| geneid | 1286 |
|---|---|
| ensemblid | ENSG00000081052.14 |
| hgncid | 2206 |
| symbol | COL4A4 |
| name | collagen type IV alpha 4 chain |
| refseq_nuc | NM_000092.5 |
| refseq_prot | NP_000083.3 |
| ensembl_nuc | ENST00000396625.5 |
| ensembl_prot | ENSP00000379866.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 227002714 |
| end | 227164205 |
| strand | - |
| ver | v1.2 |
| region | chr2:227002714-227164205 |
| region5000 | chr2:226997714-227169205 |
| regionname0 | COL4A4_chr2_227002714_227164205 |
| regionname5000 | COL4A4_chr2_226997714_227169205 |
| 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 | 1/0 | 1690 | 80 | 16 | 14 | 39 | 3 | 7 | 26 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002 | 0/0 | 1690 | 63 | 6 | 14 | 26 | 5 | 12 | 21 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003 | 0/1 | 1690 | 30 | 2 | 4 | 15 | 1 | 7 | 12 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004 | 0/0 | 1690 | 15 | 7 | 3 | 5 | 0 | 0 | 4 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005 | 0/0 | 1690 | 9 | 1 | 1 | 4 | 1 | 2 | 2 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0006 | 0/0 | 1690 | 9 | 8 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0007 | 0/0 | 1690 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0008 | 0/0 | 1690 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0009 | 0/0 | 1690 | 5 | 0 | 3 | 2 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0010 | 0/0 | 1690 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0011 | 0/0 | 1690 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0012 | 0/0 | 1690 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0013 | 0/0 | 1690 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0014 | 0/0 | 1690 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0015 | 0/0 | 1690 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0016 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0017 | 0/0 | 1690 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0018 | 0/0 | 1690 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0019 | 0/0 | 1690 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0020 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0021 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0022 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0023 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0024 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0025 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0026 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0027 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0028 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0029 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0030 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0031 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0032 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0033 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0034 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0035 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0036 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0037 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0038 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0039 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0040 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0041 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0042 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0043 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0044 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0045 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 5073 | 72 | 11 | 14 | 36 | 3 | 7 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0002 | 0/0 | 5073 | 56 | 3 | 11 | 25 | 5 | 12 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0003 | 0/1 | 5073 | 22 | 1 | 4 | 11 | 1 | 4 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0004 | 0/0 | 5073 | 13 | 5 | 3 | 5 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0005 | 0/0 | 5073 | 8 | 7 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0006 | 0/0 | 5073 | 7 | 7 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0007 | 0/0 | 5073 | 6 | 0 | 1 | 3 | 1 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0008 | 0/0 | 5073 | 5 | 5 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0009 | 0/0 | 5073 | 5 | 0 | 3 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0010 | 0/0 | 5073 | 4 | 4 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0011 | 0/0 | 5073 | 4 | 3 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0012 | 0/0 | 5073 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0013 | 0/0 | 5073 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0014 | 0/0 | 5073 | 3 | 0 | 0 | 0 | 0 | 3 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0015 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0016 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0017 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0018 | 0/0 | 5073 | 2 | 1 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0019 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0020 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0021 | 0/0 | 5073 | 2 | 0 | 2 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0022 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0023 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0024 | 0/0 | 5073 | 2 | 0 | 1 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0025 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0026 | 0/0 | 5073 | 2 | 1 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0027 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0028 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0029 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0030 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0031 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0032 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0033 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0034 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0035 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0036 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0037 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0038 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0039 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0040 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0041 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0042 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0043 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0044 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0045 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0046 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0047 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0048 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0049 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0050 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0051 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0052 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0053 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0054 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0055 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0056 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0057 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0058 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0059 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0060 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0061 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0062 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0063 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0064 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0065 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0066 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0067 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0068 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0069 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0070 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0071 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0072 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0073 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| c0074 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 4912 | 79 | 11 | 16 | 39 | 5 | 7 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0002 | 0/0 | 4911 | 73 | 3 | 18 | 33 | 4 | 15 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0003 | 0/1 | 4912 | 36 | 3 | 5 | 21 | 1 | 5 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0004 | 0/0 | 4912 | 23 | 22 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0005 | 0/0 | 4912 | 21 | 13 | 1 | 4 | 1 | 2 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0006 | 0/0 | 4915 | 6 | 6 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0007 | 0/0 | 4911 | 4 | 0 | 0 | 4 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0008 | 0/0 | 4912 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0009 | 0/0 | 4911 | 3 | 2 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0010 | 0/0 | 4916 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0011 | 0/0 | 4914 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0012 | 0/0 | 4912 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0013 | 0/0 | 4911 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0014 | 0/0 | 4915 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0015 | 0/0 | 4915 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0016 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0017 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0018 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0019 | 0/0 | 4912 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0020 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0021 | 0/0 | 4913 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0022 | 0/0 | 4912 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0023 | 0/0 | 4912 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0024 | 0/0 | 4913 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0025 | 0/0 | 4912 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0026 | 0/0 | 4913 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0027 | 0/0 | 4911 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0028 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0029 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0030 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0031 | 0/0 | 4912 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0032 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0033 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0034 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0035 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0036 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0037 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0038 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| t0039 | 0/0 | 4912 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| 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 | 0 | 0 | 2 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5073 | 72 | 11 | 14 | 36 | 3 | 7 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0010 | 0/0 | 5073 | 4 | 4 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0049 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0068 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0070 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0072 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002 | 0/0 | 5073 | 56 | 3 | 11 | 25 | 5 | 12 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0019 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0021 | 0/0 | 5073 | 2 | 0 | 2 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0058 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0059 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0060 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0003 | 0/1 | 5073 | 22 | 1 | 4 | 11 | 1 | 4 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0014 | 0/0 | 5073 | 3 | 0 | 0 | 0 | 0 | 3 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0026 | 0/0 | 5073 | 2 | 1 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0027 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0073 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0004 | 0/0 | 5073 | 13 | 5 | 3 | 5 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0040 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0051 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0007 | 0/0 | 5073 | 6 | 0 | 1 | 3 | 1 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0045 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0046 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0071 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0006c0005 | 0/0 | 5073 | 8 | 7 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0006c0035 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0007c0006 | 0/0 | 5073 | 7 | 7 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0007c0031 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0008c0008 | 0/0 | 5073 | 5 | 5 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0008c0028 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0009c0009 | 0/0 | 5073 | 5 | 0 | 3 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0010c0017 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0010c0018 | 0/0 | 5073 | 2 | 1 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0010c0032 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0011c0012 | 0/0 | 5073 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0011c0053 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0012c0011 | 0/0 | 5073 | 4 | 3 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0013c0013 | 0/0 | 5073 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0014c0020 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0014c0052 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0015c0024 | 0/0 | 5073 | 2 | 0 | 1 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0015c0042 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0016c0064 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0016c0065 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0017c0022 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0018c0023 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0019c0025 | 0/0 | 5073 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0020c0041 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0020c0054 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0021c0016 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0022c0015 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0023c0039 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0024c0069 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0025c0044 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0026c0050 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0027c0047 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0028c0048 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0029c0063 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0030c0062 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0031c0061 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0032c0057 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0033c0043 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0034c0056 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0035c0037 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0036c0055 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0037c0066 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0038c0038 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0039c0067 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0040c0074 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0041c0029 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0042c0034 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0043c0036 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0044c0033 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0045c0030 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 9984 | 66 | 10 | 13 | 32 | 3 | 7 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0001t0017 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0001t0019 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0001t0021 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0001t0022 | 0/0 | 9984 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0001t0023 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0001t0024 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0010t0005 | 0/0 | 9984 | 4 | 4 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0049t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0068t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0070t0039 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0001c0072t0001 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002t0002 | 0/0 | 9983 | 47 | 1 | 10 | 21 | 4 | 11 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002t0004 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002t0005 | 0/0 | 9984 | 2 | 0 | 0 | 1 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002t0007 | 0/0 | 9983 | 3 | 0 | 0 | 3 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002t0011 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002t0026 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0002t0027 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0019t0005 | 0/0 | 9984 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0021t0002 | 0/0 | 9983 | 2 | 0 | 2 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0058t0005 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0059t0025 | 0/0 | 9984 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0002c0060t0002 | 0/0 | 9983 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0003t0003 | 0/1 | 9984 | 20 | 0 | 4 | 10 | 1 | 4 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0003t0030 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0003t0031 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0014t0002 | 0/0 | 9983 | 3 | 0 | 0 | 0 | 0 | 3 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0026t0001 | 0/0 | 9984 | 2 | 1 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0027t0003 | 0/0 | 9984 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0003c0073t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0004t0002 | 0/0 | 9983 | 9 | 1 | 3 | 5 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0004t0005 | 0/0 | 9984 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0004t0020 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0004t0037 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0040t0002 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0004c0051t0005 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0007t0002 | 0/0 | 9983 | 2 | 0 | 1 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0007t0005 | 0/0 | 9984 | 4 | 0 | 0 | 2 | 1 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0045t0003 | 0/0 | 9984 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0046t0005 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0005c0071t0005 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0006c0005t0004 | 0/0 | 9984 | 6 | 6 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0006c0005t0009 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0006c0005t0013 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0006c0035t0036 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0007c0006t0004 | 0/0 | 9984 | 6 | 6 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0007c0006t0035 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0007c0031t0004 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0008c0008t0004 | 0/0 | 9984 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0008c0008t0009 | 0/0 | 9983 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0008c0028t0034 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0009c0009t0001 | 0/0 | 9984 | 5 | 0 | 3 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0010c0017t0008 | 0/0 | 9984 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0010c0018t0004 | 0/0 | 9984 | 2 | 1 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0010c0032t0008 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0011c0012t0006 | 0/0 | 9987 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0011c0053t0015 | 0/0 | 9987 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0012c0011t0003 | 0/0 | 9984 | 4 | 3 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0013c0013t0006 | 0/0 | 9987 | 3 | 3 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0014c0020t0001 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0014c0020t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0014c0052t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0015c0024t0002 | 0/0 | 9983 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0015c0024t0012 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0015c0042t0013 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0016c0064t0005 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0016c0065t0005 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0017c0022t0003 | 0/0 | 9984 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0018c0023t0002 | 0/0 | 9983 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0019c0025t0002 | 0/0 | 9983 | 2 | 0 | 0 | 2 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0020c0041t0010 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0020c0054t0010 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0021c0016t0014 | 0/0 | 9987 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0022c0015t0004 | 0/0 | 9984 | 2 | 2 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0023c0039t0007 | 0/0 | 9983 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0024c0069t0002 | 0/0 | 9983 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0025c0044t0001 | 0/0 | 9984 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0026c0050t0001 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0027c0047t0015 | 0/0 | 9987 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0028c0048t0001 | 0/0 | 9984 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0029c0063t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0030c0062t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0031c0061t0002 | 0/0 | 9983 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0032c0057t0002 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0033c0043t0011 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0034c0056t0001 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0035c0037t0016 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0036c0055t0029 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0037c0066t0012 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0038c0038t0005 | 0/0 | 9984 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0039c0067t0028 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0040c0074t0018 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0041c0029t0004 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0042c0034t0004 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0043c0036t0038 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0044c0033t0032 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| a0045c0030t0033 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | copy fasta | chr2 | 226997714 | 227169205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0017g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0019g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0021g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0022g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0023g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0001t0024g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0010t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0010t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0010t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0010t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0049t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0068t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0070t0039g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0001c0072t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0026g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0002t0027g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0019t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0019t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0021t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0021t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0058t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0059t0025g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0002c0060t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0030g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0003t0031g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0014t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0014t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0014t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0026t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0026t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0027t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0027t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0003c0073t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0020g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0004t0037g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0040t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0004c0051t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0007t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0007t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0007t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0007t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0007t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0007t0005g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0045t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0046t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0005c0071t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0009g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0005t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0006c0035t0036g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0006t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0006t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0006t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0006t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0006t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0006t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0006t0035g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0007c0031t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0008c0008t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0008c0008t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0008c0008t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0008c0008t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0008c0008t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0008c0028t0034g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0009c0009t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0009c0009t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0009c0009t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0009c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0009c0009t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0010c0017t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0010c0017t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0010c0018t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0010c0018t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0010c0032t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0011c0012t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0011c0012t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0011c0012t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0011c0053t0015g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0012c0011t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0012c0011t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0012c0011t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0012c0011t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0013c0013t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0013c0013t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0013c0013t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0014c0020t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0014c0020t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0014c0052t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0015c0024t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0015c0024t0012g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0015c0042t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0016c0064t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0016c0065t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0017c0022t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0017c0022t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0018c0023t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0018c0023t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0019c0025t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0019c0025t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0020c0041t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0020c0054t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0021c0016t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0021c0016t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0022c0015t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0022c0015t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0023c0039t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0024c0069t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0025c0044t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0026c0050t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0027c0047t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0028c0048t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0029c0063t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0030c0062t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0031c0061t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0032c0057t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0033c0043t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0034c0056t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0035c0037t0016g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0036c0055t0029g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0037c0066t0012g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0038c0038t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0039c0067t0028g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0040c0074t0018g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0041c0029t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0042c0034t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0043c0036t0038g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0044c0033t0032g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| a0045c0030t0033g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0072 | EUR | GBR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00140 | hp1 | a0003 | c0003 | t0003 | g0228 | EUR | GBR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00323 | hp1 | a0005 | c0007 | t0005 | g0137 | EUR | FIN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0267 | EUR | FIN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00408 | hp2 | a0014 | c0020 | t0003 | g0103 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00438 | hp1 | a0001 | c0001 | t0019 | g0126 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00558 | hp1 | a0018 | c0023 | t0002 | g0052 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00609 | hp1 | a0003 | c0027 | t0003 | g0096 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00639 | hp1 | a0002 | c0021 | t0002 | g0246 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00639 | hp2 | a0003 | c0003 | t0003 | g0116 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00673 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00673 | hp2 | a0005 | c0071 | t0005 | g0237 | EAS | CHS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00738 | hp1 | a0004 | c0004 | t0002 | g0218 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG00741 | hp2 | a0004 | c0004 | t0002 | g0095 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01099 | hp2 | a0002 | c0021 | t0002 | g0245 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01106 | hp1 | a0038 | c0038 | t0005 | g0024 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0236 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01167 | hp2 | a0009 | c0009 | t0001 | g0017 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01169 | hp1 | a0009 | c0009 | t0001 | g0016 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01175 | hp2 | a0005 | c0007 | t0002 | g0240 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01192 | hp1 | a0001 | c0001 | t0022 | g0119 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01243 | hp1 | a0010 | c0018 | t0004 | g0162 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01255 | hp2 | a0003 | c0003 | t0003 | g0099 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01257 | hp1 | a0003 | c0003 | t0003 | g0093 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01258 | hp1 | a0004 | c0004 | t0002 | g0202 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01258 | hp2 | a0003 | c0003 | t0003 | g0004 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01261 | hp1 | a0015 | c0024 | t0002 | g0120 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01261 | hp2 | a0002 | c0002 | t0026 | g0232 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0239 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01496 | hp1 | a0009 | c0009 | t0001 | g0022 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0248 | EUR | IBS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01515 | hp2 | a0028 | c0048 | t0001 | g0114 | EUR | IBS | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01884 | hp1 | a0003 | c0003 | t0030 | g0169 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01884 | hp2 | a0004 | c0040 | t0002 | g0035 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01891 | hp1 | a0012 | c0011 | t0003 | g0233 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01934 | hp1 | a0012 | c0011 | t0003 | g0138 | AMR | PEL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | PEL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | PEL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PEL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02040 | hp2 | a0004 | c0004 | t0002 | g0260 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02055 | hp1 | a0004 | c0004 | t0002 | g0147 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0149 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02056 | hp1 | a0014 | c0052 | t0003 | g0089 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02071 | hp2 | a0003 | c0003 | t0003 | g0076 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02074 | hp2 | a0002 | c0002 | t0007 | g0225 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02080 | hp1 | a0005 | c0007 | t0002 | g0053 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02080 | hp2 | a0034 | c0056 | t0001 | g0064 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02145 | hp1 | a0027 | c0047 | t0015 | g0025 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02145 | hp2 | a0013 | c0013 | t0006 | g0155 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02165 | hp1 | a0018 | c0023 | t0002 | g0127 | EAS | CDX | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02165 | hp2 | a0009 | c0009 | t0001 | g0055 | EAS | CDX | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02257 | hp1 | a0001 | c0010 | t0005 | g0275 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02257 | hp2 | a0007 | c0006 | t0004 | g0172 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02258 | hp1 | a0013 | c0013 | t0006 | g0144 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02280 | hp2 | a0006 | c0005 | t0004 | g0148 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02451 | hp1 | a0035 | c0037 | t0016 | g0003 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02451 | hp2 | a0012 | c0011 | t0003 | g0219 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02572 | hp2 | a0007 | c0006 | t0004 | g0181 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02622 | hp1 | a0022 | c0015 | t0004 | g0145 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02630 | hp1 | a0005 | c0046 | t0005 | g0159 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02630 | hp2 | a0006 | c0005 | t0004 | g0195 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02647 | hp1 | a0008 | c0008 | t0004 | g0027 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0002 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0177 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0092 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02717 | hp1 | a0041 | c0029 | t0004 | g0026 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02717 | hp2 | a0022 | c0015 | t0004 | g0146 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0205 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02809 | hp1 | a0008 | c0008 | t0004 | g0164 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02809 | hp2 | a0012 | c0011 | t0003 | g0231 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02818 | hp1 | a0036 | c0055 | t0029 | g0174 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02818 | hp2 | a0011 | c0012 | t0006 | g0032 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02886 | hp1 | a0007 | c0031 | t0004 | g0170 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02896 | hp1 | a0006 | c0005 | t0004 | g0193 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02896 | hp2 | a0011 | c0012 | t0006 | g0256 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02897 | hp1 | a0011 | c0012 | t0006 | g0257 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02897 | hp2 | a0006 | c0035 | t0036 | g0270 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02922 | hp1 | a0004 | c0004 | t0020 | g0217 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02922 | hp2 | a0015 | c0042 | t0013 | g0041 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02965 | hp1 | a0011 | c0053 | t0015 | g0152 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02970 | hp1 | a0039 | c0067 | t0028 | g0235 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02970 | hp2 | a0016 | c0064 | t0005 | g0178 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02976 | hp1 | a0008 | c0008 | t0004 | g0161 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0241 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0268 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03041 | hp1 | a0007 | c0006 | t0035 | g0163 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03041 | hp2 | a0013 | c0013 | t0006 | g0212 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03098 | hp1 | a0033 | c0043 | t0011 | g0279 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03098 | hp2 | a0001 | c0070 | t0039 | g0204 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03130 | hp1 | a0008 | c0028 | t0034 | g0160 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03130 | hp2 | a0006 | c0005 | t0013 | g0154 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03139 | hp1 | a0002 | c0002 | t0011 | g0222 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03139 | hp2 | a0044 | c0033 | t0032 | g0168 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03195 | hp1 | a0010 | c0017 | t0008 | g0183 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03195 | hp2 | a0004 | c0051 | t0005 | g0023 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03209 | hp1 | a0045 | c0030 | t0033 | g0192 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03209 | hp2 | a0002 | c0019 | t0005 | g0029 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03225 | hp2 | a0008 | c0008 | t0009 | g0271 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03453 | hp1 | a0002 | c0019 | t0005 | g0166 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03453 | hp2 | a0001 | c0010 | t0005 | g0272 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03486 | hp1 | a0006 | c0005 | t0004 | g0156 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03486 | hp2 | a0042 | c0034 | t0004 | g0274 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03491 | hp1 | a0032 | c0057 | t0002 | g0220 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03516 | hp1 | a0010 | c0032 | t0008 | g0167 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03516 | hp2 | a0006 | c0005 | t0004 | g0158 | AFR | ESN | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03540 | hp2 | a0021 | c0016 | t0014 | g0278 | AFR | GWD | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03688 | hp1 | a0005 | c0045 | t0003 | g0061 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03704 | hp2 | a0003 | c0014 | t0002 | g0242 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03710 | hp1 | a0003 | c0003 | t0003 | g0101 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03831 | hp2 | a0003 | c0003 | t0003 | g0057 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0266 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03834 | hp2 | a0003 | c0003 | t0003 | g0071 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0203 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0182 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG04115 | hp2 | a0006 | c0005 | t0009 | g0283 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG04204 | hp1 | a0005 | c0007 | t0005 | g0067 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG04204 | hp2 | a0003 | c0014 | t0002 | g0094 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG04228 | hp1 | a0002 | c0002 | t0005 | g0142 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG04228 | hp2 | a0003 | c0014 | t0002 | g0069 | SAS | STU | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18522 | hp1 | a0007 | c0006 | t0004 | g0173 | AFR | YRI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18522 | hp2 | a0010 | c0018 | t0004 | g0157 | AFR | YRI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18906 | hp1 | a0020 | c0041 | t0010 | g0028 | AFR | YRI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18906 | hp2 | a0001 | c0010 | t0005 | g0277 | AFR | YRI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18939 | hp2 | a0003 | c0003 | t0031 | g0250 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18941 | hp1 | a0002 | c0002 | t0007 | g0184 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18945 | hp1 | a0002 | c0002 | t0005 | g0215 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18946 | hp1 | a0004 | c0004 | t0002 | g0042 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18952 | hp1 | a0019 | c0025 | t0002 | g0261 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18962 | hp1 | a0017 | c0022 | t0003 | g0254 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18965 | hp1 | a0023 | c0039 | t0007 | g0012 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18968 | hp1 | a0024 | c0069 | t0002 | g0015 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18975 | hp1 | a0014 | c0020 | t0001 | g0007 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18979 | hp1 | a0001 | c0072 | t0001 | g0238 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18979 | hp2 | a0005 | c0007 | t0005 | g0134 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0084 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18995 | hp1 | a0001 | c0049 | t0003 | g0253 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18999 | hp2 | a0005 | c0007 | t0005 | g0121 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19000 | hp1 | a0003 | c0003 | t0003 | g0190 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19000 | hp2 | a0001 | c0001 | t0024 | g0132 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19001 | hp1 | a0001 | c0001 | t0023 | g0131 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19002 | hp2 | a0003 | c0003 | t0003 | g0269 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19006 | hp1 | a0001 | c0001 | t0021 | g0141 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19007 | hp1 | a0030 | c0062 | t0003 | g0265 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19007 | hp2 | a0026 | c0050 | t0001 | g0081 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19009 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19011 | hp1 | a0015 | c0024 | t0012 | g0221 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19012 | hp1 | a0037 | c0066 | t0012 | g0059 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19012 | hp2 | a0003 | c0026 | t0001 | g0010 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19030 | hp1 | a0002 | c0058 | t0005 | g0214 | AFR | LWK | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19030 | hp2 | a0007 | c0006 | t0004 | g0176 | AFR | LWK | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19043 | hp1 | a0004 | c0004 | t0005 | g0234 | AFR | LWK | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19043 | hp2 | a0001 | c0010 | t0005 | g0276 | AFR | LWK | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19057 | hp1 | a0003 | c0073 | t0003 | g0018 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19057 | hp2 | a0004 | c0004 | t0002 | g0189 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19060 | hp1 | a0029 | c0063 | t0003 | g0082 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19064 | hp2 | a0019 | c0025 | t0002 | g0198 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19066 | hp1 | a0017 | c0022 | t0003 | g0255 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19066 | hp2 | a0002 | c0002 | t0007 | g0049 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19068 | hp2 | a0003 | c0003 | t0003 | g0128 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19082 | hp1 | a0003 | c0027 | t0003 | g0133 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19082 | hp2 | a0009 | c0009 | t0001 | g0083 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19083 | hp1 | a0004 | c0004 | t0002 | g0075 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19084 | hp1 | a0002 | c0060 | t0002 | g0252 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19084 | hp2 | a0001 | c0068 | t0003 | g0199 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19087 | hp2 | a0003 | c0003 | t0003 | g0130 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19088 | hp2 | a0003 | c0003 | t0003 | g0129 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19091 | hp1 | a0003 | c0003 | t0003 | g0223 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19240 | hp1 | a0004 | c0004 | t0005 | g0030 | AFR | YRI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA19240 | hp2 | a0006 | c0005 | t0004 | g0191 | AFR | YRI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA20752 | hp1 | a0025 | c0044 | t0001 | g0060 | EUR | TSI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0151 | EUR | TSI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA20805 | hp2 | a0002 | c0002 | t0027 | g0201 | EUR | TSI | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01123 | hp1 | a0002 | c0059 | t0025 | g0037 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG01123 | hp2 | a0031 | c0061 | t0002 | g0021 | AMR | CLM | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02486 | hp1 | a0004 | c0004 | t0037 | g0062 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02486 | hp2 | a0007 | c0006 | t0004 | g0171 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02559 | hp1 | a0040 | c0074 | t0018 | g0045 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG02559 | hp2 | a0008 | c0008 | t0009 | g0165 | AFR | ACB | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03471 | hp1 | a0043 | c0036 | t0038 | g0153 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG03471 | hp2 | a0010 | c0017 | t0008 | g0179 | AFR | MSL | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | USA | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| HG06807 | hp2 | a0003 | c0026 | t0001 | g0230 | AFR | USA | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18955 | hp1 | a0004 | c0004 | t0002 | g0187 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA20300 | hp1 | a0021 | c0016 | t0014 | g0019 | AFR | USA | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA20300 | hp2 | a0007 | c0006 | t0004 | g0175 | AFR | USA | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA21309 | hp1 | a0020 | c0054 | t0010 | g0020 | AFR | LWK | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| NA21309 | hp2 | a0016 | c0065 | t0005 | g0150 | AFR | LWK | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0003 | g0118 | REF | REF | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0039 | REF | REF | COL4A4_chr2_226997714_227169205 | COL4A4 | chr2 | 226997714 | 227169205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227007448
|
G | C | 1 | a0028 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.4950C>G | p.Phe1650Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 5250/9984 | 4950/5073 | 1650/1690 | chr2 | 227007448 | ||
| chr2:227008112
|
G | A | 1 | a0034 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.4715C>T | p.Pro1572Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/48 | 5015/9984 | 4715/5073 | 1572/1690 | chr2 | 227008112 | ||
| chr2:227008171
|
C | T | 3 | a0020a0035a0044 | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.4656G>A | p.Met1552Ile | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/48 | 4956/9984 | 4656/5073 | 1552/1690 | chr2 | 227008171 | ||
| chr2:227022057
|
A | G | 30 | a0002a0004a0005others(27): Show | 147 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
missense_variant | MODERATE | c.4207T>C | p.Ser1403Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/48 | 4507/9984 | 4207/5073 | 1403/1690 | chr2 | 227022057 | ||
| chr2:227022069
|
T | A | 1 | a0026 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.4195A>T | p.Met1399Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/48 | 4495/9984 | 4195/5073 | 1399/1690 | chr2 | 227022069 | ||
| chr2:227028004
|
C | T | 21 | a0002a0004a0005others(18): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
missense_variant | MODERATE | c.3979G>A | p.Val1327Met | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/48 | 4279/9984 | 3979/5073 | 1327/1690 | chr2 | 227028004 | ||
| chr2:227030545
|
G | C | 2 | a0011a0041 | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.3871C>G | p.Pro1291Ala | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/48 | 4171/9984 | 3871/5073 | 1291/1690 | chr2 | 227030545 | ||
| chr2:227032210
|
G | A | 1 | a0031 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.3644C>T | p.Pro1215Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 39/48 | 3944/9984 | 3644/5073 | 1215/1690 | chr2 | 227032210 | ||
| chr2:227032273
|
A | G | 1 | a0032 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.3581T>C | p.Leu1194Ser | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 39/48 | 3881/9984 | 3581/5073 | 1194/1690 | chr2 | 227032273 | ||
| chr2:227047531
|
G | A | 3 | a0020a0035a0036 | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
missense_variant | MODERATE | c.3233C>T | p.Ala1078Val | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/48 | 3533/9984 | 3233/5073 | 1078/1690 | chr2 | 227047531 | ||
| chr2:227047532
|
C | T | 1 | a0016 | 2 | HG02970.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.3232G>A | p.Ala1078Thr | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/48 | 3532/9984 | 3232/5073 | 1078/1690 | chr2 | 227047532 | ||
| chr2:227051098
|
G | A | 1 | a0030 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.3029C>T | p.Pro1010Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 33/48 | 3329/9984 | 3029/5073 | 1010/1690 | chr2 | 227051098 | ||
| chr2:227051116
|
G | A | 24 | a0002a0003a0004others(21): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
missense_variant | MODERATE | c.3011C>T | p.Pro1004Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 33/48 | 3311/9984 | 3011/5073 | 1004/1690 | chr2 | 227051116 | ||
| chr2:227051131
|
C | T | 1 | a0025 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.2996G>A | p.Gly999Glu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 33/48 | 3296/9984 | 2996/5073 | 999/1690 | chr2 | 227051131 | ||
| chr2:227052374
|
T | C | 2 | a0020a0036 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.2899A>G | p.Ile967Val | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/48 | 3199/9984 | 2899/5073 | 967/1690 | chr2 | 227052374 | ||
| chr2:227054663
|
C | T | 2 | a0011a0041 | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.2791G>A | p.Ala931Thr | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/48 | 3091/9984 | 2791/5073 | 931/1690 | chr2 | 227054663 | ||
| chr2:227055951
|
G | C | 1 | a0029 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.2710C>G | p.Pro904Ala | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/48 | 3010/9984 | 2710/5073 | 904/1690 | chr2 | 227055951 | ||
| chr2:227056031
|
C | T | 1 | a0018 | 2 | HG00558.hp1 HG02165.hp1 |
missense_variant | MODERATE | c.2630G>A | p.Arg877Gln | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/48 | 2930/9984 | 2630/5073 | 877/1690 | chr2 | 227056031 | ||
| chr2:227057474
|
C | G | 1 | a0017 | 2 | NA18962.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.2510G>C | p.Gly837Ala | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/48 | 2810/9984 | 2510/5073 | 837/1690 | chr2 | 227057474 | ||
| chr2:227059512
|
G | A | 5 | a0011a0013a0016others(2): Show | 12 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
missense_variant | MODERATE | c.2276C>T | p.Pro759Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/48 | 2576/9984 | 2276/5073 | 759/1690 | chr2 | 227059512 | ||
| chr2:227062541
|
T | C | 1 | a0037 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.2045A>G | p.Asp682Gly | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/48 | 2345/9984 | 2045/5073 | 682/1690 | chr2 | 227062541 | ||
| chr2:227062578
|
C | T | 2 | a0013a0021 | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
missense_variant | MODERATE | c.2008G>A | p.Val670Ile | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/48 | 2308/9984 | 2008/5073 | 670/1690 | chr2 | 227062578 | ||
| chr2:227078062
|
C | T | 1 | a0039 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1819G>A | p.Ala607Thr | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/48 | 2119/9984 | 1819/5073 | 607/1690 | chr2 | 227078062 | ||
| chr2:227080465
|
T | C | 3 | a0007a0038a0039 | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
missense_variant | MODERATE | c.1781A>G | p.Glu594Gly | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/48 | 2081/9984 | 1781/5073 | 594/1690 | chr2 | 227080465 | ||
| chr2:227082177
|
C | G | 1 | a0012 | 4 | HG01891.hp1 HG01934.hp1 HG02451.hp2 others(1): Show |
missense_variant | MODERATE | c.1634G>C | p.Gly545Ala | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/48 | 1934/9984 | 1634/5073 | 545/1690 | chr2 | 227082177 | ||
| chr2:227089883
|
G | A | 29 | a0002a0003a0006others(26): Show | 149 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(146): Show |
missense_variant | MODERATE | c.1444C>T | p.Pro482Ser | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/48 | 1744/9984 | 1444/5073 | 482/1690 | chr2 | 227089883 | ||
| chr2:227094181
|
G | A | 1 | a0024 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1313C>T | p.Pro438Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/48 | 1613/9984 | 1313/5073 | 438/1690 | chr2 | 227094181 | ||
| chr2:227103187
|
C | G | 1 | a0023 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.827G>C | p.Gly276Ala | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 14/48 | 1127/9984 | 827/5073 | 276/1690 | chr2 | 227103187 | ||
| chr2:227147434
|
T | C | 1 | a0040 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.50A>G | p.Lys17Arg | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/48 | 350/9984 | 50/5073 | 17/1690 | chr2 | 227147434 | ||
| chr2:227147467
|
A | G | 11 | a0006a0007a0008others(8): Show | 37 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(34): Show |
missense_variant | MODERATE | c.17T>C | p.Ile6Thr | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/48 | 317/9984 | 17/5073 | 6/1690 | chr2 | 227147467 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227007466
|
G | A | 44 | a0001c0010a0002c0002a0002c0019others(41): Show | 150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
synonymous_variant | LOW | c.4932C>T | p.Phe1644Phe | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 5232/9984 | 4932/5073 | 1644/1690 | chr2 | 227007466 | ||
| chr2:227007541
|
A | G | 1 | a0002c0060 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.4857T>C | p.Pro1619Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 5157/9984 | 4857/5073 | 1619/1690 | chr2 | 227007541 | ||
| chr2:227008192
|
G | A | 1 | a0004c0051 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.4635C>T | p.Ser1545Ser | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/48 | 4935/9984 | 4635/5073 | 1545/1690 | chr2 | 227008192 | ||
| chr2:227008279
|
T | C | 61 | a0001c0010a0001c0049a0001c0068others(58): Show | 194 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(191): Show |
synonymous_variant | LOW | c.4548A>G | p.Val1516Val | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/48 | 4848/9984 | 4548/5073 | 1516/1690 | chr2 | 227008279 | ||
| chr2:227022112
|
C | T | 1 | a0016c0064 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.4152G>A | p.Ala1384Ala | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/48 | 4452/9984 | 4152/5073 | 1384/1690 | chr2 | 227022112 | ||
| chr2:227027903
|
C | T | 37 | a0002c0002a0002c0019a0002c0021others(34): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
splice_region_variant&synonymous_variant | LOW | c.4080G>A | p.Pro1360Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/48 | 4380/9984 | 4080/5073 | 1360/1690 | chr2 | 227027903 | ||
| chr2:227027942
|
T | C | 4 | a0007c0006a0007c0031a0038c0038others(1): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.4041A>G | p.Leu1347Leu | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/48 | 4341/9984 | 4041/5073 | 1347/1690 | chr2 | 227027942 | ||
| chr2:227030453
|
A | G | 3 | a0002c0058a0006c0035a0022c0015 | 4 | HG02622.hp1 HG02717.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.3963T>C | p.Asp1321Asp | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/48 | 4263/9984 | 3963/5073 | 1321/1690 | chr2 | 227030453 | ||
| chr2:227032170
|
C | T | 36 | a0002c0002a0002c0019a0002c0021others(33): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
synonymous_variant | LOW | c.3684G>A | p.Lys1228Lys | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 39/48 | 3984/9984 | 3684/5073 | 1228/1690 | chr2 | 227032170 | ||
| chr2:227032188
|
A | G | 1 | a0035c0037 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.3666T>C | p.Pro1222Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 39/48 | 3966/9984 | 3666/5073 | 1222/1690 | chr2 | 227032188 | ||
| chr2:227032260
|
C | T | 36 | a0002c0002a0002c0019a0002c0021others(33): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
synonymous_variant | LOW | c.3594G>A | p.Gly1198Gly | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 39/48 | 3894/9984 | 3594/5073 | 1198/1690 | chr2 | 227032260 | ||
| chr2:227042167
|
T | C | 2 | a0013c0013a0021c0016 | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.3486A>G | p.Pro1162Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/48 | 3786/9984 | 3486/5073 | 1162/1690 | chr2 | 227042167 | ||
| chr2:227052366
|
T | G | 2 | a0016c0064a0016c0065 | 2 | HG02970.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.2907A>C | p.Ser969Ser | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/48 | 3207/9984 | 2907/5073 | 969/1690 | chr2 | 227052366 | ||
| chr2:227052396
|
G | A | 2 | a0003c0027a0014c0052 | 3 | HG00609.hp1 HG02056.hp1 NA19082.hp1 |
synonymous_variant | LOW | c.2877C>T | p.Pro959Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/48 | 3177/9984 | 2877/5073 | 959/1690 | chr2 | 227052396 | ||
| chr2:227054658
|
C | T | 3 | a0011c0012a0011c0053a0041c0029 | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.2796G>A | p.Lys932Lys | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/48 | 3096/9984 | 2796/5073 | 932/1690 | chr2 | 227054658 | ||
| chr2:227057545
|
T | A | 2 | a0013c0013a0021c0016 | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.2439A>T | p.Gly813Gly | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/48 | 2739/9984 | 2439/5073 | 813/1690 | chr2 | 227057545 | ||
| chr2:227059547
|
G | A | 1 | a0035c0037 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.2241C>T | p.Pro747Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/48 | 2541/9984 | 2241/5073 | 747/1690 | chr2 | 227059547 | ||
| chr2:227078048
|
A | G | 1 | a0002c0021 | 2 | HG00639.hp1 HG01099.hp2 |
synonymous_variant | LOW | c.1833T>C | p.Gly611Gly | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/48 | 2133/9984 | 1833/5073 | 611/1690 | chr2 | 227078048 | ||
| chr2:227078060
|
C | T | 3 | a0020c0041a0020c0054a0036c0055 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.1821G>A | p.Ala607Ala | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/48 | 2121/9984 | 1821/5073 | 607/1690 | chr2 | 227078060 | ||
| chr2:227094141
|
G | A | 1 | a0001c0068 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.1353C>T | p.Gly451Gly | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/48 | 1653/9984 | 1353/5073 | 451/1690 | chr2 | 227094141 | ||
| chr2:227094171
|
A | G | 4 | a0002c0019a0010c0032a0035c0037others(1): Show | 5 | HG02451.hp1 HG03139.hp2 HG03209.hp2 others(2): Show |
synonymous_variant | LOW | c.1323T>C | p.Pro441Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/48 | 1623/9984 | 1323/5073 | 441/1690 | chr2 | 227094171 | ||
| chr2:227101892
|
A | G | 9 | a0004c0040a0007c0031a0011c0012others(6): Show | 12 | HG01884.hp2 HG02622.hp1 HG02717.hp1 others(9): Show |
synonymous_variant | LOW | c.948T>C | p.Tyr316Tyr | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 16/48 | 1248/9984 | 948/5073 | 316/1690 | chr2 | 227101892 | ||
| chr2:227108860
|
C | T | 3 | a0008c0028a0035c0037a0038c0038 | 3 | HG01106.hp1 HG02451.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.666G>A | p.Pro222Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 11/48 | 966/9984 | 666/5073 | 222/1690 | chr2 | 227108860 | ||
| chr2:227121143
|
T | C | 1 | a0001c0070 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.198A>G | p.Pro66Pro | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/48 | 498/9984 | 198/5073 | 66/1690 | chr2 | 227121143 | ||
| chr2:227144528
|
T | C | 3 | a0001c0072a0003c0073a0005c0071 | 3 | HG00673.hp2 NA18979.hp1 NA19057.hp1 |
synonymous_variant | LOW | c.102A>G | p.Gln34Gln | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/48 | 402/9984 | 102/5073 | 34/1690 | chr2 | 227144528 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227002723
|
G | C | 13 | a0001c0049t0003a0001c0068t0003a0003c0003t0003others(10): Show | 37 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4602C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 4602 | chr2 | 227002723 | |||||
| chr2:227002830
|
G | GTCTT | 4 | a0020c0041t0010a0020c0054t0010a0035c0037t0016others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4491_*4494dupAAGA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 4494 | chr2 | 227002830 | |||||
| chr2:227002978
|
G | A | 2 | a0015c0024t0012a0037c0066t0012 | 2 | NA19011.hp1 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4347C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 4347 | chr2 | 227002978 | |||||
| chr2:227003003
|
G | A | 63 | a0001c0010t0005a0002c0002t0002a0002c0002t0004others(60): Show | 154 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*4322C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 4322 | chr2 | 227003003 | |||||
| chr2:227003143
|
C | G | 1 | a0006c0035t0036 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4182G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 4182 | chr2 | 227003143 | |||||
| chr2:227003689
|
G | A | 3 | a0004c0004t0037a0006c0005t0013a0015c0042t0013 | 3 | HG02486.hp1 HG02922.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3636C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 3636 | chr2 | 227003689 | |||||
| chr2:227004056
|
T | C | 1 | a0002c0059t0025 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3269A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 3269 | chr2 | 227004056 | |||||
| chr2:227004138
|
C | T | 49 | a0001c0010t0005a0002c0002t0002a0002c0002t0004others(46): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*3187G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 3187 | chr2 | 227004138 | |||||
| chr2:227004407
|
G | A | 2 | a0004c0004t0020a0008c0028t0034 | 2 | HG02922.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2918C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 2918 | chr2 | 227004407 | |||||
| chr2:227004470
|
G | A | 1 | a0002c0002t0026 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2855C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 2855 | chr2 | 227004470 | |||||
| chr2:227004477
|
G | A | 1 | a0035c0037t0016 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2848C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 2848 | chr2 | 227004477 | |||||
| chr2:227004980
|
A | G | 1 | a0007c0006t0035 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2345T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 2345 | chr2 | 227004980 | |||||
| chr2:227005204
|
G | GT | 7 | a0001c0001t0024a0002c0002t0011a0002c0002t0026others(4): Show | 7 | HG01261.hp2 HG02922.hp1 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2120dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 2120 | chr2 | 227005204 | |||||
| chr2:227005204
|
G | GTT | 5 | a0011c0012t0006a0011c0053t0015a0013c0013t0006others(2): Show | 10 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2119_*2120dupAA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 2120 | chr2 | 227005204 | |||||
| chr2:227005204
|
GT | G | 21 | a0002c0002t0002a0002c0002t0007a0002c0002t0027others(18): Show | 84 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2120delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 2120 | chr2 | 227005204 | |||||
| chr2:227005630
|
C | T | 1 | a0001c0001t0023 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1695G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 1695 | chr2 | 227005630 | |||||
| chr2:227005860
|
A | T | 2 | a0002c0002t0007a0023c0039t0007 | 4 | HG02074.hp2 NA18941.hp1 NA18965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1465T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 1465 | chr2 | 227005860 | |||||
| chr2:227006334
|
G | C | 1 | a0039c0067t0028 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*991C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 991 | chr2 | 227006334 | |||||
| chr2:227006409
|
A | G | 1 | a0001c0001t0022 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*916T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 916 | chr2 | 227006409 | |||||
| chr2:227006466
|
T | G | 1 | a0040c0074t0018 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*859A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 859 | chr2 | 227006466 | |||||
| chr2:227006468
|
C | T | 1 | a0002c0002t0027 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*857G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 857 | chr2 | 227006468 | |||||
| chr2:227006550
|
A | AT | 59 | a0001c0001t0021a0001c0010t0005a0002c0002t0002others(56): Show | 150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*774dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 774 | chr2 | 227006550 | |||||
| chr2:227006620
|
A | G | 1 | a0002c0002t0026 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*705T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 705 | chr2 | 227006620 | |||||
| chr2:227006744
|
C | T | 4 | a0020c0041t0010a0020c0054t0010a0035c0037t0016others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*581G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 581 | chr2 | 227006744 | |||||
| chr2:227006758
|
AT | A | 49 | a0001c0010t0005a0002c0002t0002a0002c0002t0004others(46): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*566delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 566 | chr2 | 227006758 | |||||
| chr2:227006767
|
T | C | 1 | a0003c0003t0031 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 558 | chr2 | 227006767 | |||||
| chr2:227007055
|
A | T | 1 | a0001c0001t0019 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*270T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 270 | chr2 | 227007055 | |||||
| chr2:227007063
|
A | G | 2 | a0003c0003t0030a0043c0036t0038 | 2 | HG01884.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*262T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 262 | chr2 | 227007063 | |||||
| chr2:227007081
|
G | A | 15 | a0001c0049t0003a0001c0068t0003a0003c0003t0003others(12): Show | 39 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 244 | chr2 | 227007081 | |||||
| chr2:227007081
|
G | T | 1 | a0040c0074t0018 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 48/48 | 244 | chr2 | 227007081 | |||||
| chr2:227147485
|
G | A | 21 | a0002c0002t0004a0004c0004t0037a0006c0005t0004others(18): Show | 38 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-2C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/48 | 2 | chr2 | 227147485 | |||||
| chr2:227147562
|
G | A | 3 | a0001c0070t0039a0011c0053t0015a0027c0047t0015 | 3 | HG02145.hp1 HG02965.hp1 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/48 | 79 | chr2 | 227147562 | |||||
| chr2:227164020
|
C | G | 2 | a0001c0001t0017a0035c0037t0016 | 2 | HG02451.hp1 HG02647.hp2 |
5_prime_UTR_variant | MODIFIER | c.-115G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/48 | 16537 | chr2 | 227164020 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227007819
|
A | G | 1 | a0008c0028t0034g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4809+199T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/47 | chr2 | 227007819 | ||||||
| chr2:227007898
|
C | T | 1 | a0002c0002t0002g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4809+120G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/47 | chr2 | 227007898 | ||||||
| chr2:227007901
|
A | G | 154 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(151): Show | 154 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.4809+117T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/47 | chr2 | 227007901 | ||||||
| chr2:227007918
|
G | A | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4809+100C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 47/47 | chr2 | 227007918 | ||||||
| chr2:227008312
|
A | G | 150 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(147): Show | 150 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(147): Show |
splice_region_variant&intron_variant | LOW | c.4523-8T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227008312 | ||||||
| chr2:227008505
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4523-201G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227008505 | ||||||
| chr2:227008635
|
T | G | 3 | a0012c0011t0003g0138a0012c0011t0003g0219a0012c0011t0003g0231 | 3 | HG01934.hp1 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4523-331A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227008635 | ||||||
| chr2:227008736
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0017g0002a0001c0070t0039g0204 | 3 | HG02647.hp2 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4523-432C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227008736 | ||||||
| chr2:227008744
|
T | G | 1 | a0002c0002t0005g0215 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4523-440A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227008744 | ||||||
| chr2:227008794
|
G | A | 15 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160others(12): Show | 15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.4523-490C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227008794 | ||||||
| chr2:227009040
|
G | A | 1 | a0002c0019t0005g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4523-736C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009040 | ||||||
| chr2:227009337
|
C | T | 1 | a0002c0002t0002g0073 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4522+976G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009337 | ||||||
| chr2:227009354
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0023g0131 | 2 | HG00544.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.4522+959G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009354 | ||||||
| chr2:227009360
|
C | T | 1 | a0002c0002t0005g0215 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4522+953G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009360 | ||||||
| chr2:227009392
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4522+921G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009392 | ||||||
| chr2:227009516
|
C | T | 136 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.4522+797G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009516 | ||||||
| chr2:227009697
|
C | CA | 15 | a0001c0001t0021g0141a0001c0001t0023g0131a0002c0002t0011g0222others(12): Show | 15 | HG02071.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.4522+615dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009697 | ||||||
| chr2:227009709
|
AAGAGGAA others(5): Show |
A | 4 | a0011c0012t0006g0032a0011c0012t0006g0257a0011c0053t0015g0152others(1): Show | 4 | HG02818.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4522+592_4522+603d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009709 | ||||||
| chr2:227009711
|
GAGGAAAA others(12): Show |
G | 1 | a0002c0002t0004g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4522+583_4522+601d others(21): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009711 | ||||||
| chr2:227009713
|
G | GGAAAAGA others(10): Show |
4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4522+583_4522+599d others(19): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009713 | ||||||
| chr2:227009713
|
GGAAAAGA others(10): Show |
G | 145 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(142): Show | 145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.4522+583_4522+599d others(19): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009713 | ||||||
| chr2:227009717
|
AAGAGAAG others(22): Show |
A | 1 | a0002c0002t0002g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4522+567_4522+595d others(31): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009717 | ||||||
| chr2:227009726
|
GAAGA | G | 4 | a0011c0012t0006g0032a0011c0012t0006g0257a0011c0053t0015g0152others(1): Show | 4 | HG02818.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4522+583_4522+586d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009726 | ||||||
| chr2:227009913
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4522+400C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227009913 | ||||||
| chr2:227010126
|
T | G | 1 | a0002c0002t0011g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4522+187A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227010126 | ||||||
| chr2:227010186
|
T | C | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4522+127A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227010186 | ||||||
| chr2:227010241
|
C | T | 151 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(148): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.4522+72G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 46/47 | chr2 | 227010241 | ||||||
| chr2:227010556
|
A | ATATGTTA others(19): Show |
1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4334-81_4334-56dup others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227010556 | ||||||
| chr2:227010644
|
G | A | 151 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(148): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.4334-143C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227010644 | ||||||
| chr2:227010653
|
T | A | 151 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(148): Show | 151 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.4334-152A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227010653 | ||||||
| chr2:227011046
|
C | T | 22 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(19): Show | 22 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.4334-545G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011046 | ||||||
| chr2:227011078
|
T | G | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4334-577A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011078 | ||||||
| chr2:227011297
|
T | C | 1 | a0038c0038t0005g0024 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4334-796A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011297 | ||||||
| chr2:227011311
|
G | A | 1 | a0027c0047t0015g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4334-810C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011311 | ||||||
| chr2:227011348
|
C | T | 1 | a0006c0005t0004g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4333+833G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011348 | ||||||
| chr2:227011413
|
G | A | 134 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(131): Show | 134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.4333+768C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011413 | ||||||
| chr2:227011558
|
G | T | 152 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(149): Show | 152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.4333+623C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011558 | ||||||
| chr2:227011772
|
G | C | 1 | a0004c0004t0037g0062 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4333+409C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011772 | ||||||
| chr2:227011809
|
G | A | 83 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(80): Show | 83 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.4333+372C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011809 | ||||||
| chr2:227011821
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4333+360A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011821 | ||||||
| chr2:227011866
|
C | T | 1 | a0001c0001t0021g0141 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4333+315G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011866 | ||||||
| chr2:227011943
|
T | C | 14 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(11): Show | 14 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.4333+238A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011943 | ||||||
| chr2:227011971
|
G | A | 10 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0117others(7): Show | 10 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.4333+210C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227011971 | ||||||
| chr2:227012091
|
A | C | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4333+90T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227012091 | ||||||
| chr2:227012175
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG01943.hp1 | splice_region_variant&intron_variant | LOW | c.4333+6G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 45/47 | chr2 | 227012175 | ||||||
| chr2:227012321
|
G | A | 152 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(149): Show | 152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.4217-24C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012321 | ||||||
| chr2:227012539
|
C | T | 6 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0051t0005g0023others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4217-242G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012539 | ||||||
| chr2:227012579
|
G | T | 1 | a0002c0002t0027g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4217-282C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012579 | ||||||
| chr2:227012632
|
C | CAAA | 7 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160others(4): Show | 7 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.4217-338_4217-336d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012632 | ||||||
| chr2:227012632
|
C | CAAAA | 24 | a0002c0002t0002g0086a0002c0002t0002g0113a0002c0002t0002g0247others(21): Show | 24 | HG00741.hp2 HG01169.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.4217-339_4217-336d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012632 | ||||||
| chr2:227012632
|
C | CAAAAA | 104 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(101): Show | 104 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.4217-340_4217-336d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012632 | ||||||
| chr2:227012632
|
C | CAAAAAA | 16 | a0002c0002t0002g0043a0002c0002t0002g0051a0002c0002t0002g0074others(13): Show | 16 | HG00673.hp2 HG01175.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.4217-341_4217-336d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012632 | ||||||
| chr2:227012719
|
G | C | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0042c0034t0004g0274 | 3 | HG03209.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4217-422C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012719 | ||||||
| chr2:227012876
|
G | C | 1 | a0002c0002t0002g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4217-579C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227012876 | ||||||
| chr2:227013075
|
G | A | 1 | a0007c0006t0004g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4217-778C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013075 | ||||||
| chr2:227013202
|
T | C | 9 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0087others(6): Show | 9 | HG00408.hp1 HG00438.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.4217-905A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013202 | ||||||
| chr2:227013259
|
C | A | 1 | a0002c0002t0005g0215 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4217-962G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013259 | ||||||
| chr2:227013273
|
T | A | 6 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(3): Show | 6 | HG02922.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.4217-976A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013273 | ||||||
| chr2:227013587
|
G | A | 8 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(5): Show | 8 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4217-1290C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013587 | ||||||
| chr2:227013623
|
C | T | 8 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(5): Show | 8 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4217-1326G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013623 | ||||||
| chr2:227013763
|
C | T | 4 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4217-1466G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013763 | ||||||
| chr2:227013776
|
C | T | 1 | a0036c0055t0029g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4217-1479G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013776 | ||||||
| chr2:227013846
|
C | G | 156 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(153): Show | 156 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.4217-1549G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013846 | ||||||
| chr2:227013950
|
C | T | 3 | a0027c0047t0015g0025a0033c0043t0011g0279a0045c0030t0033g0192 | 3 | HG02145.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4217-1653G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013950 | ||||||
| chr2:227013965
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4217-1668G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227013965 | ||||||
| chr2:227014068
|
C | A | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4217-1771G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014068 | ||||||
| chr2:227014102
|
A | C | 149 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(146): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.4217-1805T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014102 | ||||||
| chr2:227014210
|
C | T | 1 | a0001c0010t0005g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4217-1913G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014210 | ||||||
| chr2:227014220
|
G | C | 134 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(131): Show | 134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.4217-1923C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014220 | ||||||
| chr2:227014265
|
C | T | 1 | a0002c0002t0002g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4217-1968G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014265 | ||||||
| chr2:227014417
|
T | G | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4217-2120A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014417 | ||||||
| chr2:227014530
|
C | A | 3 | a0027c0047t0015g0025a0033c0043t0011g0279a0045c0030t0033g0192 | 3 | HG02145.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4217-2233G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014530 | ||||||
| chr2:227014714
|
TTTTG | T | 3 | a0027c0047t0015g0025a0033c0043t0011g0279a0045c0030t0033g0192 | 3 | HG02145.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4217-2421_4217-241 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014714 | ||||||
| chr2:227014892
|
C | CT | 16 | a0001c0001t0001g0206a0001c0001t0001g0216a0002c0002t0002g0051others(13): Show | 16 | HG00741.hp1 HG01175.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.4217-2596dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014892 | ||||||
| chr2:227014892
|
CT | C | 11 | a0001c0001t0001g0136a0001c0001t0021g0141a0002c0002t0002g0074others(8): Show | 11 | HG01169.hp2 HG01255.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.4217-2596delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227014892 | ||||||
| chr2:227015147
|
T | C | 149 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(146): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.4217-2850A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015147 | ||||||
| chr2:227015162
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4217-2865A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015162 | ||||||
| chr2:227015422
|
G | T | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4217-3125C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015422 | ||||||
| chr2:227015439
|
G | C | 1 | a0002c0002t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4217-3142C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015439 | ||||||
| chr2:227015717
|
AGTG | A | 15 | a0001c0049t0003g0253a0003c0003t0003g0006a0003c0003t0003g0076others(12): Show | 15 | HG00609.hp1 HG00673.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.4217-3423_4217-342 others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015717 | ||||||
| chr2:227015795
|
C | T | 217 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.4217-3498G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015795 | ||||||
| chr2:227015827
|
A | G | 146 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(143): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.4217-3530T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015827 | ||||||
| chr2:227015838
|
A | G | 146 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(143): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.4217-3541T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227015838 | ||||||
| chr2:227016015
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4217-3718G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016015 | ||||||
| chr2:227016053
|
G | A | 131 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(128): Show | 131 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.4217-3756C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016053 | ||||||
| chr2:227016064
|
G | A | 2 | a0002c0002t0002g0112a0005c0007t0002g0240 | 2 | HG00621.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4217-3767C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016064 | ||||||
| chr2:227016088
|
C | T | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0042c0034t0004g0274 | 3 | HG03209.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4217-3791G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016088 | ||||||
| chr2:227016266
|
C | T | 10 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.4217-3969G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016266 | ||||||
| chr2:227016272
|
A | C | 2 | a0003c0003t0030g0169a0043c0036t0038g0153 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4217-3975T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016272 | ||||||
| chr2:227016304
|
C | T | 41 | a0001c0049t0003g0253a0001c0068t0003g0199a0003c0003t0003g0004others(38): Show | 41 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.4217-4007G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016304 | ||||||
| chr2:227016495
|
G | A | 1 | a0005c0046t0005g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4217-4198C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016495 | ||||||
| chr2:227016574
|
G | A | 1 | a0009c0009t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4217-4277C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016574 | ||||||
| chr2:227016721
|
C | T | 1 | a0040c0074t0018g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4217-4424G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016721 | ||||||
| chr2:227016816
|
A | C | 1 | a0003c0026t0001g0010 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4217-4519T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227016816 | ||||||
| chr2:227017196
|
A | G | 1 | a0002c0002t0002g0014 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4216+4852T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017196 | ||||||
| chr2:227017286
|
C | G | 4 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4216+4762G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017286 | ||||||
| chr2:227017290
|
C | T | 145 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(142): Show | 145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.4216+4758G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017290 | ||||||
| chr2:227017424
|
A | T | 1 | a0001c0001t0017g0002 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4216+4624T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017424 | ||||||
| chr2:227017447
|
A | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0180a0010c0032t0008g0167 | 3 | HG03516.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4216+4601T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017447 | ||||||
| chr2:227017464
|
G | A | 144 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(141): Show | 144 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.4216+4584C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017464 | ||||||
| chr2:227017588
|
G | A | 5 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4216+4460C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017588 | ||||||
| chr2:227017588
|
G | T | 1 | a0011c0053t0015g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4216+4460C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017588 | ||||||
| chr2:227017661
|
T | A | 5 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4216+4387A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017661 | ||||||
| chr2:227017694
|
A | G | 1 | a0002c0002t0002g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4216+4354T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017694 | ||||||
| chr2:227017743
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0216a0001c0001t0001g0280others(1): Show | 4 | HG00741.hp1 HG01257.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.4216+4305G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017743 | ||||||
| chr2:227017833
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4216+4215A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017833 | ||||||
| chr2:227017991
|
T | C | 1 | a0003c0003t0003g0099 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4216+4057A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227017991 | ||||||
| chr2:227018174
|
G | A | 5 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4216+3874C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018174 | ||||||
| chr2:227018261
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0022g0119 | 2 | HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.4216+3787G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018261 | ||||||
| chr2:227018539
|
A | G | 6 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0051t0005g0023others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.4216+3509T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018539 | ||||||
| chr2:227018601
|
G | A | 1 | a0015c0024t0012g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4216+3447C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018601 | ||||||
| chr2:227018800
|
G | A | 4 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4216+3248C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018800 | ||||||
| chr2:227018877
|
A | T | 1 | a0044c0033t0032g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4216+3171T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018877 | ||||||
| chr2:227018932
|
C | G | 130 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(127): Show | 130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.4216+3116G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018932 | ||||||
| chr2:227018965
|
A | C | 23 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(20): Show | 23 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.4216+3083T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018965 | ||||||
| chr2:227018988
|
T | C | 40 | a0001c0049t0003g0253a0001c0068t0003g0199a0003c0003t0003g0004others(37): Show | 40 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.4216+3060A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227018988 | ||||||
| chr2:227019050
|
C | T | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4216+2998G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019050 | ||||||
| chr2:227019194
|
G | C | 145 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(142): Show | 145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.4216+2854C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019194 | ||||||
| chr2:227019270
|
A | G | 1 | a0001c0010t0005g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4216+2778T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019270 | ||||||
| chr2:227019340
|
A | G | 1 | a0003c0026t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4216+2708T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019340 | ||||||
| chr2:227019389
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4216+2659G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019389 | ||||||
| chr2:227019390
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4216+2658C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019390 | ||||||
| chr2:227019402
|
G | A | 134 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(131): Show | 134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.4216+2646C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019402 | ||||||
| chr2:227019808
|
C | T | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4216+2240G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019808 | ||||||
| chr2:227019929
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4216+2119T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227019929 | ||||||
| chr2:227020254
|
C | CACA | 153 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(150): Show | 153 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.4216+1791_4216+179 others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020254 | ||||||
| chr2:227020392
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4216+1656T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020392 | ||||||
| chr2:227020515
|
A | C | 1 | a0019c0025t0002g0198 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4216+1533T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020515 | ||||||
| chr2:227020562
|
C | T | 1 | a0010c0018t0004g0162 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4216+1486G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020562 | ||||||
| chr2:227020671
|
A | AG | 9 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(6): Show | 9 | HG02451.hp1 HG02818.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.4216+1376dupC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020671 | ||||||
| chr2:227020678
|
G | A | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4216+1370C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020678 | ||||||
| chr2:227020717
|
G | A | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4216+1331C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020717 | ||||||
| chr2:227020757
|
A | G | 1 | a0042c0034t0004g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4216+1291T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020757 | ||||||
| chr2:227020839
|
A | T | 1 | a0002c0002t0002g0107 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4216+1209T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020839 | ||||||
| chr2:227020872
|
A | ACTTCTTT others(1): Show |
8 | a0002c0002t0002g0013a0002c0002t0002g0043a0002c0002t0002g0080others(5): Show | 8 | HG00544.hp1 HG01167.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.4216+1175_4216+117 others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020872 | ||||||
| chr2:227020873
|
C | CTTCTTTT others(2): Show |
106 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0014others(103): Show | 106 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.4216+1174_4216+117 others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020873 | ||||||
| chr2:227020873
|
C | CTTCTTTT others(3): Show |
15 | a0002c0002t0002g0033a0002c0002t0002g0036a0002c0002t0002g0092others(12): Show | 15 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.4216+1174_4216+117 others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020873 | ||||||
| chr2:227020873
|
C | CTTCTTTT others(4): Show |
8 | a0002c0019t0005g0029a0008c0028t0034g0160a0011c0012t0006g0032others(5): Show | 8 | HG02145.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.4216+1174_4216+117 others(15): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020873 | ||||||
| chr2:227020873
|
C | CTTCTTTT others(5): Show |
2 | a0002c0002t0011g0222a0002c0019t0005g0166 | 2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4216+1174_4216+117 others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020873 | ||||||
| chr2:227020880
|
C | CTTTTTTT | 7 | a0020c0041t0010g0028a0020c0054t0010g0020a0027c0047t0015g0025others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.4216+1161_4216+116 others(11): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020880 | ||||||
| chr2:227020880
|
C | T | 139 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(136): Show | 139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.4216+1168G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020880 | ||||||
| chr2:227020909
|
C | T | 8 | a0020c0041t0010g0028a0020c0054t0010g0020a0027c0047t0015g0025others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4216+1139G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020909 | ||||||
| chr2:227020910
|
G | A | 4 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4216+1138C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227020910 | ||||||
| chr2:227021015
|
G | C | 1 | a0002c0002t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4216+1033C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227021015 | ||||||
| chr2:227021310
|
C | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0117others(6): Show | 9 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.4216+738G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227021310 | ||||||
| chr2:227021370
|
G | A | 5 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4216+678C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227021370 | ||||||
| chr2:227021559
|
C | A | 1 | a0002c0002t0002g0014 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4216+489G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227021559 | ||||||
| chr2:227021825
|
A | AAAAAT | 121 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(118): Show | 121 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.4216+218_4216+222d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227021825 | ||||||
| chr2:227021825
|
AAAAAT | A | 3 | a0007c0006t0004g0175a0007c0006t0004g0176a0041c0029t0004g0026 | 3 | HG02717.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4216+218_4216+222d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 44/47 | chr2 | 227021825 | ||||||
| chr2:227022209
|
C | T | 124 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(121): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4091-36G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227022209 | ||||||
| chr2:227022376
|
G | T | 4 | a0002c0058t0005g0214a0006c0035t0036g0270a0022c0015t0004g0145others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4091-203C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227022376 | ||||||
| chr2:227022471
|
C | T | 2 | a0003c0003t0030g0169a0043c0036t0038g0153 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4091-298G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227022471 | ||||||
| chr2:227022478
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0273 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4091-305C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227022478 | ||||||
| chr2:227022618
|
A | T | 5 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4091-445T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227022618 | ||||||
| chr2:227022932
|
GGTTT | G | 4 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(1): Show | 4 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.4091-763_4091-760d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227022932 | ||||||
| chr2:227023083
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0021g0141 | 2 | HG00438.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.4091-910C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023083 | ||||||
| chr2:227023089
|
A | G | 3 | a0027c0047t0015g0025a0033c0043t0011g0279a0045c0030t0033g0192 | 3 | HG02145.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4091-916T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023089 | ||||||
| chr2:227023112
|
A | G | 124 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(121): Show | 124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4091-939T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023112 | ||||||
| chr2:227023127
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4091-954C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023127 | ||||||
| chr2:227023167
|
A | G | 3 | a0003c0003t0003g0116a0003c0003t0003g0118a0003c0003t0003g0228 | 3 | HG00140.hp1 HG00639.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4091-994T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023167 | ||||||
| chr2:227023212
|
G | A | 2 | a0004c0004t0002g0095a0004c0004t0002g0202 | 2 | HG00741.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.4091-1039C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023212 | ||||||
| chr2:227023237
|
T | A | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4091-1064A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023237 | ||||||
| chr2:227023279
|
TA | T | 12 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.4091-1107delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023279 | ||||||
| chr2:227023441
|
C | CA | 6 | a0002c0002t0002g0112a0011c0012t0006g0032a0011c0012t0006g0256others(3): Show | 6 | HG00621.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4091-1269dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023441 | ||||||
| chr2:227023441
|
C | CAA | 123 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(120): Show | 123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.4091-1270_4091-126 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023441 | ||||||
| chr2:227023503
|
CTTTCACA others(14): Show |
C | 5 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(2): Show | 5 | HG02922.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4091-1351_4091-133 others(25): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023503 | ||||||
| chr2:227023782
|
G | A | 1 | a0002c0002t0002g0110 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4091-1609C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227023782 | ||||||
| chr2:227024004
|
CAA | C | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.4090+1796_4090+179 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024004 | ||||||
| chr2:227024028
|
C | CA | 44 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0049t0003g0253others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.4090+1773dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024028 | ||||||
| chr2:227024082
|
C | T | 1 | a0025c0044t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4090+1720G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024082 | ||||||
| chr2:227024122
|
T | C | 138 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(135): Show | 138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.4090+1680A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024122 | ||||||
| chr2:227024260
|
C | T | 8 | a0002c0002t0004g0149a0002c0058t0005g0214a0006c0005t0004g0148others(5): Show | 8 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4090+1542G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024260 | ||||||
| chr2:227024332
|
G | A | 1 | a0002c0002t0011g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4090+1470C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024332 | ||||||
| chr2:227024542
|
T | C | 8 | a0001c0068t0003g0199a0003c0003t0003g0005a0003c0003t0003g0190others(5): Show | 8 | HG00408.hp2 NA18962.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.4090+1260A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024542 | ||||||
| chr2:227024843
|
A | C | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.4090+959T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227024843 | ||||||
| chr2:227025067
|
T | G | 121 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(118): Show | 121 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.4090+735A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227025067 | ||||||
| chr2:227025078
|
AGAAACT | A | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4090+718_4090+723d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227025078 | ||||||
| chr2:227025264
|
G | A | 18 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0051t0005g0023others(15): Show | 18 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.4090+538C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227025264 | ||||||
| chr2:227025493
|
C | T | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4090+309G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227025493 | ||||||
| chr2:227025567
|
A | T | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.4090+235T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 43/47 | chr2 | 227025567 | ||||||
| chr2:227025865
|
A | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4082-55T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227025865 | ||||||
| chr2:227026023
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0085 | 3 | HG03491.hp2 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.4082-213G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026023 | ||||||
| chr2:227026044
|
G | C | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4082-234C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026044 | ||||||
| chr2:227026370
|
C | T | 7 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(4): Show | 7 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4082-560G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026370 | ||||||
| chr2:227026415
|
C | T | 5 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(2): Show | 5 | HG02922.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4082-605G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026415 | ||||||
| chr2:227026452
|
T | A | 1 | a0031c0061t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4082-642A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026452 | ||||||
| chr2:227026498
|
C | CA | 13 | a0001c0001t0001g0040a0001c0001t0001g0180a0001c0070t0039g0204others(10): Show | 13 | HG02080.hp2 HG02922.hp1 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.4082-689dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026498 | ||||||
| chr2:227026527
|
T | C | 7 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(4): Show | 7 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4082-717A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026527 | ||||||
| chr2:227026616
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4082-806C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026616 | ||||||
| chr2:227026738
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4082-928C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026738 | ||||||
| chr2:227026824
|
G | A | 10 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0113others(7): Show | 10 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.4082-1014C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026824 | ||||||
| chr2:227026860
|
G | A | 2 | a0001c0001t0001g0139a0001c0072t0001g0238 | 2 | HG00621.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.4081+1042C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026860 | ||||||
| chr2:227026972
|
G | A | 7 | a0020c0041t0010g0028a0020c0054t0010g0020a0027c0047t0015g0025others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4081+930C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227026972 | ||||||
| chr2:227027074
|
G | A | 6 | a0002c0002t0004g0149a0002c0058t0005g0214a0006c0005t0004g0148others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.4081+828C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027074 | ||||||
| chr2:227027098
|
A | G | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4081+804T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027098 | ||||||
| chr2:227027145
|
T | C | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.4081+757A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027145 | ||||||
| chr2:227027216
|
C | T | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.4081+686G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027216 | ||||||
| chr2:227027241
|
G | C | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.4081+661C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027241 | ||||||
| chr2:227027249
|
CA | C | 123 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(120): Show | 123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.4081+652delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027249 | ||||||
| chr2:227027321
|
T | C | 3 | a0027c0047t0015g0025a0033c0043t0011g0279a0045c0030t0033g0192 | 3 | HG02145.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4081+581A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027321 | ||||||
| chr2:227027420
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4081+482A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027420 | ||||||
| chr2:227027435
|
C | T | 3 | a0027c0047t0015g0025a0033c0043t0011g0279a0045c0030t0033g0192 | 3 | HG02145.hp1 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4081+467G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027435 | ||||||
| chr2:227027484
|
G | C | 119 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(116): Show | 119 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.4081+418C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027484 | ||||||
| chr2:227027491
|
G | A | 1 | a0002c0002t0002g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4081+411C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027491 | ||||||
| chr2:227027501
|
G | A | 109 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(106): Show | 109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.4081+401C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027501 | ||||||
| chr2:227027540
|
G | C | 7 | a0020c0041t0010g0028a0020c0054t0010g0020a0027c0047t0015g0025others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4081+362C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027540 | ||||||
| chr2:227027580
|
A | G | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4081+322T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027580 | ||||||
| chr2:227027638
|
AAT | A | 135 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(132): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.4081+262_4081+263d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027638 | ||||||
| chr2:227027650
|
T | G | 1 | a0002c0002t0002g0080 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.4081+252A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027650 | ||||||
| chr2:227027667
|
ATAAAG | A | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4081+230_4081+234d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027667 | ||||||
| chr2:227027681
|
A | T | 1 | a0002c0002t0002g0205 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4081+221T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027681 | ||||||
| chr2:227027712
|
T | C | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.4081+190A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027712 | ||||||
| chr2:227027782
|
A | G | 16 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(13): Show | 16 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.4081+120T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 42/47 | chr2 | 227027782 | ||||||
| chr2:227028149
|
G | A | 1 | a0002c0002t0002g0110 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3974-140C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028149 | ||||||
| chr2:227028301
|
G | A | 119 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(116): Show | 119 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.3974-292C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028301 | ||||||
| chr2:227028411
|
C | T | 1 | a0008c0008t0009g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3974-402G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028411 | ||||||
| chr2:227028447
|
C | T | 3 | a0010c0017t0008g0179a0010c0017t0008g0183a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3974-438G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028447 | ||||||
| chr2:227028644
|
T | TTTA | 47 | a0001c0001t0001g0206a0001c0001t0001g0244a0001c0049t0003g0253others(44): Show | 47 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.3974-638_3974-636d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028644 | ||||||
| chr2:227028644
|
T | TTTATTA | 20 | a0001c0001t0001g0109a0001c0001t0001g0115a0002c0002t0011g0222others(17): Show | 20 | HG01257.hp1 HG01258.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.3974-641_3974-636d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028644 | ||||||
| chr2:227028644
|
T | TTTATTAT others(5): Show |
2 | a0035c0037t0016g0003a0036c0055t0029g0174 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3974-647_3974-636d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028644 | ||||||
| chr2:227028644
|
TTTA | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(57): Show | 61 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.3974-638_3974-636d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028644 | ||||||
| chr2:227028644
|
TTTATTA | T | 5 | a0002c0002t0002g0205a0002c0002t0002g0239a0002c0002t0026g0232others(2): Show | 5 | HG01261.hp1 HG01261.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.3974-641_3974-636d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028644 | ||||||
| chr2:227028644
|
TTTATTAT others(2): Show |
T | 104 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(101): Show | 104 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.3974-644_3974-636d others(11): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028644 | ||||||
| chr2:227028676
|
T | G | 1 | a0002c0002t0002g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3974-667A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028676 | ||||||
| chr2:227028806
|
C | T | 1 | a0044c0033t0032g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3974-797G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028806 | ||||||
| chr2:227028845
|
T | G | 187 | a0001c0049t0003g0253a0001c0068t0003g0199a0002c0002t0002g0008others(184): Show | 187 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.3974-836A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028845 | ||||||
| chr2:227028944
|
A | G | 109 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(106): Show | 109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.3974-935T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227028944 | ||||||
| chr2:227029031
|
G | C | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.3974-1022C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227029031 | ||||||
| chr2:227029043
|
A | T | 4 | a0004c0004t0005g0030a0004c0004t0005g0234a0008c0008t0004g0161others(1): Show | 4 | HG02809.hp1 HG02976.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.3974-1034T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227029043 | ||||||
| chr2:227029147
|
C | T | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.3974-1138G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227029147 | ||||||
| chr2:227029442
|
C | T | 6 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0051t0005g0023others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3973+1001G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227029442 | ||||||
| chr2:227029716
|
C | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0087others(6): Show | 9 | HG00408.hp1 HG00438.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.3973+727G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227029716 | ||||||
| chr2:227029823
|
T | G | 1 | a0002c0002t0002g0205 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3973+620A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227029823 | ||||||
| chr2:227030092
|
ATATAT | A | 10 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.3973+346_3973+350d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227030092 | ||||||
| chr2:227030143
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.3973+300G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227030143 | ||||||
| chr2:227030409
|
A | G | 136 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.3973+34T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 41/47 | chr2 | 227030409 | ||||||
| chr2:227030751
|
G | GAAATAGA others(5): Show |
1 | a0003c0003t0003g0130 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3818-165_3818-154d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030751 | ||||||
| chr2:227030800
|
G | A | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3818-202C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030800 | ||||||
| chr2:227030842
|
T | C | 1 | a0002c0002t0002g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3818-244A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030842 | ||||||
| chr2:227030916
|
A | AGATG | 139 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0050others(136): Show | 139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.3818-322_3818-319d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030916 | ||||||
| chr2:227030916
|
A | AGATGGAT others(1): Show |
33 | a0001c0001t0001g0065a0001c0001t0001g0087a0001c0001t0001g0091others(30): Show | 33 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.3818-326_3818-319d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030916 | ||||||
| chr2:227030916
|
A | AGATGGAT others(5): Show |
4 | a0002c0002t0002g0047a0003c0003t0003g0004a0003c0003t0003g0093others(1): Show | 4 | HG00639.hp2 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.3818-330_3818-319d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030916 | ||||||
| chr2:227030916
|
AGATG | A | 10 | a0001c0001t0001g0106a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG01071.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.3818-322_3818-319d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030916 | ||||||
| chr2:227030916
|
AGATGGAT others(5): Show |
A | 4 | a0002c0002t0002g0072a0002c0002t0002g0073a0002c0021t0002g0245others(1): Show | 4 | HG00099.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.3818-330_3818-319d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030916 | ||||||
| chr2:227030979
|
CGGTT | C | 10 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0117others(7): Show | 10 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.3818-385_3818-382d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227030979 | ||||||
| chr2:227031031
|
T | TTGGATGG others(5): Show |
1 | a0016c0065t0005g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3818-434_3818-433i others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031031 | ||||||
| chr2:227031040
|
C | CGGATGGA others(13): Show |
2 | a0020c0041t0010g0028a0036c0055t0029g0174 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3818-443_3818-442i others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031040 | ||||||
| chr2:227031040
|
C | CGGATGGA others(17): Show |
2 | a0020c0054t0010g0020a0035c0037t0016g0003 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3818-443_3818-442i others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031040 | ||||||
| chr2:227031040
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3818-442G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031040 | ||||||
| chr2:227031041
|
A | AGATGGAT others(1): Show |
3 | a0001c0001t0001g0229a0001c0001t0001g0273a0003c0003t0003g0269 | 3 | HG02280.hp1 HG03225.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.3818-451_3818-444d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031041 | ||||||
| chr2:227031041
|
A | AGATGGAT others(5): Show |
55 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(52): Show | 55 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.3818-455_3818-444d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031041 | ||||||
| chr2:227031041
|
A | AGATGGAT others(9): Show |
111 | a0001c0001t0001g0108a0002c0002t0002g0008a0002c0002t0002g0014others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.3818-459_3818-444d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031041 | ||||||
| chr2:227031041
|
A | AGATGGAT others(13): Show |
27 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0033others(24): Show | 27 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.3818-463_3818-444d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031041 | ||||||
| chr2:227031041
|
A | AGATGGAT others(17): Show |
1 | a0004c0004t0020g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3818-467_3818-444d others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031041 | ||||||
| chr2:227031041
|
A | G | 6 | a0016c0064t0005g0178a0016c0065t0005g0150a0020c0041t0010g0028others(3): Show | 6 | HG02451.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3818-443T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031041 | ||||||
| chr2:227031069
|
G | GGATGGAT others(9): Show |
5 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0051t0005g0023others(2): Show | 5 | HG02809.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3818-472_3818-471i others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031069 | ||||||
| chr2:227031069
|
G | GGATGGAT others(13): Show |
1 | a0008c0008t0004g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3818-472_3818-471i others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031069 | ||||||
| chr2:227031231
|
G | A | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3818-633C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031231 | ||||||
| chr2:227031473
|
G | A | 6 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(3): Show | 6 | HG01243.hp1 HG02257.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3817+472C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031473 | ||||||
| chr2:227031614
|
C | T | 135 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(132): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.3817+331G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031614 | ||||||
| chr2:227031666
|
T | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3817+279A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031666 | ||||||
| chr2:227031672
|
G | A | 2 | a0002c0002t0002g0066a0002c0002t0002g0259 | 2 | NA18952.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3817+273C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031672 | ||||||
| chr2:227031676
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3817+269G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031676 | ||||||
| chr2:227031707
|
C | G | 5 | a0002c0002t0002g0047a0002c0002t0002g0239a0002c0002t0002g0267others(2): Show | 5 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.3817+238G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031707 | ||||||
| chr2:227031716
|
A | T | 118 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(115): Show | 118 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.3817+229T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031716 | ||||||
| chr2:227031827
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3817+118C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031827 | ||||||
| chr2:227031866
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3817+79G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031866 | ||||||
| chr2:227031936
|
C | G | 135 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(132): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.3817+9G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 40/47 | chr2 | 227031936 | ||||||
| chr2:227032360
|
A | G | 135 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(132): Show | 135 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.3578-84T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 38/47 | chr2 | 227032360 | ||||||
| chr2:227032464
|
A | G | 1 | a0005c0046t0005g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3578-188T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 38/47 | chr2 | 227032464 | ||||||
| chr2:227032571
|
T | A | 4 | a0002c0002t0007g0049a0002c0002t0007g0184a0002c0002t0007g0225others(1): Show | 4 | HG02074.hp2 NA18941.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3578-295A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 38/47 | chr2 | 227032571 | ||||||
| chr2:227032636
|
T | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3578-360A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 38/47 | chr2 | 227032636 | ||||||
| chr2:227032737
|
A | G | 1 | a0003c0003t0003g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3578-461T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 38/47 | chr2 | 227032737 | ||||||
| chr2:227032873
|
G | T | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3577+537C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 38/47 | chr2 | 227032873 | ||||||
| chr2:227033068
|
A | C | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3577+342T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 38/47 | chr2 | 227033068 | ||||||
| chr2:227033602
|
C | T | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3506-121G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227033602 | ||||||
| chr2:227033662
|
G | A | 1 | a0027c0047t0015g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3506-181C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227033662 | ||||||
| chr2:227033717
|
A | T | 1 | a0002c0002t0002g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3506-236T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227033717 | ||||||
| chr2:227033718
|
C | T | 116 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3506-237G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227033718 | ||||||
| chr2:227033906
|
TC | T | 208 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3506-426delG | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227033906 | ||||||
| chr2:227033942
|
T | C | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3506-461A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227033942 | ||||||
| chr2:227033995
|
G | A | 6 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(3): Show | 6 | HG01243.hp1 HG02257.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.3506-514C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227033995 | ||||||
| chr2:227034084
|
T | A | 1 | a0007c0006t0004g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3506-603A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034084 | ||||||
| chr2:227034118
|
G | A | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3506-637C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034118 | ||||||
| chr2:227034170
|
TTC | T | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3506-691_3506-690d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034170 | ||||||
| chr2:227034246
|
T | A | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3506-765A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034246 | ||||||
| chr2:227034457
|
C | T | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3506-976G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034457 | ||||||
| chr2:227034541
|
CT | C | 11 | a0002c0002t0002g0043a0002c0002t0002g0110a0002c0002t0002g0185others(8): Show | 11 | HG00408.hp2 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.3506-1061delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034541 | ||||||
| chr2:227034551
|
TTTAA | T | 6 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.3506-1074_3506-107 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034551 | ||||||
| chr2:227034566
|
A | T | 7 | a0002c0019t0005g0029a0002c0019t0005g0166a0004c0004t0002g0147others(4): Show | 7 | HG01106.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3506-1085T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034566 | ||||||
| chr2:227034570
|
A | T | 144 | a0001c0001t0001g0031a0001c0001t0001g0106a0001c0001t0001g0143others(141): Show | 144 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.3506-1089T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034570 | ||||||
| chr2:227034574
|
T | A | 3 | a0003c0003t0003g0190a0003c0003t0003g0223a0025c0044t0001g0060 | 3 | NA19000.hp1 NA19091.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3506-1093A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034574 | ||||||
| chr2:227034663
|
C | A | 1 | a0002c0002t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3506-1182G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034663 | ||||||
| chr2:227034835
|
C | T | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3506-1354G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227034835 | ||||||
| chr2:227035105
|
A | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3506-1624T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227035105 | ||||||
| chr2:227035397
|
G | A | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3506-1916C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227035397 | ||||||
| chr2:227035523
|
G | A | 2 | a0001c0001t0001g0143a0010c0032t0008g0167 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3506-2042C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227035523 | ||||||
| chr2:227035529
|
C | CA | 35 | a0001c0001t0001g0040a0001c0001t0001g0125a0001c0001t0001g0282others(32): Show | 35 | HG00323.hp1 HG00673.hp2 HG02074.hp1 others(32): Show |
intron_variant | MODIFIER | c.3506-2049dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227035529 | ||||||
| chr2:227035529
|
CA | C | 38 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0135others(35): Show | 38 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.3506-2049delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227035529 | ||||||
| chr2:227035529
|
CAA | C | 9 | a0001c0068t0003g0199a0003c0003t0003g0005a0003c0003t0003g0071others(6): Show | 9 | HG00408.hp2 HG03710.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.3506-2050_3506-204 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227035529 | ||||||
| chr2:227035703
|
G | A | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3506-2222C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227035703 | ||||||
| chr2:227036082
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3506-2601T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227036082 | ||||||
| chr2:227036196
|
G | A | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3506-2715C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227036196 | ||||||
| chr2:227036458
|
ACTCAGGC others(5): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3506-2989_3506-297 others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227036458 | ||||||
| chr2:227036553
|
T | A | 1 | a0001c0001t0017g0002 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3506-3072A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227036553 | ||||||
| chr2:227036626
|
C | T | 116 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3506-3145G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227036626 | ||||||
| chr2:227036708
|
G | A | 2 | a0012c0011t0003g0138a0012c0011t0003g0219 | 2 | HG01934.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3506-3227C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227036708 | ||||||
| chr2:227036869
|
G | A | 1 | a0008c0008t0004g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3506-3388C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227036869 | ||||||
| chr2:227037089
|
G | T | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3506-3608C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037089 | ||||||
| chr2:227037103
|
C | T | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3506-3622G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037103 | ||||||
| chr2:227037381
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3506-3900G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037381 | ||||||
| chr2:227037457
|
G | A | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3506-3976C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037457 | ||||||
| chr2:227037569
|
C | T | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3506-4088G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037569 | ||||||
| chr2:227037787
|
CA | C | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3506-4307delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037787 | ||||||
| chr2:227037793
|
G | A | 1 | a0002c0002t0002g0080 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3506-4312C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037793 | ||||||
| chr2:227037914
|
C | T | 1 | a0011c0012t0006g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3505+4234G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227037914 | ||||||
| chr2:227038223
|
C | T | 4 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(1): Show | 4 | HG02257.hp1 HG03453.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3505+3925G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227038223 | ||||||
| chr2:227038224
|
G | A | 133 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.3505+3924C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227038224 | ||||||
| chr2:227038588
|
T | C | 7 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(4): Show | 7 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+3560A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227038588 | ||||||
| chr2:227038677
|
A | G | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3505+3471T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227038677 | ||||||
| chr2:227038966
|
G | A | 10 | a0002c0002t0002g0014a0002c0002t0002g0077a0002c0002t0002g0078others(7): Show | 10 | NA18939.hp1 NA18944.hp1 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.3505+3182C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227038966 | ||||||
| chr2:227039047
|
T | G | 10 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.3505+3101A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039047 | ||||||
| chr2:227039160
|
AGTTTTGT others(3): Show |
A | 1 | a0023c0039t0007g0012 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3505+2978_3505+298 others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039160 | ||||||
| chr2:227039315
|
C | T | 1 | a0010c0017t0008g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3505+2833G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039315 | ||||||
| chr2:227039323
|
C | T | 1 | a0020c0054t0010g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3505+2825G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039323 | ||||||
| chr2:227039463
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0024g0132a0003c0026t0001g0010 | 3 | HG02040.hp1 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.3505+2685C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039463 | ||||||
| chr2:227039520
|
A | C | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3505+2628T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039520 | ||||||
| chr2:227039731
|
G | A | 116 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(113): Show | 116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.3505+2417C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039731 | ||||||
| chr2:227039735
|
A | G | 4 | a0005c0007t0005g0121a0005c0007t0005g0134a0005c0007t0005g0137others(1): Show | 4 | HG00323.hp1 HG00673.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.3505+2413T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227039735 | ||||||
| chr2:227040125
|
T | C | 5 | a0007c0006t0004g0175a0007c0006t0004g0176a0007c0006t0004g0181others(2): Show | 5 | HG01106.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+2023A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040125 | ||||||
| chr2:227040176
|
T | C | 7 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(4): Show | 7 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+1972A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040176 | ||||||
| chr2:227040223
|
G | A | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.3505+1925C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040223 | ||||||
| chr2:227040294
|
T | G | 1 | a0006c0005t0004g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3505+1854A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040294 | ||||||
| chr2:227040386
|
C | G | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3505+1762G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040386 | ||||||
| chr2:227040514
|
G | C | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3505+1634C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040514 | ||||||
| chr2:227040518
|
G | A | 1 | a0002c0002t0002g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3505+1630C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040518 | ||||||
| chr2:227040568
|
C | CT | 10 | a0001c0001t0001g0046a0001c0001t0001g0109a0001c0001t0001g0125others(7): Show | 10 | HG02074.hp1 HG03098.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.3505+1579dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040568 | ||||||
| chr2:227040568
|
CT | C | 127 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(124): Show | 127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.3505+1579delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040568 | ||||||
| chr2:227040769
|
G | A | 1 | a0002c0002t0002g0210 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3505+1379C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040769 | ||||||
| chr2:227040799
|
A | C | 7 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(4): Show | 7 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+1349T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040799 | ||||||
| chr2:227040807
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3505+1341C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040807 | ||||||
| chr2:227040858
|
CA | C | 3 | a0003c0003t0003g0006a0003c0003t0003g0084a0029c0063t0003g0082 | 3 | HG00673.hp1 NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.3505+1289delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227040858 | ||||||
| chr2:227041028
|
G | T | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3505+1120C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041028 | ||||||
| chr2:227041077
|
A | G | 5 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(2): Show | 5 | HG02922.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+1071T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041077 | ||||||
| chr2:227041114
|
G | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG00609.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.3505+1034C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041114 | ||||||
| chr2:227041274
|
G | C | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3505+874C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041274 | ||||||
| chr2:227041374
|
C | T | 1 | a0002c0002t0002g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3505+774G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041374 | ||||||
| chr2:227041671
|
G | A | 1 | a0002c0002t0002g0073 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3505+477C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041671 | ||||||
| chr2:227041684
|
AAGACAG | A | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3505+458_3505+463d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041684 | ||||||
| chr2:227041701
|
AGAGAAGG others(8): Show |
A | 1 | a0004c0004t0020g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3505+432_3505+446d others(17): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041701 | ||||||
| chr2:227041703
|
AGAAGGAA others(32): Show |
A | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3505+406_3505+444d others(41): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041703 | ||||||
| chr2:227041705
|
A | G | 8 | a0002c0002t0011g0222a0008c0028t0034g0160a0013c0013t0006g0144others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.3505+443T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041705 | ||||||
| chr2:227041707
|
G | A | 1 | a0017c0022t0003g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3505+441C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041707 | ||||||
| chr2:227041709
|
A | G | 1 | a0017c0022t0003g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3505+439T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041709 | ||||||
| chr2:227041709
|
AAGGAAGG others(4): Show |
A | 2 | a0002c0002t0011g0222a0008c0028t0034g0160 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3505+428_3505+438d others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041709 | ||||||
| chr2:227041713
|
AAGGGAGG | A | 4 | a0001c0001t0001g0011a0013c0013t0006g0155a0013c0013t0006g0212others(1): Show | 4 | HG02145.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3505+428_3505+434d others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041713 | ||||||
| chr2:227041720
|
G | A | 2 | a0013c0013t0006g0144a0021c0016t0014g0019 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3505+428C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
G | GAGGA | 15 | a0001c0001t0001g0058a0001c0001t0001g0102a0001c0001t0001g0216others(12): Show | 15 | HG00609.hp1 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.3505+424_3505+427d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
G | GAGGAAGG others(1): Show |
9 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0001g0227others(6): Show | 9 | HG01106.hp2 HG01255.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.3505+420_3505+427d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
G | GAGGAAGG others(5): Show |
4 | a0001c0049t0003g0253a0003c0003t0003g0084a0003c0003t0031g0250others(1): Show | 4 | NA18939.hp2 NA18993.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.3505+416_3505+427d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
G | GAGGAAGG others(9): Show |
2 | a0019c0025t0002g0198a0019c0025t0002g0261 | 2 | NA18952.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3505+412_3505+427d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
G | GAGGAAGG others(13): Show |
1 | a0014c0020t0001g0007 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3505+408_3505+427d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
GAGGA | G | 9 | a0001c0001t0001g0206a0001c0001t0001g0229a0001c0001t0001g0273others(6): Show | 9 | HG01515.hp2 HG02056.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3505+424_3505+427d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
GAGGAAGG others(1): Show |
G | 8 | a0001c0001t0001g0038a0001c0001t0001g0136a0001c0001t0001g0209others(5): Show | 8 | HG01255.hp1 HG02809.hp2 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.3505+420_3505+427d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
GAGGAAGG others(5): Show |
G | 6 | a0002c0002t0002g0043a0002c0002t0002g0107a0002c0002t0002g0205others(3): Show | 6 | HG01943.hp2 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.3505+416_3505+427d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
GAGGAAGG others(9): Show |
G | 5 | a0002c0002t0002g0014a0002c0002t0002g0140a0002c0002t0002g0177others(2): Show | 5 | HG02683.hp1 HG03491.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+412_3505+427d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
GAGGAAGG others(13): Show |
G | 2 | a0006c0005t0004g0193a0018c0023t0002g0127 | 2 | HG02165.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3505+408_3505+427d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041720
|
GAGGAAGG others(17): Show |
G | 3 | a0001c0001t0001g0034a0002c0002t0002g0264a0044c0033t0032g0168 | 3 | HG02976.hp2 HG03139.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.3505+404_3505+427d others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041720 | ||||||
| chr2:227041744
|
A | G | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3505+404T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041744 | ||||||
| chr2:227041759
|
GAAGGAAG others(33): Show |
G | 1 | a0002c0002t0005g0215 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3505+349_3505+388d others(42): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041759 | ||||||
| chr2:227041759
|
GAAGGAAG others(37): Show |
G | 1 | a0002c0002t0007g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3505+345_3505+388d others(46): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041759 | ||||||
| chr2:227041763
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0017g0002a0042c0034t0004g0274 | 3 | HG02622.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3505+385C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041763 | ||||||
| chr2:227041763
|
GAAGGAAG others(29): Show |
G | 1 | a0002c0002t0002g0263 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3505+349_3505+384d others(38): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041763 | ||||||
| chr2:227041766
|
GGAAGGAA others(4): Show |
G | 1 | a0018c0023t0002g0052 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3505+371_3505+381d others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041766 | ||||||
| chr2:227041767
|
G | A | 5 | a0001c0001t0001g0108a0001c0001t0017g0002a0010c0017t0008g0179others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+381C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041767 | ||||||
| chr2:227041767
|
GAAGGAAG others(21): Show |
G | 1 | a0002c0002t0002g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3505+353_3505+380d others(30): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041767 | ||||||
| chr2:227041767
|
GAAGGAAG others(25): Show |
G | 1 | a0006c0005t0004g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3505+349_3505+380d others(34): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041767 | ||||||
| chr2:227041767
|
GAAGGAAG others(41): Show |
G | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3505+333_3505+380d others(50): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041767 | ||||||
| chr2:227041769
|
A | AG | 4 | a0002c0002t0002g0066a0004c0004t0002g0095a0004c0004t0002g0202others(1): Show | 4 | HG00741.hp2 HG01258.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.3505+378dupC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041769 | ||||||
| chr2:227041770
|
GGAA | G | 4 | a0001c0001t0001g0143a0008c0008t0009g0165a0008c0008t0009g0271others(1): Show | 4 | HG02559.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3505+375_3505+377d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041770 | ||||||
| chr2:227041771
|
G | A | 7 | a0001c0001t0001g0108a0001c0001t0001g0194a0001c0001t0017g0002others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+377C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041771
|
G | GGA | 7 | a0001c0001t0001g0050a0001c0001t0001g0117a0001c0001t0001g0180others(4): Show | 7 | HG00099.hp2 HG00673.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3505+376_3505+377i others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041771
|
GAAGGAAG others(13): Show |
G | 6 | a0002c0002t0002g0080a0002c0002t0007g0049a0004c0004t0002g0147others(3): Show | 6 | HG01175.hp2 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3505+357_3505+376d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041771
|
GAAGGAAG others(17): Show |
G | 7 | a0002c0002t0002g0074a0002c0002t0002g0077a0002c0002t0002g0078others(4): Show | 7 | HG00323.hp2 HG01358.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+353_3505+376d others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041771
|
GAAGGAAG others(21): Show |
G | 5 | a0002c0002t0002g0008a0002c0002t0002g0047a0002c0002t0002g0185others(2): Show | 5 | HG01175.hp1 HG01884.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+349_3505+376d others(30): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041771
|
GAAGGAAG others(25): Show |
G | 3 | a0002c0002t0002g0203a0002c0002t0002g0210a0002c0002t0002g0211 | 3 | HG03927.hp2 NA18995.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3505+345_3505+376d others(34): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041771
|
GAAGGAAG others(29): Show |
G | 1 | a0002c0002t0027g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3505+341_3505+376d others(38): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041771
|
GAAGGAAG others(33): Show |
G | 1 | a0002c0002t0002g0079 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3505+337_3505+376d others(42): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041771 | ||||||
| chr2:227041772
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3505+376T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041772 | ||||||
| chr2:227041773
|
A | AG | 6 | a0002c0002t0002g0073a0002c0021t0002g0245a0005c0007t0002g0053others(3): Show | 6 | HG01099.hp2 HG02004.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.3505+374dupC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041773 | ||||||
| chr2:227041774
|
G | A | 5 | a0001c0001t0001g0046a0002c0002t0002g0066a0004c0004t0002g0095others(2): Show | 5 | HG00741.hp2 HG01258.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+374C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041774 | ||||||
| chr2:227041774
|
GGAA | G | 3 | a0001c0001t0001g0065a0002c0021t0002g0246a0004c0004t0002g0260 | 3 | HG00639.hp1 HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.3505+371_3505+373d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041774 | ||||||
| chr2:227041775
|
G | A | 13 | a0001c0001t0001g0050a0001c0001t0001g0108a0001c0001t0001g0117others(10): Show | 13 | HG00099.hp2 HG00621.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3505+373C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
G | GGA | 6 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0251others(3): Show | 6 | HG02132.hp1 NA18979.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.3505+372_3505+373i others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
G | GGAAAGA | 4 | a0001c0001t0001g0040a0001c0001t0022g0119a0001c0072t0001g0238others(1): Show | 4 | HG01192.hp1 HG02165.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.3505+372_3505+373i others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
G | GGAAAGAA others(3): Show |
2 | a0001c0001t0001g0258a0026c0050t0001g0081 | 2 | HG02572.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3505+372_3505+373i others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
GAAGGAAG others(9): Show |
G | 2 | a0001c0001t0001g0087a0002c0002t0002g0112 | 2 | HG00438.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.3505+357_3505+372d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
GAAGGAAG others(13): Show |
G | 4 | a0002c0002t0002g0036a0002c0002t0002g0188a0004c0004t0002g0187others(1): Show | 4 | HG01243.hp2 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.3505+353_3505+372d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
GAAGGAAG others(17): Show |
G | 2 | a0002c0002t0002g0098a0002c0002t0002g0110 | 2 | HG01934.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3505+349_3505+372d others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
GAAGGAAG others(21): Show |
G | 1 | a0004c0004t0002g0218 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3505+345_3505+372d others(30): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
GAAGGAAG others(29): Show |
G | 1 | a0002c0002t0002g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3505+337_3505+372d others(38): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041775
|
GAAGGAAG others(33): Show |
G | 1 | a0002c0002t0002g0051 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3505+333_3505+372d others(42): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041775 | ||||||
| chr2:227041777
|
A | AG | 9 | a0001c0001t0001g0001a0001c0001t0021g0141a0002c0002t0002g0072others(6): Show | 10 | HG00099.hp1 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3505+370dupC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041777 | ||||||
| chr2:227041778
|
G | A | 15 | a0001c0001t0001g0143a0001c0001t0001g0213a0002c0002t0002g0066others(12): Show | 15 | HG00741.hp2 HG01099.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.3505+370C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041778 | ||||||
| chr2:227041779
|
G | A | 23 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0050others(20): Show | 23 | HG00099.hp2 HG00673.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.3505+369C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
G | GGA | 4 | a0001c0001t0001g0197a0007c0006t0004g0176a0009c0009t0001g0016others(1): Show | 4 | HG01106.hp1 HG01169.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3505+368_3505+369i others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
G | GGAAAGA | 7 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0124others(4): Show | 7 | HG00558.hp2 HG00609.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.3505+368_3505+369i others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
GAAGGAAG others(5): Show |
G | 2 | a0001c0001t0001g0054a0001c0001t0001g0207 | 2 | NA18946.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3505+357_3505+368d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
GAAGGAAG others(9): Show |
G | 2 | a0002c0002t0002g0236a0002c0059t0025g0037 | 2 | HG01123.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.3505+353_3505+368d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
GAAGGAAG others(13): Show |
G | 1 | a0002c0002t0002g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3505+349_3505+368d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
GAAGGAAG others(17): Show |
G | 1 | a0002c0002t0002g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3505+345_3505+368d others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
GAAGGAAG others(29): Show |
G | 2 | a0001c0001t0001g0208a0002c0002t0002g0182 | 2 | HG04115.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3505+333_3505+368d others(38): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
GAAGGAAG others(41): Show |
G | 2 | a0001c0001t0001g0111a0009c0009t0001g0083 | 2 | NA18971.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3505+321_3505+368d others(50): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041779
|
GAAGGAAG others(45): Show |
G | 1 | a0001c0001t0001g0100 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3505+317_3505+368d others(54): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041779 | ||||||
| chr2:227041780
|
A | G | 1 | a0009c0009t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3505+368T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041780 | ||||||
| chr2:227041782
|
G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0143others(29): Show | 33 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.3505+366C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041782 | ||||||
| chr2:227041782
|
GGAAGGGA others(53): Show |
G | 1 | a0013c0013t0006g0155 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3505+306_3505+365d others(62): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041782 | ||||||
| chr2:227041783
|
G | A | 33 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0050others(30): Show | 33 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.3505+365C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041783
|
G | GGAAAGAA others(3): Show |
5 | a0001c0001t0001g0044a0001c0001t0001g0125a0001c0001t0001g0196others(2): Show | 5 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+364_3505+365i others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041783
|
GAAGGGAA others(17): Show |
G | 1 | a0002c0002t0002g0113 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3505+341_3505+364d others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041783
|
GAAGGGAA others(21): Show |
G | 1 | a0002c0002t0002g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3505+337_3505+364d others(30): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041783
|
GAAGGGAA others(25): Show |
G | 1 | a0002c0002t0002g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3505+333_3505+364d others(34): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041783
|
GAAGGGAA others(37): Show |
G | 1 | a0013c0013t0006g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3505+321_3505+364d others(46): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041783
|
GAAGGGAA others(63): Show |
G | 1 | a0020c0041t0010g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3505+295_3505+364d others(72): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041783
|
GAAGGGAA others(67): Show |
G | 1 | a0021c0016t0014g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3505+291_3505+364d others(76): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041783 | ||||||
| chr2:227041784
|
A | G | 7 | a0001c0001t0001g0106a0001c0001t0001g0262a0001c0001t0001g0282others(4): Show | 7 | HG00323.hp1 HG01071.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+364T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041784 | ||||||
| chr2:227041785
|
AG | A | 38 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0109others(35): Show | 39 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.3505+362delC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041785 | ||||||
| chr2:227041785
|
AGG | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0108a0001c0001t0001g0194others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3505+361_3505+362d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041785 | ||||||
| chr2:227041786
|
G | A | 11 | a0001c0001t0001g0106a0001c0001t0001g0262a0001c0001t0001g0282others(8): Show | 11 | HG00323.hp1 HG00438.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3505+362C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041786 | ||||||
| chr2:227041786
|
G | GAA | 18 | a0001c0001t0001g0139a0001c0001t0001g0197a0001c0072t0001g0238others(15): Show | 18 | HG00621.hp2 HG00673.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3505+361_3505+362i others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041786 | ||||||
| chr2:227041786
|
G | GGAAGGAA others(13): Show |
1 | a0017c0022t0003g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3505+361_3505+362i others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041786 | ||||||
| chr2:227041787
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0106others(53): Show | 57 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.3505+361C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
G | GAA | 20 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0050others(17): Show | 20 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.3505+360_3505+361i others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
G | GAAAGAAA others(4): Show |
1 | a0009c0009t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3505+360_3505+361i others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
G | GAAAGAAA others(20): Show |
1 | a0001c0001t0023g0131 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3505+360_3505+361i others(29): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
G | GAAGGAAG others(13): Show |
1 | a0001c0001t0001g0244 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3505+360_3505+361i others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
G | GAAGGAAG others(13): Show |
1 | a0001c0010t0005g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3505+360_3505+361i others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
G | GAAGGAAG others(17): Show |
1 | a0001c0010t0005g0277 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3505+360_3505+361i others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
G | GAAGGAAG others(9): Show |
2 | a0001c0010t0005g0276a0010c0018t0004g0157 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3505+360_3505+361i others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
GGA | G | 5 | a0003c0003t0003g0004a0003c0003t0003g0076a0003c0003t0003g0093others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3505+359_3505+360d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
GGAAAGAA others(47): Show |
G | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3505+307_3505+360d others(56): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041787
|
GGAAAGAA others(55): Show |
G | 1 | a0013c0013t0006g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3505+299_3505+360d others(64): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041787 | ||||||
| chr2:227041788
|
G | A | 11 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0010t0005g0272others(8): Show | 11 | HG00140.hp2 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.3505+360C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041788 | ||||||
| chr2:227041789
|
A | G | 4 | a0001c0001t0001g0197a0001c0001t0019g0126a0001c0010t0005g0277others(1): Show | 4 | HG00438.hp1 HG01169.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3505+359T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041789 | ||||||
| chr2:227041790
|
A | G | 11 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0010t0005g0272others(8): Show | 11 | HG00140.hp2 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.3505+358T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041790 | ||||||
| chr2:227041790
|
AAGAAAGA others(51): Show |
A | 2 | a0016c0065t0005g0150a0021c0016t0014g0019 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3505+300_3505+357d others(60): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041790 | ||||||
| chr2:227041791
|
A | G | 21 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0010t0005g0272others(18): Show | 21 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.3505+357T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041791 | ||||||
| chr2:227041792
|
GAAAGAAA others(28): Show |
G | 2 | a0011c0012t0006g0256a0011c0012t0006g0257 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3505+321_3505+355d others(37): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041792 | ||||||
| chr2:227041793
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0143others(11): Show | 15 | HG00140.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3505+355T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041793 | ||||||
| chr2:227041794
|
A | AG | 6 | a0001c0068t0003g0199a0003c0003t0003g0101a0003c0003t0003g0116others(3): Show | 6 | HG00639.hp2 HG02451.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.3505+353_3505+354i others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041794 | ||||||
| chr2:227041795
|
A | G | 8 | a0001c0068t0003g0199a0003c0003t0003g0006a0003c0003t0003g0101others(5): Show | 8 | HG00639.hp2 HG00673.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3505+353T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041795 | ||||||
| chr2:227041796
|
GAA | G | 5 | a0003c0003t0003g0004a0003c0003t0003g0076a0003c0003t0003g0093others(2): Show | 5 | HG00140.hp1 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3505+350_3505+351d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041796 | ||||||
| chr2:227041797
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0109a0001c0001t0001g0122others(4): Show | 7 | HG01433.hp2 HG01884.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+351T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041797 | ||||||
| chr2:227041799
|
A | G | 8 | a0003c0003t0003g0004a0003c0003t0003g0006a0003c0003t0003g0076others(5): Show | 8 | HG00140.hp1 HG00673.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3505+349T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041799 | ||||||
| chr2:227041801
|
A | G | 6 | a0001c0001t0001g0038a0001c0001t0001g0106a0001c0001t0001g0123others(3): Show | 6 | HG01071.hp2 HG04204.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.3505+347T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041801 | ||||||
| chr2:227041802
|
AAGGAAGA others(39): Show |
A | 2 | a0011c0012t0006g0032a0011c0053t0015g0152 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3505+300_3505+345d others(48): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041802 | ||||||
| chr2:227041803
|
A | G | 1 | a0041c0029t0004g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3505+345T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041803 | ||||||
| chr2:227041804
|
G | A | 1 | a0017c0022t0003g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3505+344C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041804 | ||||||
| chr2:227041805
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0038others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3505+343C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041805 | ||||||
| chr2:227041805
|
G | GAAGAAAG others(5): Show |
1 | a0001c0001t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3505+331_3505+342d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041805 | ||||||
| chr2:227041805
|
GAAGA | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0207a0014c0052t0003g0089 | 3 | HG00438.hp2 HG02056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.3505+339_3505+342d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041805 | ||||||
| chr2:227041805
|
GAAGAAAG others(5): Show |
G | 1 | a0003c0003t0003g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3505+331_3505+342d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041805 | ||||||
| chr2:227041805
|
GAAGAAAG others(47): Show |
G | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3505+289_3505+342d others(56): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041805 | ||||||
| chr2:227041806
|
A | AAGAAAGA others(53): Show |
1 | a0004c0051t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3505+341_3505+342i others(62): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041806 | ||||||
| chr2:227041806
|
A | AAGAAAGA others(49): Show |
1 | a0008c0008t0004g0164 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3505+341_3505+342i others(58): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041806 | ||||||
| chr2:227041806
|
A | AAGAAAGA others(41): Show |
1 | a0008c0008t0004g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3505+341_3505+342i others(50): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041806 | ||||||
| chr2:227041806
|
AAGAAAGA others(35): Show |
A | 2 | a0001c0001t0001g0097a0020c0054t0010g0020 | 2 | NA18945.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3505+300_3505+341d others(44): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041806 | ||||||
| chr2:227041809
|
A | G | 5 | a0001c0001t0001g0104a0003c0003t0003g0071a0003c0003t0003g0269others(2): Show | 5 | HG00140.hp2 HG01891.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3505+339T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041809 | ||||||
| chr2:227041810
|
A | AAGAAAGA others(45): Show |
1 | a0004c0004t0005g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3505+337_3505+338i others(54): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041810 | ||||||
| chr2:227041810
|
AAGAAAGA others(31): Show |
A | 2 | a0036c0055t0029g0174a0041c0029t0004g0026 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3505+300_3505+337d others(40): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041810 | ||||||
| chr2:227041812
|
GAAAGAAA others(7): Show |
G | 1 | a0002c0002t0007g0184 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.3505+322_3505+335d others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041812 | ||||||
| chr2:227041813
|
A | G | 6 | a0001c0068t0003g0199a0003c0003t0003g0101a0003c0003t0003g0116others(3): Show | 6 | HG00639.hp2 HG02451.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.3505+335T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041813 | ||||||
| chr2:227041817
|
A | G | 7 | a0003c0003t0003g0004a0003c0003t0003g0006a0003c0003t0003g0076others(4): Show | 7 | HG00140.hp1 HG00673.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3505+331T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041817 | ||||||
| chr2:227041818
|
A | G | 1 | a0001c0001t0017g0002 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3505+330T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041818 | ||||||
| chr2:227041820
|
GAA | G | 7 | a0002c0002t0002g0066a0002c0002t0007g0049a0002c0021t0002g0246others(4): Show | 7 | HG00558.hp1 HG00639.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+326_3505+327d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041820 | ||||||
| chr2:227041820
|
GAAAGAAA others(7): Show |
G | 2 | a0002c0002t0002g0009a0004c0004t0002g0075 | 2 | HG02004.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3505+314_3505+327d others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041820 | ||||||
| chr2:227041820
|
GAAAGAAA others(11): Show |
G | 1 | a0004c0004t0002g0042 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3505+310_3505+327d others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041820 | ||||||
| chr2:227041822
|
A | AAG | 9 | a0002c0002t0002g0013a0002c0002t0002g0014a0002c0002t0002g0043others(6): Show | 9 | HG00544.hp1 HG01943.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.3505+324_3505+325d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041822 | ||||||
| chr2:227041822
|
A | G | 1 | a0001c0001t0017g0002 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3505+326T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041822 | ||||||
| chr2:227041824
|
GAA | G | 7 | a0002c0002t0002g0088a0002c0002t0002g0151a0002c0002t0002g0205others(4): Show | 7 | HG01123.hp1 HG02040.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.3505+322_3505+323d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041824 | ||||||
| chr2:227041825
|
A | G | 1 | a0003c0014t0002g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3505+323T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041825 | ||||||
| chr2:227041826
|
A | G | 3 | a0001c0001t0017g0002a0015c0042t0013g0041a0042c0034t0004g0274 | 3 | HG02647.hp2 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3505+322T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041826 | ||||||
| chr2:227041828
|
GAA | G | 6 | a0002c0002t0002g0177a0002c0002t0002g0264a0002c0021t0002g0245others(3): Show | 6 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.3505+318_3505+319d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041828 | ||||||
| chr2:227041829
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3505+319T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041829 | ||||||
| chr2:227041830
|
A | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0108a0001c0001t0017g0002others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3505+318T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041830 | ||||||
| chr2:227041832
|
GAA | G | 40 | a0001c0001t0001g0085a0002c0002t0002g0013a0002c0002t0002g0014others(37): Show | 40 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.3505+314_3505+315d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041832 | ||||||
| chr2:227041834
|
A | AAG | 6 | a0001c0001t0001g0139a0001c0001t0001g0196a0002c0002t0002g0073others(3): Show | 6 | HG00408.hp1 HG00621.hp2 HG00673.hp2 others(3): Show |
intron_variant | MODIFIER | c.3505+312_3505+313d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041834 | ||||||
| chr2:227041834
|
A | AAGAAAGA others(3): Show |
1 | a0003c0003t0003g0129 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3505+304_3505+313d others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041834 | ||||||
| chr2:227041834
|
A | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0108a0001c0001t0001g0200others(5): Show | 8 | HG00099.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3505+314T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041834 | ||||||
| chr2:227041836
|
G | GAGAAAGA others(1): Show |
3 | a0002c0002t0004g0149a0002c0058t0005g0214a0006c0035t0036g0270 | 3 | HG02055.hp2 HG02897.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3505+311_3505+312i others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041836 | ||||||
| chr2:227041836
|
GAA | G | 17 | a0002c0002t0002g0088a0002c0002t0002g0092a0002c0002t0002g0098others(14): Show | 17 | HG00621.hp1 HG01123.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.3505+310_3505+311d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041836 | ||||||
| chr2:227041836
|
GAAAGAAA others(13): Show |
G | 1 | a0012c0011t0003g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3505+292_3505+311d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041836 | ||||||
| chr2:227041838
|
A | AAG | 16 | a0001c0001t0001g0251a0001c0001t0021g0141a0001c0049t0003g0253others(13): Show | 16 | HG00099.hp1 HG02280.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.3505+308_3505+309d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041838 | ||||||
| chr2:227041838
|
A | AAGAAAG | 3 | a0001c0001t0001g0115a0003c0003t0031g0250a0005c0007t0005g0137 | 3 | HG00323.hp1 HG01433.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.3505+304_3505+309d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041838 | ||||||
| chr2:227041838
|
A | AAGAAAGA others(9): Show |
1 | a0002c0002t0026g0232 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3505+309_3505+310i others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041838 | ||||||
| chr2:227041838
|
A | AAGAGAGA others(3): Show |
1 | a0010c0017t0008g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3505+309_3505+310i others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041838 | ||||||
| chr2:227041838
|
A | AAGAGAGA others(15): Show |
1 | a0001c0001t0001g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3505+309_3505+310i others(24): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041838 | ||||||
| chr2:227041838
|
A | G | 12 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0050others(9): Show | 12 | HG00099.hp2 HG02055.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3505+310T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041838 | ||||||
| chr2:227041838
|
AAGAAAGA others(3): Show |
A | 2 | a0002c0002t0011g0222a0008c0028t0034g0160 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3505+300_3505+309d others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041838 | ||||||
| chr2:227041840
|
GAA | G | 7 | a0002c0002t0002g0110a0002c0002t0002g0113a0002c0002t0002g0263others(4): Show | 7 | HG00738.hp1 HG01169.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+306_3505+307d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041840 | ||||||
| chr2:227041840
|
GAAAGAAA others(5): Show |
G | 1 | a0012c0011t0003g0233 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3505+296_3505+307d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041840 | ||||||
| chr2:227041841
|
A | G | 2 | a0001c0001t0001g0111a0009c0009t0001g0083 | 2 | NA18971.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.3505+307T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041841 | ||||||
| chr2:227041842
|
A | AAG | 10 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0102others(7): Show | 11 | HG01099.hp1 HG01496.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.3505+304_3505+305d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041842 | ||||||
| chr2:227041842
|
A | AAGAGAAA others(5): Show |
1 | a0006c0005t0004g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3505+305_3505+306i others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041842 | ||||||
| chr2:227041842
|
A | G | 21 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0050others(18): Show | 21 | HG00099.hp2 HG00408.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.3505+306T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041842 | ||||||
| chr2:227041844
|
G | A | 11 | a0001c0001t0001g0108a0001c0001t0001g0226a0002c0002t0002g0177others(8): Show | 11 | HG00408.hp2 HG00609.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.3505+304C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041844 | ||||||
| chr2:227041844
|
GAAAGAGA others(9): Show |
G | 1 | a0003c0003t0003g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3505+288_3505+303d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041844 | ||||||
| chr2:227041845
|
A | G | 2 | a0001c0001t0001g0100a0016c0064t0005g0178 | 2 | HG02071.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3505+303T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041845 | ||||||
| chr2:227041846
|
A | AAGAAGAG others(24): Show |
1 | a0001c0001t0001g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3505+301_3505+302i others(33): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041846 | ||||||
| chr2:227041846
|
A | G | 58 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0050others(55): Show | 58 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.3505+302T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041846 | ||||||
| chr2:227041846
|
AAG | A | 46 | a0001c0001t0001g0085a0001c0001t0001g0100a0001c0001t0001g0105others(43): Show | 46 | HG00544.hp1 HG00558.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.3505+300_3505+301d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041846 | ||||||
| chr2:227041848
|
G | A | 52 | a0001c0001t0001g0038a0001c0001t0001g0108a0001c0001t0001g0109others(49): Show | 52 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.3505+300C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAA | 40 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0102others(37): Show | 41 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.3505+299_3505+300i others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAAA others(22): Show |
1 | a0005c0046t0005g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(31): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAAA others(22): Show |
1 | a0001c0001t0001g0262 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3505+299_3505+300i others(31): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAAA others(5): Show |
1 | a0001c0001t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAAA others(21): Show |
1 | a0001c0001t0001g0123 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3505+299_3505+300i others(30): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAAA others(27): Show |
1 | a0001c0001t0001g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(36): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAGA others(5): Show |
1 | a0014c0020t0001g0007 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAGA others(21): Show |
1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3505+299_3505+300i others(30): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAAAGAGA others(22): Show |
1 | a0001c0001t0001g0136 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(31): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAA | 7 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0091others(4): Show | 7 | HG00323.hp1 HG01257.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.3505+296_3505+299d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAAAGA others(1): Show |
5 | a0001c0001t0001g0040a0001c0010t0005g0275a0006c0005t0004g0195others(2): Show | 5 | HG02257.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+292_3505+299d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAAAGA others(5): Show |
2 | a0001c0001t0001g0056a0026c0050t0001g0081 | 2 | HG02056.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3505+288_3505+299d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAAAGA others(9): Show |
1 | a0001c0001t0001g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3505+284_3505+299d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAAAGA others(7): Show |
2 | a0005c0007t0005g0121a0005c0007t0005g0134 | 2 | NA18979.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.3505+299_3505+300i others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAAAGA others(11): Show |
2 | a0007c0006t0004g0175a0038c0038t0005g0024 | 2 | HG01106.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3505+299_3505+300i others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAAAGA others(15): Show |
1 | a0005c0045t0003g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(24): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAGAGA others(11): Show |
1 | a0001c0001t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAGAGA others(15): Show |
1 | a0001c0001t0001g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3505+299_3505+300i others(24): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
G | GAGAGAGA others(20): Show |
1 | a0001c0001t0022g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3505+299_3505+300i others(29): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
GAGAAAGA others(1): Show |
G | 3 | a0001c0001t0001g0058a0001c0001t0001g0216a0003c0026t0001g0230 | 3 | HG00738.hp2 HG00741.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3505+292_3505+299d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3505+288_3505+299d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041848
|
GAGAAAGA others(32): Show |
G | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3505+261_3505+299d others(41): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041848 | ||||||
| chr2:227041849
|
A | G | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3505+299T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041849 | ||||||
| chr2:227041850
|
G | A | 21 | a0001c0001t0001g0122a0001c0001t0001g0197a0001c0001t0001g0244others(18): Show | 21 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.3505+298C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041850 | ||||||
| chr2:227041852
|
A | AAGAAAG | 3 | a0002c0002t0002g0086a0006c0005t0009g0283a0037c0066t0012g0059 | 3 | HG02258.hp2 HG04115.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3505+290_3505+295d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041852 | ||||||
| chr2:227041852
|
A | AAGAAAGA others(41): Show |
1 | a0008c0008t0004g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3505+295_3505+296i others(50): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041852 | ||||||
| chr2:227041852
|
A | G | 26 | a0001c0001t0001g0034a0001c0001t0001g0122a0001c0001t0001g0143others(23): Show | 26 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3505+296T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041852 | ||||||
| chr2:227041854
|
G | A | 1 | a0003c0014t0002g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3505+294C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041854 | ||||||
| chr2:227041854
|
GAA | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0249a0007c0006t0004g0171others(2): Show | 5 | HG01106.hp2 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+292_3505+293d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041854 | ||||||
| chr2:227041856
|
A | AAG | 6 | a0002c0002t0002g0008a0002c0002t0002g0079a0002c0002t0002g0182others(3): Show | 6 | HG01515.hp1 HG02572.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.3505+290_3505+291d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041856 | ||||||
| chr2:227041856
|
A | AAGAAAGA others(27): Show |
1 | a0004c0004t0005g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3505+258_3505+291d others(36): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041856 | ||||||
| chr2:227041856
|
A | G | 7 | a0001c0001t0001g0034a0001c0001t0001g0143a0001c0001t0001g0180others(4): Show | 7 | HG02886.hp2 HG02976.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.3505+292T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041856 | ||||||
| chr2:227041858
|
GAAAGAA | G | 3 | a0002c0002t0002g0090a0002c0002t0002g0210a0002c0002t0002g0211 | 3 | HG02735.hp2 NA18995.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.3505+284_3505+289d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041858 | ||||||
| chr2:227041858
|
GAAAGAAA others(3): Show |
G | 2 | a0002c0002t0002g0048a0002c0002t0002g0051 | 2 | HG02129.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.3505+280_3505+289d others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041858 | ||||||
| chr2:227041860
|
A | AAGAGAGA others(3): Show |
1 | a0025c0044t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3505+287_3505+288i others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041860 | ||||||
| chr2:227041860
|
A | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0143a0001c0001t0001g0213others(2): Show | 5 | HG02886.hp2 HG02976.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3505+288T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041860 | ||||||
| chr2:227041864
|
A | G | 3 | a0001c0001t0001g0143a0025c0044t0001g0060a0044c0033t0032g0168 | 3 | HG03139.hp2 HG06807.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3505+284T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041864 | ||||||
| chr2:227041868
|
A | G | 1 | a0044c0033t0032g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3505+280T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041868 | ||||||
| chr2:227041886
|
G | A | 1 | a0002c0002t0011g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3505+262C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041886 | ||||||
| chr2:227041890
|
G | A | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3505+258C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041890 | ||||||
| chr2:227041906
|
G | A | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3505+242C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041906 | ||||||
| chr2:227041908
|
A | G | 1 | a0002c0002t0002g0107 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3505+240T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041908 | ||||||
| chr2:227041915
|
A | G | 1 | a0040c0074t0018g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3505+233T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 37/47 | chr2 | 227041915 | ||||||
| chr2:227042340
|
T | C | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3398-85A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227042340 | ||||||
| chr2:227042560
|
AAAACAAA others(1): Show |
A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3398-313_3398-306d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227042560 | ||||||
| chr2:227042670
|
C | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3397+407G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227042670 | ||||||
| chr2:227042772
|
G | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3397+305C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227042772 | ||||||
| chr2:227042805
|
G | C | 1 | a0007c0006t0004g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3397+272C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227042805 | ||||||
| chr2:227042911
|
G | T | 10 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.3397+166C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227042911 | ||||||
| chr2:227042995
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3397+82C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227042995 | ||||||
| chr2:227043036
|
C | A | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3397+41G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 36/47 | chr2 | 227043036 | ||||||
| chr2:227043218
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-34C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043218 | ||||||
| chr2:227043322
|
G | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3290-138C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043322 | ||||||
| chr2:227043337
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.3290-153T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043337 | ||||||
| chr2:227043397
|
C | T | 1 | a0024c0069t0002g0015 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3290-213G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043397 | ||||||
| chr2:227043425
|
G | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-241C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043425 | ||||||
| chr2:227043497
|
A | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-313T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043497 | ||||||
| chr2:227043552
|
A | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-368T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043552 | ||||||
| chr2:227043567
|
A | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-383T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043567 | ||||||
| chr2:227043598
|
A | G | 3 | a0003c0003t0003g0006a0003c0003t0003g0084a0029c0063t0003g0082 | 3 | HG00673.hp1 NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.3290-414T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043598 | ||||||
| chr2:227043666
|
A | C | 1 | a0016c0065t0005g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3290-482T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043666 | ||||||
| chr2:227043753
|
C | A | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3290-569G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043753 | ||||||
| chr2:227043754
|
G | A | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3290-570C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043754 | ||||||
| chr2:227043776
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-592A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043776 | ||||||
| chr2:227043811
|
G | A | 162 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.3290-627C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043811 | ||||||
| chr2:227043840
|
G | A | 10 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.3290-656C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043840 | ||||||
| chr2:227043949
|
C | T | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.3290-765G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227043949 | ||||||
| chr2:227044061
|
T | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-877A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044061 | ||||||
| chr2:227044062
|
C | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-878G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044062 | ||||||
| chr2:227044096
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3290-912A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044096 | ||||||
| chr2:227044217
|
T | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-1033A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044217 | ||||||
| chr2:227044348
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-1164G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044348 | ||||||
| chr2:227044617
|
T | TA | 159 | a0001c0001t0001g0186a0002c0002t0002g0008a0002c0002t0002g0009others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.3290-1434dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044617 | ||||||
| chr2:227044623
|
T | A | 171 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.3290-1439A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044623 | ||||||
| chr2:227044685
|
C | T | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3290-1501G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044685 | ||||||
| chr2:227044699
|
T | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3290-1515A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044699 | ||||||
| chr2:227044748
|
TA | T | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3290-1565delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044748 | ||||||
| chr2:227044806
|
A | C | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3290-1622T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044806 | ||||||
| chr2:227044836
|
T | C | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3290-1652A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227044836 | ||||||
| chr2:227045062
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-1878G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045062 | ||||||
| chr2:227045152
|
A | G | 21 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3290-1968T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045152 | ||||||
| chr2:227045284
|
C | G | 1 | a0002c0002t0002g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3290-2100G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045284 | ||||||
| chr2:227045284
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3290-2100G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045284 | ||||||
| chr2:227045452
|
G | A | 1 | a0004c0004t0005g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3289+2023C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045452 | ||||||
| chr2:227045455
|
A | G | 84 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(81): Show | 84 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3289+2020T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045455 | ||||||
| chr2:227045481
|
ATG | A | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1992_3289+199 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045481 | ||||||
| chr2:227045484
|
T | C | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.3289+1991A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045484 | ||||||
| chr2:227045574
|
A | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1901T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045574 | ||||||
| chr2:227045768
|
CA | C | 27 | a0002c0002t0011g0222a0002c0019t0005g0166a0003c0003t0003g0004others(24): Show | 27 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.3289+1706delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045768 | ||||||
| chr2:227045779
|
A | ATACAT | 36 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(33): Show | 36 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.3289+1695_3289+169 others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045779 | ||||||
| chr2:227045781
|
T | A | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+1694A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045781 | ||||||
| chr2:227045783
|
C | CAT | 4 | a0002c0002t0005g0215a0002c0002t0007g0049a0002c0002t0007g0184others(1): Show | 4 | NA18941.hp1 NA18945.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3289+1690_3289+169 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045783 | ||||||
| chr2:227045783
|
C | T | 46 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(43): Show | 46 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.3289+1692G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045783 | ||||||
| chr2:227045783
|
CAT | C | 15 | a0002c0002t0011g0222a0004c0004t0002g0147a0004c0004t0005g0030others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3289+1690_3289+169 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045783 | ||||||
| chr2:227045785
|
T | C | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+1690A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045785 | ||||||
| chr2:227045787
|
TATATATA others(7): Show |
T | 24 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(21): Show | 24 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.3289+1674_3289+168 others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045787 | ||||||
| chr2:227045789
|
T | TACAC | 36 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(33): Show | 36 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.3289+1685_3289+168 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045789 | ||||||
| chr2:227045789
|
TATATATA others(5): Show |
T | 3 | a0001c0001t0001g0213a0001c0001t0001g0273a0042c0034t0004g0274 | 3 | HG02886.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3289+1674_3289+168 others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045789 | ||||||
| chr2:227045797
|
T | C | 20 | a0002c0019t0005g0029a0002c0019t0005g0166a0003c0003t0003g0004others(17): Show | 20 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.3289+1678A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045797 | ||||||
| chr2:227045799
|
C | T | 1 | a0002c0002t0007g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3289+1676G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045799 | ||||||
| chr2:227045801
|
C | T | 20 | a0002c0019t0005g0029a0002c0019t0005g0166a0003c0003t0003g0004others(17): Show | 20 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.3289+1674G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045801 | ||||||
| chr2:227045803
|
T | C | 1 | a0002c0002t0007g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3289+1672A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045803 | ||||||
| chr2:227045803
|
T | TATATATA others(7): Show |
1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3289+1671_3289+167 others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045803 | ||||||
| chr2:227045806
|
A | ATACACAT others(24): Show |
2 | a0003c0003t0031g0250a0003c0027t0003g0133 | 2 | NA18939.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3289+1668_3289+166 others(35): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045806 | ||||||
| chr2:227045808
|
A | ACACATAT others(32): Show |
2 | a0012c0011t0003g0138a0012c0011t0003g0219 | 2 | HG01934.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3289+1666_3289+166 others(43): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045808 | ||||||
| chr2:227045808
|
A | ATACACAT others(33): Show |
12 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0086others(9): Show | 12 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3289+1666_3289+166 others(44): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045808 | ||||||
| chr2:227045808
|
A | ATACACAT others(57): Show |
2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3289+1666_3289+166 others(68): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045808 | ||||||
| chr2:227045808
|
A | ATACACAT others(91): Show |
1 | a0006c0005t0004g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3289+1666_3289+166 others(102): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045808 | ||||||
| chr2:227045809
|
T | C | 8 | a0003c0003t0003g0004a0003c0003t0003g0093a0003c0003t0003g0099others(5): Show | 8 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3289+1666A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045809 | ||||||
| chr2:227045809
|
T | TACAC | 60 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.3289+1665_3289+166 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045809 | ||||||
| chr2:227045810
|
A | ACACATAT others(31): Show |
7 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(4): Show | 7 | NA18939.hp1 NA18941.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.3289+1664_3289+166 others(42): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045810 | ||||||
| chr2:227045810
|
A | G | 39 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.3289+1665T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045810 | ||||||
| chr2:227045811
|
T | C | 24 | a0002c0002t0002g0177a0002c0019t0005g0029a0002c0019t0005g0166others(21): Show | 24 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.3289+1664A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045811 | ||||||
| chr2:227045813
|
T | C | 26 | a0002c0002t0002g0177a0002c0002t0007g0225a0002c0002t0011g0222others(23): Show | 26 | HG01884.hp2 HG02055.hp1 HG02074.hp2 others(23): Show |
intron_variant | MODIFIER | c.3289+1662A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045813 | ||||||
| chr2:227045813
|
TATACACA others(13): Show |
T | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3289+1642_3289+166 others(24): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045813 | ||||||
| chr2:227045815
|
T | C | 2 | a0001c0001t0001g0087a0002c0002t0007g0225 | 2 | HG00438.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3289+1660A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045815 | ||||||
| chr2:227045816
|
A | ATATTTAG others(4): Show |
25 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0071others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.3289+1658_3289+165 others(15): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045816 | ||||||
| chr2:227045816
|
A | G | 2 | a0003c0003t0031g0250a0003c0027t0003g0133 | 2 | NA18939.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3289+1659T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045816 | ||||||
| chr2:227045816
|
A | T | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3289+1659T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045816 | ||||||
| chr2:227045817
|
C | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1658G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045817 | ||||||
| chr2:227045818
|
A | G | 75 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(72): Show | 75 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.3289+1657T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045818 | ||||||
| chr2:227045819
|
C | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1656G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045819 | ||||||
| chr2:227045820
|
A | G | 10 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(7): Show | 10 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+1655T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045820 | ||||||
| chr2:227045820
|
A | T | 14 | a0003c0003t0003g0057a0003c0003t0003g0076a0003c0003t0003g0116others(11): Show | 14 | HG00140.hp1 HG00639.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.3289+1655T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045820 | ||||||
| chr2:227045821
|
TATATATA others(9): Show |
T | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3289+1638_3289+165 others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045821 | ||||||
| chr2:227045822
|
A | G | 21 | a0002c0002t0002g0177a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG02257.hp2 HG02486.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.3289+1653T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045822 | ||||||
| chr2:227045823
|
T | G | 14 | a0003c0003t0003g0057a0003c0003t0003g0076a0003c0003t0003g0116others(11): Show | 14 | HG00140.hp1 HG00639.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.3289+1652A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045823 | ||||||
| chr2:227045824
|
A | ATAG | 14 | a0003c0003t0003g0057a0003c0003t0003g0076a0003c0003t0003g0116others(11): Show | 14 | HG00140.hp1 HG00639.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.3289+1650_3289+165 others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045824 | ||||||
| chr2:227045824
|
A | G | 30 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0086others(27): Show | 30 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.3289+1651T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045824 | ||||||
| chr2:227045826
|
A | ATTTAGAT others(2): Show |
60 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.3289+1648_3289+164 others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045826 | ||||||
| chr2:227045826
|
A | G | 37 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(34): Show | 37 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.3289+1649T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045826 | ||||||
| chr2:227045830
|
A | T | 3 | a0003c0003t0003g0004a0003c0003t0003g0093a0003c0003t0003g0099 | 3 | HG01255.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3289+1645T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045830 | ||||||
| chr2:227045831
|
T | TTTAGATA | 11 | a0002c0019t0005g0029a0002c0019t0005g0166a0004c0004t0020g0217others(8): Show | 11 | HG02559.hp2 HG02717.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.3289+1643_3289+164 others(11): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045831 | ||||||
| chr2:227045832
|
A | AGATAG | 3 | a0003c0003t0003g0004a0003c0003t0003g0093a0003c0003t0003g0099 | 3 | HG01255.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3289+1642_3289+164 others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045832 | ||||||
| chr2:227045832
|
A | ATTTAGAT others(62): Show |
5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3289+1642_3289+164 others(73): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045832 | ||||||
| chr2:227045832
|
A | ATTTAGAT others(108): Show |
1 | a0002c0002t0011g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3289+1642_3289+164 others(119): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045832 | ||||||
| chr2:227045832
|
A | G | 27 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0086others(24): Show | 27 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.3289+1643T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045832 | ||||||
| chr2:227045832
|
A | T | 10 | a0002c0002t0002g0177a0007c0006t0004g0171a0007c0006t0004g0172others(7): Show | 10 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+1643T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045832 | ||||||
| chr2:227045833
|
C | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1642G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045833 | ||||||
| chr2:227045834
|
A | AG | 60 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.3289+1640_3289+164 others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045834 | ||||||
| chr2:227045834
|
A | G | 23 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(20): Show | 23 | HG00140.hp1 HG00639.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.3289+1641T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045834 | ||||||
| chr2:227045834
|
A | T | 11 | a0002c0002t0007g0225a0004c0004t0002g0147a0004c0004t0005g0030others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.3289+1641T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045834 | ||||||
| chr2:227045835
|
C | G | 9 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3289+1640G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045835 | ||||||
| chr2:227045835
|
C | T | 156 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(153): Show | 156 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.3289+1640G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045835 | ||||||
| chr2:227045836
|
A | G | 25 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0071others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.3289+1639T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045836 | ||||||
| chr2:227045837
|
C | G | 10 | a0002c0002t0007g0225a0004c0004t0002g0147a0004c0004t0005g0030others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+1638G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045837 | ||||||
| chr2:227045837
|
C | T | 183 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.3289+1638G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045837 | ||||||
| chr2:227045837
|
CAT | C | 6 | a0001c0001t0001g0054a0001c0001t0001g0097a0001c0001t0001g0100others(3): Show | 6 | HG02071.hp1 NA18945.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.3289+1636_3289+163 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045837 | ||||||
| chr2:227045838
|
A | AG | 9 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3289+1636_3289+163 others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045838 | ||||||
| chr2:227045840
|
A | G | 2 | a0003c0003t0031g0250a0003c0027t0003g0133 | 2 | NA18939.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3289+1635T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045840 | ||||||
| chr2:227045840
|
A | T | 20 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0086others(17): Show | 20 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.3289+1635T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045840 | ||||||
| chr2:227045840
|
AT | A | 9 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.3289+1634delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045840 | ||||||
| chr2:227045842
|
A | G | 46 | a0002c0019t0005g0029a0002c0019t0005g0166a0003c0003t0003g0004others(43): Show | 46 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.3289+1633T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045842 | ||||||
| chr2:227045842
|
A | T | 9 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(6): Show | 9 | HG02896.hp1 NA18939.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.3289+1633T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045842 | ||||||
| chr2:227045844
|
A | G | 77 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.3289+1631T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045844 | ||||||
| chr2:227045847
|
TACAC | T | 9 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3289+1624_3289+162 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045847 | ||||||
| chr2:227045848
|
A | T | 2 | a0003c0003t0031g0250a0003c0027t0003g0133 | 2 | NA18939.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.3289+1627T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045848 | ||||||
| chr2:227045849
|
C | T | 159 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.3289+1626G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045849 | ||||||
| chr2:227045850
|
A | G | 117 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.3289+1625T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045850 | ||||||
| chr2:227045851
|
C | T | 155 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.3289+1624G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045851 | ||||||
| chr2:227045852
|
A | G | 46 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0177others(43): Show | 46 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.3289+1623T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045852 | ||||||
| chr2:227045858
|
A | G | 111 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.3289+1617T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045858 | ||||||
| chr2:227045858
|
A | T | 23 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0071others(20): Show | 23 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.3289+1617T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045858 | ||||||
| chr2:227045860
|
A | G | 11 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(8): Show | 11 | HG02896.hp1 HG02970.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.3289+1615T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045860 | ||||||
| chr2:227045860
|
A | T | 1 | a0006c0005t0004g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3289+1615T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045860 | ||||||
| chr2:227045862
|
A | G | 19 | a0002c0002t0007g0225a0004c0004t0002g0147a0004c0004t0005g0030others(16): Show | 19 | HG01884.hp2 HG02055.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3289+1613T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045862 | ||||||
| chr2:227045863
|
C | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1612G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045863 | ||||||
| chr2:227045865
|
C | CATATATA others(13): Show |
1 | a0001c0001t0021g0141 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3289+1590_3289+160 others(24): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045865 | ||||||
| chr2:227045865
|
C | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1610G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045865 | ||||||
| chr2:227045866
|
A | G | 22 | a0002c0002t0002g0177a0002c0019t0005g0029a0002c0019t0005g0166others(19): Show | 22 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.3289+1609T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045866 | ||||||
| chr2:227045866
|
A | T | 89 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.3289+1609T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045866 | ||||||
| chr2:227045868
|
A | G | 45 | a0002c0002t0007g0225a0003c0003t0003g0005a0003c0003t0003g0006others(42): Show | 45 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.3289+1607T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045868 | ||||||
| chr2:227045868
|
A | T | 9 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(6): Show | 9 | HG02896.hp1 NA18939.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.3289+1607T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045868 | ||||||
| chr2:227045874
|
A | T | 22 | a0002c0002t0002g0177a0002c0019t0005g0029a0002c0019t0005g0166others(19): Show | 22 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.3289+1601T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045874 | ||||||
| chr2:227045875
|
C | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1600G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045875 | ||||||
| chr2:227045876
|
A | G | 132 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.3289+1599T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045876 | ||||||
| chr2:227045876
|
A | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1599T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045876 | ||||||
| chr2:227045878
|
A | G | 9 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(6): Show | 9 | HG02896.hp1 NA18939.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.3289+1597T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045878 | ||||||
| chr2:227045884
|
G | A | 9 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(6): Show | 9 | HG02896.hp1 NA18939.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.3289+1591C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045884 | ||||||
| chr2:227045884
|
G | T | 43 | a0002c0002t0007g0225a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3289+1591C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045884 | ||||||
| chr2:227045886
|
A | ATATATG | 4 | a0004c0004t0020g0217a0008c0028t0034g0160a0016c0064t0005g0178others(1): Show | 4 | HG02922.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3289+1588_3289+158 others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045886 | ||||||
| chr2:227045886
|
A | G | 9 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(6): Show | 9 | HG02896.hp1 NA18939.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.3289+1589T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045886 | ||||||
| chr2:227045892
|
A | G | 21 | a0002c0002t0002g0177a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.3289+1583T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045892 | ||||||
| chr2:227045892
|
A | T | 88 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.3289+1583T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045892 | ||||||
| chr2:227045894
|
T | A | 109 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.3289+1581A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045894 | ||||||
| chr2:227045894
|
T | G | 43 | a0002c0002t0007g0225a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3289+1581A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045894 | ||||||
| chr2:227045897
|
G | T | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3289+1578C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045897 | ||||||
| chr2:227045899
|
TA | T | 16 | a0002c0002t0002g0177a0002c0019t0005g0029a0002c0019t0005g0166others(13): Show | 16 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.3289+1575delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045899 | ||||||
| chr2:227045900
|
A | AT | 144 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.3289+1574_3289+157 others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045900 | ||||||
| chr2:227045900
|
AG | A | 3 | a0006c0005t0004g0156a0006c0005t0004g0158a0008c0008t0004g0161 | 3 | HG02976.hp1 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3289+1574delC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045900 | ||||||
| chr2:227045901
|
G | A | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3289+1574C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045901 | ||||||
| chr2:227045901
|
G | T | 17 | a0002c0002t0002g0177a0002c0019t0005g0029a0002c0019t0005g0166others(14): Show | 17 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.3289+1574C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045901 | ||||||
| chr2:227045903
|
A | G | 5 | a0004c0004t0020g0217a0006c0005t0004g0156a0006c0005t0004g0158others(2): Show | 5 | HG02922.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.3289+1572T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045903 | ||||||
| chr2:227045909
|
A | G | 100 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.3289+1566T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045909 | ||||||
| chr2:227045909
|
A | T | 43 | a0002c0002t0007g0225a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.3289+1566T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045909 | ||||||
| chr2:227045911
|
G | A | 144 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.3289+1564C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045911 | ||||||
| chr2:227045912
|
T | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1563A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045912 | ||||||
| chr2:227045915
|
G | A | 164 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(161): Show | 164 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.3289+1560C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045915 | ||||||
| chr2:227045915
|
GTATATGT others(7): Show |
G | 2 | a0010c0017t0008g0179a0010c0017t0008g0183 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3289+1546_3289+155 others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045915 | ||||||
| chr2:227045917
|
A | ATG | 4 | a0002c0002t0002g0177a0003c0003t0003g0004a0003c0003t0003g0093others(1): Show | 4 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3289+1557_3289+155 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045917 | ||||||
| chr2:227045917
|
A | T | 100 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.3289+1558T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045917 | ||||||
| chr2:227045919
|
A | G | 52 | a0002c0002t0007g0225a0002c0019t0005g0029a0002c0019t0005g0166others(49): Show | 52 | HG00408.hp2 HG00609.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.3289+1556T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045919 | ||||||
| chr2:227045919
|
A | T | 4 | a0004c0004t0020g0217a0006c0005t0004g0156a0006c0005t0004g0158others(1): Show | 4 | HG02922.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3289+1556T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045919 | ||||||
| chr2:227045920
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1555A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045920 | ||||||
| chr2:227045921
|
G | A | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3289+1554C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045921 | ||||||
| chr2:227045921
|
GTATATGT others(1): Show |
G | 30 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(27): Show | 30 | HG00099.hp2 HG00621.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.3289+1546_3289+155 others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045921 | ||||||
| chr2:227045925
|
A | T | 4 | a0002c0002t0002g0177a0003c0003t0003g0004a0003c0003t0003g0093others(1): Show | 4 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3289+1550T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045925 | ||||||
| chr2:227045927
|
G | A | 7 | a0002c0002t0002g0177a0003c0003t0003g0004a0003c0003t0003g0093others(4): Show | 7 | HG01106.hp1 HG01255.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.3289+1548C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045927 | ||||||
| chr2:227045927
|
G | T | 7 | a0002c0019t0005g0029a0002c0019t0005g0166a0011c0012t0006g0032others(4): Show | 7 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3289+1548C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045927 | ||||||
| chr2:227045929
|
A | ATATATGT others(15): Show |
4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3289+1524_3289+154 others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045929 | ||||||
| chr2:227045935
|
G | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1540C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045935 | ||||||
| chr2:227045935
|
G | GTA | 10 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(7): Show | 10 | HG02630.hp2 HG02896.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.3289+1538_3289+153 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045935 | ||||||
| chr2:227045935
|
G | T | 11 | a0002c0002t0007g0225a0007c0006t0004g0171a0007c0006t0004g0172others(8): Show | 11 | HG01106.hp1 HG02074.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3289+1540C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045935 | ||||||
| chr2:227045938
|
T | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1537A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045938 | ||||||
| chr2:227045941
|
A | ATT | 11 | a0002c0019t0005g0029a0002c0019t0005g0166a0004c0004t0020g0217others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.3289+1533_3289+153 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045941 | ||||||
| chr2:227045943
|
G | A | 11 | a0002c0019t0005g0029a0002c0019t0005g0166a0004c0004t0020g0217others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.3289+1532C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045943 | ||||||
| chr2:227045943
|
G | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1532C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045943 | ||||||
| chr2:227045943
|
G | GTA | 6 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(3): Show | 6 | HG01106.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3289+1530_3289+153 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045943 | ||||||
| chr2:227045943
|
G | T | 70 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(67): Show | 70 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.3289+1532C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045943 | ||||||
| chr2:227045949
|
A | ATT | 11 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3289+1525_3289+152 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045949 | ||||||
| chr2:227045951
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1524C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045951 | ||||||
| chr2:227045952
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1523A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045952 | ||||||
| chr2:227045957
|
ATG | A | 8 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(5): Show | 8 | HG02630.hp2 NA18939.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.3289+1516_3289+151 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045957 | ||||||
| chr2:227045959
|
G | A | 5 | a0001c0001t0001g0034a0006c0005t0004g0191a0006c0005t0004g0193others(2): Show | 5 | HG02896.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3289+1516C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045959 | ||||||
| chr2:227045959
|
G | T | 10 | a0002c0002t0007g0225a0007c0006t0004g0171a0007c0006t0004g0172others(7): Show | 10 | HG02074.hp2 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+1516C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045959 | ||||||
| chr2:227045960
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1515A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045960 | ||||||
| chr2:227045961
|
A | ATATATAT others(27): Show |
1 | a0002c0002t0007g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3289+1513_3289+151 others(38): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045961 | ||||||
| chr2:227045965
|
A | ATATG | 7 | a0006c0005t0004g0156a0006c0005t0004g0158a0013c0013t0006g0144others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.3289+1509_3289+151 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045965 | ||||||
| chr2:227045965
|
A | ATATTTAT others(35): Show |
9 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3289+1509_3289+151 others(46): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045965 | ||||||
| chr2:227045965
|
A | G | 10 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(7): Show | 10 | HG02630.hp2 HG02896.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.3289+1510T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045965 | ||||||
| chr2:227045967
|
T | A | 30 | a0002c0002t0002g0077a0002c0002t0002g0140a0002c0002t0002g0185others(27): Show | 30 | HG01106.hp1 HG02074.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.3289+1508A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(35): Show |
1 | a0002c0002t0002g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3289+1507_3289+150 others(46): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(33): Show |
3 | a0002c0002t0002g0267a0002c0002t0002g0268a0003c0026t0001g0230 | 3 | HG00323.hp2 HG03017.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3289+1507_3289+150 others(44): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(35): Show |
1 | a0002c0002t0002g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3289+1507_3289+150 others(46): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(43): Show |
59 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(56): Show | 59 | HG00099.hp1 HG00544.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.3289+1507_3289+150 others(54): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(41): Show |
48 | a0002c0002t0002g0047a0002c0002t0002g0239a0003c0003t0003g0004others(45): Show | 48 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.3289+1507_3289+150 others(52): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(41): Show |
5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3289+1507_3289+150 others(52): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(49): Show |
2 | a0003c0003t0030g0169a0043c0036t0038g0153 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3289+1507_3289+150 others(60): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(51): Show |
2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3289+1507_3289+150 others(62): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045967
|
T | TTATATAT others(87): Show |
2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3289+1507_3289+150 others(98): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045967 | ||||||
| chr2:227045968
|
T | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1507A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045968 | ||||||
| chr2:227045971
|
A | ATATATGT others(63): Show |
11 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3289+1503_3289+150 others(74): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045971 | ||||||
| chr2:227045973
|
G | A | 13 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.3289+1502C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045973 | ||||||
| chr2:227045975
|
G | A | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1500C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045975 | ||||||
| chr2:227045976
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1499A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045976 | ||||||
| chr2:227045981
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1494C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045981 | ||||||
| chr2:227045984
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1491A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045984 | ||||||
| chr2:227045984
|
TATATTTA others(1): Show |
T | 139 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.3289+1483_3289+149 others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045984 | ||||||
| chr2:227045989
|
T | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1486A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045989 | ||||||
| chr2:227045989
|
T | G | 1 | a0002c0002t0007g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3289+1486A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045989 | ||||||
| chr2:227045992
|
G | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1483C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045992 | ||||||
| chr2:227045992
|
G | T | 24 | a0002c0002t0007g0225a0002c0019t0005g0029a0002c0019t0005g0166others(21): Show | 24 | HG01884.hp2 HG02055.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.3289+1483C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045992 | ||||||
| chr2:227045997
|
T | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1478A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227045997 | ||||||
| chr2:227046000
|
G | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1475C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046000 | ||||||
| chr2:227046007
|
T | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1468A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046007 | ||||||
| chr2:227046008
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1467A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046008 | ||||||
| chr2:227046010
|
G | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1465C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046010 | ||||||
| chr2:227046017
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1458A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046017 | ||||||
| chr2:227046022
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1453C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046022 | ||||||
| chr2:227046025
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1450A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046025 | ||||||
| chr2:227046030
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1445C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046030 | ||||||
| chr2:227046043
|
C | CATATATA others(20): Show |
21 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.3289+1431_3289+143 others(31): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046043 | ||||||
| chr2:227046043
|
C | CATATATA others(20): Show |
137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.3289+1431_3289+143 others(31): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046043 | ||||||
| chr2:227046054
|
T | TCTAAATA others(16): Show |
5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3289+1420_3289+142 others(27): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046054 | ||||||
| chr2:227046060
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1415G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046060 | ||||||
| chr2:227046064
|
T | C | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3289+1411A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046064 | ||||||
| chr2:227046079
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1396A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046079 | ||||||
| chr2:227046082
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1393C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046082 | ||||||
| chr2:227046082
|
G | GAT | 13 | a0002c0019t0005g0029a0002c0019t0005g0166a0004c0004t0002g0147others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.3289+1391_3289+139 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046082 | ||||||
| chr2:227046082
|
G | GATAT | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3289+1389_3289+139 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046082 | ||||||
| chr2:227046084
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1391A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046084 | ||||||
| chr2:227046091
|
G | A | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3289+1384C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046091 | ||||||
| chr2:227046092
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1383A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046092 | ||||||
| chr2:227046094
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+1381G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046094 | ||||||
| chr2:227046239
|
AATAAAAT others(1140): Show |
A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3289+89_3289+1235d others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046239 | ||||||
| chr2:227046305
|
C | T | 11 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3289+1170G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046305 | ||||||
| chr2:227046321
|
T | G | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3289+1154A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046321 | ||||||
| chr2:227046353
|
T | TA | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3289+1121dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046353 | ||||||
| chr2:227046553
|
A | G | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3289+922T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046553 | ||||||
| chr2:227046684
|
A | G | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3289+791T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046684 | ||||||
| chr2:227046771
|
G | T | 14 | a0002c0002t0011g0222a0004c0004t0002g0147a0004c0004t0005g0030others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.3289+704C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046771 | ||||||
| chr2:227046850
|
A | T | 16 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(13): Show | 16 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.3289+625T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046850 | ||||||
| chr2:227046913
|
A | T | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3289+562T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046913 | ||||||
| chr2:227046945
|
G | A | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.3289+530C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046945 | ||||||
| chr2:227046967
|
G | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3289+508C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227046967 | ||||||
| chr2:227047009
|
G | A | 195 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3289+466C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047009 | ||||||
| chr2:227047022
|
C | T | 1 | a0015c0024t0002g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3289+453G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047022 | ||||||
| chr2:227047023
|
G | A | 6 | a0001c0001t0001g0135a0013c0013t0006g0144a0013c0013t0006g0155others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3289+452C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047023 | ||||||
| chr2:227047024
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3289+451G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047024 | ||||||
| chr2:227047113
|
G | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3289+362C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047113 | ||||||
| chr2:227047122
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3289+353T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047122 | ||||||
| chr2:227047133
|
T | C | 3 | a0002c0002t0002g0072a0002c0021t0002g0245a0002c0021t0002g0246 | 3 | HG00099.hp1 HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.3289+342A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047133 | ||||||
| chr2:227047391
|
G | A | 2 | a0003c0003t0031g0250a0003c0073t0003g0018 | 2 | NA18939.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3289+84C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 35/47 | chr2 | 227047391 | ||||||
| chr2:227047615
|
G | A | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3215-66C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047615 | ||||||
| chr2:227047627
|
G | A | 1 | a0003c0003t0003g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3215-78C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047627 | ||||||
| chr2:227047677
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3215-128A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047677 | ||||||
| chr2:227047731
|
C | CACACACA others(4): Show |
1 | a0003c0003t0003g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3215-183_3215-182i others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCA | 30 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0040others(27): Show | 30 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.3215-184_3215-183d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACA | 14 | a0001c0001t0001g0282a0002c0002t0002g0014a0002c0002t0002g0077others(11): Show | 14 | HG00673.hp1 HG03927.hp1 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.3215-186_3215-183d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACACA | 8 | a0002c0002t0002g0072a0012c0011t0003g0231a0013c0013t0006g0144others(5): Show | 8 | HG00099.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3215-188_3215-183d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACACAC others(1): Show |
37 | a0002c0002t0002g0036a0002c0002t0002g0043a0002c0002t0002g0110others(34): Show | 37 | HG00408.hp2 HG00609.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.3215-190_3215-183d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACACAC others(3): Show |
36 | a0002c0002t0002g0066a0002c0002t0002g0086a0002c0002t0002g0151others(33): Show | 36 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.3215-192_3215-183d others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACACAC others(5): Show |
44 | a0002c0002t0002g0008a0002c0002t0002g0047a0002c0002t0002g0051others(41): Show | 44 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.3215-194_3215-183d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACACAC others(7): Show |
12 | a0002c0002t0002g0033a0002c0002t0002g0048a0002c0002t0002g0092others(9): Show | 12 | HG01123.hp1 HG02040.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.3215-196_3215-183d others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACACAC others(9): Show |
10 | a0002c0002t0002g0009a0002c0002t0002g0113a0002c0002t0002g0205others(7): Show | 10 | HG01123.hp2 HG01169.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.3215-198_3215-183d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
C | CCACACAC others(11): Show |
1 | a0002c0002t0002g0013 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3215-200_3215-183d others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
CCA | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0226a0026c0050t0001g0081 | 3 | HG00609.hp2 HG02132.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3215-184_3215-183d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
CCACACAC others(3): Show |
C | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3215-192_3215-183d others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047731
|
CCACACAC others(5): Show |
C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3215-194_3215-183d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047731 | ||||||
| chr2:227047828
|
G | GA | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3215-280dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047828 | ||||||
| chr2:227047835
|
T | A | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3215-286A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047835 | ||||||
| chr2:227047883
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3215-334A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047883 | ||||||
| chr2:227047934
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3215-385C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227047934 | ||||||
| chr2:227048077
|
A | G | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3215-528T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048077 | ||||||
| chr2:227048235
|
T | C | 28 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(25): Show | 28 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.3215-686A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048235 | ||||||
| chr2:227048362
|
C | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3215-813G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048362 | ||||||
| chr2:227048376
|
C | T | 1 | a0003c0014t0002g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3215-827G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048376 | ||||||
| chr2:227048406
|
T | C | 21 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3215-857A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048406 | ||||||
| chr2:227048408
|
G | A | 21 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3215-859C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048408 | ||||||
| chr2:227048424
|
G | A | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3215-875C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048424 | ||||||
| chr2:227048582
|
G | A | 11 | a0002c0002t0002g0086a0002c0002t0004g0149a0002c0002t0005g0142others(8): Show | 11 | HG01261.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3215-1033C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048582 | ||||||
| chr2:227048598
|
A | C | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3215-1049T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048598 | ||||||
| chr2:227048726
|
T | A | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3215-1177A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048726 | ||||||
| chr2:227048786
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3215-1237C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048786 | ||||||
| chr2:227048823
|
A | G | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+1245T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048823 | ||||||
| chr2:227048990
|
G | A | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3214+1078C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227048990 | ||||||
| chr2:227049000
|
C | T | 2 | a0002c0002t0002g0263a0002c0002t0002g0264 | 2 | NA18999.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3214+1068G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049000 | ||||||
| chr2:227049001
|
A | G | 154 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.3214+1067T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049001 | ||||||
| chr2:227049559
|
T | A | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+509A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049559 | ||||||
| chr2:227049709
|
C | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+359G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049709 | ||||||
| chr2:227049719
|
G | A | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3214+349C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049719 | ||||||
| chr2:227049733
|
A | G | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+335T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049733 | ||||||
| chr2:227049741
|
C | T | 1 | a0001c0049t0003g0253 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3214+327G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049741 | ||||||
| chr2:227049742
|
G | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+326C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049742 | ||||||
| chr2:227049768
|
T | C | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.3214+300A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049768 | ||||||
| chr2:227049771
|
C | T | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3214+297G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049771 | ||||||
| chr2:227049841
|
G | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3214+227C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049841 | ||||||
| chr2:227049845
|
C | T | 84 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(81): Show | 84 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3214+223G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049845 | ||||||
| chr2:227049909
|
T | C | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+159A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049909 | ||||||
| chr2:227049939
|
C | G | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.3214+129G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049939 | ||||||
| chr2:227049964
|
T | C | 2 | a0002c0002t0002g0092a0002c0002t0002g0203 | 2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3214+104A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 34/47 | chr2 | 227049964 | ||||||
| chr2:227050259
|
T | G | 199 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.3151-128A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 33/47 | chr2 | 227050259 | ||||||
| chr2:227050441
|
T | C | 11 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3151-310A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 33/47 | chr2 | 227050441 | ||||||
| chr2:227050500
|
G | A | 2 | a0002c0002t0002g0239a0004c0004t0002g0218 | 2 | HG00738.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.3151-369C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 33/47 | chr2 | 227050500 | ||||||
| chr2:227050885
|
G | T | 163 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3150+92C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 33/47 | chr2 | 227050885 | ||||||
| chr2:227051208
|
T | C | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.2969-50A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051208 | ||||||
| chr2:227051290
|
G | A | 1 | a0003c0003t0003g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2969-132C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051290 | ||||||
| chr2:227051317
|
A | G | 1 | a0030c0062t0003g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2969-159T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051317 | ||||||
| chr2:227051323
|
T | C | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2969-165A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051323 | ||||||
| chr2:227051398
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2969-240C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051398 | ||||||
| chr2:227051565
|
T | C | 1 | a0005c0007t0005g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2969-407A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051565 | ||||||
| chr2:227051588
|
G | T | 1 | a0002c0002t0002g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2969-430C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051588 | ||||||
| chr2:227051717
|
A | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2969-559T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051717 | ||||||
| chr2:227051817
|
G | A | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2968+488C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051817 | ||||||
| chr2:227051971
|
C | T | 1 | a0002c0002t0002g0009 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2968+334G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227051971 | ||||||
| chr2:227052084
|
G | A | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2968+221C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052084 | ||||||
| chr2:227052115
|
C | T | 1 | a0003c0014t0002g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2968+190G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052115 | ||||||
| chr2:227052188
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0017g0002a0001c0070t0039g0204 | 3 | HG02647.hp2 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2968+117A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052188 | ||||||
| chr2:227052191
|
C | CA | 6 | a0001c0001t0001g0087a0001c0001t0001g0251a0001c0001t0019g0126others(3): Show | 6 | HG00438.hp1 HG00438.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.2968+113dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052191 | ||||||
| chr2:227052206
|
C | A | 3 | a0011c0012t0006g0256a0011c0012t0006g0257a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2968+99G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052206 | ||||||
| chr2:227052246
|
A | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2968+59T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052246 | ||||||
| chr2:227052261
|
A | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2968+44T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052261 | ||||||
| chr2:227052279
|
A | T | 1 | a0006c0005t0013g0154 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2968+26T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 32/47 | chr2 | 227052279 | ||||||
| chr2:227052524
|
C | G | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2861-112G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052524 | ||||||
| chr2:227052554
|
T | C | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2861-142A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052554 | ||||||
| chr2:227052594
|
G | A | 2 | a0001c0001t0001g0104a0018c0023t0002g0127 | 2 | HG00140.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2861-182C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052594 | ||||||
| chr2:227052607
|
T | C | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2861-195A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052607 | ||||||
| chr2:227052632
|
G | A | 28 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(25): Show | 28 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.2861-220C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052632 | ||||||
| chr2:227052722
|
A | AC | 264 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2861-311_2861-310i others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052722 | ||||||
| chr2:227052862
|
G | A | 21 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2861-450C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052862 | ||||||
| chr2:227052961
|
C | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0206a0001c0001t0001g0282 | 3 | HG01255.hp1 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2861-549G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227052961 | ||||||
| chr2:227053010
|
C | G | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2861-598G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053010 | ||||||
| chr2:227053084
|
C | CTT | 21 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(18): Show | 21 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2861-674_2861-673d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053084 | ||||||
| chr2:227053105
|
G | A | 1 | a0025c0044t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2861-693C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053105 | ||||||
| chr2:227053169
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2861-757A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053169 | ||||||
| chr2:227053221
|
CTCTTTGA others(1): Show |
C | 84 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(81): Show | 84 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2861-817_2861-810d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053221 | ||||||
| chr2:227053430
|
A | T | 165 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(162): Show | 165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.2861-1018T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053430 | ||||||
| chr2:227053433
|
C | T | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2861-1021G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053433 | ||||||
| chr2:227053479
|
T | C | 1 | a0015c0024t0012g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2861-1067A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053479 | ||||||
| chr2:227053543
|
CT | C | 23 | a0001c0001t0001g0068a0001c0001t0001g0224a0001c0001t0001g0282others(20): Show | 23 | HG01884.hp2 HG01943.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2860+1050delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053543 | ||||||
| chr2:227053543
|
CTT | C | 36 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.2860+1049_2860+105 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053543 | ||||||
| chr2:227053543
|
CTTT | C | 133 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0014others(130): Show | 133 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.2860+1048_2860+105 others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053543 | ||||||
| chr2:227053543
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0002g0008 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2860+1040_2860+105 others(15): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053543 | ||||||
| chr2:227053549
|
T | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+1045A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053549 | ||||||
| chr2:227053579
|
A | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+1015T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053579 | ||||||
| chr2:227053599
|
G | A | 1 | a0004c0004t0002g0075 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2860+995C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053599 | ||||||
| chr2:227053610
|
T | C | 144 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.2860+984A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053610 | ||||||
| chr2:227053735
|
GAC | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+857_2860+858d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053735 | ||||||
| chr2:227053739
|
G | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+855C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053739 | ||||||
| chr2:227053745
|
C | T | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2860+849G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053745 | ||||||
| chr2:227053852
|
CT | C | 9 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2860+741delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053852 | ||||||
| chr2:227053928
|
T | G | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+666A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053928 | ||||||
| chr2:227053964
|
T | C | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+630A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227053964 | ||||||
| chr2:227054005
|
C | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+589G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054005 | ||||||
| chr2:227054046
|
A | G | 1 | a0003c0003t0003g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2860+548T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054046 | ||||||
| chr2:227054053
|
A | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+541T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054053 | ||||||
| chr2:227054180
|
G | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+414C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054180 | ||||||
| chr2:227054183
|
G | T | 139 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2860+411C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054183 | ||||||
| chr2:227054194
|
C | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+400G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054194 | ||||||
| chr2:227054246
|
G | A | 139 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2860+348C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054246 | ||||||
| chr2:227054322
|
T | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+272A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054322 | ||||||
| chr2:227054394
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2860+200G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054394 | ||||||
| chr2:227054425
|
G | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+169C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054425 | ||||||
| chr2:227054436
|
T | G | 22 | a0002c0002t0011g0222a0002c0019t0005g0029a0002c0019t0005g0166others(19): Show | 22 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2860+158A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 31/47 | chr2 | 227054436 | ||||||
| chr2:227054752
|
G | T | 2 | a0007c0006t0004g0175a0007c0006t0004g0176 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2717-15C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227054752 | ||||||
| chr2:227054753
|
C | T | 2 | a0007c0006t0004g0175a0007c0006t0004g0176 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2717-16G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227054753 | ||||||
| chr2:227054893
|
A | G | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2717-156T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227054893 | ||||||
| chr2:227054914
|
C | T | 137 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.2717-177G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227054914 | ||||||
| chr2:227054935
|
G | A | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2717-198C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227054935 | ||||||
| chr2:227055234
|
G | C | 28 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(25): Show | 28 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.2717-497C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055234 | ||||||
| chr2:227055243
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2717-506C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055243 | ||||||
| chr2:227055348
|
T | TA | 140 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.2716+596dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055348 | ||||||
| chr2:227055348
|
T | TAAAAAAA others(299): Show |
4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2716+596_2716+597i others(308): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055348 | ||||||
| chr2:227055369
|
G | A | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2716+576C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055369 | ||||||
| chr2:227055551
|
C | T | 49 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(46): Show | 49 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.2716+394G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055551 | ||||||
| chr2:227055554
|
C | A | 1 | a0005c0007t0005g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2716+391G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055554 | ||||||
| chr2:227055573
|
C | G | 1 | a0042c0034t0004g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2716+372G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055573 | ||||||
| chr2:227055587
|
T | C | 4 | a0012c0011t0003g0138a0012c0011t0003g0219a0012c0011t0003g0231others(1): Show | 4 | HG01891.hp1 HG01934.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2716+358A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055587 | ||||||
| chr2:227055615
|
T | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2716+330A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055615 | ||||||
| chr2:227055757
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2716+188G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055757 | ||||||
| chr2:227055758
|
G | A | 144 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.2716+187C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055758 | ||||||
| chr2:227055781
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2716+164C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055781 | ||||||
| chr2:227055803
|
G | C | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2716+142C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 30/47 | chr2 | 227055803 | ||||||
| chr2:227056230
|
G | A | 1 | a0015c0024t0002g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2546-115C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056230 | ||||||
| chr2:227056313
|
G | C | 1 | a0002c0002t0026g0232 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2546-198C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056313 | ||||||
| chr2:227056349
|
TA | T | 167 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.2546-235delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056349 | ||||||
| chr2:227056379
|
A | T | 155 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.2546-264T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056379 | ||||||
| chr2:227056390
|
A | AT | 166 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(163): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.2546-276dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056390 | ||||||
| chr2:227056492
|
A | G | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2546-377T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056492 | ||||||
| chr2:227056523
|
G | A | 4 | a0012c0011t0003g0138a0012c0011t0003g0219a0012c0011t0003g0231others(1): Show | 4 | HG01891.hp1 HG01934.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546-408C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056523 | ||||||
| chr2:227056562
|
C | T | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2546-447G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056562 | ||||||
| chr2:227056563
|
G | A | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2546-448C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056563 | ||||||
| chr2:227056598
|
T | G | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2546-483A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056598 | ||||||
| chr2:227056683
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2546-568T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056683 | ||||||
| chr2:227056784
|
G | C | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2545+655C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056784 | ||||||
| chr2:227056857
|
A | G | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2545+582T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056857 | ||||||
| chr2:227056963
|
G | A | 43 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(40): Show | 43 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.2545+476C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227056963 | ||||||
| chr2:227057210
|
G | A | 182 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2545+229C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227057210 | ||||||
| chr2:227057225
|
G | A | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2545+214C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227057225 | ||||||
| chr2:227057261
|
A | G | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2545+178T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227057261 | ||||||
| chr2:227057299
|
A | G | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2545+140T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227057299 | ||||||
| chr2:227057388
|
T | C | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2545+51A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227057388 | ||||||
| chr2:227057393
|
T | A | 182 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2545+46A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 29/47 | chr2 | 227057393 | ||||||
| chr2:227057605
|
A | G | 44 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.2384-5T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057605 | ||||||
| chr2:227057672
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2384-72G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057672 | ||||||
| chr2:227057686
|
GGA | G | 10 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0004t0037g0062others(7): Show | 10 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2384-88_2384-87del others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057686 | ||||||
| chr2:227057738
|
G | A | 198 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2384-138C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057738 | ||||||
| chr2:227057750
|
A | G | 1 | a0002c0002t0002g0079 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2384-150T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057750 | ||||||
| chr2:227057754
|
T | C | 71 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(68): Show | 71 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2384-154A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057754 | ||||||
| chr2:227057830
|
C | T | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2384-230G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057830 | ||||||
| chr2:227057907
|
T | C | 198 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2384-307A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227057907 | ||||||
| chr2:227058072
|
CTTTG | C | 10 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2384-476_2384-473d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058072 | ||||||
| chr2:227058157
|
G | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2384-557C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058157 | ||||||
| chr2:227058184
|
T | C | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2384-584A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058184 | ||||||
| chr2:227058242
|
G | C | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2384-642C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058242 | ||||||
| chr2:227058257
|
A | G | 43 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(40): Show | 43 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.2384-657T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058257 | ||||||
| chr2:227058272
|
A | ATG | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2384-674_2384-673d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058272 | ||||||
| chr2:227058288
|
C | A | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2384-688G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058288 | ||||||
| chr2:227058300
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2384-700A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058300 | ||||||
| chr2:227058338
|
G | A | 1 | a0002c0002t0002g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2384-738C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058338 | ||||||
| chr2:227058552
|
C | T | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2383+853G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058552 | ||||||
| chr2:227058604
|
G | A | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2383+801C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058604 | ||||||
| chr2:227058641
|
T | A | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2383+764A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058641 | ||||||
| chr2:227058758
|
C | T | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2383+647G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058758 | ||||||
| chr2:227058807
|
A | G | 12 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2383+598T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058807 | ||||||
| chr2:227058832
|
G | A | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2383+573C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058832 | ||||||
| chr2:227058848
|
T | C | 194 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2383+557A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058848 | ||||||
| chr2:227058914
|
T | TG | 198 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2383+490_2383+491i others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227058914 | ||||||
| chr2:227059136
|
G | A | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2383+269C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227059136 | ||||||
| chr2:227059236
|
A | G | 198 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2383+169T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 28/47 | chr2 | 227059236 | ||||||
| chr2:227059635
|
CA | C | 11 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2165-13delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227059635 | ||||||
| chr2:227059638
|
A | C | 12 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2165-15T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227059638 | ||||||
| chr2:227059644
|
A | AT | 11 | a0002c0002t0002g0086a0002c0002t0004g0149a0002c0002t0005g0142others(8): Show | 11 | HG01261.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2165-22dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227059644 | ||||||
| chr2:227059645
|
T | A | 1 | a0008c0028t0034g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2165-22A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227059645 | ||||||
| chr2:227060017
|
T | C | 4 | a0020c0041t0010g0028a0020c0054t0010g0020a0035c0037t0016g0003others(1): Show | 4 | HG02451.hp1 HG02818.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164+119A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060017 | ||||||
| chr2:227060058
|
C | T | 40 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(37): Show | 40 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.2164+78G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060058 | ||||||
| chr2:227060101
|
G | GA | 8 | a0001c0001t0001g0046a0001c0001t0001g0087a0001c0001t0001g0109others(5): Show | 8 | HG00438.hp1 HG00438.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2164+34dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAA | 7 | a0001c0001t0001g0207a0016c0065t0005g0150a0020c0041t0010g0028others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2164+33_2164+34dup others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAA | 11 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.2164+31_2164+34dup others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAA | 67 | a0001c0001t0001g0200a0001c0001t0001g0273a0001c0001t0022g0119others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2164+30_2164+34dup others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAA | 30 | a0001c0001t0001g0136a0001c0001t0001g0143a0001c0001t0001g0180others(27): Show | 30 | HG00558.hp1 HG00741.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.2164+29_2164+34dup others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAAA | 18 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(15): Show | 18 | HG01071.hp1 HG01106.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.2164+28_2164+34dup others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAAA others(1): Show |
33 | a0001c0001t0001g0108a0001c0001t0001g0194a0002c0002t0002g0086others(30): Show | 33 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.2164+27_2164+34dup others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAAA others(2): Show |
13 | a0003c0003t0003g0076a0003c0003t0003g0099a0003c0003t0003g0128others(10): Show | 13 | HG01255.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2164+26_2164+34dup others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAAA others(3): Show |
3 | a0003c0003t0003g0071a0003c0014t0002g0094a0012c0011t0003g0231 | 3 | HG02809.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2164+25_2164+34dup others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAAA others(4): Show |
1 | a0003c0003t0003g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2164+24_2164+34dup others(11): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAAA others(5): Show |
1 | a0043c0036t0038g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2164+23_2164+34dup others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060101
|
G | GAAAAAAA others(6): Show |
1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2164+22_2164+34dup others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060101 | ||||||
| chr2:227060115
|
A | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0227a0005c0007t0002g0240 | 3 | HG01106.hp2 HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2164+21T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 27/47 | chr2 | 227060115 | ||||||
| chr2:227060381
|
C | T | 197 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2057-138G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060381 | ||||||
| chr2:227060688
|
A | G | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.2057-445T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060688 | ||||||
| chr2:227060723
|
G | T | 80 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(77): Show | 80 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2057-480C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060723 | ||||||
| chr2:227060725
|
A | AT | 9 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0001g0115others(6): Show | 9 | HG01433.hp1 HG01433.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.2057-483dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060725 | ||||||
| chr2:227060725
|
ATT | A | 149 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.2057-484_2057-483d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060725 | ||||||
| chr2:227060725
|
ATTT | A | 41 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(38): Show | 41 | HG00544.hp1 HG00639.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.2057-485_2057-483d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060725 | ||||||
| chr2:227060758
|
T | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2057-515A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060758 | ||||||
| chr2:227060876
|
C | T | 1 | a0005c0046t0005g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2057-633G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060876 | ||||||
| chr2:227060993
|
T | G | 181 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2057-750A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060993 | ||||||
| chr2:227060999
|
T | G | 40 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(37): Show | 40 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.2057-756A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227060999 | ||||||
| chr2:227061020
|
C | T | 10 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0004t0037g0062others(7): Show | 10 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2057-777G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061020 | ||||||
| chr2:227061159
|
C | T | 12 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2057-916G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061159 | ||||||
| chr2:227061188
|
T | A | 1 | a0032c0057t0002g0220 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2057-945A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061188 | ||||||
| chr2:227061195
|
C | T | 1 | a0025c0044t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2057-952G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061195 | ||||||
| chr2:227061253
|
T | C | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2057-1010A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061253 | ||||||
| chr2:227061262
|
G | A | 12 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2057-1019C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061262 | ||||||
| chr2:227061275
|
C | T | 40 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(37): Show | 40 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.2057-1032G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061275 | ||||||
| chr2:227061728
|
ATATCT | A | 10 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0004t0037g0062others(7): Show | 10 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2056+797_2056+801d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061728 | ||||||
| chr2:227061851
|
C | T | 28 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(25): Show | 28 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.2056+679G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061851 | ||||||
| chr2:227061905
|
G | T | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2056+625C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061905 | ||||||
| chr2:227061989
|
C | A | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2056+541G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227061989 | ||||||
| chr2:227062036
|
A | G | 199 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2056+494T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062036 | ||||||
| chr2:227062095
|
G | A | 58 | a0001c0001t0001g0180a0002c0002t0002g0008a0002c0002t0002g0014others(55): Show | 58 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2056+435C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062095 | ||||||
| chr2:227062100
|
C | T | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2056+430G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062100 | ||||||
| chr2:227062144
|
G | A | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2056+386C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062144 | ||||||
| chr2:227062154
|
T | C | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2056+376A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062154 | ||||||
| chr2:227062157
|
A | G | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2056+373T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062157 | ||||||
| chr2:227062236
|
CA | C | 44 | a0001c0001t0001g0282a0003c0003t0003g0004a0003c0003t0003g0005others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.2056+293delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062236 | ||||||
| chr2:227062236
|
CAA | C | 147 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.2056+292_2056+293d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062236 | ||||||
| chr2:227062244
|
A | T | 2 | a0003c0003t0003g0190a0003c0003t0003g0223 | 2 | NA19000.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2056+286T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062244 | ||||||
| chr2:227062282
|
T | C | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2056+248A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062282 | ||||||
| chr2:227062454
|
T | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2056+76A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062454 | ||||||
| chr2:227062473
|
GT | G | 144 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2056+56delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062473 | ||||||
| chr2:227062473
|
GTT | G | 10 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2056+55_2056+56del others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 26/47 | chr2 | 227062473 | ||||||
| chr2:227062820
|
C | T | 181 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1988-222G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227062820 | ||||||
| chr2:227062986
|
T | C | 4 | a0002c0019t0005g0029a0002c0019t0005g0166a0042c0034t0004g0274others(1): Show | 4 | HG03139.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1988-388A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227062986 | ||||||
| chr2:227063081
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1988-483C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227063081 | ||||||
| chr2:227063220
|
G | C | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1988-622C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227063220 | ||||||
| chr2:227063235
|
A | T | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1988-637T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227063235 | ||||||
| chr2:227063391
|
T | C | 1 | a0002c0002t0002g0259 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1988-793A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227063391 | ||||||
| chr2:227063807
|
C | G | 1 | a0002c0002t0002g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1988-1209G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227063807 | ||||||
| chr2:227063861
|
G | C | 1 | a0002c0002t0002g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1988-1263C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227063861 | ||||||
| chr2:227064181
|
T | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-1583A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227064181 | ||||||
| chr2:227064261
|
A | G | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-1663T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227064261 | ||||||
| chr2:227064839
|
G | A | 1 | a0002c0002t0002g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1988-2241C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227064839 | ||||||
| chr2:227064928
|
G | A | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1988-2330C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227064928 | ||||||
| chr2:227064931
|
C | A | 197 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1988-2333G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227064931 | ||||||
| chr2:227064932
|
G | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0044others(43): Show | 47 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1988-2334C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227064932 | ||||||
| chr2:227064937
|
G | T | 1 | a0001c0010t0005g0276 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1988-2339C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227064937 | ||||||
| chr2:227065023
|
GGTGCGCG others(4): Show |
G | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1988-2436_1988-242 others(15): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065023 | ||||||
| chr2:227065039
|
A | T | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1988-2441T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065039 | ||||||
| chr2:227065118
|
G | C | 2 | a0009c0009t0001g0055a0034c0056t0001g0064 | 2 | HG02080.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1988-2520C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065118 | ||||||
| chr2:227065144
|
C | T | 84 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(81): Show | 84 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1988-2546G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065144 | ||||||
| chr2:227065152
|
T | C | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1988-2554A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065152 | ||||||
| chr2:227065219
|
C | T | 14 | a0002c0019t0005g0029a0002c0019t0005g0166a0007c0006t0004g0171others(11): Show | 14 | HG01106.hp1 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1988-2621G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065219 | ||||||
| chr2:227065271
|
T | C | 5 | a0016c0064t0005g0178a0016c0065t0005g0150a0020c0041t0010g0028others(2): Show | 5 | HG02818.hp1 HG02970.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1988-2673A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065271 | ||||||
| chr2:227065285
|
G | T | 28 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(25): Show | 28 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.1988-2687C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065285 | ||||||
| chr2:227065290
|
C | T | 1 | a0006c0005t0004g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1988-2692G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065290 | ||||||
| chr2:227065293
|
G | C | 1 | a0006c0005t0004g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1988-2695C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065293 | ||||||
| chr2:227065368
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0023g0131 | 2 | NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1988-2770C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065368 | ||||||
| chr2:227065387
|
G | A | 5 | a0016c0064t0005g0178a0016c0065t0005g0150a0020c0041t0010g0028others(2): Show | 5 | HG02818.hp1 HG02970.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1988-2789C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065387 | ||||||
| chr2:227065398
|
G | A | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1988-2800C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065398 | ||||||
| chr2:227065472
|
T | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1988-2874A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065472 | ||||||
| chr2:227065539
|
G | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-2941C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065539 | ||||||
| chr2:227065546
|
T | C | 2 | a0006c0005t0004g0156a0006c0005t0004g0158 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1988-2948A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065546 | ||||||
| chr2:227065579
|
C | A | 88 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1988-2981G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065579 | ||||||
| chr2:227065618
|
G | C | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1988-3020C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065618 | ||||||
| chr2:227065620
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1988-3022G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065620 | ||||||
| chr2:227065633
|
G | C | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1988-3035C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065633 | ||||||
| chr2:227065634
|
G | A | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1988-3036C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065634 | ||||||
| chr2:227065637
|
C | A | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1988-3039G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065637 | ||||||
| chr2:227065638
|
C | G | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1988-3040G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065638 | ||||||
| chr2:227065639
|
A | G | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1988-3041T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065639 | ||||||
| chr2:227065643
|
C | T | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1988-3045G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065643 | ||||||
| chr2:227065837
|
C | T | 1 | a0015c0024t0012g0221 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1988-3239G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065837 | ||||||
| chr2:227065926
|
C | T | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1988-3328G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065926 | ||||||
| chr2:227065991
|
A | C | 2 | a0002c0002t0002g0092a0002c0002t0002g0203 | 2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1988-3393T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227065991 | ||||||
| chr2:227066044
|
C | G | 1 | a0002c0002t0002g0266 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1988-3446G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066044 | ||||||
| chr2:227066127
|
G | A | 4 | a0002c0019t0005g0029a0002c0019t0005g0166a0042c0034t0004g0274others(1): Show | 4 | HG03139.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1988-3529C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066127 | ||||||
| chr2:227066146
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1988-3548G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066146 | ||||||
| chr2:227066181
|
A | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-3583T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066181 | ||||||
| chr2:227066340
|
C | T | 5 | a0016c0064t0005g0178a0016c0065t0005g0150a0020c0041t0010g0028others(2): Show | 5 | HG02818.hp1 HG02970.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1988-3742G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066340 | ||||||
| chr2:227066341
|
A | G | 5 | a0016c0064t0005g0178a0016c0065t0005g0150a0020c0041t0010g0028others(2): Show | 5 | HG02818.hp1 HG02970.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1988-3743T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066341 | ||||||
| chr2:227066357
|
T | C | 1 | a0002c0002t0002g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1988-3759A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066357 | ||||||
| chr2:227066717
|
C | T | 1 | a0003c0003t0003g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1988-4119G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066717 | ||||||
| chr2:227066718
|
G | A | 13 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0004t0037g0062others(10): Show | 13 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1988-4120C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066718 | ||||||
| chr2:227066965
|
C | G | 112 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1988-4367G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066965 | ||||||
| chr2:227066989
|
A | G | 1 | a0002c0002t0002g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1988-4391T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066989 | ||||||
| chr2:227066992
|
C | T | 2 | a0003c0003t0030g0169a0043c0036t0038g0153 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1988-4394G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227066992 | ||||||
| chr2:227067033
|
A | C | 2 | a0001c0001t0001g0038a0003c0014t0002g0094 | 2 | HG04204.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1988-4435T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067033 | ||||||
| chr2:227067109
|
A | C | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1988-4511T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067109 | ||||||
| chr2:227067252
|
C | A | 15 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0091others(12): Show | 15 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.1988-4654G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067252 | ||||||
| chr2:227067371
|
T | C | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1988-4773A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067371 | ||||||
| chr2:227067525
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1988-4927G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067525 | ||||||
| chr2:227067537
|
C | G | 1 | a0001c0010t0005g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1988-4939G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067537 | ||||||
| chr2:227067737
|
T | C | 40 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(37): Show | 40 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.1988-5139A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067737 | ||||||
| chr2:227067752
|
T | A | 3 | a0001c0010t0005g0275a0001c0010t0005g0276a0001c0010t0005g0277 | 3 | HG02257.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1988-5154A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067752 | ||||||
| chr2:227067882
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1988-5284T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227067882 | ||||||
| chr2:227068106
|
T | C | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1988-5508A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068106 | ||||||
| chr2:227068137
|
C | G | 57 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(54): Show | 57 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.1988-5539G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068137 | ||||||
| chr2:227068149
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0024g0132 | 2 | HG02040.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1988-5551A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068149 | ||||||
| chr2:227068203
|
A | C | 5 | a0016c0064t0005g0178a0016c0065t0005g0150a0020c0041t0010g0028others(2): Show | 5 | HG02818.hp1 HG02970.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1988-5605T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068203 | ||||||
| chr2:227068204
|
T | G | 57 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1988-5606A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068204 | ||||||
| chr2:227068387
|
A | C | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1988-5789T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068387 | ||||||
| chr2:227068485
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1988-5887G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068485 | ||||||
| chr2:227068539
|
C | T | 71 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(68): Show | 71 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1988-5941G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068539 | ||||||
| chr2:227068568
|
C | T | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-5970G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068568 | ||||||
| chr2:227068667
|
A | AC | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1988-6070dupG | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068667 | ||||||
| chr2:227068669
|
T | C | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1988-6071A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068669 | ||||||
| chr2:227068696
|
A | C | 1 | a0003c0014t0002g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1988-6098T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068696 | ||||||
| chr2:227068697
|
G | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-6099C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068697 | ||||||
| chr2:227068715
|
T | C | 32 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(29): Show | 32 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1988-6117A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068715 | ||||||
| chr2:227068819
|
C | T | 32 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(29): Show | 32 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1988-6221G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068819 | ||||||
| chr2:227068906
|
G | A | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1988-6308C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068906 | ||||||
| chr2:227068921
|
C | A | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1988-6323G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068921 | ||||||
| chr2:227068971
|
T | C | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1988-6373A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068971 | ||||||
| chr2:227068972
|
T | C | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1988-6374A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227068972 | ||||||
| chr2:227069216
|
G | C | 1 | a0002c0060t0002g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1988-6618C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069216 | ||||||
| chr2:227069217
|
A | G | 13 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0108others(10): Show | 13 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1988-6619T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069217 | ||||||
| chr2:227069272
|
C | T | 38 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(35): Show | 38 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1988-6674G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069272 | ||||||
| chr2:227069400
|
G | C | 2 | a0010c0017t0008g0179a0010c0017t0008g0183 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1988-6802C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069400 | ||||||
| chr2:227069438
|
C | T | 1 | a0004c0004t0002g0218 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1988-6840G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069438 | ||||||
| chr2:227069439
|
G | A | 27 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(24): Show | 27 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1988-6841C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069439 | ||||||
| chr2:227069451
|
C | T | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1988-6853G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069451 | ||||||
| chr2:227069522
|
T | C | 1 | a0002c0002t0002g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1988-6924A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069522 | ||||||
| chr2:227069583
|
G | C | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1988-6985C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069583 | ||||||
| chr2:227069667
|
C | T | 16 | a0001c0001t0001g0229a0001c0001t0001g0273a0002c0002t0011g0222others(13): Show | 16 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1988-7069G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069667 | ||||||
| chr2:227069696
|
T | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988-7098A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069696 | ||||||
| chr2:227069705
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1988-7107A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069705 | ||||||
| chr2:227069724
|
C | T | 1 | a0003c0073t0003g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1988-7126G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069724 | ||||||
| chr2:227069786
|
T | A | 199 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1988-7188A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227069786 | ||||||
| chr2:227070056
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1988-7458C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070056 | ||||||
| chr2:227070222
|
A | G | 3 | a0001c0068t0003g0199a0003c0003t0030g0169a0043c0036t0038g0153 | 3 | HG01884.hp1 HG03471.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1988-7624T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070222 | ||||||
| chr2:227070263
|
T | G | 37 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(34): Show | 37 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.1987+7631A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070263 | ||||||
| chr2:227070349
|
A | C | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1987+7545T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070349 | ||||||
| chr2:227070429
|
T | C | 5 | a0016c0064t0005g0178a0016c0065t0005g0150a0020c0041t0010g0028others(2): Show | 5 | HG02818.hp1 HG02970.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1987+7465A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070429 | ||||||
| chr2:227070433
|
G | A | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+7461C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070433 | ||||||
| chr2:227070548
|
A | G | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1987+7346T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070548 | ||||||
| chr2:227070613
|
G | A | 1 | a0003c0003t0003g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1987+7281C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070613 | ||||||
| chr2:227070636
|
A | G | 43 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(40): Show | 43 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.1987+7258T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070636 | ||||||
| chr2:227070692
|
G | A | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+7202C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070692 | ||||||
| chr2:227070725
|
G | T | 37 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(34): Show | 37 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.1987+7169C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070725 | ||||||
| chr2:227070731
|
A | AG | 17 | a0001c0001t0001g0196a0001c0001t0001g0206a0001c0001t0001g0251others(14): Show | 17 | HG00408.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1987+7162dupC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070731 | ||||||
| chr2:227070731
|
A | G | 1 | a0002c0002t0002g0110 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1987+7163T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070731 | ||||||
| chr2:227070738
|
A | G | 2 | a0001c0001t0001g0125a0002c0002t0002g0203 | 2 | HG02074.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1987+7156T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070738 | ||||||
| chr2:227070739
|
G | A | 37 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(34): Show | 37 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.1987+7155C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070739 | ||||||
| chr2:227070875
|
T | TAATA | 48 | a0001c0001t0021g0141a0002c0002t0002g0009a0002c0002t0002g0013others(45): Show | 48 | HG00544.hp1 HG01106.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.1987+7015_1987+701 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070875 | ||||||
| chr2:227070875
|
T | TAATAAAT others(1): Show |
43 | a0002c0002t0004g0149a0003c0003t0003g0004a0003c0003t0003g0005others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1987+7011_1987+701 others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070875 | ||||||
| chr2:227070875
|
T | TAATAAAT others(5): Show |
1 | a0003c0003t0003g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1987+7007_1987+701 others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227070875 | ||||||
| chr2:227071179
|
A | G | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+6715T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227071179 | ||||||
| chr2:227071194
|
A | G | 70 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(67): Show | 70 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1987+6700T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227071194 | ||||||
| chr2:227071453
|
G | A | 2 | a0011c0012t0006g0256a0011c0012t0006g0257 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1987+6441C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227071453 | ||||||
| chr2:227071502
|
C | T | 1 | a0002c0002t0002g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1987+6392G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227071502 | ||||||
| chr2:227071545
|
ATTAAC | A | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.1987+6344_1987+634 others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227071545 | ||||||
| chr2:227071815
|
A | G | 1 | a0001c0068t0003g0199 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1987+6079T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227071815 | ||||||
| chr2:227071848
|
G | C | 1 | a0016c0065t0005g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1987+6046C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227071848 | ||||||
| chr2:227072113
|
G | A | 6 | a0002c0002t0004g0149a0002c0058t0005g0214a0006c0005t0004g0148others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1987+5781C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227072113 | ||||||
| chr2:227072385
|
A | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+5509T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227072385 | ||||||
| chr2:227072386
|
G | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+5508C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227072386 | ||||||
| chr2:227072614
|
A | C | 11 | a0004c0004t0002g0147a0004c0004t0005g0030a0004c0004t0005g0234others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1987+5280T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227072614 | ||||||
| chr2:227072752
|
C | T | 2 | a0012c0011t0003g0138a0012c0011t0003g0219 | 2 | HG01934.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1987+5142G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227072752 | ||||||
| chr2:227072845
|
A | T | 2 | a0007c0006t0004g0181a0038c0038t0005g0024 | 2 | HG01106.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1987+5049T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227072845 | ||||||
| chr2:227072895
|
C | T | 57 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1987+4999G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227072895 | ||||||
| chr2:227073068
|
A | T | 1 | a0005c0045t0003g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1987+4826T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073068 | ||||||
| chr2:227073092
|
G | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1987+4802C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073092 | ||||||
| chr2:227073104
|
CT | C | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+4789delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073104 | ||||||
| chr2:227073297
|
CA | C | 36 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(33): Show | 36 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1987+4596delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073297 | ||||||
| chr2:227073512
|
C | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+4382G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073512 | ||||||
| chr2:227073516
|
T | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0180a0010c0032t0008g0167 | 3 | HG03516.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1987+4378A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073516 | ||||||
| chr2:227073622
|
A | C | 1 | a0002c0002t0007g0049 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1987+4272T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073622 | ||||||
| chr2:227073759
|
G | T | 2 | a0002c0002t0002g0113a0002c0002t0002g0248 | 2 | HG01169.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1987+4135C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073759 | ||||||
| chr2:227073760
|
A | T | 2 | a0002c0002t0002g0113a0002c0002t0002g0248 | 2 | HG01169.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1987+4134T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073760 | ||||||
| chr2:227073790
|
T | C | 1 | a0032c0057t0002g0220 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1987+4104A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073790 | ||||||
| chr2:227073806
|
C | T | 1 | a0020c0054t0010g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1987+4088G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073806 | ||||||
| chr2:227073824
|
T | A | 1 | a0002c0002t0002g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1987+4070A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227073824 | ||||||
| chr2:227074022
|
A | C | 1 | a0003c0003t0003g0269 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1987+3872T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227074022 | ||||||
| chr2:227074152
|
C | T | 2 | a0009c0009t0001g0016a0009c0009t0001g0017 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1987+3742G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227074152 | ||||||
| chr2:227074164
|
A | G | 38 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(35): Show | 38 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1987+3730T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227074164 | ||||||
| chr2:227074203
|
G | GA | 5 | a0002c0002t0002g0086a0002c0002t0005g0142a0002c0002t0026g0232others(2): Show | 5 | HG01261.hp2 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+3690dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227074203 | ||||||
| chr2:227074690
|
G | A | 3 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160 | 3 | HG02922.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1987+3204C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227074690 | ||||||
| chr2:227074714
|
C | T | 13 | a0002c0002t0011g0222a0004c0004t0005g0030a0004c0004t0005g0234others(10): Show | 13 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1987+3180G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227074714 | ||||||
| chr2:227074901
|
A | G | 1 | a0002c0002t0002g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1987+2993T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227074901 | ||||||
| chr2:227075267
|
C | T | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1987+2627G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227075267 | ||||||
| chr2:227075336
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1987+2558A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227075336 | ||||||
| chr2:227075482
|
C | A | 1 | a0002c0002t0005g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1987+2412G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227075482 | ||||||
| chr2:227075678
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1987+2216T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227075678 | ||||||
| chr2:227075945
|
C | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+1949G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227075945 | ||||||
| chr2:227076017
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1987+1877G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076017 | ||||||
| chr2:227076022
|
G | A | 28 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(25): Show | 28 | HG00544.hp1 HG01123.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1987+1872C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076022 | ||||||
| chr2:227076124
|
T | A | 14 | a0002c0019t0005g0029a0002c0019t0005g0166a0007c0006t0004g0171others(11): Show | 14 | HG01106.hp1 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1987+1770A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076124 | ||||||
| chr2:227076151
|
C | T | 112 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1987+1743G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076151 | ||||||
| chr2:227076289
|
G | C | 1 | a0003c0073t0003g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1987+1605C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076289 | ||||||
| chr2:227076298
|
G | T | 1 | a0005c0007t0002g0053 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1987+1596C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076298 | ||||||
| chr2:227076384
|
T | C | 2 | a0002c0002t0002g0036a0002c0059t0025g0037 | 2 | HG01123.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1987+1510A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076384 | ||||||
| chr2:227076449
|
G | C | 1 | a0005c0007t0005g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1987+1445C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076449 | ||||||
| chr2:227076592
|
T | A | 5 | a0013c0013t0006g0144a0013c0013t0006g0155a0013c0013t0006g0212others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1987+1302A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076592 | ||||||
| chr2:227076667
|
T | C | 39 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(36): Show | 39 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1987+1227A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076667 | ||||||
| chr2:227076919
|
C | T | 11 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(8): Show | 11 | HG01106.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1987+975G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076919 | ||||||
| chr2:227076921
|
A | C | 1 | a0036c0055t0029g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1987+973T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227076921 | ||||||
| chr2:227077075
|
G | A | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1987+819C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077075 | ||||||
| chr2:227077129
|
C | T | 1 | a0002c0002t0002g0080 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1987+765G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077129 | ||||||
| chr2:227077265
|
C | T | 32 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(29): Show | 32 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1987+629G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077265 | ||||||
| chr2:227077364
|
T | C | 88 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1987+530A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077364 | ||||||
| chr2:227077375
|
G | C | 1 | a0010c0018t0004g0162 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1987+519C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077375 | ||||||
| chr2:227077451
|
T | G | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1987+443A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077451 | ||||||
| chr2:227077533
|
T | C | 3 | a0020c0041t0010g0028a0020c0054t0010g0020a0036c0055t0029g0174 | 3 | HG02818.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1987+361A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077533 | ||||||
| chr2:227077663
|
TAAAGAA | T | 10 | a0004c0004t0005g0030a0004c0004t0005g0234a0004c0004t0037g0062others(7): Show | 10 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1987+225_1987+230d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077663 | ||||||
| chr2:227077669
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1987+225T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077669 | ||||||
| chr2:227077699
|
G | GA | 36 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(33): Show | 36 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1987+194dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077699 | ||||||
| chr2:227077779
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1987+115C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077779 | ||||||
| chr2:227077803
|
A | G | 39 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(36): Show | 39 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1987+91T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 25/47 | chr2 | 227077803 | ||||||
| chr2:227078162
|
G | A | 2 | a0003c0003t0030g0169a0043c0036t0038g0153 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1804-85C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078162 | ||||||
| chr2:227078164
|
A | G | 1 | a0003c0003t0003g0006 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1804-87T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078164 | ||||||
| chr2:227078235
|
T | C | 193 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1804-158A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078235 | ||||||
| chr2:227078304
|
G | C | 2 | a0005c0007t0005g0137a0014c0052t0003g0089 | 2 | HG00323.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1804-227C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078304 | ||||||
| chr2:227078344
|
G | T | 10 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0087others(7): Show | 10 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.1804-267C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078344 | ||||||
| chr2:227078525
|
G | A | 2 | a0003c0026t0001g0010a0030c0062t0003g0265 | 2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1804-448C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078525 | ||||||
| chr2:227078526
|
C | T | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1804-449G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078526 | ||||||
| chr2:227078527
|
G | A | 1 | a0031c0061t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1804-450C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078527 | ||||||
| chr2:227078735
|
C | T | 20 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0065others(17): Show | 20 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.1804-658G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078735 | ||||||
| chr2:227078764
|
C | T | 34 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(31): Show | 34 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.1804-687G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078764 | ||||||
| chr2:227078805
|
C | A | 1 | a0002c0002t0005g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1804-728G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078805 | ||||||
| chr2:227078825
|
A | G | 11 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(8): Show | 11 | HG01106.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1804-748T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078825 | ||||||
| chr2:227078854
|
G | T | 1 | a0002c0002t0005g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1804-777C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078854 | ||||||
| chr2:227078996
|
C | A | 56 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(53): Show | 56 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1804-919G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227078996 | ||||||
| chr2:227079122
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0200a0001c0001t0022g0119others(1): Show | 4 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1804-1045C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227079122 | ||||||
| chr2:227079192
|
C | CT | 57 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1804-1116dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227079192 | ||||||
| chr2:227079262
|
C | T | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1803+1181G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227079262 | ||||||
| chr2:227079321
|
C | T | 13 | a0002c0002t0011g0222a0004c0004t0005g0030a0004c0004t0005g0234others(10): Show | 13 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1803+1122G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227079321 | ||||||
| chr2:227079923
|
A | G | 1 | a0002c0002t0002g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1803+520T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227079923 | ||||||
| chr2:227079989
|
C | T | 43 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(40): Show | 43 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.1803+454G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227079989 | ||||||
| chr2:227080194
|
T | C | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1803+249A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227080194 | ||||||
| chr2:227080207
|
A | G | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1803+236T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227080207 | ||||||
| chr2:227080377
|
G | A | 1 | a0003c0073t0003g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1803+66C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 24/47 | chr2 | 227080377 | ||||||
| chr2:227080692
|
T | C | 1 | a0028c0048t0001g0114 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1697-143A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227080692 | ||||||
| chr2:227080785
|
G | A | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1697-236C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227080785 | ||||||
| chr2:227080882
|
G | A | 2 | a0002c0002t0011g0222a0015c0042t0013g0041 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1697-333C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227080882 | ||||||
| chr2:227081163
|
T | G | 1 | a0008c0008t0009g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1697-614A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081163 | ||||||
| chr2:227081259
|
G | C | 4 | a0002c0002t0011g0222a0004c0004t0020g0217a0008c0028t0034g0160others(1): Show | 4 | HG02922.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1697-710C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081259 | ||||||
| chr2:227081446
|
G | C | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1696+669C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081446 | ||||||
| chr2:227081477
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0206a0001c0001t0001g0282 | 3 | HG01255.hp1 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1696+638G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081477 | ||||||
| chr2:227081747
|
C | CTTAAAAA others(322): Show |
1 | a0008c0028t0034g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1696+367_1696+368i others(331): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081747 | ||||||
| chr2:227081747
|
C | CTTAAAAA others(321): Show |
1 | a0004c0004t0020g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1696+367_1696+368i others(330): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081747 | ||||||
| chr2:227081747
|
C | CTTAAAAA others(320): Show |
1 | a0002c0002t0011g0222 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1696+367_1696+368i others(329): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081747 | ||||||
| chr2:227081747
|
C | CTTAAAAA others(319): Show |
1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1696+367_1696+368i others(328): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 23/47 | chr2 | 227081747 | ||||||
| chr2:227082337
|
C | G | 54 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(51): Show | 54 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1624-150G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227082337 | ||||||
| chr2:227082375
|
C | T | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1624-188G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227082375 | ||||||
| chr2:227082741
|
G | A | 1 | a0010c0018t0004g0162 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1624-554C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227082741 | ||||||
| chr2:227082789
|
T | G | 5 | a0002c0002t0002g0113a0002c0002t0002g0247a0002c0002t0002g0248others(2): Show | 5 | HG01123.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1624-602A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227082789 | ||||||
| chr2:227082914
|
G | C | 44 | a0001c0001t0001g0180a0003c0003t0003g0004a0003c0003t0003g0005others(41): Show | 44 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1624-727C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227082914 | ||||||
| chr2:227083126
|
G | A | 2 | a0003c0003t0030g0169a0043c0036t0038g0153 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1624-939C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083126 | ||||||
| chr2:227083207
|
T | C | 1 | a0003c0027t0003g0096 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1624-1020A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083207 | ||||||
| chr2:227083220
|
C | T | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1624-1033G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083220 | ||||||
| chr2:227083301
|
A | G | 13 | a0002c0019t0005g0029a0002c0019t0005g0166a0007c0006t0004g0171others(10): Show | 13 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1624-1114T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083301 | ||||||
| chr2:227083346
|
A | G | 51 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(48): Show | 51 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.1624-1159T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083346 | ||||||
| chr2:227083427
|
A | T | 1 | a0018c0023t0002g0052 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1624-1240T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083427 | ||||||
| chr2:227083545
|
C | G | 13 | a0002c0019t0005g0029a0002c0019t0005g0166a0007c0006t0004g0171others(10): Show | 13 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1624-1358G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083545 | ||||||
| chr2:227083722
|
A | G | 2 | a0005c0007t0005g0067a0005c0045t0003g0061 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1624-1535T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083722 | ||||||
| chr2:227083809
|
C | T | 195 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1624-1622G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083809 | ||||||
| chr2:227083952
|
A | G | 1 | a0002c0002t0002g0112 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1624-1765T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227083952 | ||||||
| chr2:227084010
|
A | T | 57 | a0002c0019t0005g0029a0002c0019t0005g0166a0003c0003t0003g0004others(54): Show | 57 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1624-1823T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084010 | ||||||
| chr2:227084030
|
G | A | 52 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(49): Show | 52 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1624-1843C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084030 | ||||||
| chr2:227084134
|
G | C | 2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1624-1947C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084134 | ||||||
| chr2:227084150
|
G | A | 143 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1624-1963C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084150 | ||||||
| chr2:227084210
|
C | T | 23 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(20): Show | 23 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.1624-2023G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084210 | ||||||
| chr2:227084264
|
T | A | 56 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(53): Show | 56 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1624-2077A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084264 | ||||||
| chr2:227084297
|
T | C | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1624-2110A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084297 | ||||||
| chr2:227084476
|
T | C | 2 | a0002c0002t0011g0222a0015c0042t0013g0041 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1624-2289A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084476 | ||||||
| chr2:227084551
|
AT | A | 61 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(58): Show | 61 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1624-2365delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084551 | ||||||
| chr2:227084674
|
C | A | 6 | a0002c0002t0011g0222a0006c0005t0004g0191a0006c0005t0004g0193others(3): Show | 6 | HG02896.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-2487G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084674 | ||||||
| chr2:227084712
|
A | T | 2 | a0006c0005t0004g0156a0006c0005t0004g0158 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1624-2525T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084712 | ||||||
| chr2:227084849
|
G | A | 1 | a0002c0002t0002g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1624-2662C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084849 | ||||||
| chr2:227084880
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1624-2693G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227084880 | ||||||
| chr2:227085023
|
CGA | C | 18 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(15): Show | 18 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.1624-2838_1624-283 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085023 | ||||||
| chr2:227085129
|
C | CA | 128 | a0001c0001t0001g0105a0001c0072t0001g0238a0002c0002t0002g0008others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1624-2943dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085129 | ||||||
| chr2:227085157
|
CA | C | 142 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1624-2971delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085157 | ||||||
| chr2:227085305
|
C | T | 61 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(58): Show | 61 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1624-3118G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085305 | ||||||
| chr2:227085339
|
A | G | 1 | a0006c0005t0013g0154 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1624-3152T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085339 | ||||||
| chr2:227085508
|
G | A | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1623+3145C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085508 | ||||||
| chr2:227085566
|
G | A | 1 | a0014c0052t0003g0089 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1623+3087C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085566 | ||||||
| chr2:227085635
|
G | C | 1 | a0002c0002t0002g0259 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1623+3018C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085635 | ||||||
| chr2:227085734
|
G | A | 3 | a0012c0011t0003g0138a0012c0011t0003g0219a0012c0011t0003g0231 | 3 | HG01934.hp1 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1623+2919C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085734 | ||||||
| chr2:227085750
|
T | G | 1 | a0040c0074t0018g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1623+2903A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085750 | ||||||
| chr2:227085752
|
G | A | 119 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1623+2901C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227085752 | ||||||
| chr2:227086057
|
G | A | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1623+2596C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086057 | ||||||
| chr2:227086168
|
T | C | 5 | a0020c0041t0010g0028a0020c0054t0010g0020a0033c0043t0011g0279others(2): Show | 5 | HG02818.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+2485A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086168 | ||||||
| chr2:227086325
|
G | A | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1623+2328C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086325 | ||||||
| chr2:227086347
|
C | T | 199 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1623+2306G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086347 | ||||||
| chr2:227086537
|
A | G | 45 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(42): Show | 45 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1623+2116T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086537 | ||||||
| chr2:227086564
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1623+2089T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086564 | ||||||
| chr2:227086584
|
A | G | 1 | a0015c0024t0002g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1623+2069T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086584 | ||||||
| chr2:227086740
|
C | T | 1 | a0003c0003t0003g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1623+1913G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086740 | ||||||
| chr2:227086741
|
G | A | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1623+1912C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086741 | ||||||
| chr2:227086777
|
G | A | 1 | a0003c0014t0002g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1623+1876C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086777 | ||||||
| chr2:227086796
|
A | G | 18 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(15): Show | 18 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.1623+1857T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086796 | ||||||
| chr2:227086827
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1623+1826C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086827 | ||||||
| chr2:227086946
|
C | T | 1 | a0005c0046t0005g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1623+1707G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227086946 | ||||||
| chr2:227087091
|
C | G | 1 | a0040c0074t0018g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1623+1562G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087091 | ||||||
| chr2:227087116
|
G | A | 1 | a0028c0048t0001g0114 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1623+1537C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087116 | ||||||
| chr2:227087137
|
C | T | 13 | a0002c0019t0005g0029a0002c0019t0005g0166a0007c0006t0004g0171others(10): Show | 13 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1623+1516G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087137 | ||||||
| chr2:227087314
|
T | C | 1 | a0020c0054t0010g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1623+1339A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087314 | ||||||
| chr2:227087388
|
T | C | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623+1265A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087388 | ||||||
| chr2:227087395
|
C | T | 10 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1623+1258G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087395 | ||||||
| chr2:227087438
|
G | A | 64 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(61): Show | 64 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1623+1215C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087438 | ||||||
| chr2:227087529
|
C | T | 6 | a0002c0002t0004g0149a0002c0058t0005g0214a0006c0005t0004g0148others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+1124G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087529 | ||||||
| chr2:227087862
|
G | T | 6 | a0002c0002t0011g0222a0006c0005t0004g0191a0006c0005t0004g0193others(3): Show | 6 | HG02896.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+791C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087862 | ||||||
| chr2:227087926
|
G | C | 5 | a0002c0002t0002g0036a0002c0002t0002g0074a0002c0002t0002g0092others(2): Show | 5 | HG01123.hp1 HG01243.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1623+727C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087926 | ||||||
| chr2:227087933
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0186a0002c0002t0002g0086 | 3 | HG02258.hp2 NA18941.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1623+720G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227087933 | ||||||
| chr2:227088083
|
T | C | 23 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(20): Show | 23 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.1623+570A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088083 | ||||||
| chr2:227088089
|
T | C | 1 | a0010c0018t0004g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1623+564A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088089 | ||||||
| chr2:227088112
|
C | T | 2 | a0003c0003t0031g0250a0003c0073t0003g0018 | 2 | NA18939.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1623+541G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088112 | ||||||
| chr2:227088117
|
G | T | 58 | a0002c0019t0005g0029a0002c0019t0005g0166a0003c0003t0003g0004others(55): Show | 58 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1623+536C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088117 | ||||||
| chr2:227088221
|
C | T | 2 | a0004c0004t0020g0217a0008c0028t0034g0160 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1623+432G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088221 | ||||||
| chr2:227088308
|
G | A | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1623+345C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088308 | ||||||
| chr2:227088349
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0186 | 2 | NA18941.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1623+304C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088349 | ||||||
| chr2:227088620
|
T | C | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1623+33A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 22/47 | chr2 | 227088620 | ||||||
| chr2:227088869
|
A | G | 2 | a0013c0013t0006g0144a0021c0016t0014g0019 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1460-53T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227088869 | ||||||
| chr2:227088949
|
G | A | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1460-133C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227088949 | ||||||
| chr2:227089178
|
G | GA | 125 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1460-363dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089178 | ||||||
| chr2:227089226
|
A | G | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1460-410T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089226 | ||||||
| chr2:227089340
|
T | A | 45 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(42): Show | 45 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1460-524A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089340 | ||||||
| chr2:227089473
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0207a0001c0001t0001g0209others(1): Show | 4 | HG00438.hp1 NA18944.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+395C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089473 | ||||||
| chr2:227089588
|
C | CAT | 14 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0123others(11): Show | 14 | HG01099.hp1 HG02132.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1459+278_1459+279d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATAT | 5 | a0013c0013t0006g0144a0013c0013t0006g0212a0021c0016t0014g0019others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1459+276_1459+279d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(3): Show |
1 | a0002c0002t0002g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1459+270_1459+279d others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(5): Show |
29 | a0002c0002t0002g0008a0002c0002t0002g0033a0002c0002t0002g0036others(26): Show | 29 | HG00558.hp1 HG01123.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1459+268_1459+279d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(7): Show |
11 | a0002c0002t0002g0014a0002c0002t0002g0073a0002c0002t0002g0079others(8): Show | 11 | HG00621.hp1 HG01261.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1459+266_1459+279d others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(9): Show |
15 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0210others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.1459+264_1459+279d others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(11): Show |
4 | a0002c0002t0002g0078a0002c0002t0002g0090a0002c0002t0002g0211others(1): Show | 4 | HG02165.hp2 HG02735.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+262_1459+279d others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(13): Show |
1 | a0012c0011t0003g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1459+260_1459+279d others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(15): Show |
4 | a0003c0003t0030g0169a0012c0011t0003g0233a0016c0064t0005g0178others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+279_1459+280i others(24): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(17): Show |
2 | a0002c0002t0002g0047a0012c0011t0003g0219 | 2 | HG01175.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1459+279_1459+280i others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(19): Show |
2 | a0002c0002t0002g0140a0012c0011t0003g0138 | 2 | HG01934.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1459+279_1459+280i others(28): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(23): Show |
1 | a0002c0002t0002g0077 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1459+279_1459+280i others(32): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089588
|
C | CATATATA others(25): Show |
2 | a0002c0002t0002g0185a0002c0002t0002g0188 | 2 | NA18944.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1459+279_1459+280i others(34): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089588 | ||||||
| chr2:227089608
|
T | C | 3 | a0004c0004t0020g0217a0005c0007t0002g0053a0008c0028t0034g0160 | 3 | HG02080.hp1 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1459+260A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089608 | ||||||
| chr2:227089608
|
T | TATATATA others(15): Show |
1 | a0044c0033t0032g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1459+259_1459+260i others(24): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089608 | ||||||
| chr2:227089608
|
T | TATATATA others(19): Show |
2 | a0002c0019t0005g0029a0002c0019t0005g0166 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1459+259_1459+260i others(28): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089608 | ||||||
| chr2:227089608
|
TAC | T | 22 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(19): Show | 22 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.1459+258_1459+259d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089608 | ||||||
| chr2:227089610
|
C | T | 123 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1459+258G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089610 | ||||||
| chr2:227089611
|
A | ATATATAT others(31): Show |
2 | a0007c0006t0004g0171a0007c0006t0004g0172 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1459+256_1459+257i others(40): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089611 | ||||||
| chr2:227089611
|
A | ATATATAT others(29): Show |
1 | a0007c0006t0004g0173 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1459+256_1459+257i others(38): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089611 | ||||||
| chr2:227089611
|
A | ATATATAT others(27): Show |
1 | a0007c0031t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1459+256_1459+257i others(36): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089611 | ||||||
| chr2:227089611
|
A | ATATATAT others(25): Show |
2 | a0038c0038t0005g0024a0039c0067t0028g0235 | 2 | HG01106.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1459+256_1459+257i others(34): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089611 | ||||||
| chr2:227089611
|
A | ATATATAT others(23): Show |
2 | a0007c0006t0004g0176a0007c0006t0035g0163 | 2 | HG03041.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1459+256_1459+257i others(32): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089611 | ||||||
| chr2:227089611
|
A | ATATATAT others(21): Show |
1 | a0007c0006t0004g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1459+256_1459+257i others(30): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089611 | ||||||
| chr2:227089611
|
A | ATATATAT others(19): Show |
1 | a0007c0006t0004g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1459+256_1459+257i others(28): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089611 | ||||||
| chr2:227089612
|
T | C | 2 | a0016c0064t0005g0178a0016c0065t0005g0150 | 2 | HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1459+256A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089612 | ||||||
| chr2:227089614
|
C | T | 33 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(30): Show | 33 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1459+254G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089614 | ||||||
| chr2:227089624
|
A | T | 33 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(30): Show | 33 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1459+244T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089624 | ||||||
| chr2:227089630
|
TA | T | 3 | a0003c0003t0003g0004a0003c0003t0003g0093a0003c0003t0003g0099 | 3 | HG01255.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1459+237delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089630 | ||||||
| chr2:227089631
|
A | AT | 26 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(23): Show | 26 | HG00639.hp2 HG00673.hp1 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1459+236_1459+237i others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089631 | ||||||
| chr2:227089631
|
A | ATAT | 3 | a0003c0003t0003g0084a0003c0003t0003g0269a0003c0014t0002g0094 | 3 | HG04204.hp2 NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1459+236_1459+237i others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089631 | ||||||
| chr2:227089631
|
A | T | 1 | a0003c0003t0003g0223 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1459+237T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089631 | ||||||
| chr2:227089633
|
G | T | 33 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(30): Show | 33 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1459+235C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089633 | ||||||
| chr2:227089635
|
C | T | 28 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(25): Show | 28 | HG00673.hp1 HG02071.hp2 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.1459+233G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089635 | ||||||
| chr2:227089637
|
C | T | 30 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(27): Show | 30 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1459+231G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089637 | ||||||
| chr2:227089638
|
AAGG | A | 7 | a0003c0003t0003g0005a0003c0003t0003g0076a0003c0003t0003g0101others(4): Show | 7 | HG02071.hp2 HG03710.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1459+227_1459+229d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089638 | ||||||
| chr2:227089638
|
AAGGCT | A | 14 | a0003c0003t0003g0006a0003c0003t0003g0057a0003c0003t0003g0128others(11): Show | 14 | HG00673.hp1 HG03017.hp1 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.1459+225_1459+229d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089638 | ||||||
| chr2:227089638
|
AAGGCTTT | A | 3 | a0003c0003t0003g0084a0003c0014t0002g0069a0003c0014t0002g0094 | 3 | HG04204.hp2 HG04228.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1459+223_1459+229d others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089638 | ||||||
| chr2:227089638
|
AAGGCTTT others(4): Show |
A | 5 | a0003c0003t0003g0004a0003c0003t0003g0093a0003c0003t0003g0099others(2): Show | 5 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1459+219_1459+229d others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089638 | ||||||
| chr2:227089639
|
A | T | 2 | a0003c0003t0003g0071a0019c0025t0002g0261 | 2 | HG03834.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1459+229T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089639 | ||||||
| chr2:227089640
|
G | A | 2 | a0003c0003t0003g0071a0019c0025t0002g0261 | 2 | HG03834.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1459+228C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089640 | ||||||
| chr2:227089640
|
G | T | 2 | a0003c0003t0003g0223a0003c0003t0003g0269 | 2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1459+228C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089640 | ||||||
| chr2:227089641
|
G | A | 2 | a0003c0003t0003g0223a0003c0003t0003g0269 | 2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1459+227C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089641 | ||||||
| chr2:227089641
|
G | T | 2 | a0003c0003t0003g0071a0019c0025t0002g0261 | 2 | HG03834.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1459+227C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089641 | ||||||
| chr2:227089642
|
C | A | 2 | a0003c0003t0003g0071a0019c0025t0002g0261 | 2 | HG03834.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1459+226G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089642 | ||||||
| chr2:227089642
|
C | T | 9 | a0003c0003t0003g0005a0003c0003t0003g0076a0003c0003t0003g0101others(6): Show | 9 | HG02071.hp2 HG03710.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.1459+226G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089642 | ||||||
| chr2:227089643
|
T | A | 9 | a0003c0003t0003g0005a0003c0003t0003g0076a0003c0003t0003g0101others(6): Show | 9 | HG02071.hp2 HG03710.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.1459+225A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089643 | ||||||
| chr2:227089644
|
T | A | 2 | a0003c0003t0003g0071a0019c0025t0002g0261 | 2 | HG03834.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1459+224A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089644 | ||||||
| chr2:227089645
|
T | A | 23 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(20): Show | 23 | HG00673.hp1 HG02071.hp2 HG03017.hp1 others(20): Show |
intron_variant | MODIFIER | c.1459+223A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089645 | ||||||
| chr2:227089646
|
G | C | 4 | a0003c0003t0003g0057a0003c0003t0003g0241a0003c0003t0031g0250others(1): Show | 4 | HG03017.hp1 HG03831.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+222C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089646 | ||||||
| chr2:227089646
|
G | T | 22 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0076others(19): Show | 22 | HG00673.hp1 HG02071.hp2 HG03491.hp1 others(19): Show |
intron_variant | MODIFIER | c.1459+222C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089646 | ||||||
| chr2:227089648
|
C | T | 7 | a0003c0003t0003g0057a0003c0003t0003g0084a0003c0003t0003g0241others(4): Show | 7 | HG03017.hp1 HG03831.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459+220G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089648 | ||||||
| chr2:227089649
|
T | A | 28 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(25): Show | 28 | HG00673.hp1 HG02071.hp2 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.1459+219A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089649 | ||||||
| chr2:227089651
|
T | A | 33 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(30): Show | 33 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1459+217A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089651 | ||||||
| chr2:227089653
|
AT | A | 3 | a0003c0003t0003g0084a0003c0014t0002g0069a0003c0014t0002g0094 | 3 | HG04204.hp2 HG04228.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1459+214delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089653 | ||||||
| chr2:227089654
|
T | TA | 9 | a0003c0003t0003g0004a0003c0003t0003g0057a0003c0003t0003g0093others(6): Show | 9 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1459+213dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089654 | ||||||
| chr2:227089654
|
T | TATA | 21 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0071others(18): Show | 21 | HG00673.hp1 HG02071.hp2 HG03491.hp1 others(18): Show |
intron_variant | MODIFIER | c.1459+213_1459+214i others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089654 | ||||||
| chr2:227089654
|
TAATATAT others(18): Show |
T | 5 | a0003c0003t0003g0118a0003c0003t0003g0228a0003c0027t0003g0096others(2): Show | 5 | HG00140.hp1 HG00609.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.1459+189_1459+213d others(27): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089654 | ||||||
| chr2:227089673
|
C | CTTTGACT | 33 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(30): Show | 33 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1459+194_1459+195i others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089673 | ||||||
| chr2:227089678
|
TA | T | 33 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(30): Show | 33 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1459+189delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 21/47 | chr2 | 227089678 | ||||||
| chr2:227090055
|
G | A | 1 | a0002c0002t0002g0088 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1370-98C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090055 | ||||||
| chr2:227090188
|
C | A | 2 | a0010c0017t0008g0179a0010c0017t0008g0183 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1370-231G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090188 | ||||||
| chr2:227090282
|
T | A | 2 | a0002c0002t0005g0142a0006c0005t0009g0283 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1370-325A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090282 | ||||||
| chr2:227090305
|
C | T | 3 | a0013c0013t0006g0144a0021c0016t0014g0019a0021c0016t0014g0278 | 3 | HG02258.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1370-348G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090305 | ||||||
| chr2:227090347
|
G | T | 44 | a0003c0003t0003g0004a0003c0003t0003g0005a0003c0003t0003g0006others(41): Show | 44 | HG00140.hp1 HG00609.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1370-390C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090347 | ||||||
| chr2:227090368
|
C | T | 43 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(40): Show | 43 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.1370-411G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090368 | ||||||
| chr2:227090375
|
G | A | 1 | a0040c0074t0018g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1370-418C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090375 | ||||||
| chr2:227090427
|
C | T | 2 | a0002c0002t0011g0222a0015c0042t0013g0041 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1370-470G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090427 | ||||||
| chr2:227090549
|
G | A | 2 | a0013c0013t0006g0144a0021c0016t0014g0019 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1370-592C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090549 | ||||||
| chr2:227090573
|
A | C | 5 | a0002c0002t0002g0203a0002c0002t0004g0149a0002c0058t0005g0214others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1370-616T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090573 | ||||||
| chr2:227090576
|
C | G | 1 | a0009c0009t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1370-619G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090576 | ||||||
| chr2:227090581
|
C | T | 8 | a0002c0002t0002g0086a0002c0002t0005g0142a0002c0002t0026g0232others(5): Show | 8 | HG01261.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1370-624G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090581 | ||||||
| chr2:227090587
|
T | C | 122 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1370-630A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090587 | ||||||
| chr2:227090623
|
G | A | 21 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(18): Show | 21 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(18): Show |
intron_variant | MODIFIER | c.1370-666C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090623 | ||||||
| chr2:227090667
|
G | A | 1 | a0008c0008t0004g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1370-710C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090667 | ||||||
| chr2:227090668
|
C | T | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1370-711G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090668 | ||||||
| chr2:227090729
|
G | A | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1370-772C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090729 | ||||||
| chr2:227090731
|
A | G | 155 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1370-774T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090731 | ||||||
| chr2:227090874
|
T | TA | 33 | a0001c0001t0001g0136a0003c0003t0003g0005a0003c0003t0003g0006others(30): Show | 33 | HG00609.hp1 HG00673.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1370-918dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090874 | ||||||
| chr2:227090874
|
TA | T | 22 | a0001c0001t0001g0054a0001c0001t0001g0085a0001c0010t0005g0276others(19): Show | 22 | HG01106.hp1 HG01167.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1370-918delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227090874 | ||||||
| chr2:227091247
|
C | CAGAT | 7 | a0001c0001t0001g0038a0001c0001t0001g0251a0001c0001t0021g0141others(4): Show | 7 | HG00323.hp1 HG02056.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1370-1294_1370-129 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091247
|
C | CAGATAGA others(3): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0196 | 2 | HG00408.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.1370-1291_1370-129 others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091247
|
C | CAGATAT | 37 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0001g0227others(34): Show | 37 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1370-1296_1370-129 others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091247
|
C | CAGATATA others(5): Show |
4 | a0002c0002t0005g0142a0010c0017t0008g0179a0010c0017t0008g0183others(1): Show | 4 | HG02922.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370-1302_1370-129 others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091247
|
C | CAGATATA others(11): Show |
2 | a0002c0002t0004g0149a0006c0005t0004g0148 | 2 | HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1370-1308_1370-129 others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091247
|
CAGATAT | C | 71 | a0001c0001t0001g0054a0001c0001t0001g0102a0001c0001t0001g0124others(68): Show | 71 | HG00558.hp2 HG00609.hp1 HG01099.hp1 others(68): Show |
intron_variant | MODIFIER | c.1370-1296_1370-129 others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091247
|
CAGATATA others(5): Show |
C | 10 | a0004c0004t0037g0062a0006c0005t0004g0158a0007c0006t0004g0171others(7): Show | 10 | HG01106.hp1 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1370-1302_1370-129 others(16): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091247
|
CAGATATA others(11): Show |
C | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1370-1308_1370-129 others(22): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091247 | ||||||
| chr2:227091303
|
A | G | 2 | a0004c0004t0002g0218a0015c0042t0013g0041 | 2 | HG00738.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1370-1346T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091303 | ||||||
| chr2:227091311
|
A | G | 23 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(20): Show | 23 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.1370-1354T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091311 | ||||||
| chr2:227091324
|
T | A | 4 | a0002c0019t0005g0029a0002c0019t0005g0166a0010c0032t0008g0167others(1): Show | 4 | HG03139.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-1367A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091324 | ||||||
| chr2:227091351
|
T | C | 123 | a0002c0002t0002g0008a0002c0002t0002g0014a0002c0002t0002g0033others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1370-1394A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091351 | ||||||
| chr2:227091422
|
T | TA | 49 | a0001c0001t0001g0194a0001c0001t0001g0262a0002c0019t0005g0029others(46): Show | 49 | HG00609.hp1 HG00673.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.1370-1466dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091422 | ||||||
| chr2:227091422
|
TA | T | 6 | a0001c0001t0001g0244a0001c0010t0005g0276a0002c0002t0002g0088others(3): Show | 6 | HG01515.hp1 HG01515.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370-1466delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091422 | ||||||
| chr2:227091468
|
G | GAT | 4 | a0002c0019t0005g0029a0002c0019t0005g0166a0010c0032t0008g0167others(1): Show | 4 | HG03139.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370-1513_1370-151 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091468 | ||||||
| chr2:227091474
|
G | T | 1 | a0025c0044t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1370-1517C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091474 | ||||||
| chr2:227091516
|
C | T | 1 | a0002c0002t0005g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370-1559G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091516 | ||||||
| chr2:227091622
|
G | A | 34 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(31): Show | 34 | HG00609.hp1 HG00673.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1370-1665C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091622 | ||||||
| chr2:227091902
|
AAAAG | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0180a0027c0047t0015g0025 | 3 | HG02145.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1370-1949_1370-194 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091902 | ||||||
| chr2:227091906
|
G | A | 145 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1370-1949C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091906 | ||||||
| chr2:227091918
|
GAAAGAAA others(2): Show |
G | 145 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1370-1970_1370-196 others(13): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091918 | ||||||
| chr2:227091918
|
GAAAGAAA others(7): Show |
G | 9 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(6): Show | 9 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1370-1975_1370-196 others(18): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091918 | ||||||
| chr2:227091922
|
G | GA | 33 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0108others(30): Show | 33 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1370-1966dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091922 | ||||||
| chr2:227091922
|
G | GAAAAGA | 6 | a0001c0001t0001g0136a0005c0046t0005g0159a0008c0008t0004g0161others(3): Show | 6 | HG01255.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-1966_1370-196 others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091922 | ||||||
| chr2:227091922
|
G | GAAAAGAA others(4): Show |
1 | a0001c0001t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1370-1966_1370-196 others(15): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091922 | ||||||
| chr2:227091922
|
G | GAAAGA | 5 | a0001c0001t0001g0104a0001c0001t0001g0224a0004c0004t0002g0187others(2): Show | 5 | HG00140.hp2 HG01243.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-1970_1370-196 others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091922 | ||||||
| chr2:227091931
|
G | T | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1370-1974C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091931 | ||||||
| chr2:227091943
|
A | C | 1 | a0002c0002t0007g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1370-1986T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091943 | ||||||
| chr2:227091948
|
A | AAAGAC | 9 | a0007c0006t0004g0171a0007c0006t0004g0172a0007c0006t0004g0173others(6): Show | 9 | HG01106.hp1 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1370-1996_1370-199 others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091948 | ||||||
| chr2:227091948
|
A | C | 100 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0013others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1370-1991T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227091948 | ||||||
| chr2:227092066
|
C | CA | 5 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1369+2058dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092066 | ||||||
| chr2:227092070
|
A | C | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1369+2055T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092070 | ||||||
| chr2:227092082
|
C | T | 30 | a0003c0003t0003g0005a0003c0003t0003g0006a0003c0003t0003g0057others(27): Show | 30 | HG00609.hp1 HG00673.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1369+2043G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092082 | ||||||
| chr2:227092728
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1369+1397A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092728 | ||||||
| chr2:227092767
|
G | C | 195 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1369+1358C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092767 | ||||||
| chr2:227092828
|
T | C | 1 | a0005c0007t0005g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1369+1297A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092828 | ||||||
| chr2:227092898
|
A | C | 23 | a0002c0002t0002g0009a0002c0002t0002g0013a0002c0002t0002g0048others(20): Show | 23 | HG00544.hp1 HG01261.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.1369+1227T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092898 | ||||||
| chr2:227092991
|
G | C | 2 | a0033c0043t0011g0279a0045c0030t0033g0192 | 2 | HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1369+1134C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227092991 | ||||||
| chr2:227093236
|
A | G | 10 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0087others(7): Show | 10 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+889T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093236 | ||||||
| chr2:227093273
|
A | G | 9 | a0002c0002t0011g0222a0006c0005t0004g0191a0006c0005t0004g0193others(6): Show | 9 | HG02717.hp1 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1369+852T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093273 | ||||||
| chr2:227093290
|
TAAACAAA others(3): Show |
T | 1 | a0038c0038t0005g0024 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1369+825_1369+834d others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093290 | ||||||
| chr2:227093386
|
G | A | 39 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(36): Show | 39 | HG00099.hp2 HG01071.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.1369+739C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093386 | ||||||
| chr2:227093484
|
G | A | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1369+641C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093484 | ||||||
| chr2:227093610
|
C | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0104 | 2 | HG00140.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1369+515G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093610 | ||||||
| chr2:227093753
|
C | T | 154 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0087others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1369+372G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093753 | ||||||
| chr2:227093772
|
C | T | 1 | a0015c0024t0002g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1369+353G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093772 | ||||||
| chr2:227093789
|
C | T | 39 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0050others(36): Show | 39 | HG00099.hp2 HG00438.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1369+336G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093789 | ||||||
| chr2:227093824
|
C | T | 2 | a0001c0001t0001g0106a0004c0004t0002g0202 | 2 | HG01071.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1369+301G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093824 | ||||||
| chr2:227093828
|
C | A | 20 | a0001c0001t0001g0194a0002c0002t0002g0009a0002c0002t0002g0013others(17): Show | 20 | HG00544.hp1 HG02004.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.1369+297G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093828 | ||||||
| chr2:227093936
|
A | G | 9 | a0002c0002t0011g0222a0006c0005t0004g0191a0006c0005t0004g0193others(6): Show | 9 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1369+189T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227093936 | ||||||
| chr2:227094027
|
T | C | 1 | a0003c0003t0003g0228 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1369+98A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227094027 | ||||||
| chr2:227094045
|
A | T | 15 | a0002c0002t0011g0222a0006c0005t0004g0191a0006c0005t0004g0193others(12): Show | 15 | HG02622.hp1 HG02717.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.1369+80T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 20/47 | chr2 | 227094045 | ||||||
| chr2:227094407
|
C | T | 4 | a0006c0005t0004g0191a0006c0005t0004g0193a0010c0017t0008g0179others(1): Show | 4 | HG02896.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205-118G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227094407 | ||||||
| chr2:227094411
|
G | A | 5 | a0003c0003t0030g0169a0006c0005t0004g0191a0006c0005t0004g0193others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1205-122C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227094411 | ||||||
| chr2:227094533
|
C | T | 1 | a0003c0003t0003g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1205-244G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227094533 | ||||||
| chr2:227094649
|
A | G | 19 | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0001g0229others(16): Show | 19 | HG01106.hp1 HG01106.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1205-360T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227094649 | ||||||
| chr2:227094852
|
T | G | 1 | a0026c0050t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1205-563A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227094852 | ||||||
| chr2:227095257
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1205-968C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227095257 | ||||||
| chr2:227095365
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1205-1076C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227095365 | ||||||
| chr2:227095575
|
C | T | 1 | a0003c0003t0003g0269 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1205-1286G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227095575 | ||||||
| chr2:227095620
|
C | G | 1 | a0002c0002t0027g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1205-1331G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227095620 | ||||||
| chr2:227095636
|
C | T | 1 | a0011c0053t0015g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1205-1347G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227095636 | ||||||
| chr2:227095637
|
G | A | 29 | a0001c0001t0001g0011a0001c0001t0001g0123a0001c0001t0001g0262others(26): Show | 29 | HG00673.hp1 HG00673.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.1205-1348C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227095637 | ||||||
| chr2:227095987
|
C | G | 1 | a0036c0055t0029g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1205-1698G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227095987 | ||||||
| chr2:227096044
|
T | C | 2 | a0012c0011t0003g0138a0012c0011t0003g0219 | 2 | HG01934.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1205-1755A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227096044 | ||||||
| chr2:227096695
|
A | C | 1 | a0001c0001t0001g0224 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1204+1999T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227096695 | ||||||
| chr2:227096925
|
C | T | 2 | a0012c0011t0003g0138a0012c0011t0003g0219 | 2 | HG01934.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1204+1769G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227096925 | ||||||
| chr2:227096943
|
T | C | 6 | a0001c0001t0001g0125a0001c0001t0001g0207a0001c0001t0001g0209others(3): Show | 6 | HG00438.hp1 HG02074.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204+1751A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227096943 | ||||||
| chr2:227097079
|
T | C | 6 | a0007c0031t0004g0170a0020c0041t0010g0028a0022c0015t0004g0145others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204+1615A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097079 | ||||||
| chr2:227097105
|
T | G | 2 | a0016c0064t0005g0178a0035c0037t0016g0003 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+1589A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097105 | ||||||
| chr2:227097162
|
CAAG | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0065others(81): Show | 85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1204+1529_1204+153 others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097162 | ||||||
| chr2:227097227
|
T | C | 3 | a0001c0001t0001g0038a0017c0022t0003g0254a0017c0022t0003g0255 | 3 | NA18962.hp1 NA18971.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1204+1467A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097227 | ||||||
| chr2:227097244
|
G | C | 2 | a0011c0053t0015g0152a0027c0047t0015g0025 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1204+1450C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097244 | ||||||
| chr2:227097390
|
C | T | 1 | a0004c0040t0002g0035 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1204+1304G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097390 | ||||||
| chr2:227097501
|
T | C | 1 | a0037c0066t0012g0059 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1204+1193A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097501 | ||||||
| chr2:227097510
|
G | A | 27 | a0001c0001t0001g0034a0001c0001t0001g0050a0001c0001t0001g0117others(24): Show | 27 | HG00544.hp1 HG01071.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.1204+1184C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097510 | ||||||
| chr2:227097660
|
C | T | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1204+1034G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097660 | ||||||
| chr2:227097751
|
C | A | 69 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0100others(66): Show | 69 | HG00673.hp1 HG00673.hp2 HG01891.hp1 others(66): Show |
intron_variant | MODIFIER | c.1204+943G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097751 | ||||||
| chr2:227097915
|
T | G | 1 | a0003c0014t0002g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1204+779A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227097915 | ||||||
| chr2:227098058
|
C | T | 2 | a0010c0032t0008g0167a0044c0033t0032g0168 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1204+636G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227098058 | ||||||
| chr2:227098324
|
G | A | 68 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0100others(65): Show | 68 | HG00673.hp1 HG00673.hp2 HG01891.hp1 others(65): Show |
intron_variant | MODIFIER | c.1204+370C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227098324 | ||||||
| chr2:227098632
|
G | A | 1 | a0016c0065t0005g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1204+62C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 19/47 | chr2 | 227098632 | ||||||
| chr2:227099137
|
G | A | 1 | a0004c0004t0005g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1100-339C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 18/47 | chr2 | 227099137 | ||||||
| chr2:227099193
|
C | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0038others(162): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1100-395G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 18/47 | chr2 | 227099193 | ||||||
| chr2:227099399
|
A | G | 2 | a0040c0074t0018g0045a0042c0034t0004g0274 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1099+221T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 18/47 | chr2 | 227099399 | ||||||
| chr2:227099592
|
T | C | 4 | a0011c0012t0006g0032a0011c0012t0006g0256a0011c0012t0006g0257others(1): Show | 4 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+28A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 18/47 | chr2 | 227099592 | ||||||
| chr2:227099838
|
C | T | 49 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0100others(46): Show | 49 | HG00673.hp1 HG00673.hp2 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.1030-149G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227099838 | ||||||
| chr2:227100172
|
A | ATG | 49 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0100others(46): Show | 49 | HG00673.hp1 HG00673.hp2 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.1030-485_1030-484d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100172 | ||||||
| chr2:227100318
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1030-629G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100318 | ||||||
| chr2:227100338
|
A | G | 15 | a0001c0001t0001g0143a0001c0001t0001g0180a0001c0001t0001g0194others(12): Show | 15 | HG02258.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.1030-649T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100338 | ||||||
| chr2:227100357
|
TATG | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0065others(97): Show | 101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1030-671_1030-669d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100357 | ||||||
| chr2:227100439
|
T | A | 5 | a0006c0005t0004g0191a0006c0005t0004g0193a0010c0017t0008g0179others(2): Show | 5 | HG02896.hp1 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1030-750A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100439 | ||||||
| chr2:227100439
|
TA | T | 57 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0100others(54): Show | 57 | HG00673.hp1 HG00673.hp2 HG01891.hp1 others(54): Show |
intron_variant | MODIFIER | c.1030-751delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100439 | ||||||
| chr2:227100781
|
TG | T | 55 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0100others(52): Show | 55 | HG00673.hp1 HG00673.hp2 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.1029+722delC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100781 | ||||||
| chr2:227100789
|
G | A | 1 | a0043c0036t0038g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1029+715C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100789 | ||||||
| chr2:227100808
|
CT | C | 34 | a0001c0001t0001g0034a0001c0001t0001g0117a0001c0001t0017g0002others(31): Show | 34 | HG00544.hp1 HG01071.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.1029+695delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100808 | ||||||
| chr2:227100837
|
C | T | 1 | a0043c0036t0038g0153 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1029+667G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100837 | ||||||
| chr2:227100844
|
G | T | 8 | a0007c0031t0004g0170a0015c0042t0013g0041a0020c0041t0010g0028others(5): Show | 8 | HG02622.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029+660C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100844 | ||||||
| chr2:227100891
|
A | T | 4 | a0001c0070t0039g0204a0007c0031t0004g0170a0022c0015t0004g0145others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+613T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100891 | ||||||
| chr2:227100893
|
C | T | 4 | a0001c0070t0039g0204a0007c0031t0004g0170a0022c0015t0004g0145others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+611G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100893 | ||||||
| chr2:227100898
|
A | G | 4 | a0001c0070t0039g0204a0007c0031t0004g0170a0022c0015t0004g0145others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029+606T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100898 | ||||||
| chr2:227100954
|
A | G | 1 | a0008c0008t0009g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1029+550T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100954 | ||||||
| chr2:227100962
|
G | A | 1 | a0020c0041t0010g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1029+542C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100962 | ||||||
| chr2:227100998
|
C | T | 1 | a0007c0031t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1029+506G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227100998 | ||||||
| chr2:227101009
|
T | C | 3 | a0003c0003t0003g0006a0003c0003t0003g0084a0029c0063t0003g0082 | 3 | HG00673.hp1 NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1029+495A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227101009 | ||||||
| chr2:227101012
|
G | T | 2 | a0007c0006t0004g0175a0007c0006t0004g0176 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1029+492C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227101012 | ||||||
| chr2:227101197
|
C | T | 2 | a0006c0005t0004g0156a0021c0016t0014g0278 | 2 | HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1029+307G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227101197 | ||||||
| chr2:227101428
|
A | C | 1 | a0002c0002t0002g0009 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1029+76T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227101428 | ||||||
| chr2:227101432
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(164): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1029+72G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 17/47 | chr2 | 227101432 | ||||||
| chr2:227101582
|
T | TA | 171 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.976-26dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 16/47 | chr2 | 227101582 | ||||||
| chr2:227102200
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.931-291A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 15/47 | chr2 | 227102200 | ||||||
| chr2:227102307
|
T | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(167): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.931-398A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 15/47 | chr2 | 227102307 | ||||||
| chr2:227102389
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.930+400C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 15/47 | chr2 | 227102389 | ||||||
| chr2:227102549
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(209): Show | 213 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.930+240C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 15/47 | chr2 | 227102549 | ||||||
| chr2:227102614
|
C | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.930+175G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 15/47 | chr2 | 227102614 | ||||||
| chr2:227102667
|
G | A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.930+122C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 15/47 | chr2 | 227102667 | ||||||
| chr2:227102885
|
ACAATATT others(16): Show |
A | 168 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(165): Show | 169 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.871-60_871-38delCT others(21): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 14/47 | chr2 | 227102885 | ||||||
| chr2:227102905
|
AAAGCAAT others(15): Show |
A | 1 | a0001c0001t0001g0262 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.871-79_871-58delCC others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 14/47 | chr2 | 227102905 | ||||||
| chr2:227102950
|
A | G | 2 | a0005c0046t0005g0159a0016c0065t0005g0150 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.871-102T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 14/47 | chr2 | 227102950 | ||||||
| chr2:227103114
|
G | A | 1 | a0003c0003t0003g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.870+30C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 14/47 | chr2 | 227103114 | ||||||
| chr2:227103114
|
GA | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(185): Show | 189 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.870+29delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 14/47 | chr2 | 227103114 | ||||||
| chr2:227103115
|
A | T | 1 | a0003c0003t0003g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.870+29T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 14/47 | chr2 | 227103115 | ||||||
| chr2:227103276
|
C | G | 1 | a0003c0003t0003g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.817-79G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103276 | ||||||
| chr2:227103284
|
A | C | 4 | a0001c0001t0001g0213a0002c0058t0005g0214a0013c0013t0006g0212others(1): Show | 4 | HG02886.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-87T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103284 | ||||||
| chr2:227103298
|
T | TA | 11 | a0006c0005t0004g0156a0006c0005t0004g0158a0006c0005t0004g0195others(8): Show | 11 | HG01106.hp1 HG01169.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.817-102dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103298 | ||||||
| chr2:227103317
|
A | G | 10 | a0004c0004t0020g0217a0006c0005t0004g0156a0006c0005t0004g0158others(7): Show | 10 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-120T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103317 | ||||||
| chr2:227103417
|
G | A | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-220C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103417 | ||||||
| chr2:227103504
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(180): Show | 184 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.817-307A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103504 | ||||||
| chr2:227103525
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(180): Show | 184 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.817-328A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103525 | ||||||
| chr2:227103561
|
C | T | 1 | a0008c0008t0009g0271 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.817-364G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103561 | ||||||
| chr2:227103837
|
A | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(165): Show | 169 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.816+135T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103837 | ||||||
| chr2:227103875
|
T | C | 1 | a0002c0002t0007g0049 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.816+97A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103875 | ||||||
| chr2:227103876
|
G | T | 4 | a0006c0005t0004g0158a0007c0006t0004g0181a0008c0008t0009g0165others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+96C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 13/47 | chr2 | 227103876 | ||||||
| chr2:227104061
|
A | G | 1 | a0002c0002t0002g0077 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.736-9T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104061 | ||||||
| chr2:227104085
|
A | G | 1 | a0032c0057t0002g0220 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.736-33T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104085 | ||||||
| chr2:227104121
|
T | A | 10 | a0003c0003t0030g0169a0007c0031t0004g0170a0011c0012t0006g0256others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-69A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104121 | ||||||
| chr2:227104397
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(164): Show | 168 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.736-345G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104397 | ||||||
| chr2:227104414
|
C | CA | 26 | a0001c0001t0001g0087a0001c0001t0001g0224a0001c0001t0001g0251others(23): Show | 26 | HG00438.hp2 HG02071.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.736-363dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104414 | ||||||
| chr2:227104414
|
C | CAA | 133 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(130): Show | 134 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.736-364_736-363dup others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104414 | ||||||
| chr2:227104414
|
C | CAAA | 21 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0123others(18): Show | 21 | HG00438.hp1 HG00544.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.736-365_736-363dup others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104414 | ||||||
| chr2:227104414
|
C | CAAAA | 18 | a0001c0001t0001g0034a0001c0001t0001g0180a0001c0001t0001g0281others(15): Show | 18 | HG00639.hp2 HG01192.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.736-366_736-363dup others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104414 | ||||||
| chr2:227104414
|
C | CAAAAA | 7 | a0001c0001t0001g0117a0001c0001t0001g0258a0001c0070t0039g0204others(4): Show | 7 | HG01071.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.736-367_736-363dup others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104414 | ||||||
| chr2:227104490
|
G | A | 1 | a0009c0009t0001g0083 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.736-438C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104490 | ||||||
| chr2:227104549
|
T | A | 6 | a0001c0001t0021g0141a0002c0002t0002g0077a0002c0002t0002g0078others(3): Show | 6 | NA18939.hp1 NA19006.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.736-497A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104549 | ||||||
| chr2:227104569
|
G | A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.736-517C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104569 | ||||||
| chr2:227104581
|
CAATAAAT others(1): Show |
C | 167 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(164): Show | 168 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.736-537_736-530del others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104581 | ||||||
| chr2:227104638
|
C | CT | 104 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(101): Show | 105 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.736-587dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104638 | ||||||
| chr2:227104638
|
CT | C | 10 | a0001c0001t0001g0139a0002c0002t0002g0043a0002c0002t0002g0079others(7): Show | 10 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-587delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104638 | ||||||
| chr2:227104706
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(164): Show | 168 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.736-654A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104706 | ||||||
| chr2:227104797
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-745A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104797 | ||||||
| chr2:227104829
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.736-777C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104829 | ||||||
| chr2:227104867
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.736-815G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104867 | ||||||
| chr2:227104887
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-835G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104887 | ||||||
| chr2:227104921
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-869C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104921 | ||||||
| chr2:227104932
|
C | CA | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-881dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104932 | ||||||
| chr2:227104937
|
G | A | 1 | a0003c0003t0031g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.736-885C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104937 | ||||||
| chr2:227104998
|
T | C | 1 | a0003c0003t0003g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.736-946A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227104998 | ||||||
| chr2:227105101
|
T | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-1049A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105101 | ||||||
| chr2:227105115
|
A | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-1063T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105115 | ||||||
| chr2:227105188
|
A | AT | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-1137dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105188 | ||||||
| chr2:227105188
|
A | ATT | 13 | a0001c0001t0001g0108a0001c0001t0001g0197a0001c0001t0001g0273others(10): Show | 13 | HG01175.hp2 HG02622.hp2 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.736-1138_736-1137d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105188 | ||||||
| chr2:227105188
|
AT | A | 23 | a0001c0001t0001g0034a0001c0001t0001g0117a0001c0001t0001g0180others(20): Show | 23 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.736-1137delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105188 | ||||||
| chr2:227105232
|
T | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-1180A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105232 | ||||||
| chr2:227105283
|
C | T | 1 | a0005c0007t0005g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.736-1231G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105283 | ||||||
| chr2:227105295
|
A | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-1243T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105295 | ||||||
| chr2:227105307
|
C | T | 10 | a0004c0004t0020g0217a0006c0005t0004g0158a0007c0006t0004g0181others(7): Show | 10 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-1255G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105307 | ||||||
| chr2:227105334
|
A | T | 2 | a0001c0010t0005g0275a0001c0010t0005g0277 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.736-1282T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105334 | ||||||
| chr2:227105742
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-1690C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105742 | ||||||
| chr2:227105857
|
C | T | 1 | a0002c0002t0005g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.736-1805G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105857 | ||||||
| chr2:227105906
|
A | C | 1 | a0020c0054t0010g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.736-1854T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105906 | ||||||
| chr2:227105917
|
A | G | 1 | a0025c0044t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.736-1865T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105917 | ||||||
| chr2:227105951
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-1899T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227105951 | ||||||
| chr2:227106047
|
G | GA | 170 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(167): Show | 171 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.736-1996dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106047 | ||||||
| chr2:227106125
|
G | GT | 142 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(139): Show | 143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.736-2074dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106125 | ||||||
| chr2:227106153
|
C | T | 3 | a0008c0028t0034g0160a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.736-2101G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106153 | ||||||
| chr2:227106198
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.736-2146A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106198 | ||||||
| chr2:227106460
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.735+2121G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106460 | ||||||
| chr2:227106514
|
C | A | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.735+2067G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106514 | ||||||
| chr2:227106554
|
TTTATC | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.735+2022_735+2026d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106554 | ||||||
| chr2:227106559
|
CTTATT | C | 24 | a0001c0001t0001g0034a0001c0001t0001g0117a0001c0001t0001g0180others(21): Show | 24 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.735+2017_735+2021d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106559 | ||||||
| chr2:227106648
|
T | C | 10 | a0003c0003t0030g0169a0007c0031t0004g0170a0011c0012t0006g0256others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.735+1933A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106648 | ||||||
| chr2:227106714
|
C | T | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.735+1867G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106714 | ||||||
| chr2:227106717
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.735+1864G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106717 | ||||||
| chr2:227106727
|
G | A | 1 | a0002c0002t0002g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.735+1854C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106727 | ||||||
| chr2:227106765
|
C | T | 29 | a0001c0001t0001g0034a0001c0001t0001g0117a0001c0001t0001g0180others(26): Show | 29 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.735+1816G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106765 | ||||||
| chr2:227106799
|
G | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(140): Show | 144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.735+1782C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106799 | ||||||
| chr2:227106814
|
C | G | 7 | a0006c0005t0004g0158a0007c0006t0004g0181a0008c0008t0009g0165others(4): Show | 7 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1767G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106814 | ||||||
| chr2:227106845
|
C | T | 9 | a0001c0001t0001g0180a0004c0004t0005g0030a0004c0051t0005g0023others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+1736G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106845 | ||||||
| chr2:227106904
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.735+1677A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227106904 | ||||||
| chr2:227107015
|
G | A | 1 | a0024c0069t0002g0015 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.735+1566C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107015 | ||||||
| chr2:227107068
|
C | T | 1 | a0018c0023t0002g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.735+1513G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107068 | ||||||
| chr2:227107089
|
T | C | 4 | a0001c0001t0001g0143a0013c0013t0006g0144a0021c0016t0014g0019others(1): Show | 4 | HG02258.hp1 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+1492A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107089 | ||||||
| chr2:227107160
|
C | T | 55 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(52): Show | 55 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.735+1421G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107160 | ||||||
| chr2:227107192
|
A | T | 1 | a0001c0001t0001g0224 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.735+1389T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107192 | ||||||
| chr2:227107202
|
G | C | 5 | a0004c0004t0005g0234a0007c0006t0035g0163a0008c0008t0004g0161others(2): Show | 5 | HG02809.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+1379C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107202 | ||||||
| chr2:227107291
|
T | C | 2 | a0010c0032t0008g0167a0044c0033t0032g0168 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.735+1290A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107291 | ||||||
| chr2:227107383
|
C | A | 1 | a0002c0002t0002g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.735+1198G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107383 | ||||||
| chr2:227107507
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(155): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.735+1074A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107507 | ||||||
| chr2:227107527
|
C | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0056a0009c0009t0001g0055 | 3 | HG02056.hp2 HG02165.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.735+1054G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107527 | ||||||
| chr2:227107572
|
C | T | 52 | a0001c0001t0001g0034a0001c0001t0001g0117a0001c0001t0001g0180others(49): Show | 52 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(49): Show |
intron_variant | MODIFIER | c.735+1009G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107572 | ||||||
| chr2:227107756
|
C | CT | 9 | a0001c0001t0001g0251a0002c0002t0002g0107a0002c0002t0002g0113others(6): Show | 9 | HG00738.hp1 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.735+824dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107756 | ||||||
| chr2:227107756
|
CT | C | 44 | a0001c0001t0001g0034a0001c0001t0001g0117a0001c0001t0001g0180others(41): Show | 44 | HG00639.hp2 HG01071.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.735+824delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107756 | ||||||
| chr2:227107756
|
CTT | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(146): Show | 150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.735+823_735+824del others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107756 | ||||||
| chr2:227107790
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(145): Show | 149 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.735+791C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107790 | ||||||
| chr2:227107819
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(148): Show | 152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.735+762T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107819 | ||||||
| chr2:227107839
|
G | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(210): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.735+742C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107839 | ||||||
| chr2:227107844
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(184): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.735+737T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107844 | ||||||
| chr2:227107882
|
C | T | 1 | a0017c0022t0003g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.735+699G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107882 | ||||||
| chr2:227107888
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.735+693G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107888 | ||||||
| chr2:227107904
|
C | T | 1 | a0005c0046t0005g0159 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.735+677G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107904 | ||||||
| chr2:227107992
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.735+589T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107992 | ||||||
| chr2:227107998
|
C | T | 2 | a0003c0027t0003g0096a0009c0009t0001g0083 | 2 | HG00609.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.735+583G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227107998 | ||||||
| chr2:227108143
|
G | A | 70 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(67): Show | 70 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.735+438C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227108143 | ||||||
| chr2:227108379
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(203): Show | 207 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.735+202T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227108379 | ||||||
| chr2:227108477
|
G | A | 70 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(67): Show | 70 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.735+104C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227108477 | ||||||
| chr2:227108482
|
T | A | 1 | a0012c0011t0003g0233 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.735+99A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 12/47 | chr2 | 227108482 | ||||||
| chr2:227108694
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(76): Show | 80 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.694-72G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 11/47 | chr2 | 227108694 | ||||||
| chr2:227108790
|
T | C | 2 | a0003c0003t0003g0005a0003c0003t0003g0190 | 2 | NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.693+43A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 11/47 | chr2 | 227108790 | ||||||
| chr2:227108907
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(166): Show | 170 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.658-39T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 10/47 | chr2 | 227108907 | ||||||
| chr2:227108942
|
C | T | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.658-74G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 10/47 | chr2 | 227108942 | ||||||
| chr2:227109157
|
T | C | 100 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(97): Show | 100 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.657+67A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 10/47 | chr2 | 227109157 | ||||||
| chr2:227109162
|
C | T | 99 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(96): Show | 99 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.657+62G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 10/47 | chr2 | 227109162 | ||||||
| chr2:227109176
|
T | C | 117 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(114): Show | 117 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.657+48A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 10/47 | chr2 | 227109176 | ||||||
| chr2:227109397
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(198): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.595-111T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109397 | ||||||
| chr2:227109475
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(207): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.595-189T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109475 | ||||||
| chr2:227109477
|
G | A | 95 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.595-191C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109477 | ||||||
| chr2:227109541
|
G | A | 2 | a0010c0032t0008g0167a0044c0033t0032g0168 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.595-255C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109541 | ||||||
| chr2:227109544
|
C | G | 3 | a0001c0001t0001g0262a0002c0002t0002g0263a0002c0002t0002g0264 | 3 | NA18999.hp1 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.595-258G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109544 | ||||||
| chr2:227109544
|
C | T | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-258G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109544 | ||||||
| chr2:227109562
|
C | T | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.595-276G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109562 | ||||||
| chr2:227109590
|
T | TA | 95 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.595-305dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109590 | ||||||
| chr2:227109620
|
G | A | 15 | a0001c0001t0001g0143a0001c0001t0001g0194a0002c0019t0005g0029others(12): Show | 15 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.595-334C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109620 | ||||||
| chr2:227109663
|
C | T | 95 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.595-377G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109663 | ||||||
| chr2:227109695
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.595-409G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109695 | ||||||
| chr2:227109696
|
G | A | 95 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.595-410C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109696 | ||||||
| chr2:227109703
|
T | C | 95 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.595-417A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109703 | ||||||
| chr2:227109710
|
GC | G | 3 | a0008c0028t0034g0160a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.595-425delG | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109710 | ||||||
| chr2:227109745
|
C | CA | 11 | a0001c0001t0001g0108a0003c0003t0003g0093a0007c0031t0004g0170others(8): Show | 11 | HG01257.hp1 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.595-460dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227109745 | ||||||
| chr2:227110017
|
A | G | 1 | a0003c0027t0003g0096 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.595-731T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110017 | ||||||
| chr2:227110183
|
C | T | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.595-897G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110183 | ||||||
| chr2:227110184
|
G | C | 20 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(17): Show | 20 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.595-898C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110184 | ||||||
| chr2:227110206
|
G | A | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.595-920C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110206 | ||||||
| chr2:227110216
|
T | C | 24 | a0001c0001t0001g0143a0001c0001t0001g0194a0001c0001t0001g0273others(21): Show | 24 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.595-930A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110216 | ||||||
| chr2:227110339
|
C | T | 2 | a0035c0037t0016g0003a0038c0038t0005g0024 | 2 | HG01106.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.595-1053G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110339 | ||||||
| chr2:227110350
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.595-1064C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110350 | ||||||
| chr2:227110403
|
G | C | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-1117C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110403 | ||||||
| chr2:227110422
|
C | T | 20 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(17): Show | 20 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.595-1136G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110422 | ||||||
| chr2:227110446
|
A | C | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.595-1160T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110446 | ||||||
| chr2:227110526
|
C | G | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.594+1152G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110526 | ||||||
| chr2:227110529
|
C | T | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.594+1149G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110529 | ||||||
| chr2:227110680
|
C | CT | 72 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0065others(69): Show | 72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.594+997dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110680 | ||||||
| chr2:227110680
|
C | CTTT | 7 | a0004c0004t0020g0217a0007c0006t0004g0181a0008c0008t0009g0165others(4): Show | 7 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+995_594+997dup others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110680 | ||||||
| chr2:227110680
|
CT | C | 85 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(82): Show | 85 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.594+997delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110680 | ||||||
| chr2:227110680
|
CTT | C | 8 | a0001c0001t0001g0229a0003c0003t0003g0118a0006c0005t0004g0191others(5): Show | 8 | HG02280.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+996_594+997del others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110680 | ||||||
| chr2:227110723
|
G | A | 1 | a0002c0002t0002g0268 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.594+955C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110723 | ||||||
| chr2:227110830
|
G | A | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.594+848C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110830 | ||||||
| chr2:227110854
|
G | A | 16 | a0001c0001t0001g0143a0001c0001t0001g0194a0002c0019t0005g0029others(13): Show | 16 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.594+824C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110854 | ||||||
| chr2:227110867
|
A | T | 1 | a0002c0002t0007g0049 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.594+811T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110867 | ||||||
| chr2:227110953
|
T | C | 1 | a0003c0003t0003g0076 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.594+725A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110953 | ||||||
| chr2:227110981
|
G | A | 2 | a0011c0053t0015g0152a0027c0047t0015g0025 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.594+697C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227110981 | ||||||
| chr2:227111002
|
G | A | 95 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(92): Show | 95 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.594+676C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111002 | ||||||
| chr2:227111011
|
A | T | 2 | a0035c0037t0016g0003a0038c0038t0005g0024 | 2 | HG01106.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.594+667T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111011 | ||||||
| chr2:227111013
|
A | T | 4 | a0004c0004t0005g0234a0007c0006t0035g0163a0008c0008t0004g0161others(1): Show | 4 | HG02809.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+665T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111013 | ||||||
| chr2:227111068
|
C | A | 6 | a0001c0010t0005g0272a0001c0010t0005g0275a0001c0010t0005g0276others(3): Show | 6 | HG02257.hp1 HG03453.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+610G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111068 | ||||||
| chr2:227111073
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0024g0132 | 2 | HG00544.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.594+605G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111073 | ||||||
| chr2:227111204
|
C | T | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.594+474G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111204 | ||||||
| chr2:227111218
|
A | G | 3 | a0002c0002t0002g0107a0002c0002t0002g0113a0028c0048t0001g0114 | 3 | HG01169.hp2 HG01515.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.594+460T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111218 | ||||||
| chr2:227111331
|
A | G | 3 | a0001c0001t0001g0034a0033c0043t0011g0279a0045c0030t0033g0192 | 3 | HG02976.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.594+347T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111331 | ||||||
| chr2:227111344
|
G | C | 20 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(17): Show | 20 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.594+334C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111344 | ||||||
| chr2:227111397
|
G | A | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.594+281C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111397 | ||||||
| chr2:227111402
|
C | A | 94 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(91): Show | 94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.594+276G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111402 | ||||||
| chr2:227111503
|
T | C | 1 | a0002c0002t0002g0205 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.594+175A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111503 | ||||||
| chr2:227111510
|
T | C | 92 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.594+168A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111510 | ||||||
| chr2:227111514
|
C | A | 92 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0054others(89): Show | 92 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.594+164G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111514 | ||||||
| chr2:227111582
|
G | A | 22 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(19): Show | 22 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.594+96C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111582 | ||||||
| chr2:227111592
|
T | C | 4 | a0001c0001t0001g0143a0013c0013t0006g0144a0021c0016t0014g0019others(1): Show | 4 | HG02258.hp1 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+86A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111592 | ||||||
| chr2:227111615
|
A | G | 15 | a0001c0001t0001g0143a0001c0001t0001g0194a0002c0019t0005g0029others(12): Show | 15 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.594+63T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 9/47 | chr2 | 227111615 | ||||||
| chr2:227111734
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0022g0119a0003c0003t0003g0116 | 3 | HG00639.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.559-21A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227111734 | ||||||
| chr2:227111831
|
T | A | 1 | a0007c0006t0004g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.559-118A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227111831 | ||||||
| chr2:227111868
|
G | A | 9 | a0001c0070t0039g0204a0003c0003t0030g0169a0007c0031t0004g0170others(6): Show | 9 | HG01884.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.559-155C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227111868 | ||||||
| chr2:227112033
|
G | C | 72 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0056others(69): Show | 72 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.559-320C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112033 | ||||||
| chr2:227112135
|
C | G | 1 | a0003c0003t0003g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.559-422G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112135 | ||||||
| chr2:227112160
|
T | C | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.559-447A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112160 | ||||||
| chr2:227112259
|
A | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.559-546T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112259 | ||||||
| chr2:227112272
|
C | CTTT | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.559-562_559-560dup others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112272 | ||||||
| chr2:227112272
|
CT | C | 7 | a0006c0005t0004g0191a0006c0005t0004g0193a0006c0035t0036g0270others(4): Show | 7 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.559-560delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112272 | ||||||
| chr2:227112299
|
G | A | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.559-586C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112299 | ||||||
| chr2:227112308
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(206): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.559-595T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112308 | ||||||
| chr2:227112357
|
C | T | 2 | a0001c0001t0001g0200a0002c0002t0002g0092 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.559-644G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112357 | ||||||
| chr2:227112469
|
A | G | 4 | a0006c0005t0004g0191a0006c0005t0004g0193a0033c0043t0011g0279others(1): Show | 4 | HG02896.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-756T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112469 | ||||||
| chr2:227112549
|
G | A | 1 | a0018c0023t0002g0127 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.559-836C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112549 | ||||||
| chr2:227112595
|
G | C | 2 | a0001c0001t0001g0111a0002c0002t0002g0112 | 2 | HG00621.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.559-882C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112595 | ||||||
| chr2:227112778
|
T | C | 1 | a0025c0044t0001g0060 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.559-1065A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112778 | ||||||
| chr2:227112791
|
T | C | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.559-1078A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112791 | ||||||
| chr2:227112806
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(75): Show | 79 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.559-1093T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112806 | ||||||
| chr2:227112961
|
CT | C | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.559-1249delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227112961 | ||||||
| chr2:227113064
|
G | A | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.559-1351C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113064 | ||||||
| chr2:227113087
|
T | C | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.559-1374A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113087 | ||||||
| chr2:227113177
|
C | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(207): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.558+1451G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113177 | ||||||
| chr2:227113316
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(91): Show | 95 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.558+1312C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113316 | ||||||
| chr2:227113337
|
C | A | 1 | a0009c0009t0001g0083 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.558+1291G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113337 | ||||||
| chr2:227113375
|
C | T | 30 | a0001c0001t0001g0143a0001c0001t0001g0194a0002c0019t0005g0029others(27): Show | 30 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.558+1253G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113375 | ||||||
| chr2:227113376
|
C | G | 30 | a0001c0001t0001g0143a0001c0001t0001g0194a0002c0019t0005g0029others(27): Show | 30 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.558+1252G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113376 | ||||||
| chr2:227113396
|
A | C | 2 | a0011c0053t0015g0152a0027c0047t0015g0025 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.558+1232T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113396 | ||||||
| chr2:227113411
|
C | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+1217G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113411 | ||||||
| chr2:227113547
|
C | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+1081G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113547 | ||||||
| chr2:227113582
|
G | GT | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+1045dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113582 | ||||||
| chr2:227113638
|
C | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+990G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113638 | ||||||
| chr2:227113667
|
C | T | 1 | a0002c0002t0002g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.558+961G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113667 | ||||||
| chr2:227113763
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(112): Show | 116 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.558+865T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113763 | ||||||
| chr2:227113908
|
C | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+720G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227113908 | ||||||
| chr2:227114032
|
C | A | 1 | a0007c0031t0004g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.558+596G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114032 | ||||||
| chr2:227114084
|
A | G | 1 | a0042c0034t0004g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.558+544T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114084 | ||||||
| chr2:227114191
|
T | C | 1 | a0038c0038t0005g0024 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.558+437A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114191 | ||||||
| chr2:227114265
|
G | A | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.558+363C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114265 | ||||||
| chr2:227114290
|
A | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+338T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114290 | ||||||
| chr2:227114296
|
T | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+332A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114296 | ||||||
| chr2:227114311
|
A | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+317T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114311 | ||||||
| chr2:227114332
|
C | CA | 20 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(17): Show | 20 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.558+295dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114332 | ||||||
| chr2:227114354
|
C | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+274G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114354 | ||||||
| chr2:227114418
|
T | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+210A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114418 | ||||||
| chr2:227114510
|
G | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.558+118C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114510 | ||||||
| chr2:227114545
|
A | G | 6 | a0001c0001t0001g0046a0001c0001t0001g0139a0002c0002t0002g0073others(3): Show | 6 | HG00621.hp2 HG02004.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+83T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 8/47 | chr2 | 227114545 | ||||||
| chr2:227114736
|
A | G | 35 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(32): Show | 35 | HG00639.hp2 HG01071.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-40T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227114736 | ||||||
| chr2:227114768
|
A | T | 1 | a0003c0003t0003g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.490-72T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227114768 | ||||||
| chr2:227114817
|
A | C | 201 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0046others(198): Show | 201 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.490-121T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227114817 | ||||||
| chr2:227114876
|
CT | C | 3 | a0001c0001t0001g0262a0002c0002t0002g0263a0002c0002t0002g0264 | 3 | NA18999.hp1 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.490-181delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227114876 | ||||||
| chr2:227114985
|
C | G | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-289G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227114985 | ||||||
| chr2:227115029
|
C | G | 10 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-333G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115029 | ||||||
| chr2:227115057
|
T | G | 1 | a0003c0073t0003g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.490-361A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115057 | ||||||
| chr2:227115057
|
TATAG | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-365_490-362del others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115057 | ||||||
| chr2:227115059
|
T | G | 158 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0044others(155): Show | 158 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.490-363A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115059 | ||||||
| chr2:227115061
|
G | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0213a0002c0002t0002g0047others(3): Show | 6 | HG01175.hp1 HG01433.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-365C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115061 | ||||||
| chr2:227115173
|
C | A | 1 | a0003c0027t0003g0133 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.490-477G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115173 | ||||||
| chr2:227115205
|
C | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-509G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115205 | ||||||
| chr2:227115269
|
C | CT | 32 | a0001c0001t0001g0044a0001c0001t0001g0143a0001c0001t0001g0194others(29): Show | 32 | HG00544.hp2 HG01169.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.490-574dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115269 | ||||||
| chr2:227115269
|
C | CTTTT | 6 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(3): Show | 6 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-577_490-574dup others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115269 | ||||||
| chr2:227115269
|
CT | C | 62 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0056others(59): Show | 62 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.490-574delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115269 | ||||||
| chr2:227115284
|
T | C | 1 | a0002c0002t0005g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.490-588A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115284 | ||||||
| chr2:227115311
|
A | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-615T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115311 | ||||||
| chr2:227115331
|
C | T | 14 | a0006c0005t0004g0158a0006c0005t0004g0195a0007c0006t0004g0181others(11): Show | 14 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-635G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115331 | ||||||
| chr2:227115356
|
T | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-660A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115356 | ||||||
| chr2:227115363
|
C | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-667G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115363 | ||||||
| chr2:227115420
|
A | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-724T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115420 | ||||||
| chr2:227115426
|
G | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-730C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115426 | ||||||
| chr2:227115437
|
A | AT | 11 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-742dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115437 | ||||||
| chr2:227115456
|
T | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-760A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115456 | ||||||
| chr2:227115463
|
G | A | 1 | a0002c0002t0005g0215 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.490-767C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115463 | ||||||
| chr2:227115474
|
A | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-778T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115474 | ||||||
| chr2:227115538
|
C | T | 10 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-842G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115538 | ||||||
| chr2:227115552
|
A | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-856T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115552 | ||||||
| chr2:227115561
|
T | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-865A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115561 | ||||||
| chr2:227115590
|
A | AT | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-895dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115590 | ||||||
| chr2:227115679
|
C | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-983G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115679 | ||||||
| chr2:227115840
|
T | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1144A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115840 | ||||||
| chr2:227115890
|
T | TTAAC | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1195_490-1194i others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115890 | ||||||
| chr2:227115900
|
G | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1204C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115900 | ||||||
| chr2:227115963
|
T | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1267A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227115963 | ||||||
| chr2:227116022
|
A | G | 17 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(14): Show | 17 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-1326T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116022 | ||||||
| chr2:227116065
|
A | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1369T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116065 | ||||||
| chr2:227116083
|
G | T | 4 | a0006c0005t0004g0191a0006c0005t0004g0193a0033c0043t0011g0279others(1): Show | 4 | HG02896.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-1387C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116083 | ||||||
| chr2:227116084
|
T | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1388A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116084 | ||||||
| chr2:227116129
|
G | A | 1 | a0002c0058t0005g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.490-1433C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116129 | ||||||
| chr2:227116150
|
AAACGT | A | 11 | a0001c0001t0001g0143a0001c0001t0001g0194a0002c0019t0005g0029others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-1459_490-1455d others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116150 | ||||||
| chr2:227116153
|
C | T | 21 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(18): Show | 21 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.490-1457G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116153 | ||||||
| chr2:227116154
|
G | A | 5 | a0001c0001t0001g0213a0002c0002t0004g0149a0002c0058t0005g0214others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-1458C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116154 | ||||||
| chr2:227116164
|
A | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1468T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116164 | ||||||
| chr2:227116240
|
T | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1544A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116240 | ||||||
| chr2:227116311
|
A | G | 23 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(20): Show | 23 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.490-1615T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116311 | ||||||
| chr2:227116313
|
A | C | 23 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(20): Show | 23 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.490-1617T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116313 | ||||||
| chr2:227116365
|
C | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1669G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116365 | ||||||
| chr2:227116435
|
G | A | 1 | a0001c0001t0017g0002 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.490-1739C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116435 | ||||||
| chr2:227116555
|
C | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1859G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116555 | ||||||
| chr2:227116585
|
A | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-1889T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116585 | ||||||
| chr2:227116748
|
G | A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.489+1897C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116748 | ||||||
| chr2:227116778
|
A | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+1867T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116778 | ||||||
| chr2:227116802
|
C | G | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+1843G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116802 | ||||||
| chr2:227116842
|
T | TAGAA | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+1802_489+1803i others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116842 | ||||||
| chr2:227116940
|
A | G | 3 | a0001c0001t0001g0280a0001c0001t0001g0281a0004c0004t0002g0218 | 3 | HG00738.hp1 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.489+1705T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116940 | ||||||
| chr2:227116941
|
T | C | 2 | a0011c0053t0015g0152a0027c0047t0015g0025 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.489+1704A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116941 | ||||||
| chr2:227116981
|
C | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+1664G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227116981 | ||||||
| chr2:227117473
|
G | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+1172C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227117473 | ||||||
| chr2:227117539
|
G | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+1106C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227117539 | ||||||
| chr2:227117625
|
T | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+1020A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227117625 | ||||||
| chr2:227117646
|
T | TA | 9 | a0001c0001t0001g0085a0001c0001t0001g0243a0001c0001t0001g0281others(6): Show | 9 | HG00639.hp1 HG01099.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+998dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227117646 | ||||||
| chr2:227117646
|
TA | T | 15 | a0001c0001t0001g0031a0001c0001t0001g0206a0001c0001t0001g0273others(12): Show | 15 | HG01106.hp1 HG01433.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.489+998delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227117646 | ||||||
| chr2:227117809
|
CTAAGA | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(62): Show | 66 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.489+831_489+835del others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227117809 | ||||||
| chr2:227118125
|
C | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+520G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227118125 | ||||||
| chr2:227118222
|
G | T | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+423C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227118222 | ||||||
| chr2:227118327
|
C | G | 2 | a0003c0003t0003g0118a0015c0024t0002g0120 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.489+318G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227118327 | ||||||
| chr2:227118346
|
A | C | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.489+299T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227118346 | ||||||
| chr2:227118483
|
A | C | 1 | a0005c0007t0005g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.489+162T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227118483 | ||||||
| chr2:227118485
|
T | C | 1 | a0040c0074t0018g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489+160A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227118485 | ||||||
| chr2:227118498
|
T | C | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+147A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 7/47 | chr2 | 227118498 | ||||||
| chr2:227118904
|
A | G | 1 | a0003c0003t0003g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.373-143T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227118904 | ||||||
| chr2:227118924
|
A | G | 1 | a0002c0002t0002g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.373-163T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227118924 | ||||||
| chr2:227118934
|
A | C | 1 | a0011c0012t0006g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.373-173T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227118934 | ||||||
| chr2:227119093
|
G | A | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-332C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227119093 | ||||||
| chr2:227119241
|
C | T | 1 | a0008c0028t0034g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.373-480G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227119241 | ||||||
| chr2:227119279
|
T | C | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-518A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227119279 | ||||||
| chr2:227119290
|
T | G | 19 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(16): Show | 19 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.373-529A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227119290 | ||||||
| chr2:227119604
|
T | C | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+291A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227119604 | ||||||
| chr2:227119745
|
T | C | 1 | a0005c0007t0002g0240 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.372+150A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 6/47 | chr2 | 227119745 | ||||||
| chr2:227120068
|
A | AT | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.328-130dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120068 | ||||||
| chr2:227120083
|
G | T | 1 | a0039c0067t0028g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.328-144C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120083 | ||||||
| chr2:227120110
|
C | T | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.328-171G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120110 | ||||||
| chr2:227120147
|
T | G | 4 | a0001c0001t0001g0186a0002c0002t0002g0188a0004c0004t0002g0187others(1): Show | 4 | NA18941.hp2 NA18944.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-208A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120147 | ||||||
| chr2:227120281
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.328-342A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120281 | ||||||
| chr2:227120415
|
T | C | 2 | a0011c0053t0015g0152a0027c0047t0015g0025 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.328-476A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120415 | ||||||
| chr2:227120481
|
G | A | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+533C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120481 | ||||||
| chr2:227120484
|
A | G | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+530T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120484 | ||||||
| chr2:227120564
|
A | G | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.327+450T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120564 | ||||||
| chr2:227120607
|
A | G | 1 | a0003c0014t0002g0242 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.327+407T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120607 | ||||||
| chr2:227120675
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0068t0003g0199others(1): Show | 4 | HG02040.hp1 NA18952.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+339G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120675 | ||||||
| chr2:227120735
|
C | T | 1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.327+279G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120735 | ||||||
| chr2:227120884
|
A | C | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.327+130T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120884 | ||||||
| chr2:227120950
|
C | A | 2 | a0011c0053t0015g0152a0027c0047t0015g0025 | 2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.327+64G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 5/47 | chr2 | 227120950 | ||||||
| chr2:227121172
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.193-24T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121172 | ||||||
| chr2:227121463
|
G | A | 1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.193-315C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121463 | ||||||
| chr2:227121496
|
C | A | 13 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.193-348G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121496 | ||||||
| chr2:227121561
|
C | CA | 41 | a0001c0001t0001g0011a0001c0001t0001g0117a0001c0001t0001g0143others(38): Show | 41 | HG01071.hp1 HG01106.hp1 HG01261.hp1 others(38): Show |
intron_variant | MODIFIER | c.193-414dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121561 | ||||||
| chr2:227121561
|
C | CAA | 6 | a0003c0003t0003g0116a0006c0005t0004g0191a0006c0005t0004g0193others(3): Show | 6 | HG00639.hp2 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-415_193-414dup others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121561 | ||||||
| chr2:227121576
|
AG | A | 3 | a0001c0001t0001g0273a0002c0002t0002g0248a0003c0003t0003g0093 | 3 | HG01257.hp1 HG01515.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.193-429delC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121576 | ||||||
| chr2:227121577
|
G | A | 126 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0046others(123): Show | 126 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.193-429C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121577 | ||||||
| chr2:227121577
|
G | GAA | 68 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(65): Show | 69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.193-431_193-430dup others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121577 | ||||||
| chr2:227121603
|
T | G | 11 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-455A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121603 | ||||||
| chr2:227121629
|
AACAAG | A | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.193-486_193-482del others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121629 | ||||||
| chr2:227121684
|
C | T | 2 | a0001c0001t0023g0131a0002c0060t0002g0252 | 2 | NA19001.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.193-536G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121684 | ||||||
| chr2:227121690
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(201): Show | 205 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.193-542A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121690 | ||||||
| chr2:227121875
|
A | G | 1 | a0004c0051t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.193-727T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121875 | ||||||
| chr2:227121963
|
G | A | 5 | a0001c0001t0001g0054a0001c0001t0001g0056a0003c0003t0003g0006others(2): Show | 5 | HG00673.hp1 HG02056.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-815C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227121963 | ||||||
| chr2:227122039
|
T | C | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-891A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122039 | ||||||
| chr2:227122145
|
A | C | 10 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0048others(7): Show | 10 | HG02040.hp2 HG02132.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.193-997T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122145 | ||||||
| chr2:227122278
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.193-1130C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122278 | ||||||
| chr2:227122283
|
G | A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-1135C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122283 | ||||||
| chr2:227122628
|
C | T | 1 | a0031c0061t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.193-1480G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122628 | ||||||
| chr2:227122791
|
C | T | 10 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-1643G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122791 | ||||||
| chr2:227122873
|
A | T | 13 | a0001c0070t0039g0204a0006c0005t0004g0191a0006c0005t0004g0193others(10): Show | 13 | HG01106.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.193-1725T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122873 | ||||||
| chr2:227122873
|
AT | A | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-1726delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122873 | ||||||
| chr2:227122889
|
G | C | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-1741C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122889 | ||||||
| chr2:227122932
|
G | A | 3 | a0001c0001t0001g0135a0002c0002t0002g0009a0002c0002t0002g0013 | 3 | HG00544.hp1 HG02004.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.193-1784C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122932 | ||||||
| chr2:227122933
|
C | T | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193-1785G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227122933 | ||||||
| chr2:227123305
|
C | T | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-2157G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123305 | ||||||
| chr2:227123412
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.193-2264A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123412 | ||||||
| chr2:227123465
|
C | A | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.193-2317G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123465 | ||||||
| chr2:227123563
|
G | A | 1 | a0016c0064t0005g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-2415C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123563 | ||||||
| chr2:227123584
|
C | T | 1 | a0002c0002t0002g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.193-2436G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123584 | ||||||
| chr2:227123666
|
C | T | 1 | a0002c0002t0002g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.193-2518G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123666 | ||||||
| chr2:227123681
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(202): Show | 206 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.193-2533A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123681 | ||||||
| chr2:227123841
|
T | C | 10 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-2693A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227123841 | ||||||
| chr2:227124056
|
T | C | 5 | a0006c0005t0004g0191a0006c0005t0004g0193a0008c0028t0034g0160others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-2908A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227124056 | ||||||
| chr2:227124395
|
A | G | 1 | a0038c0038t0005g0024 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.193-3247T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227124395 | ||||||
| chr2:227124520
|
C | G | 1 | a0035c0037t0016g0003 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193-3372G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227124520 | ||||||
| chr2:227124721
|
G | A | 1 | a0002c0002t0002g0248 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.193-3573C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227124721 | ||||||
| chr2:227124743
|
A | G | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.193-3595T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227124743 | ||||||
| chr2:227124862
|
T | C | 8 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(5): Show | 8 | HG02257.hp1 HG03130.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3714A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227124862 | ||||||
| chr2:227124929
|
G | A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-3781C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227124929 | ||||||
| chr2:227125110
|
G | A | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.193-3962C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125110 | ||||||
| chr2:227125231
|
G | A | 1 | a0008c0008t0009g0271 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.193-4083C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125231 | ||||||
| chr2:227125319
|
T | C | 14 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.193-4171A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125319 | ||||||
| chr2:227125517
|
A | G | 4 | a0002c0002t0002g0107a0002c0002t0002g0113a0002c0002t0002g0151others(1): Show | 4 | HG01169.hp2 HG01515.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-4369T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125517 | ||||||
| chr2:227125643
|
G | C | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.193-4495C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125643 | ||||||
| chr2:227125646
|
T | G | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.193-4498A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125646 | ||||||
| chr2:227125703
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.193-4555C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125703 | ||||||
| chr2:227125736
|
A | G | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.193-4588T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227125736 | ||||||
| chr2:227126026
|
G | C | 1 | a0045c0030t0033g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.193-4878C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126026 | ||||||
| chr2:227126068
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(80): Show | 84 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.193-4920G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126068 | ||||||
| chr2:227126136
|
G | A | 2 | a0011c0012t0006g0032a0041c0029t0004g0026 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.193-4988C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126136 | ||||||
| chr2:227126161
|
G | T | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.193-5013C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126161 | ||||||
| chr2:227126198
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(66): Show | 70 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.193-5050C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126198 | ||||||
| chr2:227126423
|
C | T | 10 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-5275G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126423 | ||||||
| chr2:227126517
|
C | A | 1 | a0034c0056t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.193-5369G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126517 | ||||||
| chr2:227126732
|
C | T | 1 | a0003c0003t0003g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.193-5584G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126732 | ||||||
| chr2:227126747
|
T | C | 1 | a0037c0066t0012g0059 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.193-5599A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126747 | ||||||
| chr2:227126915
|
A | G | 21 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(18): Show | 21 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.193-5767T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126915 | ||||||
| chr2:227126939
|
T | G | 5 | a0006c0005t0004g0191a0006c0005t0004g0193a0008c0028t0034g0160others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-5791A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227126939 | ||||||
| chr2:227127235
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(69): Show | 73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.193-6087C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227127235 | ||||||
| chr2:227127400
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(69): Show | 73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.193-6252C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227127400 | ||||||
| chr2:227127669
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(69): Show | 73 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.193-6521G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227127669 | ||||||
| chr2:227127878
|
A | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(70): Show | 74 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.193-6730T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227127878 | ||||||
| chr2:227127970
|
A | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(278): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.193-6822T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227127970 | ||||||
| chr2:227128395
|
C | T | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.193-7247G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227128395 | ||||||
| chr2:227128427
|
T | C | 2 | a0003c0003t0030g0169a0015c0042t0013g0041 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.193-7279A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227128427 | ||||||
| chr2:227128442
|
T | C | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.193-7294A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227128442 | ||||||
| chr2:227128752
|
G | A | 49 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0070others(46): Show | 49 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.193-7604C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227128752 | ||||||
| chr2:227129015
|
G | C | 21 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(18): Show | 21 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.193-7867C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129015 | ||||||
| chr2:227129180
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.193-8032C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129180 | ||||||
| chr2:227129221
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(71): Show | 75 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.193-8073C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129221 | ||||||
| chr2:227129331
|
A | T | 2 | a0001c0001t0001g0122a0003c0027t0003g0133 | 2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.193-8183T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129331 | ||||||
| chr2:227129370
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.193-8222T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129370 | ||||||
| chr2:227129411
|
C | CT | 77 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(74): Show | 78 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.193-8264dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129411 | ||||||
| chr2:227129411
|
CT | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0194others(17): Show | 20 | HG01884.hp2 HG02132.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.193-8264delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129411 | ||||||
| chr2:227129444
|
C | G | 1 | a0001c0001t0022g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.193-8296G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129444 | ||||||
| chr2:227129527
|
G | A | 51 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0054others(48): Show | 51 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.193-8379C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129527 | ||||||
| chr2:227129597
|
T | C | 1 | a0006c0005t0004g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.193-8449A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129597 | ||||||
| chr2:227129680
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(259): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.193-8532T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129680 | ||||||
| chr2:227129891
|
G | T | 2 | a0035c0037t0016g0003a0038c0038t0005g0024 | 2 | HG01106.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.193-8743C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129891 | ||||||
| chr2:227129986
|
C | T | 1 | a0042c0034t0004g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.193-8838G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227129986 | ||||||
| chr2:227130112
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(80): Show | 84 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.193-8964T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130112 | ||||||
| chr2:227130208
|
G | A | 21 | a0001c0001t0001g0117a0001c0001t0001g0180a0001c0001t0001g0258others(18): Show | 21 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.193-9060C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130208 | ||||||
| chr2:227130263
|
A | G | 10 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG02257.hp1 HG02970.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-9115T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130263 | ||||||
| chr2:227130352
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.193-9204A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130352 | ||||||
| chr2:227130425
|
C | A | 2 | a0003c0003t0030g0169a0015c0042t0013g0041 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.193-9277G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130425 | ||||||
| chr2:227130590
|
T | C | 5 | a0002c0002t0002g0092a0002c0002t0002g0107a0002c0002t0002g0113others(2): Show | 5 | HG01169.hp2 HG01515.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-9442A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130590 | ||||||
| chr2:227130640
|
T | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(68): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.193-9492A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130640 | ||||||
| chr2:227130655
|
A | ACAGT | 71 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(68): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.192+9505_192+9506i others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130655 | ||||||
| chr2:227130670
|
G | A | 5 | a0006c0005t0004g0191a0006c0005t0004g0193a0008c0028t0034g0160others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+9491C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130670 | ||||||
| chr2:227130684
|
C | G | 10 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(7): Show | 10 | HG02257.hp1 HG02970.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+9477G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130684 | ||||||
| chr2:227130764
|
C | T | 15 | a0001c0001t0001g0143a0001c0001t0001g0273a0001c0010t0005g0272others(12): Show | 15 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+9397G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130764 | ||||||
| chr2:227130787
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(68): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.192+9374C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130787 | ||||||
| chr2:227130874
|
T | G | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.192+9287A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130874 | ||||||
| chr2:227130875
|
C | T | 1 | a0007c0006t0004g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192+9286G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227130875 | ||||||
| chr2:227131122
|
T | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(68): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.192+9039A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131122 | ||||||
| chr2:227131138
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.192+9023A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131138 | ||||||
| chr2:227131140
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.192+9021G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131140 | ||||||
| chr2:227131151
|
T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(68): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.192+9010A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131151 | ||||||
| chr2:227131151
|
T | TC | 4 | a0003c0003t0030g0169a0011c0012t0006g0032a0015c0042t0013g0041others(1): Show | 4 | HG01884.hp1 HG02717.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+9009_192+9010i others(3): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131151 | ||||||
| chr2:227131175
|
A | T | 2 | a0003c0003t0003g0005a0003c0003t0003g0190 | 2 | NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.192+8986T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131175 | ||||||
| chr2:227131346
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(68): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.192+8815T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131346 | ||||||
| chr2:227131515
|
T | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(68): Show | 72 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.192+8646A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131515 | ||||||
| chr2:227131528
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(64): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.192+8633G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131528 | ||||||
| chr2:227131668
|
G | A | 15 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0022g0119others(12): Show | 15 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+8493C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131668 | ||||||
| chr2:227131672
|
C | T | 5 | a0006c0005t0004g0191a0006c0005t0004g0193a0008c0028t0034g0160others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+8489G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131672 | ||||||
| chr2:227131687
|
G | T | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.192+8474C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131687 | ||||||
| chr2:227131755
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(67): Show | 71 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.192+8406T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227131755 | ||||||
| chr2:227132010
|
G | A | 1 | a0002c0002t0002g0092 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.192+8151C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132010 | ||||||
| chr2:227132061
|
C | T | 1 | a0003c0003t0003g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.192+8100G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132061 | ||||||
| chr2:227132110
|
G | A | 2 | a0001c0001t0001g0085a0002c0002t0002g0086 | 2 | HG02258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.192+8051C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132110 | ||||||
| chr2:227132149
|
T | C | 5 | a0006c0005t0004g0191a0006c0005t0004g0193a0008c0028t0034g0160others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+8012A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132149 | ||||||
| chr2:227132159
|
A | G | 15 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0022g0119others(12): Show | 15 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+8002T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132159 | ||||||
| chr2:227132178
|
G | A | 2 | a0006c0005t0004g0191a0006c0005t0004g0193 | 2 | HG02896.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+7983C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132178 | ||||||
| chr2:227132250
|
A | G | 3 | a0001c0070t0039g0204a0035c0037t0016g0003a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.192+7911T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132250 | ||||||
| chr2:227132324
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(65): Show | 69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.192+7837C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132324 | ||||||
| chr2:227132383
|
G | T | 3 | a0003c0003t0030g0169a0011c0012t0006g0032a0041c0029t0004g0026 | 3 | HG01884.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.192+7778C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132383 | ||||||
| chr2:227132444
|
G | A | 2 | a0006c0005t0004g0158a0043c0036t0038g0153 | 2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.192+7717C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132444 | ||||||
| chr2:227132512
|
T | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(67): Show | 71 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.192+7649A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132512 | ||||||
| chr2:227132646
|
T | G | 5 | a0001c0001t0001g0194a0002c0019t0005g0029a0002c0019t0005g0166others(2): Show | 5 | HG01884.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+7515A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132646 | ||||||
| chr2:227132754
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(67): Show | 71 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.192+7407T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132754 | ||||||
| chr2:227132791
|
CAA | C | 17 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0022g0119others(14): Show | 17 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.192+7368_192+7369d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132791 | ||||||
| chr2:227132810
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.192+7351A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132810 | ||||||
| chr2:227132976
|
C | T | 3 | a0001c0001t0001g0262a0002c0002t0002g0263a0002c0002t0002g0264 | 3 | NA18999.hp1 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.192+7185G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227132976 | ||||||
| chr2:227133051
|
G | A | 32 | a0001c0001t0001g0011a0001c0001t0001g0117a0001c0001t0001g0273others(29): Show | 32 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.192+7110C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133051 | ||||||
| chr2:227133109
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.192+7052G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133109 | ||||||
| chr2:227133131
|
A | T | 5 | a0006c0005t0004g0191a0006c0005t0004g0193a0008c0028t0034g0160others(2): Show | 5 | HG02896.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+7030T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133131 | ||||||
| chr2:227133255
|
A | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(65): Show | 69 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.192+6906T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133255 | ||||||
| chr2:227133291
|
G | A | 1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.192+6870C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133291 | ||||||
| chr2:227133320
|
C | T | 35 | a0001c0001t0001g0011a0001c0001t0001g0117a0001c0001t0001g0273others(32): Show | 35 | HG00639.hp2 HG01071.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.192+6841G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133320 | ||||||
| chr2:227133344
|
T | C | 3 | a0001c0001t0001g0143a0013c0013t0006g0144a0036c0055t0029g0174 | 3 | HG02258.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.192+6817A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133344 | ||||||
| chr2:227133408
|
G | A | 3 | a0001c0001t0001g0227a0003c0003t0003g0228a0004c0004t0002g0202 | 3 | HG00140.hp1 HG01258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.192+6753C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133408 | ||||||
| chr2:227133643
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.192+6518C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133643 | ||||||
| chr2:227133700
|
T | C | 1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.192+6461A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133700 | ||||||
| chr2:227133756
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.192+6405C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133756 | ||||||
| chr2:227133893
|
GA | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(159): Show | 163 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.192+6267delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133893 | ||||||
| chr2:227133917
|
A | T | 1 | a0002c0002t0002g0205 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.192+6244T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133917 | ||||||
| chr2:227133997
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(105): Show | 109 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.192+6164A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227133997 | ||||||
| chr2:227134078
|
C | G | 15 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0022g0119others(12): Show | 15 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+6083G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227134078 | ||||||
| chr2:227134100
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.192+6061C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227134100 | ||||||
| chr2:227134738
|
C | T | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0048others(13): Show | 16 | HG02040.hp2 HG02132.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.192+5423G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227134738 | ||||||
| chr2:227134739
|
G | A | 1 | a0002c0002t0002g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.192+5422C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227134739 | ||||||
| chr2:227134807
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(82): Show | 86 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.192+5354T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227134807 | ||||||
| chr2:227134823
|
C | T | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192+5338G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227134823 | ||||||
| chr2:227134843
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(66): Show | 70 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.192+5318G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227134843 | ||||||
| chr2:227135227
|
C | T | 1 | a0002c0002t0002g0074 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.192+4934G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227135227 | ||||||
| chr2:227135248
|
CT | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(64): Show | 68 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.192+4912delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227135248 | ||||||
| chr2:227135466
|
C | T | 1 | a0008c0008t0009g0165 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.192+4695G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227135466 | ||||||
| chr2:227135643
|
A | AT | 131 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0040others(128): Show | 132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.192+4517dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227135643 | ||||||
| chr2:227135826
|
T | C | 97 | a0001c0001t0001g0011a0001c0001t0001g0040a0001c0001t0001g0046others(94): Show | 97 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.192+4335A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227135826 | ||||||
| chr2:227136018
|
C | CA | 28 | a0001c0001t0001g0011a0001c0070t0039g0204a0002c0002t0002g0008others(25): Show | 28 | HG02040.hp2 HG02132.hp2 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.192+4142dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136018 | ||||||
| chr2:227136098
|
A | C | 1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.192+4063T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136098 | ||||||
| chr2:227136315
|
T | G | 2 | a0004c0004t0005g0030a0015c0042t0013g0041 | 2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.192+3846A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136315 | ||||||
| chr2:227136464
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(141): Show | 145 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.192+3697C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136464 | ||||||
| chr2:227136577
|
G | A | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.192+3584C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136577 | ||||||
| chr2:227136698
|
C | T | 2 | a0002c0002t0004g0149a0004c0004t0037g0062 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.192+3463G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136698 | ||||||
| chr2:227136904
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.192+3257C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136904 | ||||||
| chr2:227136911
|
GT | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(111): Show | 115 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.192+3249delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136911 | ||||||
| chr2:227136974
|
CCTT | C | 32 | a0005c0046t0005g0159a0006c0005t0004g0148a0006c0005t0004g0158others(29): Show | 32 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(29): Show |
intron_variant | MODIFIER | c.192+3184_192+3186d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136974 | ||||||
| chr2:227136984
|
C | T | 5 | a0006c0005t0004g0148a0006c0035t0036g0270a0008c0008t0009g0271others(2): Show | 5 | HG02280.hp2 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+3177G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227136984 | ||||||
| chr2:227137074
|
C | T | 3 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020 | 3 | HG02630.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192+3087G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227137074 | ||||||
| chr2:227137221
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0024g0132 | 2 | HG00544.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.192+2940A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227137221 | ||||||
| chr2:227137428
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.192+2733A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227137428 | ||||||
| chr2:227137616
|
T | C | 1 | a0002c0002t0002g0009 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.192+2545A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227137616 | ||||||
| chr2:227137816
|
C | G | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.192+2345G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227137816 | ||||||
| chr2:227138014
|
G | A | 8 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+2147C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138014 | ||||||
| chr2:227138018
|
T | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(143): Show | 147 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.192+2143A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138018 | ||||||
| chr2:227138023
|
C | G | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192+2138G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138023 | ||||||
| chr2:227138083
|
G | A | 3 | a0010c0032t0008g0167a0021c0016t0014g0019a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.192+2078C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138083 | ||||||
| chr2:227138133
|
A | AAAT | 81 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(78): Show | 82 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.192+2025_192+2027d others(5): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138133
|
A | AAATAAT | 22 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(19): Show | 22 | HG01243.hp1 HG02280.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.192+2022_192+2027d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138133
|
A | AAATAATA others(2): Show |
10 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0171others(7): Show | 10 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+2019_192+2027d others(11): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138133
|
A | AAATAATA others(5): Show |
4 | a0003c0003t0003g0118a0011c0012t0006g0032a0015c0024t0002g0120others(1): Show | 4 | HG01261.hp1 HG02818.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+2016_192+2027d others(14): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138133
|
A | AAATAATA others(8): Show |
5 | a0001c0001t0001g0117a0001c0001t0022g0119a0003c0003t0003g0116others(2): Show | 5 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+2013_192+2027d others(17): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138133
|
A | AAATAATA others(11): Show |
3 | a0011c0053t0015g0152a0013c0013t0006g0155a0027c0047t0015g0025 | 3 | HG02145.hp1 HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.192+2010_192+2027d others(20): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138133
|
A | AAATAATA others(20): Show |
1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192+2027_192+2028i others(29): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138133
|
A | AAATAATA others(23): Show |
1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.192+2027_192+2028i others(32): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138133 | ||||||
| chr2:227138155
|
A | AATAATC | 3 | a0008c0008t0004g0161a0008c0008t0004g0164a0008c0028t0034g0160 | 3 | HG02809.hp1 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.192+2005_192+2006i others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138155 | ||||||
| chr2:227138159
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.192+2002T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138159 | ||||||
| chr2:227138237
|
G | A | 3 | a0019c0025t0002g0198a0019c0025t0002g0261a0030c0062t0003g0265 | 3 | NA18952.hp1 NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.192+1924C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138237 | ||||||
| chr2:227138261
|
T | C | 2 | a0001c0001t0001g0034a0004c0040t0002g0035 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.192+1900A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138261 | ||||||
| chr2:227138459
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(80): Show | 84 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.192+1702G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138459 | ||||||
| chr2:227138479
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(89): Show | 93 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.192+1682T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138479 | ||||||
| chr2:227138502
|
G | A | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.192+1659C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138502 | ||||||
| chr2:227138506
|
G | A | 5 | a0001c0001t0001g0180a0001c0001t0001g0258a0011c0012t0006g0256others(2): Show | 5 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+1655C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138506 | ||||||
| chr2:227138589
|
C | T | 4 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(1): Show | 4 | HG02630.hp1 HG03098.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1572G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138589 | ||||||
| chr2:227138637
|
CA | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(127): Show | 131 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.192+1523delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138637 | ||||||
| chr2:227138801
|
C | T | 1 | a0002c0060t0002g0252 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.192+1360G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138801 | ||||||
| chr2:227138926
|
C | G | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.192+1235G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227138926 | ||||||
| chr2:227139109
|
T | C | 5 | a0001c0001t0001g0117a0001c0001t0022g0119a0003c0003t0003g0116others(2): Show | 5 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+1052A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227139109 | ||||||
| chr2:227139193
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.192+968T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227139193 | ||||||
| chr2:227139755
|
C | T | 28 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(25): Show | 28 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.192+406G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227139755 | ||||||
| chr2:227139790
|
T | C | 1 | a0037c0066t0012g0059 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.192+371A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 4/47 | chr2 | 227139790 | ||||||
| chr2:227140500
|
T | A | 1 | a0002c0002t0002g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.115-262A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140500 | ||||||
| chr2:227140875
|
T | TCA | 4 | a0001c0001t0001g0031a0001c0001t0001g0115a0002c0002t0026g0232others(1): Show | 4 | HG01261.hp2 HG01433.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-639_115-638dup others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140875
|
T | TCACA | 3 | a0001c0001t0001g0258a0006c0005t0004g0156a0025c0044t0001g0060 | 3 | HG02572.hp1 HG03486.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.115-641_115-638dup others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140875
|
TCA | T | 83 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0046others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.115-639_115-638del others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140875
|
TCACA | T | 45 | a0001c0001t0001g0011a0001c0001t0001g0070a0001c0001t0001g0108others(42): Show | 45 | HG00323.hp1 HG00738.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.115-641_115-638del others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140875
|
TCACACA | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(61): Show | 65 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.115-643_115-638del others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140875
|
TCACACAC others(1): Show |
T | 17 | a0001c0001t0001g0100a0001c0001t0001g0194a0002c0002t0002g0043others(14): Show | 17 | HG01255.hp2 HG01358.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.115-645_115-638del others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140875
|
TCACACAC others(3): Show |
T | 3 | a0002c0019t0005g0029a0002c0019t0005g0166a0004c0004t0005g0030 | 3 | HG03209.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.115-647_115-638del others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140875
|
TCACACAC others(5): Show |
T | 8 | a0001c0001t0001g0273a0001c0001t0017g0002a0001c0010t0005g0272others(5): Show | 8 | HG02257.hp1 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-649_115-638del others(12): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140875 | ||||||
| chr2:227140877
|
A | T | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.115-639T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140877 | ||||||
| chr2:227140896
|
C | CAA | 8 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-659_115-658ins others(2): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140896 | ||||||
| chr2:227140921
|
A | C | 2 | a0011c0012t0006g0032a0020c0041t0010g0028 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.115-683T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227140921 | ||||||
| chr2:227141190
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(127): Show | 131 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.115-952T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141190 | ||||||
| chr2:227141228
|
C | A | 3 | a0001c0070t0039g0204a0011c0053t0015g0152a0027c0047t0015g0025 | 3 | HG02145.hp1 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.115-990G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141228 | ||||||
| chr2:227141296
|
C | G | 3 | a0001c0070t0039g0204a0011c0053t0015g0152a0027c0047t0015g0025 | 3 | HG02145.hp1 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.115-1058G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141296 | ||||||
| chr2:227141334
|
C | A | 2 | a0001c0001t0001g0111a0002c0002t0002g0112 | 2 | HG00621.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.115-1096G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141334 | ||||||
| chr2:227141455
|
C | T | 2 | a0003c0003t0030g0169a0013c0013t0006g0155 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.115-1217G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141455 | ||||||
| chr2:227141469
|
T | C | 5 | a0002c0002t0002g0072a0003c0003t0003g0071a0003c0003t0003g0093others(2): Show | 5 | HG00099.hp1 HG00741.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-1231A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141469 | ||||||
| chr2:227141539
|
A | G | 2 | a0011c0012t0006g0032a0020c0041t0010g0028 | 2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.115-1301T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141539 | ||||||
| chr2:227141842
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0022g0119a0003c0003t0003g0116others(2): Show | 5 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-1604C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141842 | ||||||
| chr2:227141921
|
G | C | 40 | a0001c0070t0039g0204a0006c0005t0004g0148a0006c0005t0004g0156others(37): Show | 40 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.115-1683C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227141921 | ||||||
| chr2:227142057
|
T | C | 8 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1819A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142057 | ||||||
| chr2:227142063
|
A | G | 8 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1825T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142063 | ||||||
| chr2:227142075
|
C | CTTTAAAA | 80 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(77): Show | 81 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.115-1844_115-1838d others(9): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142075 | ||||||
| chr2:227142097
|
CA | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0040others(64): Show | 67 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.115-1860delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142097 | ||||||
| chr2:227142097
|
CAA | C | 39 | a0001c0001t0001g0143a0001c0001t0001g0186a0002c0002t0002g0072others(36): Show | 39 | HG00099.hp1 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.115-1861_115-1860d others(4): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142097 | ||||||
| chr2:227142097
|
CAAAAAA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(74): Show | 78 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.115-1865_115-1860d others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142097 | ||||||
| chr2:227142097
|
CAAAAAAA others(1): Show |
C | 8 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1867_115-1860d others(10): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142097 | ||||||
| chr2:227142215
|
C | T | 4 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(1): Show | 4 | HG02630.hp1 HG03098.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-1977G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142215 | ||||||
| chr2:227142262
|
C | T | 14 | a0006c0005t0004g0158a0006c0005t0013g0154a0007c0006t0004g0171others(11): Show | 14 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-2024G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142262 | ||||||
| chr2:227142339
|
G | A | 8 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-2101C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142339 | ||||||
| chr2:227142412
|
C | T | 3 | a0001c0070t0039g0204a0011c0053t0015g0152a0027c0047t0015g0025 | 3 | HG02145.hp1 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.114+2104G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142412 | ||||||
| chr2:227142473
|
G | C | 2 | a0003c0003t0030g0169a0013c0013t0006g0155 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.114+2043C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142473 | ||||||
| chr2:227142482
|
G | A | 3 | a0004c0004t0005g0234a0012c0011t0003g0233a0039c0067t0028g0235 | 3 | HG01891.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+2034C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142482 | ||||||
| chr2:227142739
|
C | A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.114+1777G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142739 | ||||||
| chr2:227142740
|
AGTGAGAC others(8): Show |
A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.114+1761_114+1775d others(17): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142740 | ||||||
| chr2:227142757
|
C | A | 1 | a0003c0003t0030g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.114+1759G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142757 | ||||||
| chr2:227142757
|
C | CA | 18 | a0001c0001t0001g0097a0001c0001t0001g0135a0001c0001t0021g0141others(15): Show | 18 | HG00544.hp1 HG00609.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.114+1758dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142757 | ||||||
| chr2:227142789
|
T | A | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114+1727A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227142789 | ||||||
| chr2:227143020
|
G | GCACA | 42 | a0001c0070t0039g0204a0004c0004t0002g0147a0006c0005t0004g0148others(39): Show | 42 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(39): Show |
intron_variant | MODIFIER | c.114+1492_114+1495d others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143020 | ||||||
| chr2:227143053
|
C | G | 42 | a0001c0070t0039g0204a0004c0004t0002g0147a0006c0005t0004g0148others(39): Show | 42 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(39): Show |
intron_variant | MODIFIER | c.114+1463G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143053 | ||||||
| chr2:227143142
|
T | C | 1 | a0002c0002t0002g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.114+1374A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143142 | ||||||
| chr2:227143173
|
A | G | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114+1343T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143173 | ||||||
| chr2:227143212
|
A | G | 16 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0180others(13): Show | 16 | HG02040.hp2 HG02129.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+1304T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143212 | ||||||
| chr2:227143220
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.114+1296A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143220 | ||||||
| chr2:227143233
|
T | C | 31 | a0004c0004t0002g0147a0006c0005t0004g0148a0006c0005t0004g0156others(28): Show | 31 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(28): Show |
intron_variant | MODIFIER | c.114+1283A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143233 | ||||||
| chr2:227143412
|
C | T | 1 | a0006c0005t0004g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+1104G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143412 | ||||||
| chr2:227143413
|
G | A | 2 | a0003c0003t0030g0169a0013c0013t0006g0155 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.114+1103C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143413 | ||||||
| chr2:227143755
|
G | A | 1 | a0020c0041t0010g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.114+761C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143755 | ||||||
| chr2:227143844
|
C | G | 2 | a0003c0003t0003g0005a0003c0003t0003g0190 | 2 | NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.114+672G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143844 | ||||||
| chr2:227143915
|
T | C | 4 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(1): Show | 4 | HG02630.hp1 HG03098.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+601A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143915 | ||||||
| chr2:227143971
|
C | A | 3 | a0001c0001t0001g0143a0013c0013t0006g0144a0036c0055t0029g0174 | 3 | HG02258.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.114+545G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227143971 | ||||||
| chr2:227144011
|
T | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0044others(128): Show | 132 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.114+505A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227144011 | ||||||
| chr2:227144017
|
T | C | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114+499A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227144017 | ||||||
| chr2:227144066
|
T | G | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114+450A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227144066 | ||||||
| chr2:227144072
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0213others(8): Show | 11 | HG02040.hp2 HG02129.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+444G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227144072 | ||||||
| chr2:227144176
|
G | T | 2 | a0007c0006t0004g0175a0007c0006t0004g0176 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.114+340C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227144176 | ||||||
| chr2:227144410
|
A | G | 2 | a0003c0003t0003g0005a0003c0003t0003g0190 | 2 | NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.114+106T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227144410 | ||||||
| chr2:227144433
|
G | T | 2 | a0006c0035t0036g0270a0021c0016t0014g0278 | 2 | HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.114+83C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 3/47 | chr2 | 227144433 | ||||||
| chr2:227145036
|
T | C | 8 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(5): Show | 8 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-478A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145036 | ||||||
| chr2:227145176
|
G | A | 2 | a0002c0002t0004g0149a0004c0004t0037g0062 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.72-618C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145176 | ||||||
| chr2:227145213
|
C | T | 4 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(1): Show | 4 | HG02630.hp1 HG03098.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-655G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145213 | ||||||
| chr2:227145354
|
A | G | 2 | a0003c0003t0030g0169a0013c0013t0006g0155 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.72-796T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145354 | ||||||
| chr2:227145371
|
C | T | 1 | a0007c0006t0004g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.72-813G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145371 | ||||||
| chr2:227145384
|
T | C | 5 | a0001c0001t0001g0180a0001c0001t0001g0258a0011c0012t0006g0256others(2): Show | 5 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-826A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145384 | ||||||
| chr2:227145399
|
A | T | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.72-841T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145399 | ||||||
| chr2:227145412
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(134): Show | 138 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.72-854C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145412 | ||||||
| chr2:227145412
|
G | T | 9 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0035t0036g0270others(6): Show | 9 | HG02280.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-854C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145412 | ||||||
| chr2:227145438
|
T | C | 2 | a0003c0003t0030g0169a0013c0013t0006g0155 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.72-880A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145438 | ||||||
| chr2:227145538
|
A | G | 3 | a0001c0001t0001g0213a0002c0058t0005g0214a0013c0013t0006g0212 | 3 | HG02886.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.72-980T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145538 | ||||||
| chr2:227145541
|
G | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0117others(18): Show | 21 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.72-983C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145541 | ||||||
| chr2:227145607
|
T | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA19065.hp2 NA19068.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.72-1049A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145607 | ||||||
| chr2:227145829
|
T | C | 36 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0117others(33): Show | 36 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-1271A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145829 | ||||||
| chr2:227145937
|
C | T | 1 | a0002c0002t0002g0013 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72-1379G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145937 | ||||||
| chr2:227145986
|
C | T | 1 | a0001c0010t0005g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71+1427G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227145986 | ||||||
| chr2:227146009
|
T | A | 1 | a0003c0003t0003g0269 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.71+1404A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146009 | ||||||
| chr2:227146063
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71+1350T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146063 | ||||||
| chr2:227146283
|
CT | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(148): Show | 152 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.71+1129delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146283 | ||||||
| chr2:227146454
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(147): Show | 151 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.71+959C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146454 | ||||||
| chr2:227146514
|
A | G | 2 | a0002c0002t0002g0267a0002c0002t0002g0268 | 2 | HG00323.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.71+899T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146514 | ||||||
| chr2:227146548
|
C | T | 5 | a0001c0001t0001g0117a0001c0001t0022g0119a0003c0003t0003g0116others(2): Show | 5 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+865G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146548 | ||||||
| chr2:227146653
|
C | T | 4 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(1): Show | 4 | HG02630.hp1 HG03098.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+760G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146653 | ||||||
| chr2:227146999
|
G | A | 41 | a0005c0046t0005g0159a0006c0005t0004g0148a0006c0005t0004g0156others(38): Show | 41 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(38): Show |
intron_variant | MODIFIER | c.71+414C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227146999 | ||||||
| chr2:227147108
|
T | C | 4 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(1): Show | 4 | HG02630.hp1 HG03098.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+305A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227147108 | ||||||
| chr2:227147250
|
G | T | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.71+163C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227147250 | ||||||
| chr2:227147338
|
C | T | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.71+75G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 2/47 | chr2 | 227147338 | ||||||
| chr2:227147660
|
G | A | 3 | a0011c0012t0006g0032a0015c0042t0013g0041a0020c0041t0010g0028 | 3 | HG02818.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-101-76C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227147660 | ||||||
| chr2:227147719
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(136): Show | 140 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-101-135A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227147719 | ||||||
| chr2:227147775
|
T | A | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-101-191A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227147775 | ||||||
| chr2:227148161
|
C | A | 2 | a0002c0002t0004g0149a0004c0004t0037g0062 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-101-577G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148161 | ||||||
| chr2:227148191
|
A | G | 11 | a0006c0005t0004g0195a0007c0006t0004g0171a0007c0006t0004g0172others(8): Show | 11 | HG02257.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-101-607T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148191 | ||||||
| chr2:227148354
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-101-770C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148354 | ||||||
| chr2:227148421
|
T | C | 1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-101-837A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148421 | ||||||
| chr2:227148510
|
T | C | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-101-926A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148510 | ||||||
| chr2:227148522
|
G | T | 5 | a0007c0006t0035g0163a0008c0008t0004g0161a0008c0008t0004g0164others(2): Show | 5 | HG01243.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-938C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148522 | ||||||
| chr2:227148578
|
A | T | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-101-994T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148578 | ||||||
| chr2:227148696
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-101-1112G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148696 | ||||||
| chr2:227148819
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(130): Show | 134 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-101-1235C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148819 | ||||||
| chr2:227148840
|
C | CT | 27 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0180others(24): Show | 27 | HG01175.hp1 HG01175.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-101-1257dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148840 | ||||||
| chr2:227148945
|
G | A | 5 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-1361C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227148945 | ||||||
| chr2:227149020
|
T | A | 7 | a0006c0005t0004g0191a0006c0005t0004g0193a0007c0006t0004g0181others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101-1436A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149020 | ||||||
| chr2:227149072
|
C | T | 1 | a0004c0004t0020g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-101-1488G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149072 | ||||||
| chr2:227149080
|
C | T | 1 | a0023c0039t0007g0012 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-101-1496G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149080 | ||||||
| chr2:227149358
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-101-1774C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149358 | ||||||
| chr2:227149371
|
A | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-101-1787T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149371 | ||||||
| chr2:227149386
|
C | T | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-101-1802G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149386 | ||||||
| chr2:227149392
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-101-1808A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149392 | ||||||
| chr2:227149457
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(135): Show | 139 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-101-1873T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149457 | ||||||
| chr2:227149647
|
A | AAC | 102 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0034others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-101-2065_-101-206 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149647 | ||||||
| chr2:227149869
|
GGACA | G | 5 | a0001c0001t0001g0117a0001c0001t0022g0119a0003c0003t0003g0116others(2): Show | 5 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-2289_-101-228 others(8): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149869 | ||||||
| chr2:227149884
|
C | T | 36 | a0006c0005t0004g0148a0006c0005t0004g0156a0006c0005t0004g0158others(33): Show | 36 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(33): Show |
intron_variant | MODIFIER | c.-101-2300G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149884 | ||||||
| chr2:227149886
|
G | A | 48 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0046others(45): Show | 48 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-101-2302C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227149886 | ||||||
| chr2:227150051
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0031others(202): Show | 206 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.-101-2467T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150051 | ||||||
| chr2:227150221
|
G | C | 5 | a0005c0046t0005g0159a0016c0065t0005g0150a0020c0054t0010g0020others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-2637C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150221 | ||||||
| chr2:227150276
|
G | A | 2 | a0017c0022t0003g0254a0017c0022t0003g0255 | 2 | NA18962.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-101-2692C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150276 | ||||||
| chr2:227150299
|
C | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0258a0011c0012t0006g0256others(2): Show | 5 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-2715G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150299 | ||||||
| chr2:227150408
|
G | A | 5 | a0007c0006t0035g0163a0008c0008t0004g0161a0008c0008t0004g0164others(2): Show | 5 | HG01243.hp1 HG02809.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-2824C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150408 | ||||||
| chr2:227150535
|
C | G | 1 | a0002c0002t0002g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-101-2951G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150535 | ||||||
| chr2:227150629
|
G | A | 2 | a0001c0001t0001g0282a0002c0002t0002g0182 | 2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-101-3045C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150629 | ||||||
| chr2:227150721
|
G | T | 2 | a0003c0003t0030g0169a0013c0013t0006g0155 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-101-3137C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150721 | ||||||
| chr2:227150904
|
C | CT | 54 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0085others(51): Show | 54 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-101-3321dupA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150904 | ||||||
| chr2:227150904
|
CT | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0010t0005g0272others(8): Show | 11 | HG01175.hp2 HG02040.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.-101-3321delA | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150904 | ||||||
| chr2:227150904
|
CTT | C | 100 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0068others(97): Show | 100 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-101-3322_-101-332 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227150904 | ||||||
| chr2:227151075
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0063a0002c0002t0002g0008others(6): Show | 9 | HG02040.hp2 HG02080.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.-101-3491T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151075 | ||||||
| chr2:227151130
|
T | A | 5 | a0001c0001t0001g0117a0001c0001t0022g0119a0003c0003t0003g0116others(2): Show | 5 | HG00639.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-3546A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151130 | ||||||
| chr2:227151143
|
C | A | 141 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0044others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.-101-3559G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151143 | ||||||
| chr2:227151478
|
A | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0258a0011c0012t0006g0256others(2): Show | 5 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-3894T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151478 | ||||||
| chr2:227151485
|
T | C | 139 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0044others(136): Show | 139 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-101-3901A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151485 | ||||||
| chr2:227151553
|
GA | G | 141 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0044others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.-101-3970delT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151553 | ||||||
| chr2:227151561
|
T | C | 1 | a0006c0005t0009g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-101-3977A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151561 | ||||||
| chr2:227151613
|
G | T | 1 | a0006c0005t0004g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-101-4029C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151613 | ||||||
| chr2:227151706
|
C | T | 1 | a0038c0038t0005g0024 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-101-4122G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151706 | ||||||
| chr2:227151797
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-101-4213G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151797 | ||||||
| chr2:227151798
|
C | T | 2 | a0001c0001t0001g0070a0003c0003t0003g0004 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-101-4214G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151798 | ||||||
| chr2:227151817
|
A | C | 1 | a0002c0002t0002g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-101-4233T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151817 | ||||||
| chr2:227151907
|
G | A | 1 | a0040c0074t0018g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-101-4323C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151907 | ||||||
| chr2:227151926
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-101-4342A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227151926 | ||||||
| chr2:227152008
|
A | G | 2 | a0003c0003t0030g0169a0013c0013t0006g0155 | 2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-101-4424T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152008 | ||||||
| chr2:227152611
|
C | G | 2 | a0001c0001t0001g0068a0003c0014t0002g0069 | 2 | HG01943.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-101-5027G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152611 | ||||||
| chr2:227152660
|
G | A | 147 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0040others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-101-5076C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152660 | ||||||
| chr2:227152676
|
T | C | 150 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0040others(147): Show | 150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-101-5092A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152676 | ||||||
| chr2:227152739
|
T | C | 26 | a0001c0001t0001g0044a0001c0001t0001g0122a0001c0001t0001g0123others(23): Show | 26 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-101-5155A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152739 | ||||||
| chr2:227152775
|
C | T | 3 | a0010c0032t0008g0167a0021c0016t0014g0019a0044c0033t0032g0168 | 3 | HG03139.hp2 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-101-5191G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152775 | ||||||
| chr2:227152791
|
A | G | 2 | a0002c0002t0004g0149a0004c0004t0037g0062 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-101-5207T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152791 | ||||||
| chr2:227152817
|
G | A | 1 | a0005c0045t0003g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-101-5233C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152817 | ||||||
| chr2:227152871
|
G | C | 141 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0040others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-101-5287C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152871 | ||||||
| chr2:227152894
|
A | T | 3 | a0001c0001t0001g0258a0011c0012t0006g0256a0011c0012t0006g0257 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-101-5310T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152894 | ||||||
| chr2:227152946
|
T | C | 1 | a0004c0004t0002g0042 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-101-5362A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227152946 | ||||||
| chr2:227153312
|
G | A | 19 | a0001c0001t0001g0034a0003c0003t0030g0169a0004c0040t0002g0035others(16): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-101-5728C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227153312 | ||||||
| chr2:227153595
|
G | A | 5 | a0002c0002t0004g0149a0006c0005t0004g0148a0008c0008t0004g0027others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-6011C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227153595 | ||||||
| chr2:227153834
|
A | G | 14 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(11): Show | 14 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-101-6250T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227153834 | ||||||
| chr2:227153955
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(143): Show | 147 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-101-6371A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227153955 | ||||||
| chr2:227154048
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-101-6464T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154048 | ||||||
| chr2:227154061
|
G | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0207a0001c0001t0001g0208others(12): Show | 15 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-101-6477C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154061 | ||||||
| chr2:227154069
|
A | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(144): Show | 148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-101-6485T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154069 | ||||||
| chr2:227154119
|
G | A | 11 | a0001c0001t0001g0011a0002c0002t0002g0009a0002c0002t0002g0013others(8): Show | 11 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-101-6535C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154119 | ||||||
| chr2:227154184
|
G | C | 13 | a0001c0001t0001g0273a0001c0001t0017g0002a0001c0010t0005g0272others(10): Show | 13 | HG02257.hp1 HG02451.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.-101-6600C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154184 | ||||||
| chr2:227154244
|
T | G | 49 | a0001c0001t0001g0180a0001c0001t0001g0273a0001c0001t0017g0002others(46): Show | 49 | HG01106.hp1 HG01243.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.-101-6660A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154244 | ||||||
| chr2:227154310
|
A | G | 1 | a0006c0035t0036g0270 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-101-6726T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154310 | ||||||
| chr2:227154383
|
T | C | 2 | a0005c0007t0005g0137a0012c0011t0003g0138 | 2 | HG00323.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-101-6799A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154383 | ||||||
| chr2:227154391
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-101-6807C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154391 | ||||||
| chr2:227154596
|
T | G | 3 | a0001c0001t0001g0034a0004c0040t0002g0035a0006c0005t0004g0195 | 3 | HG01884.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-101-7012A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154596 | ||||||
| chr2:227154730
|
A | G | 13 | a0001c0001t0001g0273a0001c0001t0017g0002a0001c0010t0005g0272others(10): Show | 13 | HG02257.hp1 HG02451.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.-101-7146T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227154730 | ||||||
| chr2:227155033
|
T | C | 2 | a0001c0001t0001g0143a0013c0013t0006g0144 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-101-7449A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155033 | ||||||
| chr2:227155241
|
T | C | 3 | a0001c0001t0021g0141a0002c0002t0002g0140a0002c0002t0002g0185 | 3 | NA18939.hp1 NA19006.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-101-7657A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155241 | ||||||
| chr2:227155775
|
T | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-101-8191A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155775 | ||||||
| chr2:227155789
|
C | G | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101-8205G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155789 | ||||||
| chr2:227155813
|
T | A | 1 | a0002c0002t0002g0259 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-102+8194A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155813 | ||||||
| chr2:227155841
|
G | T | 1 | a0011c0053t0015g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-102+8166C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155841 | ||||||
| chr2:227155854
|
T | C | 1 | a0004c0051t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-102+8153A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155854 | ||||||
| chr2:227155892
|
C | T | 2 | a0001c0001t0001g0143a0013c0013t0006g0144 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-102+8115G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155892 | ||||||
| chr2:227155896
|
A | C | 1 | a0004c0051t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-102+8111T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155896 | ||||||
| chr2:227155947
|
T | C | 1 | a0003c0003t0003g0006 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-102+8060A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227155947 | ||||||
| chr2:227156063
|
G | GA | 133 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-102+7943dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156063 | ||||||
| chr2:227156121
|
G | A | 1 | a0002c0002t0005g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-102+7886C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156121 | ||||||
| chr2:227156243
|
C | A | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-102+7764G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156243 | ||||||
| chr2:227156279
|
T | G | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-102+7728A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156279 | ||||||
| chr2:227156371
|
T | C | 35 | a0001c0001t0001g0180a0002c0019t0005g0166a0003c0003t0030g0169others(32): Show | 35 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.-102+7636A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156371 | ||||||
| chr2:227156391
|
C | T | 1 | a0004c0004t0002g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-102+7616G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156391 | ||||||
| chr2:227156395
|
T | TA | 187 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0040others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-102+7611dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156395 | ||||||
| chr2:227156395
|
TAA | T | 12 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(9): Show | 12 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102+7610_-102+761 others(6): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156395 | ||||||
| chr2:227156482
|
C | G | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-102+7525G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156482 | ||||||
| chr2:227156491
|
G | GA | 35 | a0001c0001t0001g0180a0002c0019t0005g0166a0003c0003t0030g0169others(32): Show | 35 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.-102+7515dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156491 | ||||||
| chr2:227156491
|
G | GAAA | 14 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(11): Show | 14 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-102+7513_-102+751 others(7): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156491 | ||||||
| chr2:227156862
|
A | G | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-102+7145T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227156862 | ||||||
| chr2:227157120
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-102+6887T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157120 | ||||||
| chr2:227157130
|
T | G | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-102+6877A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157130 | ||||||
| chr2:227157174
|
A | G | 1 | a0001c0070t0039g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-102+6833T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157174 | ||||||
| chr2:227157402
|
A | C | 2 | a0022c0015t0004g0145a0022c0015t0004g0146 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-102+6605T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157402 | ||||||
| chr2:227157496
|
A | T | 1 | a0002c0002t0002g0043 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-102+6511T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157496 | ||||||
| chr2:227157779
|
A | C | 2 | a0001c0001t0001g0143a0013c0013t0006g0144 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-102+6228T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157779 | ||||||
| chr2:227157833
|
G | T | 12 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(9): Show | 12 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102+6174C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157833 | ||||||
| chr2:227157947
|
A | G | 2 | a0006c0035t0036g0270a0021c0016t0014g0278 | 2 | HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-102+6060T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227157947 | ||||||
| chr2:227158004
|
C | T | 1 | a0004c0004t0002g0042 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-102+6003G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158004 | ||||||
| chr2:227158049
|
C | T | 3 | a0001c0001t0001g0034a0004c0040t0002g0035a0006c0005t0004g0195 | 3 | HG01884.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-102+5958G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158049 | ||||||
| chr2:227158357
|
G | T | 2 | a0002c0019t0005g0029a0004c0004t0005g0030 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-102+5650C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158357 | ||||||
| chr2:227158411
|
T | A | 1 | a0009c0009t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-102+5596A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158411 | ||||||
| chr2:227158505
|
C | T | 2 | a0001c0001t0001g0282a0006c0005t0009g0283 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-102+5502G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158505 | ||||||
| chr2:227158580
|
A | G | 1 | a0015c0042t0013g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-102+5427T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158580 | ||||||
| chr2:227158610
|
C | A | 5 | a0001c0001t0001g0186a0002c0002t0002g0188a0003c0003t0003g0190others(2): Show | 5 | NA18941.hp2 NA18944.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102+5397G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158610 | ||||||
| chr2:227158654
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-102+5353G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158654 | ||||||
| chr2:227158656
|
G | A | 1 | a0009c0009t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-102+5351C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158656 | ||||||
| chr2:227158739
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-102+5268A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158739 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(307): Show |
1 | a0004c0051t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-102+5245_-102+524 others(318): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(320): Show |
1 | a0003c0073t0003g0018 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-102+5245_-102+524 others(331): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(321): Show |
2 | a0009c0009t0001g0016a0009c0009t0001g0017 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-102+5245_-102+524 others(332): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(325): Show |
2 | a0002c0002t0002g0014a0024c0069t0002g0015 | 2 | NA18968.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-102+5245_-102+524 others(336): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(329): Show |
1 | a0009c0009t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-102+5245_-102+524 others(340): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(336): Show |
1 | a0002c0002t0002g0013 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-102+5245_-102+524 others(347): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(337): Show |
5 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(2): Show | 5 | HG02004.hp1 NA18965.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102+5245_-102+524 others(348): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158761
|
T | TCTGGGAT others(338): Show |
1 | a0014c0020t0001g0007 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-102+5245_-102+524 others(349): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158761 | ||||||
| chr2:227158940
|
T | C | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-102+5067A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227158940 | ||||||
| chr2:227159085
|
T | C | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+4922A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227159085 | ||||||
| chr2:227159222
|
C | T | 14 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(11): Show | 14 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-102+4785G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227159222 | ||||||
| chr2:227159422
|
C | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0031a0001c0001t0001g0034others(131): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-102+4585G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227159422 | ||||||
| chr2:227159496
|
C | A | 3 | a0001c0001t0001g0180a0010c0017t0008g0179a0016c0064t0005g0178 | 3 | HG02970.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-102+4511G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227159496 | ||||||
| chr2:227159595
|
C | A | 13 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(10): Show | 13 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102+4412G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227159595 | ||||||
| chr2:227159629
|
C | T | 2 | a0002c0002t0002g0036a0002c0059t0025g0037 | 2 | HG01123.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-102+4378G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227159629 | ||||||
| chr2:227160025
|
C | T | 3 | a0001c0001t0001g0034a0004c0040t0002g0035a0006c0005t0004g0195 | 3 | HG01884.hp2 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-102+3982G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160025 | ||||||
| chr2:227160410
|
G | T | 1 | a0002c0002t0002g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-102+3597C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160410 | ||||||
| chr2:227160493
|
T | C | 1 | a0007c0006t0004g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-102+3514A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160493 | ||||||
| chr2:227160549
|
C | T | 1 | a0009c0009t0001g0022 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-102+3458G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160549 | ||||||
| chr2:227160576
|
G | A | 5 | a0001c0001t0001g0262a0002c0002t0002g0263a0002c0002t0002g0264others(2): Show | 5 | NA18952.hp1 NA18999.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.-102+3431C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160576 | ||||||
| chr2:227160647
|
G | A | 1 | a0004c0051t0005g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-102+3360C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160647 | ||||||
| chr2:227160812
|
C | T | 1 | a0011c0012t0006g0032 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-102+3195G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160812 | ||||||
| chr2:227160830
|
A | G | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+3177T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160830 | ||||||
| chr2:227160831
|
G | A | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+3176C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227160831 | ||||||
| chr2:227161040
|
T | C | 151 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0180others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.-102+2967A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161040 | ||||||
| chr2:227161044
|
G | A | 1 | a0021c0016t0014g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-102+2963C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161044 | ||||||
| chr2:227161057
|
A | G | 12 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(9): Show | 12 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102+2950T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161057 | ||||||
| chr2:227161079
|
C | T | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+2928G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161079 | ||||||
| chr2:227161081
|
T | C | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+2926A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161081 | ||||||
| chr2:227161113
|
T | C | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+2894A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161113 | ||||||
| chr2:227161269
|
C | T | 3 | a0002c0002t0002g0203a0002c0002t0027g0201a0004c0004t0002g0202 | 3 | HG01258.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-102+2738G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161269 | ||||||
| chr2:227161284
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-102+2723T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161284 | ||||||
| chr2:227161421
|
C | T | 1 | a0010c0017t0008g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-102+2586G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161421 | ||||||
| chr2:227161429
|
A | T | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+2578T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161429 | ||||||
| chr2:227161564
|
G | A | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+2443C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161564 | ||||||
| chr2:227161606
|
T | A | 1 | a0002c0002t0002g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-102+2401A>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161606 | ||||||
| chr2:227161774
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-102+2233G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161774 | ||||||
| chr2:227161864
|
G | C | 2 | a0027c0047t0015g0025a0038c0038t0005g0024 | 2 | HG01106.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-102+2143C>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161864 | ||||||
| chr2:227161935
|
C | CA | 25 | a0001c0001t0001g0011a0001c0001t0001g0186a0001c0001t0001g0281others(22): Show | 25 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-102+2071dupT | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227161935 | ||||||
| chr2:227162001
|
T | C | 3 | a0004c0051t0005g0023a0027c0047t0015g0025a0038c0038t0005g0024 | 3 | HG01106.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-102+2006A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162001 | ||||||
| chr2:227162051
|
T | C | 3 | a0002c0002t0002g0267a0002c0002t0002g0268a0003c0003t0003g0269 | 3 | HG00323.hp2 HG03017.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-102+1956A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162051 | ||||||
| chr2:227162082
|
A | G | 13 | a0001c0001t0001g0011a0001c0068t0003g0199a0002c0002t0002g0008others(10): Show | 13 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102+1925T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162082 | ||||||
| chr2:227162166
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-102+1841A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162166 | ||||||
| chr2:227162240
|
A | G | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01106.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102+1767T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162240 | ||||||
| chr2:227162262
|
A | G | 2 | a0002c0019t0005g0029a0004c0004t0005g0030 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-102+1745T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162262 | ||||||
| chr2:227162358
|
A | C | 2 | a0001c0001t0017g0002a0035c0037t0016g0003 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-102+1649T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162358 | ||||||
| chr2:227162406
|
T | G | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01106.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102+1601A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162406 | ||||||
| chr2:227162485
|
A | G | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01106.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102+1522T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162485 | ||||||
| chr2:227162576
|
C | T | 11 | a0001c0001t0001g0273a0001c0001t0017g0002a0001c0010t0005g0272others(8): Show | 11 | HG02257.hp1 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-102+1431G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162576 | ||||||
| chr2:227162577
|
G | A | 1 | a0006c0005t0004g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-102+1430C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162577 | ||||||
| chr2:227162597
|
AG | A | 9 | a0001c0001t0001g0273a0001c0010t0005g0272a0001c0010t0005g0275others(6): Show | 9 | HG02257.hp1 HG02897.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.-102+1409delC | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162597 | ||||||
| chr2:227162658
|
A | T | 16 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(13): Show | 16 | HG00544.hp1 HG01106.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-102+1349T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162658 | ||||||
| chr2:227162838
|
C | T | 3 | a0008c0008t0004g0027a0020c0041t0010g0028a0041c0029t0004g0026 | 3 | HG02647.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-102+1169G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162838 | ||||||
| chr2:227162840
|
A | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0197a0002c0002t0002g0008others(15): Show | 18 | HG00544.hp1 HG01106.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-102+1167T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227162840 | ||||||
| chr2:227163031
|
C | G | 1 | a0031c0061t0002g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-102+976G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163031 | ||||||
| chr2:227163138
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-102+869A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163138 | ||||||
| chr2:227163326
|
C | G | 2 | a0020c0054t0010g0020a0021c0016t0014g0019 | 2 | NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-102+681G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163326 | ||||||
| chr2:227163403
|
T | C | 86 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0206others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-102+604A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163403 | ||||||
| chr2:227163579
|
G | A | 1 | a0033c0043t0011g0279 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-102+428C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163579 | ||||||
| chr2:227163659
|
C | T | 12 | a0001c0001t0001g0011a0002c0002t0002g0008a0002c0002t0002g0009others(9): Show | 12 | HG00544.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102+348G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163659 | ||||||
| chr2:227163749
|
T | TAGGAGAA others(17): Show |
1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+257_-102+258i others(26): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163749 | ||||||
| chr2:227163755
|
T | G | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+252A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163755 | ||||||
| chr2:227163761
|
T | G | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+246A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163761 | ||||||
| chr2:227163765
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-102+242C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163765 | ||||||
| chr2:227163775
|
G | T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+232C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163775 | ||||||
| chr2:227163779
|
G | T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+228C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163779 | ||||||
| chr2:227163795
|
G | T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+212C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163795 | ||||||
| chr2:227163796
|
A | T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+211T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163796 | ||||||
| chr2:227163797
|
G | A | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+210C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163797 | ||||||
| chr2:227163798
|
C | T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+209G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163798 | ||||||
| chr2:227163801
|
C | G | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+206G>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163801 | ||||||
| chr2:227163804
|
A | G | 1 | a0003c0003t0003g0006 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-102+203T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163804 | ||||||
| chr2:227163807
|
T | C | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+200A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163807 | ||||||
| chr2:227163809
|
A | G | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+198T>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163809 | ||||||
| chr2:227163810
|
T | G | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+197A>C | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163810 | ||||||
| chr2:227163823
|
C | A | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+184G>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163823 | ||||||
| chr2:227163824
|
A | C | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+183T>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163824 | ||||||
| chr2:227163826
|
C | T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+181G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163826 | ||||||
| chr2:227163830
|
T | C | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+177A>G | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163830 | ||||||
| chr2:227163831
|
TAAAGCCC others(12): Show |
T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+157_-102+175d others(21): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163831 | ||||||
| chr2:227163853
|
A | T | 1 | a0003c0003t0003g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-102+154T>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163853 | ||||||
| chr2:227163853
|
AGGAGCCA others(72): Show |
A | 1 | a0003c0003t0003g0004 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-102+75_-102+153de others(80): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163853 | ||||||
| chr2:227163877
|
G | A | 2 | a0001c0001t0001g0282a0006c0005t0009g0283 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-102+130C>T | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163877 | ||||||
| chr2:227163933
|
G | T | 1 | a0003c0003t0003g0004 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-102+74C>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163933 | ||||||
| chr2:227163937
|
C | T | 1 | a0003c0003t0003g0004 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-102+70G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163937 | ||||||
| chr2:227163940
|
C | CAACAACA others(71): Show |
1 | a0003c0003t0003g0004 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-102+66_-102+67ins others(78): Show |
COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163940 | ||||||
| chr2:227163941
|
C | T | 1 | a0003c0003t0003g0004 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-102+66G>A | COL4A4 | ENSG00000081052.14 | transcript | ENST00000396625.5 | protein_coding | 1/47 | chr2 | 227163941 |