C | T | 1 | a0001c0001t0051g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-53-9719G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906528 | ||||||
| chr18:47906621
|
A | C | 1 | a0001c0001t0105g0302 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-53-9812T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906621 | ||||||
| chr18:47906624
|
G | A | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-53-9815C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906624 | ||||||
| chr18:47906711
|
G | A | 1 | a0001c0001t0150g0066 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-53-9902C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906711 | ||||||
| chr18:47906793
|
T | C | 212 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-53-9984A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906793 | ||||||
| chr18:47906887
|
G | C | 1 | a0001c0001t0143g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-53-10078C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47906887 | ||||||
| chr18:47907161
|
G | T | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-53-10352C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907161 | ||||||
| chr18:47907297
|
T | A | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.-53-10488A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907297 | ||||||
| chr18:47907624
|
G | A | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-10815C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907624 | ||||||
| chr18:47907665
|
G | A | 204 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.-53-10856C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907665 | ||||||
| chr18:47907723
|
A | G | 209 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-53-10914T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907723 | ||||||
| chr18:47907759
|
A | C | 208 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.-53-10950T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907759 | ||||||
| chr18:47907832
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-53-11023A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907832 | ||||||
| chr18:47907890
|
G | A | 1 | a0001c0001t0051g0290 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-53-11081C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47907890 | ||||||
| chr18:47908104
|
G | C | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-53-11295C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908104 | ||||||
| chr18:47908108
|
A | G | 4 | a0001c0001t0042g0254a0001c0001t0043g0255a0001c0001t0088g0232others(1): Show | 4 | HG02015.hp1 HG03834.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-11299T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908108 | ||||||
| chr18:47908169
|
G | A | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-53-11360C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908169 | ||||||
| chr18:47908292
|
A | C | 2 | a0001c0002t0253g0015a0001c0002t0254g0016 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-53-11483T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908292 | ||||||
| chr18:47908341
|
G | T | 227 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-53-11532C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908341 | ||||||
| chr18:47908452
|
A | G | 1 | a0001c0001t0180g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-53-11643T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908452 | ||||||
| chr18:47908499
|
A | C | 2 | a0001c0001t0131g0212a0001c0001t0132g0211 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-53-11690T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908499 | ||||||
| chr18:47908528
|
A | G | 1 | a0001c0001t0094g0004 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-53-11719T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908528 | ||||||
| chr18:47908604
|
T | C | 1 | a0001c0001t0014g0276 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-53-11795A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908604 | ||||||
| chr18:47908690
|
C | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-11881G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908690 | ||||||
| chr18:47908705
|
A | G | 3 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0140g0098 | 3 | HG01074.hp1 HG01975.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-53-11896T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908705 | ||||||
| chr18:47908761
|
A | G | 1 | a0001c0001t0193g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-53-11952T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908761 | ||||||
| chr18:47908831
|
C | G | 205 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.-53-12022G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47908831 | ||||||
| chr18:47909068
|
TA | T | 183 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-53-12260delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909068 | ||||||
| chr18:47909230
|
T | C | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-53-12421A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909230 | ||||||
| chr18:47909242
|
A | G | 1 | a0001c0001t0232g0129 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-53-12433T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909242 | ||||||
| chr18:47909263
|
T | C | 2 | a0001c0001t0010g0124a0001c0001t0010g0162 | 2 | NA19004.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-53-12454A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909263 | ||||||
| chr18:47909509
|
T | A | 1 | a0001c0001t0032g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-53-12700A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909509 | ||||||
| chr18:47909619
|
C | G | 202 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-53-12810G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909619 | ||||||
| chr18:47909792
|
T | C | 1 | a0001c0001t0088g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-53-12983A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909792 | ||||||
| chr18:47909855
|
C | T | 1 | a0001c0001t0195g0044 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-53-13046G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47909855 | ||||||
| chr18:47910171
|
GA | G | 189 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.-53-13363delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910171 | ||||||
| chr18:47910171
|
GAA | G | 14 | a0001c0001t0001g0300a0001c0001t0042g0254a0001c0001t0095g0176others(11): Show | 14 | HG00438.hp2 HG01891.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-53-13364_-53-1336 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910171 | ||||||
| chr18:47910231
|
T | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-13422A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910231 | ||||||
| chr18:47910281
|
TA | T | 3 | a0001c0001t0020g0191a0001c0001t0020g0192a0001c0001t0129g0190 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-53-13473delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910281 | ||||||
| chr18:47910318
|
T | G | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-53-13509A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910318 | ||||||
| chr18:47910321
|
GGAA | G | 4 | a0001c0001t0202g0220a0001c0001t0203g0233a0001c0001t0204g0295others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53-13515_-53-1351 others(7): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910321 | ||||||
| chr18:47910384
|
TA | T | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-53-13576delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910384 | ||||||
| chr18:47910663
|
G | C | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-13854C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910663 | ||||||
| chr18:47910708
|
T | C | 1 | a0001c0001t0073g0293 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-53-13899A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910708 | ||||||
| chr18:47910879
|
T | G | 2 | a0001c0001t0054g0274a0001c0001t0055g0275 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-53-14070A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910879 | ||||||
| chr18:47910906
|
C | A | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-53-14097G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47910906 | ||||||
| chr18:47911344
|
C | A | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-53-14535G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47911344 | ||||||
| chr18:47911351
|
G | GA | 9 | a0001c0001t0014g0115a0001c0001t0014g0276a0001c0001t0077g0253others(6): Show | 9 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53-14543dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47911351 | ||||||
| chr18:47911695
|
A | G | 214 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-53-14886T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47911695 | ||||||
| chr18:47912132
|
G | A | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-53-15323C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47912132 | ||||||
| chr18:47912674
|
T | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-53-15865A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47912674 | ||||||
| chr18:47912858
|
C | CA | 62 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(59): Show | 62 | HG00544.hp1 HG00609.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.-53-16050dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47912858 | ||||||
| chr18:47912858
|
C | CAA | 8 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0028g0164others(5): Show | 8 | HG02135.hp1 HG02148.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-16051_-53-1605 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47912858 | ||||||
| chr18:47912858
|
CA | C | 17 | a0001c0001t0006g0219a0001c0001t0012g0239a0001c0001t0077g0253others(14): Show | 17 | HG00558.hp2 HG00741.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-53-16050delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47912858 | ||||||
| chr18:47912858
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0205g0120others(5): Show | 8 | HG02717.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53-16057_-53-1605 others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47912858 | ||||||
| chr18:47913151
|
C | T | 1 | a0001c0002t0248g0303 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-53-16342G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913151 | ||||||
| chr18:47913173
|
G | A | 1 | a0001c0001t0095g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-53-16364C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913173 | ||||||
| chr18:47913291
|
A | G | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-53-16482T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913291 | ||||||
| chr18:47913373
|
A | G | 2 | a0001c0001t0122g0251a0001c0001t0123g0252 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-53-16564T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913373 | ||||||
| chr18:47913399
|
A | G | 1 | a0001c0001t0141g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-53-16590T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913399 | ||||||
| chr18:47913602
|
A | G | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-54+16759T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913602 | ||||||
| chr18:47913648
|
T | C | 1 | a0001c0001t0070g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-54+16713A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913648 | ||||||
| chr18:47913697
|
A | C | 2 | a0001c0001t0067g0280a0001c0001t0076g0289 | 2 | HG01069.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-54+16664T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913697 | ||||||
| chr18:47913748
|
T | C | 4 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174others(1): Show | 4 | HG00438.hp2 HG02055.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+16613A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913748 | ||||||
| chr18:47913809
|
T | TTCTCTAC others(9): Show |
1 | a0001c0001t0164g0009 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-54+16536_-54+1655 others(20): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913809 | ||||||
| chr18:47913845
|
T | C | 1 | a0001c0001t0125g0283 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-54+16516A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47913845 | ||||||
| chr18:47914002
|
A | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-54+16359T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914002 | ||||||
| chr18:47914080
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+16281A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914080 | ||||||
| chr18:47914126
|
C | A | 4 | a0001c0001t0063g0249a0001c0001t0079g0247a0001c0001t0090g0248others(1): Show | 4 | NA18950.hp1 NA18979.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+16235G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914126 | ||||||
| chr18:47914273
|
G | A | 197 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.-54+16088C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914273 | ||||||
| chr18:47914398
|
G | A | 2 | a0001c0001t0021g0056a0001c0001t0021g0057 | 2 | HG03490.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-54+15963C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914398 | ||||||
| chr18:47914673
|
C | CTAAA | 199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-54+15684_-54+1568 others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914673 | ||||||
| chr18:47914685
|
T | C | 1 | a0001c0001t0227g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-54+15676A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914685 | ||||||
| chr18:47914786
|
C | T | 1 | a0001c0001t0016g0112 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-54+15575G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914786 | ||||||
| chr18:47914925
|
C | T | 130 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-54+15436G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914925 | ||||||
| chr18:47914981
|
T | G | 130 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-54+15380A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47914981 | ||||||
| chr18:47915320
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+15041A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47915320 | ||||||
| chr18:47915717
|
A | G | 2 | a0001c0001t0146g0037a0001c0001t0147g0093 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-54+14644T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47915717 | ||||||
| chr18:47915758
|
C | A | 201 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-54+14603G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47915758 | ||||||
| chr18:47916072
|
C | T | 1 | a0001c0001t0191g0082 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-54+14289G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916072 | ||||||
| chr18:47916305
|
C | A | 127 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-54+14056G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916305 | ||||||
| chr18:47916306
|
C | T | 127 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-54+14055G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916306 | ||||||
| chr18:47916396
|
ATATT | A | 127 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-54+13961_-54+1396 others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916396 | ||||||
| chr18:47916410
|
ATTTTGTT others(3): Show |
A | 1 | a0001c0001t0175g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-54+13941_-54+1395 others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916410 | ||||||
| chr18:47916480
|
G | A | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+13881C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916480 | ||||||
| chr18:47916657
|
G | A | 3 | a0001c0002t0252g0017a0001c0002t0253g0015a0001c0002t0254g0016 | 3 | HG01891.hp2 HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-54+13704C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916657 | ||||||
| chr18:47916667
|
G | GTT | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+13693_-54+1369 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916667 | ||||||
| chr18:47916724
|
T | C | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-54+13637A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47916724 | ||||||
| chr18:47917110
|
T | A | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-54+13251A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917110 | ||||||
| chr18:47917261
|
G | A | 1 | a0001c0001t0161g0103 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-54+13100C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917261 | ||||||
| chr18:47917342
|
C | T | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+13019G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917342 | ||||||
| chr18:47917414
|
T | C | 188 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-54+12947A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917414 | ||||||
| chr18:47917414
|
T | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+12947A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917414 | ||||||
| chr18:47917644
|
A | G | 1 | a0001c0001t0065g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-54+12717T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917644 | ||||||
| chr18:47917651
|
G | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+12710C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917651 | ||||||
| chr18:47917727
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-54+12634C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917727 | ||||||
| chr18:47917897
|
G | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+12464C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917897 | ||||||
| chr18:47917959
|
C | G | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-54+12402G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917959 | ||||||
| chr18:47917973
|
C | T | 1 | a0001c0001t0126g0279 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-54+12388G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47917973 | ||||||
| chr18:47918080
|
A | G | 5 | a0001c0001t0024g0069a0001c0001t0024g0077a0001c0001t0181g0076others(2): Show | 5 | HG00099.hp1 HG01123.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+12281T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47918080 | ||||||
| chr18:47918147
|
G | A | 1 | a0001c0001t0178g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-54+12214C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47918147 | ||||||
| chr18:47918581
|
A | C | 1 | a0001c0001t0004g0125 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-54+11780T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47918581 | ||||||
| chr18:47918688
|
C | G | 1 | a0001c0001t0045g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-54+11673G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47918688 | ||||||
| chr18:47918737
|
G | GCTTGATA others(3): Show |
199 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-54+11623_-54+1162 others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47918737 | ||||||
| chr18:47918914
|
G | A | 1 | a0001c0001t0053g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-54+11447C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47918914 | ||||||
| chr18:47919143
|
G | T | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54+11218C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919143 | ||||||
| chr18:47919168
|
G | A | 71 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0257others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-54+11193C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919168 | ||||||
| chr18:47919169
|
C | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+11192G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919169 | ||||||
| chr18:47919439
|
CAG | C | 75 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0257others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.-54+10920_-54+1092 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919439 | ||||||
| chr18:47919466
|
AAATACAC others(4): Show |
A | 7 | a0001c0001t0057g0246a0001c0001t0063g0249a0001c0001t0079g0247others(4): Show | 7 | HG02145.hp2 NA18950.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54+10884_-54+1089 others(15): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919466 | ||||||
| chr18:47919466
|
AAATACAC others(8): Show |
A | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+10880_-54+1089 others(19): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919466 | ||||||
| chr18:47919466
|
AAATACAC others(10): Show |
A | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+10878_-54+1089 others(21): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919466 | ||||||
| chr18:47919469
|
T | TAC | 3 | a0001c0001t0038g0031a0001c0001t0205g0120a0001c0001t0209g0121 | 3 | HG02896.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-54+10890_-54+1089 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
T | TACAC | 3 | a0001c0001t0036g0030a0001c0001t0040g0029a0001c0001t0193g0032 | 3 | HG01109.hp2 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-54+10888_-54+1089 others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TAC | T | 6 | a0001c0001t0039g0027a0001c0001t0151g0072a0001c0001t0172g0074others(3): Show | 6 | HG01071.hp1 HG01123.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54+10890_-54+1089 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACAC | T | 14 | a0001c0001t0006g0237a0001c0001t0024g0069a0001c0001t0025g0020others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-54+10888_-54+1089 others(8): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACAC | T | 19 | a0001c0001t0013g0286a0001c0001t0016g0209a0001c0001t0023g0092others(16): Show | 19 | HG00140.hp1 HG00609.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-54+10886_-54+1089 others(10): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(1): Show |
T | 62 | a0001c0001t0001g0206a0001c0001t0002g0113a0001c0001t0005g0282others(59): Show | 63 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-54+10884_-54+1089 others(12): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(3): Show |
T | 85 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0257others(82): Show | 85 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-54+10882_-54+1089 others(14): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(5): Show |
T | 17 | a0001c0001t0009g0081a0001c0001t0009g0083a0001c0001t0009g0084others(14): Show | 17 | HG00438.hp1 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-54+10880_-54+1089 others(16): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(7): Show |
T | 11 | a0001c0001t0012g0239a0001c0001t0012g0243a0001c0001t0056g0242others(8): Show | 11 | HG00735.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-54+10878_-54+1089 others(18): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(9): Show |
T | 2 | a0001c0001t0222g0169a0001c0001t0233g0168 | 2 | NA18969.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-54+10876_-54+1089 others(20): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(11): Show |
T | 3 | a0001c0001t0003g0170a0001c0001t0212g0167a0001c0001t0244g0122 | 3 | HG02055.hp1 HG02155.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-54+10874_-54+1089 others(22): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(13): Show |
T | 46 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(43): Show | 46 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.-54+10872_-54+1089 others(24): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0060g0238 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-54+10870_-54+1089 others(26): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919469
|
TACACACA others(17): Show |
T | 5 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(2): Show | 5 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+10868_-54+1089 others(28): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919469 | ||||||
| chr18:47919475
|
C | T | 1 | a0001c0001t0211g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-54+10886G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919475 | ||||||
| chr18:47919477
|
C | T | 3 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0100g0299 | 3 | HG01074.hp1 HG01975.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-54+10884G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919477 | ||||||
| chr18:47919479
|
C | T | 7 | a0001c0001t0057g0246a0001c0001t0063g0249a0001c0001t0079g0247others(4): Show | 7 | HG02145.hp2 NA18950.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54+10882G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919479 | ||||||
| chr18:47919483
|
C | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+10878G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919483 | ||||||
| chr18:47919485
|
C | T | 1 | a0001c0001t0245g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-54+10876G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919485 | ||||||
| chr18:47919521
|
A | C | 2 | a0001c0001t0038g0031a0001c0001t0193g0032 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-54+10840T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919521 | ||||||
| chr18:47919636
|
G | A | 50 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(47): Show | 50 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-54+10725C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919636 | ||||||
| chr18:47919669
|
G | A | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-54+10692C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919669 | ||||||
| chr18:47919684
|
A | G | 2 | a0001c0001t0160g0086a0001c0001t0162g0040 | 2 | HG00741.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-54+10677T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919684 | ||||||
| chr18:47919719
|
C | T | 1 | a0001c0001t0184g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-54+10642G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919719 | ||||||
| chr18:47919793
|
CTT | C | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-54+10566_-54+1056 others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919793 | ||||||
| chr18:47919836
|
C | T | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+10525G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919836 | ||||||
| chr18:47919839
|
A | G | 7 | a0001c0001t0001g0206a0001c0001t0016g0209a0001c0001t0017g0208others(4): Show | 7 | HG00423.hp2 HG02165.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54+10522T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919839 | ||||||
| chr18:47919936
|
T | C | 74 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0257others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-54+10425A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919936 | ||||||
| chr18:47919949
|
T | C | 1 | a0001c0001t0243g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-54+10412A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47919949 | ||||||
| chr18:47920054
|
C | A | 1 | a0001c0001t0243g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-54+10307G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920054 | ||||||
| chr18:47920055
|
A | T | 1 | a0001c0001t0176g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-54+10306T>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920055 | ||||||
| chr18:47920155
|
G | A | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-54+10206C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920155 | ||||||
| chr18:47920196
|
A | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+10165T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920196 | ||||||
| chr18:47920218
|
C | T | 1 | a0001c0001t0009g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-54+10143G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920218 | ||||||
| chr18:47920329
|
T | G | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+10032A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920329 | ||||||
| chr18:47920371
|
G | A | 1 | a0001c0001t0076g0289 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-54+9990C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920371 | ||||||
| chr18:47920451
|
T | C | 6 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+9910A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920451 | ||||||
| chr18:47920780
|
G | A | 2 | a0001c0001t0051g0290a0001c0001t0081g0291 | 2 | HG02132.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-54+9581C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920780 | ||||||
| chr18:47920805
|
T | C | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54+9556A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920805 | ||||||
| chr18:47920807
|
G | T | 13 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0300others(10): Show | 13 | HG02074.hp1 HG02523.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-54+9554C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47920807 | ||||||
| chr18:47921207
|
C | T | 1 | a0001c0001t0171g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-54+9154G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47921207 | ||||||
| chr18:47921401
|
C | A | 1 | a0001c0001t0198g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-54+8960G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47921401 | ||||||
| chr18:47921448
|
G | T | 1 | a0001c0001t0184g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-54+8913C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47921448 | ||||||
| chr18:47921450
|
A | G | 1 | a0001c0001t0065g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-54+8911T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47921450 | ||||||
| chr18:47921512
|
C | T | 5 | a0001c0001t0001g0195a0001c0001t0046g0196a0001c0001t0073g0293others(2): Show | 5 | HG02074.hp1 NA18955.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+8849G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47921512 | ||||||
| chr18:47921723
|
C | T | 3 | a0001c0001t0020g0191a0001c0001t0020g0192a0001c0001t0129g0190 | 3 | HG02647.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-54+8638G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47921723 | ||||||
| chr18:47921858
|
C | T | 1 | a0001c0001t0138g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-54+8503G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47921858 | ||||||
| chr18:47922061
|
T | A | 2 | a0001c0001t0025g0019a0001c0001t0025g0020 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-54+8300A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922061 | ||||||
| chr18:47922117
|
T | C | 6 | a0001c0001t0009g0081a0001c0001t0009g0083a0001c0001t0009g0084others(3): Show | 6 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+8244A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922117 | ||||||
| chr18:47922132
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-54+8229C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922132 | ||||||
| chr18:47922269
|
C | T | 1 | a0001c0001t0257g0309 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-54+8092G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922269 | ||||||
| chr18:47922501
|
G | T | 202 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.-54+7860C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922501 | ||||||
| chr18:47922567
|
A | G | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+7794T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922567 | ||||||
| chr18:47922706
|
C | G | 1 | a0001c0001t0120g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-54+7655G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922706 | ||||||
| chr18:47922850
|
GGAAA | G | 10 | a0001c0001t0019g0183a0001c0001t0019g0187a0001c0001t0048g0182others(7): Show | 10 | HG02040.hp2 NA18942.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.-54+7507_-54+7510d others(6): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922850 | ||||||
| chr18:47922942
|
T | C | 1 | a0001c0001t0185g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-54+7419A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47922942 | ||||||
| chr18:47923055
|
AT | A | 216 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(213): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.-54+7305delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47923055 | ||||||
| chr18:47923178
|
T | TA | 8 | a0001c0001t0035g0028a0001c0001t0036g0030a0001c0001t0037g0026others(5): Show | 8 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+7182dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47923178 | ||||||
| chr18:47923335
|
G | C | 1 | a0001c0001t0184g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-54+7026C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47923335 | ||||||
| chr18:47923777
|
A | G | 1 | a0001c0001t0170g0087 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-54+6584T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47923777 | ||||||
| chr18:47923821
|
T | A | 1 | a0001c0001t0121g0292 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-54+6540A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47923821 | ||||||
| chr18:47923912
|
T | A | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+6449A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47923912 | ||||||
| chr18:47924077
|
C | T | 2 | a0001c0001t0146g0037a0001c0001t0147g0093 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-54+6284G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924077 | ||||||
| chr18:47924105
|
G | A | 7 | a0001c0001t0022g0001a0001c0001t0023g0088a0001c0001t0023g0092others(4): Show | 8 | HG00609.hp2 NA18952.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54+6256C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924105 | ||||||
| chr18:47924113
|
T | C | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+6248A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924113 | ||||||
| chr18:47924116
|
C | T | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-54+6245G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924116 | ||||||
| chr18:47924117
|
G | A | 1 | a0001c0001t0147g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-54+6244C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924117 | ||||||
| chr18:47924192
|
G | A | 1 | a0001c0001t0218g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-54+6169C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924192 | ||||||
| chr18:47924248
|
C | CA | 153 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-54+6112dupT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924248 | ||||||
| chr18:47924248
|
C | CAA | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.-54+6111_-54+6112d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924248 | ||||||
| chr18:47924450
|
C | T | 1 | a0001c0001t0083g0178 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-54+5911G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924450 | ||||||
| chr18:47924467
|
C | CT | 7 | a0001c0001t0025g0019a0001c0001t0025g0020a0001c0001t0189g0018others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54+5893dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924467 | ||||||
| chr18:47924467
|
C | CTT | 8 | a0001c0002t0247g0014a0001c0002t0248g0303a0001c0002t0249g0306others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54+5892_-54+5893d others(4): Show |
SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924467 | ||||||
| chr18:47924598
|
A | G | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54+5763T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924598 | ||||||
| chr18:47924611
|
G | A | 1 | a0001c0001t0119g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-54+5750C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924611 | ||||||
| chr18:47924743
|
G | T | 2 | a0001c0001t0211g0008a0001c0001t0245g0007 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-54+5618C>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924743 | ||||||
| chr18:47924808
|
G | A | 1 | a0001c0001t0174g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-54+5553C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47924808 | ||||||
| chr18:47925001
|
C | A | 12 | a0001c0001t0026g0110a0001c0001t0026g0111a0001c0001t0148g0109others(9): Show | 12 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54+5360G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925001 | ||||||
| chr18:47925344
|
C | T | 1 | a0001c0001t0100g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-54+5017G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925344 | ||||||
| chr18:47925419
|
T | A | 50 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(47): Show | 50 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-54+4942A>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925419 | ||||||
| chr18:47925549
|
C | T | 1 | a0001c0001t0013g0177 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-54+4812G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925549 | ||||||
| chr18:47925570
|
TA | T | 184 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-54+4790delT | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925570 | ||||||
| chr18:47925675
|
C | T | 1 | a0001c0002t0247g0014 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-54+4686G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925675 | ||||||
| chr18:47925713
|
C | T | 1 | a0001c0001t0177g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-54+4648G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925713 | ||||||
| chr18:47925892
|
G | C | 1 | a0001c0001t0069g0298 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-54+4469C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925892 | ||||||
| chr18:47925950
|
G | A | 130 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-54+4411C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47925950 | ||||||
| chr18:47926096
|
C | G | 3 | a0001c0001t0007g0097a0001c0001t0014g0115a0001c0001t0086g0116 | 3 | HG00642.hp2 HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-54+4265G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47926096 | ||||||
| chr18:47926141
|
C | A | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+4220G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47926141 | ||||||
| chr18:47926186
|
C | G | 228 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(225): Show | 228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.-54+4175G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47926186 | ||||||
| chr18:47926227
|
A | C | 1 | a0001c0001t0244g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-54+4134T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47926227 | ||||||
| chr18:47926832
|
T | C | 5 | a0001c0001t0205g0120a0001c0001t0206g0117a0001c0001t0207g0118others(2): Show | 5 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54+3529A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47926832 | ||||||
| chr18:47927177
|
T | C | 1 | a0001c0001t0184g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-54+3184A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927177 | ||||||
| chr18:47927227
|
G | A | 1 | a0001c0001t0243g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-54+3134C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927227 | ||||||
| chr18:47927319
|
G | GT | 233 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(230): Show | 233 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.-54+3041dupA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927319 | ||||||
| chr18:47927464
|
G | A | 52 | a0001c0001t0003g0140a0001c0001t0003g0146a0001c0001t0003g0149others(49): Show | 52 | HG00544.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.-54+2897C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927464 | ||||||
| chr18:47927484
|
T | C | 1 | a0001c0001t0133g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-54+2877A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927484 | ||||||
| chr18:47927860
|
T | C | 2 | a0001c0001t0196g0006a0001c0001t0197g0005 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-54+2501A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927860 | ||||||
| chr18:47927913
|
T | C | 1 | a0001c0001t0094g0004 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-54+2448A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927913 | ||||||
| chr18:47927920
|
T | C | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | HG02523.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-54+2441A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47927920 | ||||||
| chr18:47928122
|
T | C | 3 | a0001c0001t0156g0104a0001c0001t0163g0105a0001c0001t0178g0106 | 3 | HG00140.hp2 HG01361.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-54+2239A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928122 | ||||||
| chr18:47928406
|
T | C | 9 | a0001c0001t0255g0096a0001c0002t0247g0014a0001c0002t0248g0303others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-54+1955A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928406 | ||||||
| chr18:47928458
|
A | C | 153 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-54+1903T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928458 | ||||||
| chr18:47928545
|
T | C | 1 | a0001c0001t0255g0096 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54+1816A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928545 | ||||||
| chr18:47928623
|
CT | C | 10 | a0001c0001t0007g0097a0001c0001t0007g0101a0001c0001t0007g0102others(7): Show | 10 | HG00140.hp2 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-54+1737delA | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928623 | ||||||
| chr18:47928713
|
T | G | 203 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-54+1648A>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928713 | ||||||
| chr18:47928739
|
C | A | 1 | a0001c0001t0105g0302 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-54+1622G>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928739 | ||||||
| chr18:47928788
|
T | C | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-54+1573A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928788 | ||||||
| chr18:47928815
|
T | C | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-54+1546A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928815 | ||||||
| chr18:47928899
|
A | G | 1 | a0001c0001t0143g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54+1462T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47928899 | ||||||
| chr18:47929196
|
T | C | 3 | a0001c0001t0095g0176a0001c0001t0200g0175a0001c0001t0201g0174 | 3 | HG00438.hp2 HG02615.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-54+1165A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47929196 | ||||||
| chr18:47929270
|
G | A | 128 | a0001c0001t0001g0195a0001c0001t0001g0198a0001c0001t0001g0206others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-54+1091C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47929270 | ||||||
| chr18:47929690
|
T | C | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+671A>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47929690 | ||||||
| chr18:47929702
|
G | A | 4 | a0001c0002t0248g0303a0001c0002t0249g0306a0001c0002t0250g0304others(1): Show | 4 | HG02572.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+659C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47929702 | ||||||
| chr18:47929869
|
G | A | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+492C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47929869 | ||||||
| chr18:47929994
|
A | G | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+367T>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47929994 | ||||||
| chr18:47930033
|
C | T | 1 | a0001c0001t0167g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-54+328G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47930033 | ||||||
| chr18:47930144
|
C | T | 1 | a0001c0001t0243g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-54+217G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47930144 | ||||||
| chr18:47930155
|
G | C | 1 | a0001c0001t0175g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-54+206C>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47930155 | ||||||
| chr18:47930176
|
G | A | 1 | a0001c0001t0192g0308 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-54+185C>T | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47930176 | ||||||
| chr18:47930258
|
C | T | 2 | a0001c0001t0164g0009a0001c0001t0194g0010 | 2 | NA18949.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-54+103G>A | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47930258 | ||||||
| chr18:47930336
|
A | C | 4 | a0001c0001t0196g0006a0001c0001t0197g0005a0001c0001t0211g0008others(1): Show | 4 | HG02055.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-54+25T>G | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47930336 | ||||||
| chr18:47930343
|
C | G | 1 | a0001c0001t0094g0004 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-54+18G>C | SMAD2 | ENSG00000175387.16 | transcript | ENST00000262160.11 | protein_coding | 1/10 | chr18 | 47930343 |