| geneid | 55105 |
|---|---|
| ensemblid | ENSG00000092978.11 |
| hgncid | 25499 |
| symbol | GPATCH2 |
| name | G-patch domain containing 2 |
| refseq_nuc | NM_018040.5 |
| refseq_prot | NP_060510.1 |
| ensembl_nuc | ENST00000366935.8 |
| ensembl_prot | ENSP00000355902.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 217426992 |
| end | 217631090 |
| strand | - |
| ver | v1.2 |
| region | chr1:217426992-217631090 |
| region5000 | chr1:217421992-217636090 |
| regionname0 | GPATCH2_chr1_217426992_217631090 |
| regionname5000 | GPATCH2_chr1_217421992_217636090 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 528 | 172 | 67 | 39 | 36 | 6 | 22 | 19 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002 | 0/0 | 528 | 10 | 0 | 1 | 5 | 0 | 4 | 3 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0003 | 0/0 | 528 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0004 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1587 | 166 | 66 | 34 | 36 | 6 | 22 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| c0002 | 0/0 | 1587 | 10 | 0 | 1 | 5 | 0 | 4 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| c0003 | 0/0 | 1587 | 5 | 5 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| c0004 | 0/0 | 1587 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| c0005 | 0/0 | 1587 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| c0006 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| c0007 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| 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 | 4273 | 37 | 4 | 10 | 13 | 1 | 8 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0002 | 0/1 | 4273 | 30 | 10 | 7 | 8 | 1 | 3 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0003 | 0/0 | 4274 | 12 | 1 | 2 | 7 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0004 | 0/0 | 4269 | 12 | 5 | 3 | 2 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0005 | 0/0 | 4269 | 11 | 2 | 2 | 5 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0006 | 0/0 | 4267 | 10 | 8 | 1 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0007 | 0/0 | 4267 | 9 | 4 | 4 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0008 | 0/0 | 4273 | 5 | 1 | 3 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0009 | 0/0 | 4269 | 5 | 5 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0010 | 0/0 | 4273 | 5 | 5 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0011 | 0/0 | 4274 | 4 | 1 | 1 | 0 | 1 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0012 | 0/0 | 4273 | 3 | 2 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0013 | 0/0 | 4273 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0014 | 0/0 | 4270 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0015 | 0/0 | 4269 | 3 | 0 | 1 | 0 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0016 | 0/0 | 4269 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0017 | 0/0 | 4273 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0018 | 0/0 | 4273 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0019 | 0/0 | 4273 | 2 | 0 | 1 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0020 | 0/0 | 4270 | 2 | 1 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0021 | 0/0 | 4270 | 2 | 1 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0022 | 0/0 | 4270 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0023 | 0/0 | 4272 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0024 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0025 | 0/0 | 4272 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0026 | 0/0 | 4273 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0027 | 0/0 | 4272 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0028 | 0/0 | 4272 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0029 | 0/0 | 4274 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0030 | 0/0 | 4274 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0031 | 0/0 | 4273 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0032 | 0/0 | 4273 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0033 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0034 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0035 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0036 | 0/0 | 4269 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0037 | 0/0 | 4274 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0038 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0039 | 0/0 | 4274 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0040 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0041 | 0/0 | 4268 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0042 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0043 | 0/0 | 4269 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| t0044 | 0/0 | 4258 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1587 | 166 | 66 | 34 | 36 | 6 | 22 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0004 | 0/0 | 1587 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0005 | 0/0 | 1587 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0007 | 0/0 | 1587 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002 | 0/0 | 1587 | 10 | 0 | 1 | 5 | 0 | 4 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0003c0003 | 0/0 | 1587 | 5 | 5 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0004c0006 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5859 | 36 | 4 | 10 | 12 | 1 | 8 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0002 | 0/1 | 5859 | 29 | 10 | 6 | 8 | 1 | 3 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0003 | 0/0 | 5860 | 12 | 1 | 2 | 7 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0004 | 0/0 | 5855 | 11 | 5 | 2 | 2 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0005 | 0/0 | 5855 | 11 | 2 | 2 | 5 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0006 | 0/0 | 5853 | 10 | 8 | 1 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0007 | 0/0 | 5853 | 9 | 4 | 4 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0008 | 0/0 | 5859 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0009 | 0/0 | 5855 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0010 | 0/0 | 5859 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0011 | 0/0 | 5860 | 4 | 1 | 1 | 0 | 1 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0012 | 0/0 | 5859 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0014 | 0/0 | 5856 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0015 | 0/0 | 5855 | 3 | 0 | 1 | 0 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0016 | 0/0 | 5855 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0017 | 0/0 | 5859 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0018 | 0/0 | 5859 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0020 | 0/0 | 5856 | 2 | 1 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0021 | 0/0 | 5856 | 2 | 1 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0022 | 0/0 | 5856 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0023 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0024 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0025 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0026 | 0/0 | 5859 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0027 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0029 | 0/0 | 5860 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0031 | 0/0 | 5859 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0032 | 0/0 | 5859 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0033 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0034 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0035 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0036 | 0/0 | 5855 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0038 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0040 | 0/0 | 5836 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0041 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0042 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0043 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0001t0044 | 0/0 | 5844 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0004t0008 | 0/0 | 5859 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0005t0004 | 0/0 | 5855 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0005t0009 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0001c0007t0002 | 0/0 | 5859 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002t0008 | 0/0 | 5859 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002t0012 | 0/0 | 5859 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002t0013 | 0/0 | 5859 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002t0019 | 0/0 | 5859 | 2 | 0 | 1 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002t0028 | 0/0 | 5858 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002t0030 | 0/0 | 5860 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0002c0002t0039 | 0/0 | 5860 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0003c0003t0010 | 0/0 | 5859 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0003c0003t0037 | 0/0 | 5860 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| a0004c0006t0001 | 0/0 | 5859 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | copy fasta | chr1 | 217421992 | 217636090 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0011g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0011g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0015g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0015g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0015g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0016g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0016g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0017g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0017g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0018g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0018g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0020g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0020g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0021g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0021g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0022g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0023g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0024g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0025g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0026g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0027g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0029g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0031g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0032g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0033g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0034g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0035g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0036g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0038g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0040g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0041g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0042g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0043g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0044g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0004t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0004t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0004t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0005t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0005t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0007t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0008g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0012g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0013g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0013g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0013g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0019g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0019g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0028g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0030g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0039g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0003c0003t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0003c0003t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0003c0003t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0003c0003t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0003c0003t0037g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0004c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0014 | EUR | GBR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00099 | hp2 | a0001 | c0001 | t0011 | g0138 | EUR | GBR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00597 | hp1 | a0002 | c0002 | t0013 | g0087 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00609 | hp1 | a0004 | c0006 | t0001 | g0053 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | CHS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0013 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01081 | hp1 | a0002 | c0002 | t0019 | g0172 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01106 | hp1 | a0001 | c0001 | t0029 | g0042 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0128 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01109 | hp1 | a0001 | c0004 | t0008 | g0119 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01168 | hp2 | a0001 | c0001 | t0017 | g0101 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01175 | hp1 | a0001 | c0001 | t0031 | g0040 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01243 | hp1 | a0001 | c0004 | t0008 | g0097 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01261 | hp1 | a0001 | c0004 | t0008 | g0108 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0153 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01361 | hp1 | a0001 | c0007 | t0002 | g0147 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0116 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01433 | hp2 | a0001 | c0005 | t0004 | g0144 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0033 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01515 | hp2 | a0001 | c0001 | t0020 | g0160 | EUR | IBS | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0094 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01891 | hp1 | a0001 | c0001 | t0024 | g0003 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01891 | hp2 | a0001 | c0001 | t0042 | g0174 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01993 | hp1 | a0001 | c0001 | t0032 | g0056 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01993 | hp2 | a0001 | c0001 | t0011 | g0149 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02055 | hp1 | a0001 | c0005 | t0009 | g0145 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02055 | hp2 | a0001 | c0001 | t0040 | g0135 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0083 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PEL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02155 | hp1 | a0002 | c0002 | t0028 | g0070 | EAS | CDX | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | CDX | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0143 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02280 | hp2 | a0001 | c0001 | t0034 | g0027 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02615 | hp1 | a0001 | c0001 | t0038 | g0110 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0178 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02622 | hp1 | a0003 | c0003 | t0010 | g0167 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0088 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02698 | hp2 | a0001 | c0001 | t0021 | g0177 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02738 | hp2 | a0002 | c0002 | t0039 | g0162 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02886 | hp1 | a0003 | c0003 | t0010 | g0151 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0032 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02965 | hp1 | a0001 | c0001 | t0018 | g0186 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0134 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0187 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0084 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03130 | hp1 | a0001 | c0001 | t0022 | g0182 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03139 | hp1 | a0003 | c0003 | t0010 | g0188 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0079 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0109 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0031 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0086 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03225 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03486 | hp2 | a0001 | c0001 | t0033 | g0081 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03516 | hp1 | a0001 | c0001 | t0018 | g0185 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03516 | hp2 | a0001 | c0001 | t0043 | g0142 | AFR | ESN | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03540 | hp1 | a0001 | c0001 | t0041 | g0181 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | GWD | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0095 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03669 | hp1 | a0001 | c0001 | t0015 | g0175 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03688 | hp2 | a0002 | c0002 | t0008 | g0156 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03704 | hp1 | a0002 | c0002 | t0019 | g0155 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03710 | hp1 | a0001 | c0001 | t0011 | g0166 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0071 | SAS | BEB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | BEB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG04199 | hp2 | a0001 | c0001 | t0044 | g0115 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG04204 | hp1 | a0001 | c0001 | t0015 | g0176 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG04228 | hp1 | a0002 | c0002 | t0012 | g0007 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | CHB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | YRI | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18906 | hp2 | a0001 | c0001 | t0027 | g0093 | AFR | YRI | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18943 | hp2 | a0001 | c0001 | t0026 | g0090 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18966 | hp1 | a0001 | c0001 | t0036 | g0065 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18968 | hp2 | a0002 | c0002 | t0013 | g0055 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18983 | hp2 | a0002 | c0002 | t0013 | g0046 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | LWK | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19043 | hp2 | a0003 | c0003 | t0010 | g0140 | AFR | LWK | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19078 | hp1 | a0002 | c0002 | t0030 | g0047 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | YRI | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19240 | hp2 | a0001 | c0001 | t0021 | g0106 | AFR | YRI | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0105 | AFR | ASW | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0165 | EUR | TSI | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0169 | EUR | TSI | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02486 | hp2 | a0001 | c0001 | t0025 | g0001 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02559 | hp1 | a0001 | c0001 | t0035 | g0035 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03471 | hp2 | a0003 | c0003 | t0037 | g0080 | AFR | MSL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | USA | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG06807 | hp2 | a0001 | c0001 | t0022 | g0183 | AFR | USA | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0117 | REF | REF | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0015 | REF | REF | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217431150
|
C | T | 1 | a0003 | 5 | HG02622.hp1 HG02886.hp1 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.1582G>A | p.Ala528Thr | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1701/5859 | 1582/1587 | 528/528 | chr1 | 217431150 | ||
| chr1:217431312
|
T | C | 1 | a0002 | 10 | HG00597.hp1 HG01081.hp1 HG02155.hp1 others(7): Show |
missense_variant | MODERATE | c.1420A>G | p.Met474Val | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1539/5859 | 1420/1587 | 474/528 | chr1 | 217431312 | ||
| chr1:217620338
|
C | T | 1 | a0004 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.218G>A | p.Arg73Gln | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/10 | 337/5859 | 218/1587 | 73/528 | chr1 | 217620338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217431193
|
T | C | 1 | a0001c0004 | 3 | HG01109.hp1 HG01243.hp1 HG01261.hp1 |
synonymous_variant | LOW | c.1539A>G | p.Pro513Pro | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1658/5859 | 1539/1587 | 513/528 | chr1 | 217431193 | ||
| chr1:217610956
|
T | G | 1 | a0001c0007 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.951A>C | p.Val317Val | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 4/10 | 1070/5859 | 951/1587 | 317/528 | chr1 | 217610956 | ||
| chr1:217620142
|
C | T | 1 | a0001c0007 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.414G>A | p.Gly138Gly | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/10 | 533/5859 | 414/1587 | 138/528 | chr1 | 217620142 | ||
| chr1:217620376
|
A | G | 1 | a0001c0005 | 2 | HG01433.hp2 HG02055.hp1 |
synonymous_variant | LOW | c.180T>C | p.Pro60Pro | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/10 | 299/5859 | 180/1587 | 60/528 | chr1 | 217620376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217427148
|
G | A | 1 | a0001c0001t0029 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3997C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3997 | chr1 | 217427148 | |||||
| chr1:217427156
|
C | G | 2 | a0001c0001t0015a0001c0001t0035 | 4 | HG01261.hp2 HG02559.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3989G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3989 | chr1 | 217427156 | |||||
| chr1:217427261
|
T | C | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(14): Show | 46 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3884A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3884 | chr1 | 217427261 | |||||
| chr1:217427370
|
A | C | 2 | a0001c0001t0034a0001c0001t0043 | 2 | HG02280.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3775T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3775 | chr1 | 217427370 | |||||
| chr1:217427386
|
C | G | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(16): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3759G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3759 | chr1 | 217427386 | |||||
| chr1:217427439
|
C | A | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(25): Show | 79 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3706G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3706 | chr1 | 217427439 | |||||
| chr1:217427518
|
A | G | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(16): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3627T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3627 | chr1 | 217427518 | |||||
| chr1:217427604
|
T | TA | 18 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(15): Show | 48 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3540dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3540 | chr1 | 217427604 | |||||
| chr1:217427889
|
G | A | 2 | a0002c0002t0013a0002c0002t0030 | 4 | HG00597.hp1 NA18968.hp2 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3256C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3256 | chr1 | 217427889 | |||||
| chr1:217427966
|
G | A | 3 | a0001c0001t0009a0001c0001t0016a0001c0005t0009 | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3179C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 3179 | chr1 | 217427966 | |||||
| chr1:217428156
|
GTCAAGTT others(10): Show |
G | 1 | a0001c0001t0040 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2972_*2988delTTAC others(13): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 2972 | chr1 | 217428156 | |||||
| chr1:217428964
|
T | C | 1 | a0001c0001t0036 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2181A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 2181 | chr1 | 217428964 | |||||
| chr1:217429050
|
T | A | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(14): Show | 46 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2095A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 2095 | chr1 | 217429050 | |||||
| chr1:217429246
|
G | C | 10 | a0001c0001t0008a0001c0001t0012a0001c0004t0008others(7): Show | 16 | HG00597.hp1 HG01081.hp1 HG01109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1899C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1899 | chr1 | 217429246 | |||||
| chr1:217429469
|
T | G | 14 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(11): Show | 43 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1676A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1676 | chr1 | 217429469 | |||||
| chr1:217429525
|
C | T | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(16): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1620G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1620 | chr1 | 217429525 | |||||
| chr1:217429603
|
G | A | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(14): Show | 46 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1542C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1542 | chr1 | 217429603 | |||||
| chr1:217429656
|
C | T | 1 | a0001c0001t0017 | 2 | HG01168.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1489G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1489 | chr1 | 217429656 | |||||
| chr1:217429757
|
G | C | 1 | a0001c0001t0022 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1388C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1388 | chr1 | 217429757 | |||||
| chr1:217429825
|
C | CA | 6 | a0001c0001t0003a0001c0001t0011a0001c0001t0029others(3): Show | 20 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1319dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1319 | chr1 | 217429825 | |||||
| chr1:217429825
|
CA | C | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(14): Show | 43 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1319delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1319 | chr1 | 217429825 | |||||
| chr1:217429825
|
CAAA | C | 3 | a0001c0001t0006a0001c0001t0007a0001c0001t0040 | 20 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1317_*1319delTTT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1317 | chr1 | 217429825 | |||||
| chr1:217429825
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0044 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308_*1319delTTTT others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1308 | chr1 | 217429825 | |||||
| chr1:217429843
|
A | G | 1 | a0001c0001t0026 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1302T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1302 | chr1 | 217429843 | |||||
| chr1:217429935
|
C | A | 1 | a0001c0001t0031 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1210 | chr1 | 217429935 | |||||
| chr1:217429976
|
CATA | C | 24 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(21): Show | 72 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1166_*1168delTAT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 1166 | chr1 | 217429976 | |||||
| chr1:217430165
|
A | G | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(16): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*980T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 980 | chr1 | 217430165 | |||||
| chr1:217430166
|
CT | C | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(16): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*978delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 978 | chr1 | 217430166 | |||||
| chr1:217430168
|
T | C | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(16): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*977A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 977 | chr1 | 217430168 | |||||
| chr1:217430172
|
T | C | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(14): Show | 46 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*973A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 973 | chr1 | 217430172 | |||||
| chr1:217430197
|
T | C | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(25): Show | 79 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 948 | chr1 | 217430197 | |||||
| chr1:217430364
|
C | A | 1 | a0001c0001t0044 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*781G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 781 | chr1 | 217430364 | |||||
| chr1:217430505
|
C | T | 19 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(16): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*640G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 640 | chr1 | 217430505 | |||||
| chr1:217430508
|
T | C | 1 | a0001c0001t0018 | 2 | HG02965.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*637A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 637 | chr1 | 217430508 | |||||
| chr1:217430542
|
C | T | 6 | a0001c0001t0006a0001c0001t0007a0001c0001t0020others(3): Show | 24 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*603G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 603 | chr1 | 217430542 | |||||
| chr1:217430603
|
T | C | 1 | a0001c0001t0022 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*542A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 542 | chr1 | 217430603 | |||||
| chr1:217430699
|
G | A | 1 | a0002c0002t0019 | 2 | HG01081.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*446C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 446 | chr1 | 217430699 | |||||
| chr1:217430782
|
T | C | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(25): Show | 79 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*363A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 10/10 | 363 | chr1 | 217430782 | |||||
| chr1:217630983
|
G | A | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(27): Show | 96 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(93): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-12C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/10 | chr1 | 217630983 | ||||||
| chr1:217631061
|
GC | G | 3 | a0001c0001t0023a0001c0001t0024a0001c0001t0025 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-91delG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/10 | 91 | chr1 | 217631061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:217431380
|
C | A | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1367-15G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431380 | ||||||
| chr1:217431435
|
G | A | 47 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(44): Show | 47 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.1367-70C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431435 | ||||||
| chr1:217431464
|
T | C | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1367-99A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431464 | ||||||
| chr1:217431493
|
G | A | 3 | a0001c0001t0033g0081a0001c0001t0041g0181a0001c0001t0042g0174 | 3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1367-128C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431493 | ||||||
| chr1:217431649
|
G | C | 2 | a0001c0001t0014g0084a0001c0001t0021g0177 | 2 | HG02698.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1367-284C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431649 | ||||||
| chr1:217431676
|
G | A | 1 | a0001c0001t0044g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1367-311C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431676 | ||||||
| chr1:217431809
|
G | C | 3 | a0001c0001t0033g0081a0001c0001t0041g0181a0001c0001t0042g0174 | 3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1367-444C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431809 | ||||||
| chr1:217431830
|
C | T | 7 | a0001c0001t0009g0098a0001c0001t0009g0105a0001c0001t0009g0178others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1367-465G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431830 | ||||||
| chr1:217431854
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1367-489T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431854 | ||||||
| chr1:217431960
|
T | C | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1367-595A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217431960 | ||||||
| chr1:217432002
|
A | G | 1 | a0001c0001t0011g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1367-637T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432002 | ||||||
| chr1:217432119
|
C | T | 3 | a0003c0003t0010g0140a0003c0003t0010g0151a0003c0003t0010g0167 | 3 | HG02622.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1367-754G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432119 | ||||||
| chr1:217432236
|
G | T | 1 | a0003c0003t0037g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1367-871C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432236 | ||||||
| chr1:217432330
|
A | AT | 80 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(77): Show | 80 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.1367-966dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432330 | ||||||
| chr1:217432365
|
A | G | 2 | a0001c0001t0007g0011a0001c0001t0007g0013 | 2 | HG00738.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1367-1000T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432365 | ||||||
| chr1:217432484
|
C | A | 1 | a0001c0001t0038g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1367-1119G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432484 | ||||||
| chr1:217432563
|
C | T | 49 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(46): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.1367-1198G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432563 | ||||||
| chr1:217432654
|
C | A | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1367-1289G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432654 | ||||||
| chr1:217432686
|
T | C | 49 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(46): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.1367-1321A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432686 | ||||||
| chr1:217432740
|
T | A | 2 | a0003c0003t0010g0188a0003c0003t0037g0080 | 2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1367-1375A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432740 | ||||||
| chr1:217432977
|
T | C | 24 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(21): Show | 24 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1367-1612A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217432977 | ||||||
| chr1:217433048
|
T | C | 2 | a0001c0001t0004g0152a0001c0001t0010g0134 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1367-1683A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433048 | ||||||
| chr1:217433065
|
T | C | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1367-1700A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433065 | ||||||
| chr1:217433119
|
C | T | 11 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0127others(8): Show | 11 | HG01168.hp1 HG01361.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1367-1754G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433119 | ||||||
| chr1:217433169
|
T | A | 2 | a0001c0001t0004g0102a0001c0001t0004g0111 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1367-1804A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433169 | ||||||
| chr1:217433173
|
T | C | 5 | a0003c0003t0010g0140a0003c0003t0010g0151a0003c0003t0010g0167others(2): Show | 5 | HG02622.hp1 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367-1808A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433173 | ||||||
| chr1:217433271
|
G | A | 2 | a0003c0003t0010g0188a0003c0003t0037g0080 | 2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1367-1906C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433271 | ||||||
| chr1:217433361
|
C | CACATATA others(3): Show |
2 | a0001c0001t0002g0112a0001c0001t0011g0141 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1367-1997_1367-199 others(14): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433361 | ||||||
| chr1:217433361
|
C | CACATATA others(5): Show |
2 | a0001c0001t0002g0099a0001c0001t0002g0104 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1367-1997_1367-199 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433361 | ||||||
| chr1:217433361
|
C | CACATATA others(7): Show |
1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1367-1997_1367-199 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433361 | ||||||
| chr1:217433361
|
C | CAT | 4 | a0001c0001t0001g0038a0001c0001t0014g0084a0001c0001t0033g0081others(1): Show | 4 | HG01358.hp1 HG01891.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367-1998_1367-199 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433361 | ||||||
| chr1:217433361
|
C | CATAT | 4 | a0001c0001t0021g0177a0001c0001t0038g0110a0001c0005t0004g0144others(1): Show | 4 | HG01433.hp2 HG02615.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367-2000_1367-199 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433361 | ||||||
| chr1:217433361
|
C | CATATATA others(3): Show |
1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1367-2006_1367-199 others(14): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433361 | ||||||
| chr1:217433361
|
CATAT | C | 2 | a0001c0001t0001g0025a0002c0002t0013g0087 | 2 | HG00597.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1367-2000_1367-199 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433361 | ||||||
| chr1:217433370
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1367-2033_1367-200 others(32): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433370 | ||||||
| chr1:217433374
|
ATATATAT others(17): Show |
A | 36 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(33): Show | 36 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1367-2033_1367-201 others(28): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433374 | ||||||
| chr1:217433378
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1367-2025_1367-201 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433378 | ||||||
| chr1:217433378
|
ATATATAT others(9): Show |
A | 23 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(20): Show | 23 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1367-2029_1367-201 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433378 | ||||||
| chr1:217433380
|
ATATATT | A | 2 | a0001c0001t0018g0186a0001c0001t0023g0002 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1367-2021_1367-201 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433380 | ||||||
| chr1:217433380
|
ATATATTT others(7): Show |
A | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1367-2029_1367-201 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433380 | ||||||
| chr1:217433382
|
ATATT | A | 50 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0017others(47): Show | 50 | HG00558.hp1 HG00673.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1367-2021_1367-201 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433382 | ||||||
| chr1:217433382
|
ATATTTAT others(5): Show |
A | 1 | a0001c0001t0034g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1367-2029_1367-201 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433382 | ||||||
| chr1:217433382
|
ATATTTAT others(9): Show |
A | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1367-2033_1367-201 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433382 | ||||||
| chr1:217433384
|
ATT | A | 8 | a0001c0001t0001g0045a0001c0001t0001g0067a0001c0001t0001g0073others(5): Show | 8 | HG00609.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367-2021_1367-202 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433384 | ||||||
| chr1:217433384
|
ATTTATTT others(3): Show |
A | 3 | a0003c0003t0010g0140a0003c0003t0010g0151a0003c0003t0010g0167 | 3 | HG02622.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1367-2029_1367-202 others(14): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433384 | ||||||
| chr1:217433384
|
ATTTATTT others(7): Show |
A | 1 | a0001c0001t0043g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1367-2033_1367-202 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433384 | ||||||
| chr1:217433386
|
T | A | 17 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(14): Show | 17 | HG01256.hp1 HG01433.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1367-2021A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433386 | ||||||
| chr1:217433390
|
T | A | 20 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(17): Show | 20 | HG01168.hp2 HG01256.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.1367-2025A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433390 | ||||||
| chr1:217433394
|
T | A | 18 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(15): Show | 18 | HG01256.hp1 HG01433.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1367-2029A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433394 | ||||||
| chr1:217433398
|
T | A | 16 | a0001c0001t0001g0044a0001c0001t0002g0099a0001c0001t0002g0104others(13): Show | 16 | HG01256.hp1 HG01433.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1367-2033A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433398 | ||||||
| chr1:217433402
|
T | A | 1 | a0001c0001t0002g0099 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1367-2037A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433402 | ||||||
| chr1:217433465
|
T | C | 3 | a0001c0001t0033g0081a0001c0001t0041g0181a0001c0001t0042g0174 | 3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1367-2100A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433465 | ||||||
| chr1:217433689
|
C | G | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0025g0001others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367-2324G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433689 | ||||||
| chr1:217433768
|
G | A | 84 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(81): Show | 84 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.1367-2403C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217433768 | ||||||
| chr1:217434019
|
T | C | 49 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(46): Show | 49 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.1367-2654A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217434019 | ||||||
| chr1:217434067
|
A | G | 4 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0062others(1): Show | 4 | HG01358.hp1 HG01952.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367-2702T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217434067 | ||||||
| chr1:217434131
|
T | C | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1367-2766A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217434131 | ||||||
| chr1:217434737
|
C | T | 48 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(45): Show | 48 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.1367-3372G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217434737 | ||||||
| chr1:217434953
|
T | C | 1 | a0002c0002t0012g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1367-3588A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217434953 | ||||||
| chr1:217435268
|
C | T | 3 | a0001c0001t0033g0081a0001c0001t0041g0181a0001c0001t0042g0174 | 3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1367-3903G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435268 | ||||||
| chr1:217435538
|
C | T | 6 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(3): Show | 6 | HG01256.hp1 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367-4173G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435538 | ||||||
| chr1:217435590
|
C | G | 1 | a0001c0001t0004g0152 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1367-4225G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435590 | ||||||
| chr1:217435747
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(3): Show | 6 | HG01256.hp1 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367-4382T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435747 | ||||||
| chr1:217435748
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1367-4383A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435748 | ||||||
| chr1:217435831
|
T | C | 96 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(93): Show | 96 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1367-4466A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435831 | ||||||
| chr1:217435863
|
C | T | 46 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(43): Show | 46 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.1367-4498G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435863 | ||||||
| chr1:217435991
|
C | T | 50 | a0001c0001t0004g0152a0001c0001t0006g0100a0001c0001t0006g0107others(47): Show | 50 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1367-4626G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217435991 | ||||||
| chr1:217436084
|
C | T | 45 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(42): Show | 45 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.1367-4719G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217436084 | ||||||
| chr1:217436228
|
GA | G | 5 | a0001c0001t0002g0137a0001c0001t0002g0171a0001c0001t0018g0185others(2): Show | 5 | HG02486.hp1 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367-4864delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217436228 | ||||||
| chr1:217436486
|
G | C | 6 | a0001c0001t0006g0143a0001c0001t0006g0173a0001c0001t0006g0180others(3): Show | 6 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367-5121C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217436486 | ||||||
| chr1:217436566
|
T | C | 1 | a0003c0003t0037g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1367-5201A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217436566 | ||||||
| chr1:217437221
|
C | T | 87 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(84): Show | 87 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.1367-5856G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217437221 | ||||||
| chr1:217437385
|
C | T | 2 | a0001c0001t0008g0096a0001c0001t0012g0088 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1367-6020G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217437385 | ||||||
| chr1:217437645
|
A | C | 23 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0025others(20): Show | 23 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1367-6280T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217437645 | ||||||
| chr1:217438143
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0014g0084a0001c0001t0021g0177others(7): Show | 10 | HG01433.hp2 HG01891.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367-6778T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438143 | ||||||
| chr1:217438179
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1367-6814T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438179 | ||||||
| chr1:217438183
|
T | C | 10 | a0001c0001t0001g0019a0001c0001t0014g0084a0001c0001t0021g0177others(7): Show | 10 | HG01433.hp2 HG01891.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367-6818A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438183 | ||||||
| chr1:217438216
|
C | A | 2 | a0001c0001t0004g0102a0001c0001t0004g0111 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1367-6851G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438216 | ||||||
| chr1:217438221
|
T | C | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1367-6856A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438221 | ||||||
| chr1:217438232
|
C | A | 1 | a0001c0005t0004g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1367-6867G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438232 | ||||||
| chr1:217438431
|
A | C | 10 | a0001c0001t0001g0019a0001c0001t0014g0084a0001c0001t0021g0177others(7): Show | 10 | HG01433.hp2 HG01891.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1367-7066T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438431 | ||||||
| chr1:217438488
|
G | C | 1 | a0001c0001t0006g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1367-7123C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438488 | ||||||
| chr1:217438602
|
G | A | 40 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(37): Show | 40 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1367-7237C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438602 | ||||||
| chr1:217438610
|
A | C | 1 | a0001c0001t0005g0020 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1367-7245T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438610 | ||||||
| chr1:217438734
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1367-7369G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438734 | ||||||
| chr1:217438779
|
T | C | 2 | a0001c0001t0002g0114a0001c0001t0003g0077 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1367-7414A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438779 | ||||||
| chr1:217438793
|
T | TCAG | 5 | a0001c0001t0014g0084a0001c0001t0021g0177a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02698.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367-7431_1367-742 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217438793 | ||||||
| chr1:217439052
|
A | G | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1367-7687T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439052 | ||||||
| chr1:217439094
|
A | T | 1 | a0001c0001t0002g0158 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1367-7729T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439094 | ||||||
| chr1:217439111
|
G | A | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0044g0115 | 3 | HG03130.hp1 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1367-7746C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439111 | ||||||
| chr1:217439308
|
T | A | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1367-7943A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439308 | ||||||
| chr1:217439355
|
C | T | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0044g0115 | 3 | HG03130.hp1 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1367-7990G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439355 | ||||||
| chr1:217439490
|
T | C | 1 | a0003c0003t0010g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1367-8125A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439490 | ||||||
| chr1:217439545
|
C | T | 1 | a0001c0001t0005g0020 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1367-8180G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439545 | ||||||
| chr1:217439595
|
A | G | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1367-8230T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439595 | ||||||
| chr1:217439656
|
G | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1367-8291C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439656 | ||||||
| chr1:217439703
|
T | C | 5 | a0001c0001t0014g0084a0001c0001t0021g0177a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02698.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367-8338A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439703 | ||||||
| chr1:217439824
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1367-8459C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439824 | ||||||
| chr1:217439978
|
G | C | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0044g0115 | 3 | HG03130.hp1 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1367-8613C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439978 | ||||||
| chr1:217439992
|
G | A | 1 | a0003c0003t0010g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1367-8627C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217439992 | ||||||
| chr1:217440175
|
G | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0112 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1367-8810C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440175 | ||||||
| chr1:217440264
|
C | T | 9 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0010g0134others(6): Show | 9 | HG01433.hp2 HG01891.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367-8899G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440264 | ||||||
| chr1:217440693
|
C | G | 2 | a0001c0001t0006g0136a0001c0001t0007g0075 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1366+8556G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440693 | ||||||
| chr1:217440722
|
C | T | 40 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(37): Show | 40 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1366+8527G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440722 | ||||||
| chr1:217440728
|
G | T | 40 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(37): Show | 40 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1366+8521C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440728 | ||||||
| chr1:217440747
|
C | T | 40 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(37): Show | 40 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1366+8502G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440747 | ||||||
| chr1:217440797
|
A | C | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0044g0115 | 3 | HG03130.hp1 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1366+8452T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440797 | ||||||
| chr1:217440888
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1366+8361G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440888 | ||||||
| chr1:217440926
|
C | T | 7 | a0001c0001t0001g0019a0001c0001t0014g0084a0001c0001t0021g0177others(4): Show | 7 | HG01433.hp2 HG01891.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366+8323G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440926 | ||||||
| chr1:217440977
|
G | A | 6 | a0001c0001t0006g0143a0001c0001t0006g0173a0001c0001t0006g0180others(3): Show | 6 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366+8272C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217440977 | ||||||
| chr1:217441124
|
AC | A | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0044g0115 | 3 | HG03130.hp1 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1366+8124delG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441124 | ||||||
| chr1:217441304
|
T | C | 2 | a0001c0001t0004g0113a0001c0001t0004g0120 | 2 | NA18612.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1366+7945A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441304 | ||||||
| chr1:217441351
|
T | TAACTC | 55 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0006g0100others(52): Show | 55 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1366+7897_1366+789 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441351 | ||||||
| chr1:217441373
|
G | A | 54 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0006g0100others(51): Show | 54 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1366+7876C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441373 | ||||||
| chr1:217441431
|
A | T | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1366+7818T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441431 | ||||||
| chr1:217441436
|
A | G | 2 | a0001c0001t0001g0019a0001c0005t0004g0144 | 2 | HG01433.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1366+7813T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441436 | ||||||
| chr1:217441579
|
T | C | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1366+7670A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441579 | ||||||
| chr1:217441595
|
T | C | 11 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0127others(8): Show | 11 | HG01168.hp1 HG01361.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1366+7654A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441595 | ||||||
| chr1:217441628
|
A | C | 4 | a0001c0001t0001g0010a0001c0001t0002g0169a0001c0001t0011g0138others(1): Show | 4 | HG00099.hp2 HG01175.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366+7621T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441628 | ||||||
| chr1:217441732
|
T | C | 3 | a0001c0001t0033g0081a0001c0001t0041g0181a0001c0001t0042g0174 | 3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1366+7517A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441732 | ||||||
| chr1:217441759
|
C | A | 2 | a0001c0001t0004g0152a0001c0001t0010g0134 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1366+7490G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441759 | ||||||
| chr1:217441785
|
C | T | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1366+7464G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217441785 | ||||||
| chr1:217442145
|
T | C | 55 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0006g0100others(52): Show | 55 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1366+7104A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217442145 | ||||||
| chr1:217442259
|
T | C | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1366+6990A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217442259 | ||||||
| chr1:217442440
|
T | C | 55 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0006g0100others(52): Show | 55 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1366+6809A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217442440 | ||||||
| chr1:217442633
|
T | TA | 55 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0006g0100others(52): Show | 55 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1366+6615dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217442633 | ||||||
| chr1:217442664
|
C | G | 36 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0004g0113others(33): Show | 36 | HG00621.hp1 HG00673.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1366+6585G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217442664 | ||||||
| chr1:217442763
|
T | C | 39 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(36): Show | 39 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1366+6486A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217442763 | ||||||
| chr1:217443150
|
G | A | 1 | a0002c0002t0012g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1366+6099C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443150 | ||||||
| chr1:217443224
|
G | A | 1 | a0001c0001t0022g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1366+6025C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443224 | ||||||
| chr1:217443402
|
G | A | 54 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0006g0100others(51): Show | 54 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1366+5847C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443402 | ||||||
| chr1:217443418
|
T | A | 55 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0006g0100others(52): Show | 55 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1366+5831A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443418 | ||||||
| chr1:217443586
|
T | C | 2 | a0001c0001t0014g0084a0001c0001t0021g0177 | 2 | HG02698.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1366+5663A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443586 | ||||||
| chr1:217443617
|
C | G | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1366+5632G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443617 | ||||||
| chr1:217443714
|
C | G | 2 | a0001c0001t0005g0069a0001c0001t0005g0071 | 2 | HG00621.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1366+5535G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443714 | ||||||
| chr1:217443743
|
ACT | A | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1366+5504_1366+550 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443743 | ||||||
| chr1:217443779
|
A | G | 1 | a0002c0002t0028g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1366+5470T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443779 | ||||||
| chr1:217443967
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1366+5282C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217443967 | ||||||
| chr1:217444021
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1366+5228C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444021 | ||||||
| chr1:217444111
|
G | A | 2 | a0001c0001t0002g0118a0001c0001t0002g0184 | 2 | HG02040.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1366+5138C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444111 | ||||||
| chr1:217444156
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1366+5093C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444156 | ||||||
| chr1:217444204
|
A | G | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0025g0001others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+5045T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444204 | ||||||
| chr1:217444284
|
C | A | 4 | a0001c0001t0006g0143a0001c0001t0006g0180a0001c0001t0007g0078others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+4965G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444284 | ||||||
| chr1:217444360
|
A | G | 64 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(61): Show | 64 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.1366+4889T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444360 | ||||||
| chr1:217444383
|
T | C | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0025g0001others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+4866A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444383 | ||||||
| chr1:217444555
|
G | T | 1 | a0003c0003t0010g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1366+4694C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444555 | ||||||
| chr1:217444849
|
C | T | 3 | a0001c0001t0033g0081a0001c0001t0041g0181a0001c0001t0042g0174 | 3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1366+4400G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444849 | ||||||
| chr1:217444886
|
C | T | 3 | a0003c0003t0010g0140a0003c0003t0010g0151a0003c0003t0010g0167 | 3 | HG02622.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1366+4363G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444886 | ||||||
| chr1:217444895
|
T | C | 1 | a0001c0001t0044g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1366+4354A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217444895 | ||||||
| chr1:217445063
|
G | A | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0025g0001others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+4186C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217445063 | ||||||
| chr1:217445144
|
C | T | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1366+4105G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217445144 | ||||||
| chr1:217445424
|
C | T | 5 | a0001c0001t0005g0095a0001c0001t0022g0182a0001c0001t0022g0183others(2): Show | 5 | HG02486.hp2 HG03130.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366+3825G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217445424 | ||||||
| chr1:217445625
|
C | G | 59 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(56): Show | 59 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1366+3624G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217445625 | ||||||
| chr1:217445852
|
A | T | 1 | a0002c0002t0013g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1366+3397T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217445852 | ||||||
| chr1:217445916
|
T | A | 1 | a0001c0001t0024g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1366+3333A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217445916 | ||||||
| chr1:217446017
|
CTAAT | C | 5 | a0001c0001t0014g0084a0001c0001t0021g0177a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02698.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366+3228_1366+323 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446017 | ||||||
| chr1:217446064
|
G | A | 1 | a0002c0002t0019g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1366+3185C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446064 | ||||||
| chr1:217446158
|
A | G | 3 | a0003c0003t0010g0140a0003c0003t0010g0151a0003c0003t0010g0167 | 3 | HG02622.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1366+3091T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446158 | ||||||
| chr1:217446270
|
A | G | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0025g0001others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+2979T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446270 | ||||||
| chr1:217446396
|
T | C | 1 | a0001c0001t0007g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1366+2853A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446396 | ||||||
| chr1:217446429
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1366+2820A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446429 | ||||||
| chr1:217446435
|
T | C | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0025g0001others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+2814A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446435 | ||||||
| chr1:217446685
|
TGTA | T | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0044g0115 | 3 | HG03130.hp1 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1366+2561_1366+256 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446685 | ||||||
| chr1:217446783
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1366+2466T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446783 | ||||||
| chr1:217446851
|
C | T | 3 | a0001c0001t0033g0081a0001c0001t0041g0181a0001c0001t0042g0174 | 3 | HG01891.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1366+2398G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446851 | ||||||
| chr1:217446861
|
G | A | 49 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(46): Show | 49 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366+2388C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446861 | ||||||
| chr1:217446958
|
T | G | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1366+2291A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217446958 | ||||||
| chr1:217447022
|
T | C | 3 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0044g0115 | 3 | HG03130.hp1 HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1366+2227A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447022 | ||||||
| chr1:217447030
|
G | A | 2 | a0001c0001t0034g0027a0001c0001t0043g0142 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1366+2219C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447030 | ||||||
| chr1:217447088
|
G | A | 40 | a0001c0001t0006g0100a0001c0001t0006g0107a0001c0001t0006g0128others(37): Show | 40 | HG00099.hp1 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1366+2161C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447088 | ||||||
| chr1:217447405
|
T | C | 2 | a0001c0001t0004g0152a0001c0001t0010g0134 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1366+1844A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447405 | ||||||
| chr1:217447564
|
G | T | 1 | a0001c0001t0036g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1366+1685C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447564 | ||||||
| chr1:217447702
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1366+1547T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447702 | ||||||
| chr1:217447780
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1366+1469T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447780 | ||||||
| chr1:217447808
|
C | T | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1366+1441G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447808 | ||||||
| chr1:217447832
|
A | C | 4 | a0001c0001t0022g0182a0001c0001t0022g0183a0001c0001t0025g0001others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+1417T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447832 | ||||||
| chr1:217447956
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1366+1293C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447956 | ||||||
| chr1:217447974
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0063others(2): Show | 5 | HG00597.hp2 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366+1275G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447974 | ||||||
| chr1:217447989
|
T | C | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1366+1260A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217447989 | ||||||
| chr1:217448084
|
G | A | 2 | a0001c0001t0020g0160a0001c0001t0032g0056 | 2 | HG01515.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1366+1165C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448084 | ||||||
| chr1:217448089
|
A | C | 1 | a0001c0001t0007g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1366+1160T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448089 | ||||||
| chr1:217448100
|
GA | G | 38 | a0001c0001t0001g0019a0001c0001t0002g0114a0001c0001t0002g0121others(35): Show | 38 | HG00099.hp1 HG00738.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1366+1148delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448100 | ||||||
| chr1:217448383
|
A | G | 2 | a0001c0001t0002g0114a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1366+866T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448383 | ||||||
| chr1:217448422
|
TA | T | 3 | a0001c0001t0022g0182a0001c0001t0040g0135a0001c0001t0044g0115 | 3 | HG02055.hp2 HG03130.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1366+826delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448422 | ||||||
| chr1:217448515
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0066others(3): Show | 6 | HG00621.hp2 HG01071.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1366+734G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448515 | ||||||
| chr1:217448626
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1366+623T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448626 | ||||||
| chr1:217448684
|
T | G | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1366+565A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448684 | ||||||
| chr1:217448700
|
C | T | 43 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(40): Show | 43 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.1366+549G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448700 | ||||||
| chr1:217448933
|
T | G | 1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1366+316A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 9/9 | chr1 | 217448933 | ||||||
| chr1:217449802
|
A | G | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1278-465T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217449802 | ||||||
| chr1:217450150
|
G | C | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-813C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217450150 | ||||||
| chr1:217450326
|
G | A | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-989C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217450326 | ||||||
| chr1:217450490
|
C | T | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-1153G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217450490 | ||||||
| chr1:217450657
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0009g0178others(4): Show | 7 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278-1320A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217450657 | ||||||
| chr1:217450705
|
C | T | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-1368G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217450705 | ||||||
| chr1:217450865
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1278-1528C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217450865 | ||||||
| chr1:217451039
|
G | A | 3 | a0002c0002t0013g0046a0002c0002t0013g0055a0002c0002t0030g0047 | 3 | NA18968.hp2 NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1278-1702C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451039 | ||||||
| chr1:217451075
|
G | A | 1 | a0001c0001t0004g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1278-1738C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451075 | ||||||
| chr1:217451094
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1278-1757A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451094 | ||||||
| chr1:217451111
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0009g0178others(4): Show | 7 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278-1774C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451111 | ||||||
| chr1:217451342
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1278-2005C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451342 | ||||||
| chr1:217451790
|
C | G | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-2453G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451790 | ||||||
| chr1:217451791
|
T | G | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-2454A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451791 | ||||||
| chr1:217451798
|
C | T | 38 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(35): Show | 38 | HG00597.hp1 HG01109.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.1278-2461G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451798 | ||||||
| chr1:217451867
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0009g0178others(4): Show | 7 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278-2530A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451867 | ||||||
| chr1:217451916
|
T | TTGC | 9 | a0001c0001t0006g0173a0001c0001t0009g0187a0001c0001t0014g0094others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278-2582_1278-258 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217451916 | ||||||
| chr1:217452021
|
G | A | 2 | a0001c0001t0004g0152a0001c0001t0009g0178 | 2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1278-2684C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452021 | ||||||
| chr1:217452468
|
C | T | 1 | a0001c0001t0011g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1278-3131G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452468 | ||||||
| chr1:217452541
|
A | G | 9 | a0001c0001t0006g0173a0001c0001t0009g0187a0001c0001t0014g0094others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278-3204T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452541 | ||||||
| chr1:217452551
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1278-3214G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452551 | ||||||
| chr1:217452759
|
G | C | 55 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(52): Show | 55 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.1278-3422C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452759 | ||||||
| chr1:217452767
|
A | G | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1278-3430T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452767 | ||||||
| chr1:217452875
|
T | C | 1 | a0003c0003t0010g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1278-3538A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452875 | ||||||
| chr1:217452913
|
A | G | 5 | a0001c0001t0006g0173a0001c0001t0027g0093a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278-3576T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217452913 | ||||||
| chr1:217453035
|
C | A | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-3698G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453035 | ||||||
| chr1:217453049
|
T | C | 1 | a0001c0001t0004g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1278-3712A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453049 | ||||||
| chr1:217453057
|
C | A | 187 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(184): Show |
intron_variant | MODIFIER | c.1278-3720G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453057 | ||||||
| chr1:217453324
|
T | C | 1 | a0001c0001t0006g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1278-3987A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453324 | ||||||
| chr1:217453563
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1278-4226A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453563 | ||||||
| chr1:217453710
|
C | A | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1278-4373G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453710 | ||||||
| chr1:217453711
|
T | G | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1278-4374A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453711 | ||||||
| chr1:217453827
|
C | T | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-4490G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453827 | ||||||
| chr1:217453939
|
G | C | 1 | a0001c0001t0002g0159 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1278-4602C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453939 | ||||||
| chr1:217454282
|
T | G | 9 | a0001c0001t0006g0173a0001c0001t0009g0187a0001c0001t0014g0094others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278-4945A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454282 | ||||||
| chr1:217454396
|
T | C | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1278-5059A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454396 | ||||||
| chr1:217454396
|
T | G | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-5059A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454396 | ||||||
| chr1:217454457
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1278-5120A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454457 | ||||||
| chr1:217454497
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1278-5160C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454497 | ||||||
| chr1:217454525
|
C | T | 3 | a0001c0001t0006g0173a0001c0001t0033g0081a0001c0001t0042g0174 | 3 | HG01891.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1278-5188G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454525 | ||||||
| chr1:217454543
|
C | T | 1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1278-5206G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454543 | ||||||
| chr1:217454545
|
C | T | 30 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0018others(27): Show | 30 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1278-5208G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454545 | ||||||
| chr1:217454588
|
C | CA | 91 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0026others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1278-5252dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454588 | ||||||
| chr1:217454588
|
C | CAA | 55 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(52): Show | 55 | HG00597.hp2 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1278-5253_1278-525 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454588 | ||||||
| chr1:217454626
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1278-5289A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454626 | ||||||
| chr1:217454627
|
C | A | 1 | a0001c0001t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1278-5290G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454627 | ||||||
| chr1:217454660
|
C | G | 7 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0009g0178others(4): Show | 7 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278-5323G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454660 | ||||||
| chr1:217454662
|
A | G | 7 | a0001c0001t0006g0173a0001c0001t0009g0187a0001c0001t0016g0086others(4): Show | 7 | HG01891.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1278-5325T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454662 | ||||||
| chr1:217454733
|
A | G | 121 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(118): Show | 121 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.1278-5396T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454733 | ||||||
| chr1:217454871
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-5534G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454871 | ||||||
| chr1:217455777
|
G | A | 5 | a0001c0001t0006g0173a0001c0001t0027g0093a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278-6440C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217455777 | ||||||
| chr1:217455946
|
G | A | 1 | a0001c0001t0022g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1278-6609C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217455946 | ||||||
| chr1:217456017
|
G | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(49): Show | 52 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.1278-6680C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456017 | ||||||
| chr1:217456047
|
T | C | 1 | a0001c0001t0002g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1278-6710A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456047 | ||||||
| chr1:217456078
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-6741G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456078 | ||||||
| chr1:217456283
|
G | A | 9 | a0001c0001t0006g0173a0001c0001t0009g0187a0001c0001t0016g0086others(6): Show | 9 | HG01891.hp2 HG02723.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278-6946C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456283 | ||||||
| chr1:217456301
|
C | T | 32 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(29): Show | 32 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1278-6964G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456301 | ||||||
| chr1:217456404
|
C | T | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1278-7067G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456404 | ||||||
| chr1:217456592
|
C | A | 3 | a0001c0001t0006g0107a0001c0001t0006g0133a0001c0001t0006g0136 | 3 | HG02622.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1278-7255G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456592 | ||||||
| chr1:217456633
|
T | C | 3 | a0001c0001t0006g0107a0001c0001t0006g0133a0001c0001t0006g0136 | 3 | HG02622.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1278-7296A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456633 | ||||||
| chr1:217456817
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0004g0152a0001c0001t0009g0178others(4): Show | 7 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278-7480C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217456817 | ||||||
| chr1:217457036
|
G | A | 32 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(29): Show | 32 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1278-7699C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217457036 | ||||||
| chr1:217457286
|
C | T | 11 | a0001c0001t0002g0158a0001c0001t0006g0165a0001c0001t0007g0004others(8): Show | 11 | HG00738.hp1 HG01071.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1278-7949G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217457286 | ||||||
| chr1:217457768
|
C | T | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1278-8431G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217457768 | ||||||
| chr1:217458087
|
A | G | 118 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(115): Show | 118 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1278-8750T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217458087 | ||||||
| chr1:217458103
|
GCCTGTAG others(8): Show |
G | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-8781_1278-876 others(19): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217458103 | ||||||
| chr1:217458848
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0038g0110a0003c0003t0010g0140others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278-9511G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217458848 | ||||||
| chr1:217459128
|
T | C | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1278-9791A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217459128 | ||||||
| chr1:217459334
|
G | C | 2 | a0001c0001t0009g0187a0001c0001t0016g0086 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1278-9997C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217459334 | ||||||
| chr1:217459455
|
C | T | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1278-10118G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217459455 | ||||||
| chr1:217460117
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1278-10780A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217460117 | ||||||
| chr1:217460283
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1278-10946C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217460283 | ||||||
| chr1:217460474
|
A | G | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1278-11137T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217460474 | ||||||
| chr1:217460771
|
T | C | 3 | a0001c0001t0006g0173a0001c0001t0033g0081a0001c0001t0042g0174 | 3 | HG01891.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1278-11434A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217460771 | ||||||
| chr1:217460985
|
G | T | 1 | a0002c0002t0008g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1278-11648C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217460985 | ||||||
| chr1:217461182
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1278-11845T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461182 | ||||||
| chr1:217461283
|
A | G | 1 | a0001c0001t0005g0051 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1278-11946T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461283 | ||||||
| chr1:217461344
|
T | C | 34 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(31): Show | 34 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1278-12007A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461344 | ||||||
| chr1:217461556
|
T | G | 2 | a0001c0001t0001g0057a0001c0001t0003g0058 | 2 | NA18962.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1278-12219A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461556 | ||||||
| chr1:217461809
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1278-12472G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461809 | ||||||
| chr1:217461879
|
T | C | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-12542A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461879 | ||||||
| chr1:217461933
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1278-12596T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461933 | ||||||
| chr1:217461983
|
G | A | 1 | a0001c0001t0007g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1278-12646C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217461983 | ||||||
| chr1:217462140
|
T | G | 4 | a0001c0001t0007g0079a0001c0001t0018g0185a0001c0001t0018g0186others(1): Show | 4 | HG02965.hp1 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278-12803A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462140 | ||||||
| chr1:217462190
|
A | G | 34 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(31): Show | 34 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1278-12853T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462190 | ||||||
| chr1:217462237
|
T | C | 1 | a0001c0005t0004g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1278-12900A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462237 | ||||||
| chr1:217462338
|
G | C | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1278-13001C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462338 | ||||||
| chr1:217462506
|
T | TA | 4 | a0001c0001t0038g0110a0003c0003t0010g0140a0003c0003t0010g0151others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278-13170dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462506 | ||||||
| chr1:217462512
|
AC | A | 3 | a0001c0001t0004g0130a0001c0001t0009g0187a0001c0001t0016g0086 | 3 | HG02970.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1278-13176delG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462512 | ||||||
| chr1:217462513
|
C | A | 15 | a0001c0001t0001g0019a0001c0001t0006g0173a0001c0001t0014g0094others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1278-13176G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462513 | ||||||
| chr1:217462589
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-13252A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462589 | ||||||
| chr1:217462643
|
A | T | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1278-13306T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462643 | ||||||
| chr1:217462709
|
T | C | 1 | a0001c0001t0044g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1278-13372A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462709 | ||||||
| chr1:217462885
|
G | A | 1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1278-13548C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217462885 | ||||||
| chr1:217463094
|
G | A | 1 | a0001c0001t0036g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1278-13757C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463094 | ||||||
| chr1:217463110
|
C | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-13773G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463110 | ||||||
| chr1:217463266
|
C | T | 47 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(44): Show | 47 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.1278-13929G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463266 | ||||||
| chr1:217463322
|
C | A | 6 | a0001c0001t0001g0019a0001c0001t0038g0110a0001c0001t0040g0135others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278-13985G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463322 | ||||||
| chr1:217463327
|
T | C | 1 | a0001c0001t0003g0039 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1278-13990A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463327 | ||||||
| chr1:217463338
|
G | A | 45 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(42): Show | 45 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1278-14001C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463338 | ||||||
| chr1:217463367
|
T | G | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-14030A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463367 | ||||||
| chr1:217463368
|
A | G | 7 | a0001c0001t0001g0019a0001c0001t0025g0001a0001c0001t0038g0110others(4): Show | 7 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1278-14031T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463368 | ||||||
| chr1:217463641
|
C | CA | 18 | a0001c0001t0001g0019a0001c0001t0002g0122a0001c0001t0002g0161others(15): Show | 18 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.1278-14305dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
C | CAA | 5 | a0001c0001t0003g0006a0001c0001t0003g0052a0001c0001t0005g0050others(2): Show | 5 | HG00673.hp2 HG03688.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278-14306_1278-14 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CA | C | 28 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0026others(25): Show | 28 | HG01168.hp2 HG01256.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1278-14305delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAA | C | 24 | a0001c0001t0001g0024a0001c0001t0001g0092a0001c0001t0002g0099others(21): Show | 24 | HG00597.hp1 HG00673.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.1278-14306_1278-14 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAAAAA | C | 5 | a0001c0001t0016g0086a0001c0001t0022g0183a0001c0001t0027g0093others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278-14309_1278-14 others(11): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAAAAAA | C | 6 | a0001c0001t0006g0173a0001c0001t0009g0187a0001c0001t0014g0094others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278-14310_1278-14 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1278-14314_1278-14 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAAAAAAA others(8): Show |
C | 11 | a0001c0001t0002g0158a0001c0001t0006g0165a0001c0001t0007g0004others(8): Show | 11 | HG00738.hp1 HG01071.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1278-14319_1278-14 others(21): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0021g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1278-14321_1278-14 others(23): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAAAAAAA others(11): Show |
C | 3 | a0001c0001t0001g0010a0001c0001t0003g0009a0001c0001t0003g0072 | 3 | HG00558.hp2 HG01515.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1278-14322_1278-14 others(24): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463641
|
CAAAAAAA others(12): Show |
C | 48 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(45): Show | 48 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1278-14323_1278-14 others(25): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463641 | ||||||
| chr1:217463674
|
A | G | 6 | a0001c0001t0004g0102a0001c0001t0004g0111a0001c0001t0006g0143others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278-14337T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463674 | ||||||
| chr1:217463700
|
G | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0063others(2): Show | 5 | HG00597.hp2 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278-14363C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463700 | ||||||
| chr1:217463733
|
T | C | 64 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(61): Show | 64 | HG00597.hp1 HG00738.hp1 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.1278-14396A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463733 | ||||||
| chr1:217463899
|
G | C | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1278-14562C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463899 | ||||||
| chr1:217463984
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1278-14647C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217463984 | ||||||
| chr1:217464022
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1278-14685C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464022 | ||||||
| chr1:217464169
|
C | G | 52 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(49): Show | 52 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.1278-14832G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464169 | ||||||
| chr1:217464184
|
T | G | 2 | a0001c0001t0015g0175a0001c0001t0015g0176 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1278-14847A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464184 | ||||||
| chr1:217464233
|
C | G | 2 | a0001c0001t0008g0096a0001c0001t0012g0088 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1278-14896G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464233 | ||||||
| chr1:217464447
|
A | T | 8 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0022g0182others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278-15110T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464447 | ||||||
| chr1:217464477
|
A | T | 53 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(50): Show | 53 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.1278-15140T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464477 | ||||||
| chr1:217464493
|
G | A | 2 | a0001c0001t0006g0107a0001c0001t0006g0133 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1278-15156C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464493 | ||||||
| chr1:217464769
|
T | A | 3 | a0001c0001t0006g0107a0001c0001t0006g0133a0001c0001t0006g0136 | 3 | HG02622.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1278-15432A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217464769 | ||||||
| chr1:217465202
|
AT | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0002g0131others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278-15866delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217465202 | ||||||
| chr1:217465489
|
A | G | 8 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0022g0182others(5): Show | 8 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278-16152T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217465489 | ||||||
| chr1:217465676
|
G | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-16339C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217465676 | ||||||
| chr1:217465702
|
G | A | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-16365C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217465702 | ||||||
| chr1:217465753
|
A | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-16416T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217465753 | ||||||
| chr1:217465805
|
C | T | 34 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(31): Show | 34 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1278-16468G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217465805 | ||||||
| chr1:217465838
|
C | A | 3 | a0001c0001t0002g0104a0001c0001t0002g0112a0001c0001t0009g0105 | 3 | HG02723.hp1 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1278-16501G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217465838 | ||||||
| chr1:217466287
|
GA | G | 53 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0022others(50): Show | 53 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1278-16951delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466287 | ||||||
| chr1:217466295
|
A | C | 1 | a0002c0002t0039g0162 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1278-16958T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466295 | ||||||
| chr1:217466492
|
C | T | 44 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(41): Show | 44 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1278-17155G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466492 | ||||||
| chr1:217466494
|
G | A | 2 | a0001c0007t0002g0147a0002c0002t0019g0155 | 2 | HG01361.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1278-17157C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466494 | ||||||
| chr1:217466545
|
A | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-17208T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466545 | ||||||
| chr1:217466643
|
A | G | 1 | a0002c0002t0028g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1278-17306T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466643 | ||||||
| chr1:217466701
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-17364G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466701 | ||||||
| chr1:217466706
|
A | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-17369T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466706 | ||||||
| chr1:217466746
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0004g0130a0003c0003t0010g0140others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278-17409G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466746 | ||||||
| chr1:217466859
|
CAG | C | 12 | a0001c0001t0001g0036a0001c0001t0002g0158a0001c0001t0006g0165others(9): Show | 12 | HG00738.hp1 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1278-17524_1278-17 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466859 | ||||||
| chr1:217466886
|
A | G | 1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1278-17549T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466886 | ||||||
| chr1:217466972
|
A | C | 2 | a0001c0001t0005g0050a0001c0001t0005g0051 | 2 | HG00673.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1278-17635T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217466972 | ||||||
| chr1:217467006
|
C | T | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278-17669G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467006 | ||||||
| chr1:217467203
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1278-17866C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467203 | ||||||
| chr1:217467222
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-17885T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467222 | ||||||
| chr1:217467247
|
A | G | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1278-17910T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467247 | ||||||
| chr1:217467442
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1278-18105A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467442 | ||||||
| chr1:217467513
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1278-18176T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467513 | ||||||
| chr1:217467698
|
T | TA | 34 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(31): Show | 34 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1278-18362dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467698 | ||||||
| chr1:217467727
|
G | A | 1 | a0001c0001t0007g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1278-18390C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217467727 | ||||||
| chr1:217468261
|
C | T | 6 | a0001c0001t0001g0092a0001c0001t0005g0020a0002c0002t0013g0046others(3): Show | 6 | HG00597.hp1 HG02135.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278-18924G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468261 | ||||||
| chr1:217468505
|
GCACACAC others(15): Show |
G | 1 | a0001c0001t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1278-19190_1278-19 others(28): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468505 | ||||||
| chr1:217468515
|
C | CCA | 5 | a0001c0001t0005g0005a0001c0001t0018g0185a0001c0001t0018g0186others(2): Show | 5 | HG00609.hp1 HG02280.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278-19180_1278-19 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCA | C | 22 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(19): Show | 22 | HG01109.hp2 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1278-19180_1278-19 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACA | C | 21 | a0001c0001t0001g0054a0001c0001t0002g0117a0001c0001t0002g0129others(18): Show | 21 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1278-19182_1278-19 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACACA | C | 49 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0025others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1278-19184_1278-19 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACACAC others(1): Show |
C | 8 | a0001c0001t0002g0158a0001c0001t0003g0058a0001c0001t0005g0020others(5): Show | 8 | HG01071.hp2 HG01081.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1278-19186_1278-19 others(14): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACACAC others(3): Show |
C | 37 | a0001c0001t0001g0019a0001c0001t0001g0062a0001c0001t0001g0082others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.1278-19188_1278-19 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACACAC others(5): Show |
C | 3 | a0001c0001t0001g0044a0001c0001t0021g0177a0002c0002t0013g0055 | 3 | HG01256.hp1 HG02698.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1278-19190_1278-19 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACACAC others(7): Show |
C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1278-19192_1278-19 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACACAC others(15): Show |
C | 1 | a0001c0001t0005g0050 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1278-19200_1278-19 others(28): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468515
|
CCACACAC others(19): Show |
C | 29 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0018others(26): Show | 29 | HG00099.hp2 HG00558.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1278-19204_1278-19 others(32): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468515 | ||||||
| chr1:217468562
|
C | G | 42 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0064others(39): Show | 42 | HG00597.hp1 HG00597.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1278-19225G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468562 | ||||||
| chr1:217468564
|
G | C | 1 | a0001c0001t0005g0005 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1278-19227C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468564 | ||||||
| chr1:217468635
|
G | C | 1 | a0001c0001t0033g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1278-19298C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468635 | ||||||
| chr1:217468704
|
G | A | 3 | a0003c0003t0010g0140a0003c0003t0010g0151a0003c0003t0010g0167 | 3 | HG02622.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1278-19367C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468704 | ||||||
| chr1:217468750
|
T | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-19413A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468750 | ||||||
| chr1:217468834
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-19497A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468834 | ||||||
| chr1:217468886
|
T | C | 3 | a0001c0001t0006g0107a0001c0001t0006g0133a0001c0001t0006g0136 | 3 | HG02622.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1278-19549A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217468886 | ||||||
| chr1:217469774
|
A | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1278-20437T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217469774 | ||||||
| chr1:217469845
|
C | T | 1 | a0001c0001t0007g0012 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1278-20508G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217469845 | ||||||
| chr1:217470252
|
A | T | 2 | a0001c0001t0009g0098a0001c0001t0014g0084 | 2 | HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1278-20915T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217470252 | ||||||
| chr1:217470473
|
C | T | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1278-21136G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217470473 | ||||||
| chr1:217470591
|
T | G | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1277+21089A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217470591 | ||||||
| chr1:217470800
|
C | T | 1 | a0001c0001t0005g0095 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1277+20880G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217470800 | ||||||
| chr1:217470938
|
TA | T | 6 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0040g0135others(3): Show | 6 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+20741delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217470938 | ||||||
| chr1:217471604
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1277+20076G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217471604 | ||||||
| chr1:217471663
|
A | G | 1 | a0001c0001t0007g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1277+20017T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217471663 | ||||||
| chr1:217471679
|
C | A | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1277+20001G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217471679 | ||||||
| chr1:217471711
|
C | CTTTT | 6 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+19965_1277+19 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217471711 | ||||||
| chr1:217471769
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1277+19911T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217471769 | ||||||
| chr1:217471949
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277+19731A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217471949 | ||||||
| chr1:217472112
|
G | A | 34 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(31): Show | 34 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1277+19568C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472112 | ||||||
| chr1:217472117
|
A | G | 7 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277+19563T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472117 | ||||||
| chr1:217472251
|
G | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(41): Show | 44 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1277+19429C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472251 | ||||||
| chr1:217472284
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277+19396C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472284 | ||||||
| chr1:217472296
|
CT | C | 102 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(99): Show | 102 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.1277+19383delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472296 | ||||||
| chr1:217472296
|
CTT | C | 6 | a0001c0001t0006g0173a0001c0001t0009g0187a0001c0001t0016g0086others(3): Show | 6 | HG02723.hp2 HG02970.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277+19382_1277+19 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472296 | ||||||
| chr1:217472402
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+19278G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472402 | ||||||
| chr1:217472431
|
G | A | 42 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(39): Show | 42 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1277+19249C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472431 | ||||||
| chr1:217472462
|
G | A | 34 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(31): Show | 34 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1277+19218C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472462 | ||||||
| chr1:217472503
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+19177A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472503 | ||||||
| chr1:217472520
|
T | A | 1 | a0001c0001t0001g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1277+19160A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472520 | ||||||
| chr1:217472524
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(4): Show | 7 | HG01243.hp2 HG01256.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277+19156C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472524 | ||||||
| chr1:217472598
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+19082T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472598 | ||||||
| chr1:217472614
|
A | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+19066T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472614 | ||||||
| chr1:217472679
|
G | C | 1 | a0001c0001t0003g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1277+19001C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472679 | ||||||
| chr1:217472817
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0004g0130a0003c0003t0010g0140others(2): Show | 5 | HG02622.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277+18863C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472817 | ||||||
| chr1:217472897
|
G | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+18783C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217472897 | ||||||
| chr1:217473051
|
A | C | 1 | a0002c0002t0028g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1277+18629T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473051 | ||||||
| chr1:217473280
|
A | AGT | 13 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0045others(10): Show | 13 | HG01081.hp1 HG01256.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1277+18398_1277+18 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473280
|
A | AGTGT | 6 | a0001c0001t0001g0073a0001c0001t0007g0014a0001c0001t0022g0182others(3): Show | 6 | HG00099.hp1 HG00609.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+18396_1277+18 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473280
|
AGT | A | 87 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(84): Show | 87 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1277+18398_1277+18 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473280
|
AGTGT | A | 9 | a0001c0001t0004g0130a0001c0001t0008g0096a0001c0001t0009g0187others(6): Show | 9 | HG02622.hp1 HG02647.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1277+18396_1277+18 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473280
|
AGTGTGT | A | 3 | a0001c0001t0001g0057a0001c0001t0003g0058a0001c0001t0025g0001 | 3 | HG02486.hp2 NA18962.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1277+18394_1277+18 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473280
|
AGTGTGTG others(3): Show |
A | 5 | a0001c0001t0006g0173a0001c0001t0027g0093a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1277+18390_1277+18 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473280
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0003g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1277+18388_1277+18 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473280
|
AGTGTGTG others(7): Show |
A | 3 | a0001c0001t0016g0083a0001c0005t0004g0144a0001c0005t0009g0145 | 3 | HG01433.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1277+18386_1277+18 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473280 | ||||||
| chr1:217473419
|
A | T | 8 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0025g0001others(5): Show | 8 | HG02055.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1277+18261T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473419 | ||||||
| chr1:217473668
|
T | C | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1277+18012A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473668 | ||||||
| chr1:217473823
|
A | G | 2 | a0001c0001t0014g0094a0001c0001t0021g0106 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1277+17857T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473823 | ||||||
| chr1:217473997
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+17683T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473997 | ||||||
| chr1:217473998
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0025g0001others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277+17682A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217473998 | ||||||
| chr1:217474052
|
C | A | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1277+17628G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217474052 | ||||||
| chr1:217474278
|
G | C | 2 | a0001c0001t0025g0001a0001c0001t0038g0110 | 2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1277+17402C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217474278 | ||||||
| chr1:217474639
|
G | A | 1 | a0001c0001t0031g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1277+17041C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217474639 | ||||||
| chr1:217474889
|
A | C | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1277+16791T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217474889 | ||||||
| chr1:217475165
|
G | A | 1 | a0001c0001t0005g0043 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1277+16515C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217475165 | ||||||
| chr1:217475383
|
G | A | 2 | a0001c0001t0018g0185a0001c0001t0018g0186 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1277+16297C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217475383 | ||||||
| chr1:217475424
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1277+16256C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217475424 | ||||||
| chr1:217475507
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0062 | 3 | HG01358.hp1 HG01952.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1277+16173A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217475507 | ||||||
| chr1:217475690
|
T | C | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1277+15990A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217475690 | ||||||
| chr1:217475953
|
A | C | 1 | a0001c0001t0038g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1277+15727T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217475953 | ||||||
| chr1:217476022
|
A | G | 1 | a0001c0001t0005g0043 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1277+15658T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476022 | ||||||
| chr1:217476235
|
A | AGT | 8 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0004g0163others(5): Show | 8 | HG00609.hp1 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1277+15443_1277+15 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
A | AGTGT | 12 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0002g0099others(9): Show | 12 | HG01243.hp2 HG01256.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1277+15441_1277+15 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
A | AGTGTGT | 3 | a0001c0001t0009g0187a0001c0001t0012g0031a0001c0001t0016g0086 | 3 | HG02970.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1277+15439_1277+15 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
A | AGTGTGTG others(1): Show |
11 | a0001c0001t0004g0111a0001c0001t0006g0143a0001c0001t0007g0078others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1277+15437_1277+15 others(14): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0012g0088a0001c0004t0008g0108a0001c0004t0008g0119 | 3 | HG01109.hp1 HG01261.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1277+15435_1277+15 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
A | AGTGTGTG others(5): Show |
5 | a0001c0001t0002g0104a0001c0001t0002g0112a0001c0001t0004g0152others(2): Show | 5 | HG02723.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277+15433_1277+15 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
A | AGTGTGTG others(7): Show |
3 | a0001c0001t0001g0092a0001c0001t0005g0020a0002c0002t0028g0070 | 3 | HG02135.hp2 HG02155.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1277+15431_1277+15 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
A | AGTGTGTG others(9): Show |
5 | a0002c0002t0013g0046a0002c0002t0013g0055a0002c0002t0013g0087others(2): Show | 5 | HG00597.hp1 HG02738.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1277+15429_1277+15 others(22): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
AGT | A | 61 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0022others(58): Show | 61 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1277+15443_1277+15 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476235
|
AGTGT | A | 5 | a0001c0001t0006g0173a0001c0001t0027g0093a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1277+15441_1277+15 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476235 | ||||||
| chr1:217476412
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0003g0039a0001c0001t0003g0089 | 3 | HG00558.hp1 NA18962.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1277+15268G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476412 | ||||||
| chr1:217476543
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1277+15137T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476543 | ||||||
| chr1:217476555
|
C | T | 42 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(39): Show | 42 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1277+15125G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476555 | ||||||
| chr1:217476714
|
T | C | 35 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(32): Show | 35 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1277+14966A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476714 | ||||||
| chr1:217476942
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+14738G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217476942 | ||||||
| chr1:217477228
|
C | T | 3 | a0001c0001t0009g0098a0001c0001t0014g0084a0001c0001t0023g0002 | 3 | HG02896.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1277+14452G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217477228 | ||||||
| chr1:217477231
|
T | C | 1 | a0001c0001t0006g0136 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1277+14449A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217477231 | ||||||
| chr1:217477246
|
C | T | 3 | a0003c0003t0010g0140a0003c0003t0010g0151a0003c0003t0010g0167 | 3 | HG02622.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1277+14434G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217477246 | ||||||
| chr1:217477740
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0040g0135others(3): Show | 6 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+13940G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217477740 | ||||||
| chr1:217477787
|
C | T | 1 | a0001c0001t0017g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1277+13893G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217477787 | ||||||
| chr1:217478585
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1277+13095C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217478585 | ||||||
| chr1:217478670
|
T | TAAAAAGT others(284): Show |
2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1277+13009_1277+13 others(297): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217478670 | ||||||
| chr1:217478696
|
G | A | 1 | a0001c0001t0011g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1277+12984C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217478696 | ||||||
| chr1:217478759
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1277+12921A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217478759 | ||||||
| chr1:217478991
|
A | AG | 3 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0011g0138 | 3 | HG00099.hp2 HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1277+12688dupC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217478991 | ||||||
| chr1:217479348
|
A | T | 2 | a0001c0001t0025g0001a0001c0001t0038g0110 | 2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1277+12332T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217479348 | ||||||
| chr1:217479459
|
C | A | 1 | a0001c0001t0003g0052 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1277+12221G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217479459 | ||||||
| chr1:217479518
|
G | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(49): Show | 52 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.1277+12162C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217479518 | ||||||
| chr1:217479725
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1277+11955A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217479725 | ||||||
| chr1:217479782
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1277+11898T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217479782 | ||||||
| chr1:217480104
|
A | G | 32 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0018others(29): Show | 32 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1277+11576T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217480104 | ||||||
| chr1:217480600
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+11080T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217480600 | ||||||
| chr1:217480614
|
A | G | 7 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277+11066T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217480614 | ||||||
| chr1:217481206
|
C | G | 34 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(31): Show | 34 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1277+10474G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217481206 | ||||||
| chr1:217481280
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+10400G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217481280 | ||||||
| chr1:217481313
|
A | G | 7 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277+10367T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217481313 | ||||||
| chr1:217481395
|
A | T | 3 | a0001c0001t0009g0098a0001c0001t0014g0084a0001c0001t0023g0002 | 3 | HG02896.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1277+10285T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217481395 | ||||||
| chr1:217481685
|
C | T | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1277+9995G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217481685 | ||||||
| chr1:217481723
|
A | G | 117 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(114): Show | 117 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1277+9957T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217481723 | ||||||
| chr1:217482051
|
CTG | C | 3 | a0001c0001t0002g0161a0001c0001t0003g0006a0001c0001t0003g0052 | 3 | NA19009.hp1 NA19009.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1277+9627_1277+962 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217482051 | ||||||
| chr1:217482150
|
C | T | 1 | a0001c0001t0033g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1277+9530G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217482150 | ||||||
| chr1:217482965
|
G | T | 37 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1277+8715C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217482965 | ||||||
| chr1:217483333
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1277+8347G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217483333 | ||||||
| chr1:217483343
|
CCTGA | C | 4 | a0001c0001t0006g0180a0001c0001t0034g0027a0001c0001t0043g0142others(1): Show | 4 | HG01243.hp1 HG02280.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1277+8333_1277+833 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217483343 | ||||||
| chr1:217483479
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1277+8201G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217483479 | ||||||
| chr1:217483589
|
T | C | 2 | a0001c0001t0044g0115a0002c0002t0012g0007 | 2 | HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1277+8091A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217483589 | ||||||
| chr1:217483795
|
G | T | 116 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(113): Show | 116 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1277+7885C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217483795 | ||||||
| chr1:217483954
|
A | G | 43 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(40): Show | 43 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.1277+7726T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217483954 | ||||||
| chr1:217484099
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1277+7581A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484099 | ||||||
| chr1:217484506
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1277+7174T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484506 | ||||||
| chr1:217484556
|
T | A | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1277+7124A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484556 | ||||||
| chr1:217484556
|
T | TATA | 2 | a0001c0001t0001g0036a0001c0001t0001g0038 | 2 | HG01071.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1277+7123_1277+712 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484556 | ||||||
| chr1:217484556
|
T | TTA | 48 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0018others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1277+7122_1277+712 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484556 | ||||||
| chr1:217484556
|
T | TTATA | 42 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0023others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1277+7120_1277+712 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484556 | ||||||
| chr1:217484556
|
T | TTATATA | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0003g0009others(6): Show | 9 | HG00741.hp1 HG01168.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1277+7118_1277+712 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484556 | ||||||
| chr1:217484556
|
TTA | T | 16 | a0001c0001t0001g0010a0001c0001t0002g0158a0001c0001t0006g0165others(13): Show | 16 | HG00738.hp1 HG01071.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1277+7122_1277+712 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484556 | ||||||
| chr1:217484577
|
T | G | 30 | a0001c0001t0001g0044a0001c0001t0002g0104a0001c0001t0002g0112others(27): Show | 30 | HG00597.hp1 HG01109.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1277+7103A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484577 | ||||||
| chr1:217484577
|
T | TAG | 10 | a0001c0001t0001g0019a0001c0001t0001g0082a0001c0001t0001g0092others(7): Show | 10 | HG01243.hp2 HG02135.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1277+7102_1277+710 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484577 | ||||||
| chr1:217484822
|
G | T | 1 | a0001c0001t0038g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1277+6858C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217484822 | ||||||
| chr1:217485154
|
A | C | 41 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(38): Show | 41 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1277+6526T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217485154 | ||||||
| chr1:217485266
|
T | G | 41 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(38): Show | 41 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1277+6414A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217485266 | ||||||
| chr1:217485459
|
CT | C | 15 | a0001c0001t0001g0010a0001c0001t0002g0158a0001c0001t0006g0165others(12): Show | 15 | HG00738.hp1 HG01071.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1277+6220delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217485459 | ||||||
| chr1:217485459
|
CTT | C | 41 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(38): Show | 41 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1277+6219_1277+622 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217485459 | ||||||
| chr1:217485550
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1277+6130A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217485550 | ||||||
| chr1:217485842
|
A | T | 35 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(32): Show | 35 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1277+5838T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217485842 | ||||||
| chr1:217486099
|
T | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1277+5581A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217486099 | ||||||
| chr1:217486422
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+5258T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217486422 | ||||||
| chr1:217486597
|
T | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+5083A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217486597 | ||||||
| chr1:217486670
|
C | T | 35 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(32): Show | 35 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1277+5010G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217486670 | ||||||
| chr1:217486710
|
G | A | 35 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(32): Show | 35 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1277+4970C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217486710 | ||||||
| chr1:217486758
|
G | A | 35 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(32): Show | 35 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1277+4922C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217486758 | ||||||
| chr1:217486978
|
C | A | 2 | a0001c0001t0001g0057a0001c0001t0003g0058 | 2 | NA18962.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1277+4702G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217486978 | ||||||
| chr1:217487425
|
CT | C | 11 | a0001c0001t0001g0057a0001c0001t0005g0051a0001c0001t0006g0173others(8): Show | 11 | HG01891.hp2 HG02723.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1277+4254delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217487425 | ||||||
| chr1:217487425
|
CTT | C | 40 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(37): Show | 40 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.1277+4253_1277+425 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217487425 | ||||||
| chr1:217487692
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1277+3988A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217487692 | ||||||
| chr1:217487781
|
C | T | 3 | a0001c0001t0002g0104a0001c0001t0002g0112a0001c0001t0009g0105 | 3 | HG02723.hp1 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1277+3899G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217487781 | ||||||
| chr1:217488030
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1277+3650C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488030 | ||||||
| chr1:217488055
|
T | TA | 39 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(36): Show | 39 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.1277+3624dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488055 | ||||||
| chr1:217488166
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1277+3514C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488166 | ||||||
| chr1:217488232
|
G | A | 1 | a0001c0001t0011g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1277+3448C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488232 | ||||||
| chr1:217488601
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+3079A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488601 | ||||||
| chr1:217488779
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1277+2901T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488779 | ||||||
| chr1:217488861
|
AT | A | 41 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(38): Show | 41 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1277+2818delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488861 | ||||||
| chr1:217488863
|
T | A | 1 | a0003c0003t0010g0167 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1277+2817A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488863 | ||||||
| chr1:217488981
|
A | G | 1 | a0001c0001t0004g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1277+2699T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217488981 | ||||||
| chr1:217489195
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0040g0135 | 3 | HG02055.hp2 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1277+2485G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489195 | ||||||
| chr1:217489209
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1277+2471A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489209 | ||||||
| chr1:217489263
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1277+2417C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489263 | ||||||
| chr1:217489300
|
G | C | 1 | a0003c0003t0010g0188 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1277+2380C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489300 | ||||||
| chr1:217489397
|
AACTG | A | 36 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(33): Show | 36 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1277+2279_1277+228 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489397 | ||||||
| chr1:217489451
|
T | C | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1277+2229A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489451 | ||||||
| chr1:217489583
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1277+2097G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489583 | ||||||
| chr1:217489680
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0015g0175a0001c0001t0015g0176others(1): Show | 4 | HG01515.hp1 HG01993.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1277+2000A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489680 | ||||||
| chr1:217489888
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1277+1792C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489888 | ||||||
| chr1:217489935
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1277+1745T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217489935 | ||||||
| chr1:217490044
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1277+1636T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490044 | ||||||
| chr1:217490068
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1277+1612C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490068 | ||||||
| chr1:217490069
|
C | G | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1277+1611G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490069 | ||||||
| chr1:217490088
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0004g0130a0001c0001t0038g0110 | 3 | HG02615.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1277+1592G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490088 | ||||||
| chr1:217490356
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1277+1324G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490356 | ||||||
| chr1:217490688
|
T | A | 63 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0044others(60): Show | 63 | HG00597.hp1 HG00738.hp1 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.1277+992A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490688 | ||||||
| chr1:217490810
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1277+870T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490810 | ||||||
| chr1:217490899
|
C | T | 37 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1277+781G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217490899 | ||||||
| chr1:217491110
|
C | G | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1277+570G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217491110 | ||||||
| chr1:217491145
|
A | C | 1 | a0001c0001t0003g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1277+535T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217491145 | ||||||
| chr1:217491246
|
A | C | 37 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1277+434T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217491246 | ||||||
| chr1:217491862
|
CT | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0018others(65): Show | 68 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1207-113delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217491862 | ||||||
| chr1:217492409
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1207-659A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217492409 | ||||||
| chr1:217492498
|
C | T | 1 | a0001c0001t0005g0005 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1207-748G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217492498 | ||||||
| chr1:217492861
|
A | G | 50 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(47): Show | 50 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.1207-1111T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217492861 | ||||||
| chr1:217492865
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1207-1115G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217492865 | ||||||
| chr1:217492928
|
T | C | 37 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1207-1178A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217492928 | ||||||
| chr1:217492998
|
A | G | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1207-1248T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217492998 | ||||||
| chr1:217493327
|
A | G | 1 | a0001c0001t0007g0012 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1207-1577T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217493327 | ||||||
| chr1:217493398
|
T | C | 1 | a0003c0003t0010g0167 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1207-1648A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217493398 | ||||||
| chr1:217493788
|
C | G | 1 | a0001c0001t0021g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1207-2038G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217493788 | ||||||
| chr1:217493821
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1207-2071T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217493821 | ||||||
| chr1:217493948
|
C | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(41): Show | 44 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1207-2198G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217493948 | ||||||
| chr1:217493949
|
A | C | 44 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(41): Show | 44 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1207-2199T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217493949 | ||||||
| chr1:217493959
|
G | GA | 37 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1207-2210dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217493959 | ||||||
| chr1:217494011
|
A | T | 1 | a0001c0001t0015g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1207-2261T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494011 | ||||||
| chr1:217494261
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1207-2511T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494261 | ||||||
| chr1:217494275
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1207-2525C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494275 | ||||||
| chr1:217494352
|
G | C | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1207-2602C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494352 | ||||||
| chr1:217494503
|
C | T | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1207-2753G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494503 | ||||||
| chr1:217494506
|
T | C | 2 | a0001c0001t0001g0073a0002c0002t0019g0172 | 2 | HG01081.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1207-2756A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494506 | ||||||
| chr1:217494509
|
C | A | 1 | a0001c0001t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1207-2759G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494509 | ||||||
| chr1:217494730
|
T | C | 42 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(39): Show | 42 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1207-2980A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494730 | ||||||
| chr1:217494738
|
T | C | 59 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(56): Show | 59 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.1207-2988A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494738 | ||||||
| chr1:217494779
|
A | T | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1207-3029T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494779 | ||||||
| chr1:217494814
|
C | A | 1 | a0001c0001t0003g0039 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1207-3064G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494814 | ||||||
| chr1:217494855
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1207-3105G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494855 | ||||||
| chr1:217494886
|
AT | A | 42 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(39): Show | 42 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1207-3137delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494886 | ||||||
| chr1:217494988
|
G | C | 44 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(41): Show | 44 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.1207-3238C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217494988 | ||||||
| chr1:217495018
|
C | T | 37 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1207-3268G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217495018 | ||||||
| chr1:217495248
|
A | T | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1206+3108T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217495248 | ||||||
| chr1:217495339
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1206+3017G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217495339 | ||||||
| chr1:217495593
|
A | G | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1206+2763T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217495593 | ||||||
| chr1:217495769
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1206+2587T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217495769 | ||||||
| chr1:217495797
|
C | T | 38 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(35): Show | 38 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1206+2559G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217495797 | ||||||
| chr1:217495864
|
T | C | 37 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1206+2492A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217495864 | ||||||
| chr1:217496001
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1206+2355C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496001 | ||||||
| chr1:217496015
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1206+2341A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496015 | ||||||
| chr1:217496125
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1206+2231T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496125 | ||||||
| chr1:217496181
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1206+2175C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496181 | ||||||
| chr1:217496229
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1206+2127G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496229 | ||||||
| chr1:217496341
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0035g0035 | 2 | HG01256.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1206+2015G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496341 | ||||||
| chr1:217496372
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1206+1984C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496372 | ||||||
| chr1:217496560
|
G | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1206+1796C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496560 | ||||||
| chr1:217496561
|
A | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1206+1795T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496561 | ||||||
| chr1:217496698
|
T | A | 42 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0082others(39): Show | 42 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1206+1658A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496698 | ||||||
| chr1:217496836
|
A | G | 2 | a0001c0001t0022g0182a0001c0001t0022g0183 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1206+1520T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496836 | ||||||
| chr1:217496863
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1206+1493G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217496863 | ||||||
| chr1:217497185
|
T | C | 40 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(37): Show | 40 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.1206+1171A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217497185 | ||||||
| chr1:217497194
|
C | T | 2 | a0001c0001t0004g0163a0001c0001t0005g0095 | 2 | HG03491.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1206+1162G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217497194 | ||||||
| chr1:217497532
|
A | G | 169 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(166): Show | 169 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.1206+824T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217497532 | ||||||
| chr1:217497557
|
A | C | 2 | a0001c0001t0001g0019a0001c0001t0040g0135 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1206+799T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217497557 | ||||||
| chr1:217497749
|
GTA | G | 35 | a0001c0001t0001g0044a0001c0001t0001g0082a0001c0001t0001g0092others(32): Show | 35 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1206+605_1206+606d others(4): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217497749 | ||||||
| chr1:217497855
|
C | T | 5 | a0001c0001t0006g0173a0001c0001t0027g0093a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+501G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217497855 | ||||||
| chr1:217497881
|
T | C | 55 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0018others(52): Show | 55 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.1206+475A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217497881 | ||||||
| chr1:217498190
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1206+166G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 7/9 | chr1 | 217498190 | ||||||
| chr1:217498429
|
C | G | 33 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0066others(30): Show | 33 | HG00099.hp1 HG00673.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1167-34G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498429 | ||||||
| chr1:217498545
|
A | G | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1167-150T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498545 | ||||||
| chr1:217498603
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1167-208T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498603 | ||||||
| chr1:217498644
|
G | A | 5 | a0001c0001t0006g0173a0001c0001t0027g0093a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1167-249C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498644 | ||||||
| chr1:217498711
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167-316A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498711 | ||||||
| chr1:217498906
|
A | G | 1 | a0001c0001t0021g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1167-511T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498906 | ||||||
| chr1:217498942
|
C | G | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167-547G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498942 | ||||||
| chr1:217498980
|
C | T | 1 | a0001c0001t0015g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1167-585G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217498980 | ||||||
| chr1:217499004
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1167-609G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499004 | ||||||
| chr1:217499045
|
G | A | 2 | a0001c0001t0005g0043a0001c0001t0007g0014 | 2 | HG00099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1167-650C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499045 | ||||||
| chr1:217499071
|
G | A | 1 | a0001c0001t0007g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1167-676C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499071 | ||||||
| chr1:217499079
|
T | A | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1167-684A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499079 | ||||||
| chr1:217499116
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1167-721G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499116 | ||||||
| chr1:217499155
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0118others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1167-760C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499155 | ||||||
| chr1:217499157
|
T | C | 1 | a0001c0001t0017g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1167-762A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499157 | ||||||
| chr1:217499172
|
T | C | 1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1167-777A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499172 | ||||||
| chr1:217499293
|
T | A | 4 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167-898A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499293 | ||||||
| chr1:217499487
|
G | C | 3 | a0001c0001t0006g0180a0001c0001t0022g0182a0001c0001t0025g0001 | 3 | HG02486.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1167-1092C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499487 | ||||||
| chr1:217499571
|
G | A | 1 | a0001c0001t0016g0086 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1167-1176C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499571 | ||||||
| chr1:217499733
|
CT | C | 10 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0117others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1167-1339delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499733 | ||||||
| chr1:217499774
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1167-1379G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499774 | ||||||
| chr1:217499821
|
C | A | 3 | a0001c0001t0006g0180a0001c0001t0022g0182a0001c0001t0025g0001 | 3 | HG02486.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1167-1426G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499821 | ||||||
| chr1:217499830
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1167-1435C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499830 | ||||||
| chr1:217499842
|
C | G | 1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1167-1447G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499842 | ||||||
| chr1:217499901
|
T | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167-1506A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499901 | ||||||
| chr1:217499930
|
G | A | 4 | a0001c0001t0004g0152a0001c0001t0004g0179a0001c0001t0009g0178others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167-1535C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499930 | ||||||
| chr1:217499948
|
A | G | 116 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(113): Show | 116 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1167-1553T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499948 | ||||||
| chr1:217500054
|
A | G | 5 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0118others(2): Show | 5 | HG01243.hp2 HG02559.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167-1659T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500054 | ||||||
| chr1:217500063
|
A | G | 2 | a0002c0002t0013g0046a0002c0002t0030g0047 | 2 | NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1167-1668T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500063 | ||||||
| chr1:217500085
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1167-1690C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500085 | ||||||
| chr1:217500217
|
A | C | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1167-1822T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500217 | ||||||
| chr1:217500695
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1167-2300C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500695 | ||||||
| chr1:217500720
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167-2325C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500720 | ||||||
| chr1:217500751
|
T | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1167-2356A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500751 | ||||||
| chr1:217500845
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1167-2450G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217500845 | ||||||
| chr1:217501043
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1167-2648A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217501043 | ||||||
| chr1:217501174
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167-2779A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217501174 | ||||||
| chr1:217501268
|
T | G | 1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1167-2873A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217501268 | ||||||
| chr1:217501440
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1167-3045T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217501440 | ||||||
| chr1:217501706
|
C | G | 1 | a0001c0001t0002g0104 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1167-3311G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217501706 | ||||||
| chr1:217501826
|
G | T | 50 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(47): Show | 50 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1167-3431C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217501826 | ||||||
| chr1:217501877
|
G | A | 3 | a0001c0001t0006g0180a0001c0001t0022g0182a0001c0001t0025g0001 | 3 | HG02486.hp2 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1167-3482C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217501877 | ||||||
| chr1:217502021
|
T | G | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1167-3626A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502021 | ||||||
| chr1:217502032
|
C | T | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1167-3637G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502032 | ||||||
| chr1:217502257
|
A | G | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1167-3862T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502257 | ||||||
| chr1:217502396
|
G | A | 3 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124 | 3 | HG00609.hp2 HG02135.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1167-4001C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502396 | ||||||
| chr1:217502636
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1167-4241G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502636 | ||||||
| chr1:217502822
|
G | T | 2 | a0001c0001t0004g0111a0001c0001t0006g0107 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1167-4427C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502822 | ||||||
| chr1:217502905
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1167-4510A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502905 | ||||||
| chr1:217502945
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167-4550C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502945 | ||||||
| chr1:217502982
|
C | T | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167-4587G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217502982 | ||||||
| chr1:217503014
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1167-4619C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217503014 | ||||||
| chr1:217503280
|
A | G | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1167-4885T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217503280 | ||||||
| chr1:217503489
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167-5094T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217503489 | ||||||
| chr1:217503490
|
T | C | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1167-5095A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217503490 | ||||||
| chr1:217503836
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1167-5441A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217503836 | ||||||
| chr1:217503914
|
A | G | 114 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(111): Show | 114 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1167-5519T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217503914 | ||||||
| chr1:217504113
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1167-5718T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217504113 | ||||||
| chr1:217504289
|
G | A | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1167-5894C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217504289 | ||||||
| chr1:217504318
|
G | GA | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1167-5924dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217504318 | ||||||
| chr1:217504695
|
T | A | 4 | a0001c0001t0004g0111a0001c0001t0006g0107a0001c0001t0021g0106others(1): Show | 4 | HG01261.hp1 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1167-6300A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217504695 | ||||||
| chr1:217505190
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0004g0163 | 2 | HG03491.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1167-6795G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505190 | ||||||
| chr1:217505284
|
T | C | 11 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0006g0143others(8): Show | 11 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1167-6889A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505284 | ||||||
| chr1:217505412
|
G | GA | 98 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(95): Show | 98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1167-7018dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505412 | ||||||
| chr1:217505562
|
T | C | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1167-7167A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505562 | ||||||
| chr1:217505592
|
T | C | 51 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(48): Show | 51 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1167-7197A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505592 | ||||||
| chr1:217505640
|
T | C | 1 | a0001c0001t0015g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1167-7245A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505640 | ||||||
| chr1:217505747
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1167-7352T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505747 | ||||||
| chr1:217505965
|
G | A | 1 | a0001c0001t0015g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1167-7570C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505965 | ||||||
| chr1:217505980
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1167-7585C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217505980 | ||||||
| chr1:217506026
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1167-7631C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506026 | ||||||
| chr1:217506029
|
C | T | 6 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(3): Show | 6 | HG01243.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167-7634G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506029 | ||||||
| chr1:217506218
|
C | T | 6 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(3): Show | 6 | HG01243.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167-7823G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506218 | ||||||
| chr1:217506424
|
A | G | 1 | a0001c0001t0044g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1167-8029T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506424 | ||||||
| chr1:217506440
|
T | C | 2 | a0001c0001t0004g0130a0001c0001t0008g0096 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1167-8045A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506440 | ||||||
| chr1:217506509
|
A | G | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1167-8114T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506509 | ||||||
| chr1:217506693
|
C | T | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1166+8129G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506693 | ||||||
| chr1:217506738
|
A | T | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1166+8084T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506738 | ||||||
| chr1:217507042
|
TGTGA | T | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1166+7776_1166+777 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217507042 | ||||||
| chr1:217507239
|
T | C | 1 | a0001c0001t0007g0012 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1166+7583A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217507239 | ||||||
| chr1:217507335
|
C | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1166+7487G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217507335 | ||||||
| chr1:217507626
|
A | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1166+7196T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217507626 | ||||||
| chr1:217507988
|
A | T | 1 | a0001c0001t0014g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1166+6834T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217507988 | ||||||
| chr1:217508261
|
T | G | 1 | a0001c0001t0002g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1166+6561A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217508261 | ||||||
| chr1:217508625
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1166+6197T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217508625 | ||||||
| chr1:217508644
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1166+6178T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217508644 | ||||||
| chr1:217509519
|
T | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1166+5303A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217509519 | ||||||
| chr1:217509768
|
T | G | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1166+5054A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217509768 | ||||||
| chr1:217509910
|
A | G | 98 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(95): Show | 98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1166+4912T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217509910 | ||||||
| chr1:217510228
|
C | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1166+4594G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510228 | ||||||
| chr1:217510274
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1166+4548G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510274 | ||||||
| chr1:217510368
|
T | C | 6 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(3): Show | 6 | HG01243.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1166+4454A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510368 | ||||||
| chr1:217510395
|
G | A | 1 | a0001c0001t0008g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1166+4427C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510395 | ||||||
| chr1:217510592
|
A | ACGT | 2 | a0001c0001t0009g0187a0001c0001t0016g0086 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1166+4227_1166+422 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510592 | ||||||
| chr1:217510617
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0159others(2): Show | 5 | HG01167.hp1 HG01361.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166+4205G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510617 | ||||||
| chr1:217510632
|
A | G | 1 | a0001c0001t0015g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1166+4190T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510632 | ||||||
| chr1:217510896
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1166+3926G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217510896 | ||||||
| chr1:217511092
|
G | A | 1 | a0001c0001t0023g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1166+3730C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511092 | ||||||
| chr1:217511134
|
A | T | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1166+3688T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511134 | ||||||
| chr1:217511623
|
A | G | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1166+3199T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511623 | ||||||
| chr1:217511771
|
G | C | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1166+3051C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511771 | ||||||
| chr1:217511817
|
C | CTG | 91 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(88): Show | 91 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1166+3003_1166+300 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511817 | ||||||
| chr1:217511817
|
C | CTGTG | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0161 | 3 | HG02896.hp2 HG02897.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1166+3001_1166+300 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511817 | ||||||
| chr1:217511817
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1166+2995_1166+300 others(14): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511817 | ||||||
| chr1:217511817
|
C | CTGTGTGT others(7): Show |
3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+2991_1166+300 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511817 | ||||||
| chr1:217511817
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1166+2989_1166+300 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511817 | ||||||
| chr1:217511817
|
CTGTGTG | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0002g0158others(7): Show | 10 | HG00738.hp1 HG01071.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.1166+2999_1166+300 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511817 | ||||||
| chr1:217511839
|
GT | G | 2 | a0001c0001t0001g0008a0002c0002t0012g0007 | 2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1166+2982delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511839 | ||||||
| chr1:217511850
|
T | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1166+2972A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511850 | ||||||
| chr1:217511856
|
G | A | 5 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0118others(2): Show | 5 | HG01243.hp2 HG02559.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166+2966C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511856 | ||||||
| chr1:217511981
|
G | A | 1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1166+2841C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217511981 | ||||||
| chr1:217512239
|
G | T | 109 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(106): Show | 109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1166+2583C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217512239 | ||||||
| chr1:217512322
|
T | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1166+2500A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217512322 | ||||||
| chr1:217512700
|
T | C | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1166+2122A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217512700 | ||||||
| chr1:217512854
|
T | C | 1 | a0001c0001t0007g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1166+1968A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217512854 | ||||||
| chr1:217512977
|
A | C | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+1845T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217512977 | ||||||
| chr1:217513024
|
T | A | 3 | a0001c0001t0003g0059a0001c0001t0011g0149a0001c0001t0029g0042 | 3 | HG01106.hp1 HG01175.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1166+1798A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217513024 | ||||||
| chr1:217513163
|
G | A | 2 | a0001c0001t0003g0006a0001c0001t0003g0048 | 2 | HG00621.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1166+1659C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217513163 | ||||||
| chr1:217513180
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1166+1642T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217513180 | ||||||
| chr1:217513205
|
C | T | 1 | a0002c0002t0039g0162 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1166+1617G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217513205 | ||||||
| chr1:217513320
|
C | T | 1 | a0001c0001t0008g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1166+1502G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217513320 | ||||||
| chr1:217513727
|
G | A | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1166+1095C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217513727 | ||||||
| chr1:217513981
|
C | A | 98 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(95): Show | 98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1166+841G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217513981 | ||||||
| chr1:217514010
|
A | C | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1166+812T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514010 | ||||||
| chr1:217514079
|
G | T | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1166+743C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514079 | ||||||
| chr1:217514082
|
C | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0045others(9): Show | 12 | HG00738.hp1 HG01071.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1166+740G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514082 | ||||||
| chr1:217514129
|
C | T | 1 | a0002c0002t0019g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1166+693G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514129 | ||||||
| chr1:217514132
|
G | A | 4 | a0001c0001t0011g0166a0001c0001t0015g0175a0001c0001t0015g0176others(1): Show | 4 | HG02698.hp2 HG03669.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1166+690C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514132 | ||||||
| chr1:217514141
|
G | A | 98 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(95): Show | 98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1166+681C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514141 | ||||||
| chr1:217514476
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1166+346C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514476 | ||||||
| chr1:217514516
|
G | GTACGAAA others(34): Show |
1 | a0001c0001t0001g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1166+265_1166+305d others(43): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217514516 | ||||||
| chr1:217515066
|
C | T | 100 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(97): Show | 100 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1099-177G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515066 | ||||||
| chr1:217515100
|
A | AT | 10 | a0001c0001t0006g0173a0001c0001t0007g0013a0001c0001t0022g0183others(7): Show | 10 | HG00738.hp1 HG01891.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-212dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515100 | ||||||
| chr1:217515565
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-676C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515565 | ||||||
| chr1:217515600
|
C | T | 100 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(97): Show | 100 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1099-711G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515600 | ||||||
| chr1:217515614
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-725G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515614 | ||||||
| chr1:217515705
|
C | CTCAAAAT others(22): Show |
1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1099-845_1099-817d others(31): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515705 | ||||||
| chr1:217515768
|
TA | T | 8 | a0001c0001t0001g0054a0001c0001t0003g0039a0001c0001t0006g0173others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-880delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515768 | ||||||
| chr1:217515769
|
A | T | 10 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-880T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515769 | ||||||
| chr1:217515799
|
T | TA | 58 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(55): Show | 58 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1099-911dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515799 | ||||||
| chr1:217515799
|
TA | T | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1099-911delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515799 | ||||||
| chr1:217515926
|
G | C | 1 | a0001c0001t0007g0012 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1099-1037C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515926 | ||||||
| chr1:217516034
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-1145A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516034 | ||||||
| chr1:217516158
|
T | A | 11 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-1269A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516158 | ||||||
| chr1:217516211
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-1322C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516211 | ||||||
| chr1:217516227
|
AT | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(110): Show | 113 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1099-1339delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516227 | ||||||
| chr1:217516231
|
T | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-1342A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516231 | ||||||
| chr1:217516231
|
TA | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0017others(55): Show | 58 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.1099-1343delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516231 | ||||||
| chr1:217516295
|
C | T | 1 | a0001c0001t0009g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1099-1406G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516295 | ||||||
| chr1:217516694
|
C | T | 1 | a0001c0001t0006g0143 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1099-1805G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516694 | ||||||
| chr1:217516824
|
C | A | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-1935G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516824 | ||||||
| chr1:217516853
|
A | C | 1 | a0001c0001t0001g0026 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1099-1964T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516853 | ||||||
| chr1:217516867
|
T | G | 2 | a0001c0001t0003g0059a0001c0001t0011g0149 | 2 | HG01175.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1099-1978A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516867 | ||||||
| chr1:217516931
|
T | C | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-2042A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516931 | ||||||
| chr1:217517053
|
A | G | 1 | a0001c0001t0020g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1099-2164T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217517053 | ||||||
| chr1:217517065
|
ATAATCAT others(9): Show |
A | 1 | a0001c0001t0004g0154 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1099-2192_1099-217 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217517065 | ||||||
| chr1:217517066
|
T | G | 1 | a0001c0001t0002g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1099-2177A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217517066 | ||||||
| chr1:217517576
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-2687T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217517576 | ||||||
| chr1:217517765
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-2876G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217517765 | ||||||
| chr1:217518054
|
A | G | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1099-3165T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217518054 | ||||||
| chr1:217518089
|
T | C | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1099-3200A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217518089 | ||||||
| chr1:217518311
|
A | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-3422T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217518311 | ||||||
| chr1:217518560
|
A | G | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-3671T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217518560 | ||||||
| chr1:217518616
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-3727T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217518616 | ||||||
| chr1:217518617
|
G | GATTAATA others(35): Show |
1 | a0001c0001t0002g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1099-3770_1099-372 others(46): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217518617 | ||||||
| chr1:217518689
|
A | T | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-3800T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217518689 | ||||||
| chr1:217519300
|
A | C | 1 | a0001c0001t0009g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1099-4411T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217519300 | ||||||
| chr1:217519428
|
G | A | 1 | a0001c0001t0011g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1099-4539C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217519428 | ||||||
| chr1:217519695
|
C | CAAGGCTT others(5): Show |
1 | a0001c0007t0002g0147 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1099-4818_1099-480 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217519695 | ||||||
| chr1:217519710
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-4821C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217519710 | ||||||
| chr1:217519835
|
A | G | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-4946T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217519835 | ||||||
| chr1:217519947
|
A | G | 98 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(95): Show | 98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1099-5058T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217519947 | ||||||
| chr1:217520147
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-5258A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520147 | ||||||
| chr1:217520151
|
C | T | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-5262G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520151 | ||||||
| chr1:217520225
|
T | C | 2 | a0001c0001t0005g0085a0001c0001t0008g0096 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1099-5336A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520225 | ||||||
| chr1:217520499
|
T | C | 98 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(95): Show | 98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1099-5610A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520499 | ||||||
| chr1:217520504
|
A | T | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-5615T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520504 | ||||||
| chr1:217520534
|
G | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-5645C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520534 | ||||||
| chr1:217520611
|
CTGATTAT others(30): Show |
C | 1 | a0001c0001t0002g0159 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1099-5759_1099-572 others(41): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520611 | ||||||
| chr1:217520640
|
A | G | 4 | a0001c0001t0002g0118a0001c0001t0003g0077a0001c0001t0007g0075others(1): Show | 4 | HG01884.hp1 HG02735.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-5751T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520640 | ||||||
| chr1:217520760
|
C | G | 1 | a0001c0001t0038g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1099-5871G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520760 | ||||||
| chr1:217520862
|
G | A | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-5973C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520862 | ||||||
| chr1:217520884
|
G | A | 9 | a0001c0001t0004g0152a0001c0001t0004g0179a0001c0001t0009g0178others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-5995C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520884 | ||||||
| chr1:217520996
|
C | T | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-6107G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217520996 | ||||||
| chr1:217521079
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0002g0131others(3): Show | 6 | HG01109.hp2 HG02145.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-6190G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521079 | ||||||
| chr1:217521215
|
C | T | 2 | a0001c0001t0014g0084a0001c0001t0023g0002 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1099-6326G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521215 | ||||||
| chr1:217521324
|
A | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0091a0001c0001t0002g0148others(13): Show | 16 | HG00099.hp2 HG00558.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099-6435T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521324 | ||||||
| chr1:217521358
|
C | CAAAAAA | 49 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1099-6475_1099-647 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521358 | ||||||
| chr1:217521358
|
C | CAAAAAAA | 19 | a0001c0001t0002g0104a0001c0001t0002g0148a0001c0001t0003g0009others(16): Show | 19 | HG00597.hp1 HG00609.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1099-6476_1099-647 others(11): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521358 | ||||||
| chr1:217521358
|
C | CAAAAAAA others(1): Show |
78 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(75): Show | 78 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1099-6477_1099-647 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521358 | ||||||
| chr1:217521358
|
C | CAAAAAAA others(2): Show |
16 | a0001c0001t0001g0029a0001c0001t0002g0131a0001c0001t0002g0132others(13): Show | 16 | HG01106.hp1 HG01358.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099-6478_1099-647 others(13): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521358 | ||||||
| chr1:217521358
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-6479_1099-647 others(14): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521358 | ||||||
| chr1:217521529
|
T | G | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-6640A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521529 | ||||||
| chr1:217521640
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-6751G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521640 | ||||||
| chr1:217521655
|
C | T | 1 | a0001c0001t0003g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099-6766G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521655 | ||||||
| chr1:217521687
|
A | T | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-6798T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521687 | ||||||
| chr1:217521849
|
T | C | 40 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-6960A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521849 | ||||||
| chr1:217521948
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-7059A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521948 | ||||||
| chr1:217521956
|
A | T | 11 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-7067T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521956 | ||||||
| chr1:217521966
|
G | A | 1 | a0004c0006t0001g0053 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1099-7077C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217521966 | ||||||
| chr1:217522016
|
T | A | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-7127A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522016 | ||||||
| chr1:217522065
|
T | A | 1 | a0001c0001t0016g0086 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1099-7176A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522065 | ||||||
| chr1:217522119
|
A | G | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-7230T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522119 | ||||||
| chr1:217522149
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1099-7260A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522149 | ||||||
| chr1:217522299
|
GATTAATC others(7): Show |
G | 2 | a0001c0001t0004g0102a0001c0004t0008g0119 | 2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1099-7424_1099-741 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522299 | ||||||
| chr1:217522314
|
A | C | 2 | a0001c0001t0004g0102a0001c0004t0008g0119 | 2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1099-7425T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522314 | ||||||
| chr1:217522380
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-7491A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522380 | ||||||
| chr1:217522432
|
G | T | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-7543C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522432 | ||||||
| chr1:217522447
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-7558C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522447 | ||||||
| chr1:217522496
|
G | T | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(55): Show | 58 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1099-7607C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522496 | ||||||
| chr1:217522564
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1099-7675T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522564 | ||||||
| chr1:217522567
|
T | A | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-7678A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522567 | ||||||
| chr1:217522610
|
A | G | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-7721T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522610 | ||||||
| chr1:217522695
|
AGATTGGC others(1609): Show |
A | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-9422_1099-780 others(4): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522695 | ||||||
| chr1:217522767
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1099-7878A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522767 | ||||||
| chr1:217522831
|
T | TAC | 9 | a0001c0001t0002g0118a0001c0001t0004g0130a0001c0001t0004g0152others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-7944_1099-794 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522831 | ||||||
| chr1:217522831
|
T | TACACAC | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-7948_1099-794 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217522831 | ||||||
| chr1:217523124
|
A | C | 55 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(52): Show | 55 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1099-8235T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523124 | ||||||
| chr1:217523175
|
A | T | 64 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(61): Show | 64 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1099-8286T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523175 | ||||||
| chr1:217523363
|
G | T | 1 | a0001c0001t0003g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1099-8474C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523363 | ||||||
| chr1:217523411
|
A | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(37): Show | 40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-8522T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523411 | ||||||
| chr1:217523518
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-8629C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523518 | ||||||
| chr1:217523524
|
A | G | 3 | a0001c0001t0003g0006a0001c0001t0003g0039a0001c0001t0003g0048 | 3 | HG00621.hp2 NA18994.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1099-8635T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523524 | ||||||
| chr1:217523699
|
AGACGGGG others(119): Show |
A | 2 | a0001c0001t0002g0099a0001c0001t0002g0121 | 2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1099-8936_1099-881 others(4): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523699 | ||||||
| chr1:217523702
|
C | CG | 6 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0073others(3): Show | 6 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-8814dupC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523702 | ||||||
| chr1:217523703
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-8814C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523703 | ||||||
| chr1:217523707
|
TGGTGGCC others(168): Show |
T | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1099-8993_1099-881 others(4): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523707 | ||||||
| chr1:217523708
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0044g0115a0002c0002t0012g0007 | 3 | HG04199.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1099-8819C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523708 | ||||||
| chr1:217523715
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0044g0115a0002c0002t0012g0007 | 3 | HG04199.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1099-8826C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523715 | ||||||
| chr1:217523747
|
C | A | 4 | a0001c0001t0006g0173a0001c0001t0033g0081a0001c0001t0041g0181others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-8858G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523747 | ||||||
| chr1:217523747
|
C | T | 26 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0024others(23): Show | 26 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1099-8858G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523747 | ||||||
| chr1:217523780
|
G | C | 1 | a0001c0001t0002g0139 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1099-8891C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523780 | ||||||
| chr1:217523795
|
G | GC | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-8907_1099-890 others(5): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523795 | ||||||
| chr1:217523796
|
T | A | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-8907A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523796 | ||||||
| chr1:217523796
|
T | C | 62 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(59): Show | 62 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1099-8907A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523796 | ||||||
| chr1:217523806
|
A | AC | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(37): Show | 40 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1099-8918dupG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523806 | ||||||
| chr1:217523829
|
G | A | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-8940C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523829 | ||||||
| chr1:217523833
|
TGGCTGGC others(42): Show |
T | 1 | a0001c0001t0011g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1099-8993_1099-894 others(53): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523833 | ||||||
| chr1:217523885
|
CTGGCCGG others(42): Show |
C | 39 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1099-9045_1099-899 others(53): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523885 | ||||||
| chr1:217523889
|
C | T | 1 | a0002c0002t0013g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1099-9000G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523889 | ||||||
| chr1:217523905
|
CCCCCACA others(41): Show |
C | 1 | a0001c0001t0004g0154 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1099-9064_1099-901 others(52): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523905 | ||||||
| chr1:217523922
|
C | T | 1 | a0001c0001t0021g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1099-9033G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523922 | ||||||
| chr1:217523926
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1099-9037G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523926 | ||||||
| chr1:217523929
|
G | A | 2 | a0001c0001t0004g0127a0001c0001t0006g0128 | 2 | HG01106.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1099-9040C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523929 | ||||||
| chr1:217523932
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1099-9043T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523932 | ||||||
| chr1:217523934
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1099-9045A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523934 | ||||||
| chr1:217523944
|
G | A | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-9055C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523944 | ||||||
| chr1:217523971
|
C | T | 13 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0118others(10): Show | 13 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-9082G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523971 | ||||||
| chr1:217524035
|
T | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(103): Show | 106 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1099-9146A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524035 | ||||||
| chr1:217524100
|
G | A | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-9211C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524100 | ||||||
| chr1:217524102
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0004g0130 | 2 | HG02735.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1099-9213G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524102 | ||||||
| chr1:217524104
|
G | T | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-9215C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524104 | ||||||
| chr1:217524124
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1099-9235G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524124 | ||||||
| chr1:217524154
|
CGGGCGGA others(31): Show |
C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-9303_1099-926 others(42): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524154 | ||||||
| chr1:217524185
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1099-9296G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524185 | ||||||
| chr1:217524186
|
G | A | 40 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-9297C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524186 | ||||||
| chr1:217524197
|
G | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-9308C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524197 | ||||||
| chr1:217524203
|
GCTCCTCA others(33): Show |
G | 40 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-9354_1099-931 others(44): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524203 | ||||||
| chr1:217524260
|
C | T | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1099-9371G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524260 | ||||||
| chr1:217524266
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1099-9377C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524266 | ||||||
| chr1:217524283
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-9394G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524283 | ||||||
| chr1:217524316
|
A | T | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-9427T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524316 | ||||||
| chr1:217524319
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-9430G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524319 | ||||||
| chr1:217524320
|
G | A | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-9431C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524320 | ||||||
| chr1:217524321
|
C | A | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-9432G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524321 | ||||||
| chr1:217524325
|
T | C | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-9436A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524325 | ||||||
| chr1:217524349
|
T | C | 2 | a0001c0001t0004g0154a0001c0001t0020g0160 | 2 | HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1099-9460A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524349 | ||||||
| chr1:217524435
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-9546G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524435 | ||||||
| chr1:217524436
|
G | A | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-9547C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524436 | ||||||
| chr1:217524453
|
C | CG | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG00673.hp1 HG00738.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-9565dupC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524453 | ||||||
| chr1:217524480
|
A | C | 4 | a0001c0001t0001g0024a0001c0001t0003g0006a0001c0001t0003g0039others(1): Show | 4 | HG00621.hp2 HG00673.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-9591T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524480 | ||||||
| chr1:217524484
|
C | G | 4 | a0001c0001t0001g0024a0001c0001t0003g0006a0001c0001t0003g0039others(1): Show | 4 | HG00621.hp2 HG00673.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-9595G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524484 | ||||||
| chr1:217524488
|
T | A | 4 | a0001c0001t0001g0024a0001c0001t0003g0006a0001c0001t0003g0039others(1): Show | 4 | HG00621.hp2 HG00673.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-9599A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524488 | ||||||
| chr1:217524490
|
T | C | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-9601A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524490 | ||||||
| chr1:217524493
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0003g0006a0001c0001t0003g0039others(1): Show | 4 | HG00621.hp2 HG00673.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-9604T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524493 | ||||||
| chr1:217524537
|
T | C | 160 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(157): Show | 160 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.1099-9648A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524537 | ||||||
| chr1:217524564
|
C | G | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-9675G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524564 | ||||||
| chr1:217524616
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-9727G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524616 | ||||||
| chr1:217524625
|
G | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-9736C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524625 | ||||||
| chr1:217524634
|
G | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-9745C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524634 | ||||||
| chr1:217524683
|
A | T | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-9794T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524683 | ||||||
| chr1:217524706
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-9817G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524706 | ||||||
| chr1:217524707
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-9818C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524707 | ||||||
| chr1:217524754
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099-9865C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524754 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(119): Show |
1 | a0001c0001t0015g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1099-9959_1099-995 others(130): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(77): Show |
1 | a0001c0001t0002g0139 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1099-9959_1099-995 others(88): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(91): Show |
1 | a0001c0001t0005g0050 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1099-9959_1099-995 others(102): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(98): Show |
2 | a0001c0001t0003g0052a0001c0001t0005g0095 | 2 | HG03654.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1099-9959_1099-995 others(109): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(105): Show |
1 | a0001c0001t0005g0051 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1099-9959_1099-995 others(116): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(119): Show |
2 | a0001c0001t0002g0161a0001c0001t0005g0020 | 2 | NA19077.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1099-9959_1099-995 others(130): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(126): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0067 | 2 | HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1099-9959_1099-995 others(137): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(133): Show |
2 | a0001c0001t0001g0066a0001c0001t0035g0035 | 2 | HG02559.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1099-9959_1099-995 others(144): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(140): Show |
4 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0003g0072others(1): Show | 4 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-9959_1099-995 others(151): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(154): Show |
3 | a0001c0001t0001g0068a0001c0001t0002g0164a0001c0001t0003g0058 | 3 | HG02040.hp2 HG02155.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1099-9959_1099-995 others(165): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(168): Show |
2 | a0001c0001t0001g0026a0001c0001t0007g0004 | 2 | HG01167.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1099-9959_1099-995 others(179): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(182): Show |
1 | a0001c0001t0005g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1099-9959_1099-995 others(193): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGAAA others(231): Show |
1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1099-9959_1099-995 others(242): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524847
|
C | CGTGGACA others(63): Show |
1 | a0001c0001t0003g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1099-9959_1099-995 others(74): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524847 | ||||||
| chr1:217524848
|
G | GTGGAAAG others(568): Show |
1 | a0002c0002t0008g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1099-9960_1099-995 others(579): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524848 | ||||||
| chr1:217524848
|
G | GTGGAAAG others(369): Show |
1 | a0001c0001t0002g0159 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1099-9960_1099-995 others(380): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524848 | ||||||
| chr1:217524849
|
G | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(80): Show | 83 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1099-9960C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524849 | ||||||
| chr1:217524853
|
G | A | 78 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(75): Show | 78 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.1099-9964C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524853 | ||||||
| chr1:217524857
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1099-9968C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524857 | ||||||
| chr1:217524861
|
A | AGGGGAGA others(50): Show |
3 | a0001c0001t0011g0166a0001c0001t0015g0176a0001c0001t0021g0177 | 3 | HG02698.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1099-10029_1099-99 others(62): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524861 | ||||||
| chr1:217524861
|
A | G | 16 | a0001c0001t0001g0073a0001c0001t0001g0091a0001c0001t0002g0148others(13): Show | 16 | HG00099.hp2 HG00558.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099-9972T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524861 | ||||||
| chr1:217524862
|
G | GA | 6 | a0001c0001t0001g0044a0001c0001t0002g0122a0001c0001t0002g0123others(3): Show | 6 | HG00609.hp2 HG01256.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-9974_1099-997 others(5): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524862 | ||||||
| chr1:217524862
|
G | GAGA | 16 | a0001c0001t0001g0073a0001c0001t0001g0091a0001c0001t0002g0148others(13): Show | 16 | HG00099.hp2 HG00558.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099-9974_1099-997 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524862 | ||||||
| chr1:217524862
|
G | GGA | 13 | a0001c0001t0002g0099a0001c0001t0002g0118a0001c0001t0004g0154others(10): Show | 13 | HG01168.hp1 HG01891.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-9974_1099-997 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524862 | ||||||
| chr1:217524862
|
G | GGAAGAGG others(280): Show |
1 | a0001c0001t0012g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1099-9974_1099-997 others(291): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524862 | ||||||
| chr1:217524862
|
G | GGAGGGAG others(92): Show |
1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-9974_1099-997 others(103): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524862 | ||||||
| chr1:217524864
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-9975C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524864 | ||||||
| chr1:217524866
|
A | G | 34 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-9977T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524866 | ||||||
| chr1:217524868
|
AG | A | 5 | a0001c0001t0002g0159a0001c0001t0005g0033a0001c0001t0010g0134others(2): Show | 5 | HG01167.hp1 HG01496.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-9980delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524868 | ||||||
| chr1:217524869
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0004g0130 | 2 | HG03225.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1099-9980C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GA | 34 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00597.hp1 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-9981_1099-998 others(5): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGA | 5 | a0001c0001t0002g0118a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02615.hp1 HG02735.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-9981_1099-998 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(448): Show |
1 | a0001c0001t0002g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(459): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(621): Show |
1 | a0001c0001t0004g0154 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(632): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(561): Show |
1 | a0001c0001t0001g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(572): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(238): Show |
1 | a0001c0001t0011g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(249): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(304): Show |
1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(315): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(316): Show |
1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(327): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(603): Show |
1 | a0001c0001t0001g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(614): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(442): Show |
1 | a0001c0001t0004g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(453): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(472): Show |
1 | a0001c0001t0029g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(483): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(478): Show |
1 | a0001c0001t0002g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(489): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(496): Show |
1 | a0001c0001t0003g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(507): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(508): Show |
1 | a0001c0001t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(519): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(514): Show |
1 | a0001c0001t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(525): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(520): Show |
1 | a0002c0002t0019g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(531): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(592): Show |
1 | a0001c0001t0002g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(603): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(616): Show |
1 | a0001c0001t0002g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(627): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(772): Show |
1 | a0001c0001t0002g0123 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(783): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524869
|
G | GGGAGAGG others(416): Show |
1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1099-9981_1099-998 others(427): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524869 | ||||||
| chr1:217524872
|
G | A | 7 | a0001c0001t0002g0099a0001c0001t0006g0173a0001c0001t0022g0183others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-9983C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524872 | ||||||
| chr1:217524873
|
A | AGAGGGGG | 2 | a0001c0001t0011g0141a0001c0001t0012g0088 | 2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1099-9991_1099-998 others(11): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524873 | ||||||
| chr1:217524873
|
A | AGAGGGGG others(1): Show |
2 | a0001c0001t0043g0142a0001c0004t0008g0097 | 2 | HG01243.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1099-9992_1099-998 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524873 | ||||||
| chr1:217524873
|
A | AGAGGGGG others(7): Show |
1 | a0003c0003t0010g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1099-9998_1099-998 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524873 | ||||||
| chr1:217524873
|
A | AGAGGGGG others(85): Show |
1 | a0002c0002t0019g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1099-9985_1099-998 others(96): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524873 | ||||||
| chr1:217524873
|
A | G | 7 | a0001c0001t0002g0099a0001c0001t0006g0173a0001c0001t0022g0183others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-9984T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524873 | ||||||
| chr1:217524873
|
AGAGGGGG | A | 2 | a0001c0001t0009g0187a0001c0001t0017g0101 | 2 | HG01168.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1099-9991_1099-998 others(11): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524873 | ||||||
| chr1:217524875
|
A | G | 9 | a0001c0001t0002g0099a0001c0001t0003g0059a0001c0001t0006g0173others(6): Show | 9 | HG01175.hp2 HG01891.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-9986T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524875 | ||||||
| chr1:217524876
|
G | GGGAGAGG others(77): Show |
1 | a0001c0001t0005g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1099-9988_1099-998 others(88): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524876 | ||||||
| chr1:217524876
|
G | GGGGGAGG others(4): Show |
2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1099-9988_1099-998 others(15): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524876 | ||||||
| chr1:217524877
|
G | GCGAGAGG others(68): Show |
1 | a0001c0001t0001g0038 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1099-9989_1099-998 others(79): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524877 | ||||||
| chr1:217524877
|
G | GCGAGAGG others(96): Show |
1 | a0001c0001t0001g0036 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1099-9989_1099-998 others(107): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524877 | ||||||
| chr1:217524877
|
G | GCGAGAGG others(110): Show |
1 | a0001c0001t0002g0168 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1099-9989_1099-998 others(121): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524877 | ||||||
| chr1:217524877
|
G | GGGAGAGG others(89): Show |
1 | a0001c0001t0001g0041 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1099-9989_1099-998 others(100): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524877 | ||||||
| chr1:217524878
|
G | A | 7 | a0001c0001t0002g0099a0001c0001t0006g0173a0001c0001t0022g0183others(4): Show | 7 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-9989C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524878 | ||||||
| chr1:217524878
|
G | GAGA | 39 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1099-9990_1099-998 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524878 | ||||||
| chr1:217524879
|
G | A | 10 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0082others(7): Show | 10 | HG01175.hp2 HG01243.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-9990C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524879 | ||||||
| chr1:217524880
|
G | A | 31 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0037others(28): Show | 31 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1099-9991C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524880 | ||||||
| chr1:217524880
|
GGAGGGGG others(16): Show |
G | 9 | a0001c0001t0002g0104a0001c0001t0006g0146a0001c0001t0009g0105others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-10014_1099-99 others(28): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524880 | ||||||
| chr1:217524881
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-9992C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524881 | ||||||
| chr1:217524882
|
A | G | 16 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0082others(13): Show | 16 | HG01175.hp2 HG01243.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099-9993T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524882 | ||||||
| chr1:217524883
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1099-9994C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524883 | ||||||
| chr1:217524883
|
G | GA | 39 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1099-9995_1099-999 others(5): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524883 | ||||||
| chr1:217524884
|
G | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(11): Show | 14 | HG01071.hp1 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-9995C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524884 | ||||||
| chr1:217524885
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0082others(5): Show | 8 | HG01175.hp2 HG01243.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-9996C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524885 | ||||||
| chr1:217524887
|
G | A | 69 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(66): Show | 69 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1099-9998C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524887 | ||||||
| chr1:217524888
|
G | A | 1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1099-9999C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524888 | ||||||
| chr1:217524889
|
A | G | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0082others(19): Show | 22 | HG01175.hp2 HG01243.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-10000T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524889 | ||||||
| chr1:217524890
|
G | A | 10 | a0001c0001t0002g0099a0001c0001t0004g0130a0001c0001t0006g0173others(7): Show | 10 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-10001C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524890 | ||||||
| chr1:217524891
|
G | A | 12 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0036others(9): Show | 12 | HG01071.hp1 HG01175.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099-10002C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524891 | ||||||
| chr1:217524892
|
G | A | 4 | a0001c0001t0005g0033a0001c0001t0007g0075a0001c0001t0009g0098others(1): Show | 4 | HG01496.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-10003C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524892 | ||||||
| chr1:217524892
|
G | GAGA | 37 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(34): Show | 37 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1099-10004_1099-10 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524892 | ||||||
| chr1:217524893
|
G | A | 2 | a0001c0001t0002g0118a0001c0001t0002g0159 | 2 | HG01167.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1099-10004C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524893 | ||||||
| chr1:217524894
|
G | A | 32 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0037others(29): Show | 32 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1099-10005C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524894 | ||||||
| chr1:217524895
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-10006C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524895 | ||||||
| chr1:217524896
|
A | AGGGGGGA others(52): Show |
1 | a0001c0001t0015g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1099-10008_1099-10 others(65): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524896 | ||||||
| chr1:217524896
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0082others(10): Show | 13 | HG01175.hp2 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-10007T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524896 | ||||||
| chr1:217524896
|
AGGGGGGA others(8): Show |
A | 1 | a0001c0001t0002g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1099-10022_1099-10 others(21): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524896 | ||||||
| chr1:217524897
|
G | A | 9 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0082others(6): Show | 9 | HG01175.hp2 HG01243.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-10008C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524897 | ||||||
| chr1:217524898
|
G | A | 46 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(43): Show | 46 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1099-10009C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524898 | ||||||
| chr1:217524901
|
G | A | 30 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0037others(27): Show | 30 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1099-10012C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524901 | ||||||
| chr1:217524902
|
G | A | 37 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(34): Show | 37 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1099-10013C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524902 | ||||||
| chr1:217524903
|
A | G | 41 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(38): Show | 41 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-10014T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524903 | ||||||
| chr1:217524904
|
G | A | 60 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(57): Show | 60 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1099-10015C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524904 | ||||||
| chr1:217524904
|
G | GGGGGA | 6 | a0001c0001t0001g0082a0001c0001t0002g0121a0001c0001t0002g0131others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-10016_1099-10 others(11): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524904 | ||||||
| chr1:217524904
|
G | GGGGGAGG others(28): Show |
1 | a0001c0001t0003g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1099-10016_1099-10 others(41): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524904 | ||||||
| chr1:217524904
|
G | GGGGGAGG others(40): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1099-10016_1099-10 others(53): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524904 | ||||||
| chr1:217524904
|
G | GGGGGAGG others(46): Show |
1 | a0001c0001t0011g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1099-10016_1099-10 others(59): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524904 | ||||||
| chr1:217524905
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(1): Show | 4 | HG01071.hp1 HG01358.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-10016C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524905 | ||||||
| chr1:217524906
|
G | A | 1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1099-10017C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524906 | ||||||
| chr1:217524907
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-10018C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524907 | ||||||
| chr1:217524908
|
G | A | 67 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(64): Show | 67 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1099-10019C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524908 | ||||||
| chr1:217524910
|
A | AG | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0017others(8): Show | 11 | HG00738.hp1 HG01071.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-10022dupC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524910 | ||||||
| chr1:217524910
|
A | AGGGGGGA others(8): Show |
1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1099-10022_1099-10 others(21): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524910 | ||||||
| chr1:217524910
|
A | G | 2 | a0001c0001t0017g0116a0001c0001t0032g0056 | 2 | HG01433.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1099-10021T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524910 | ||||||
| chr1:217524910
|
AG | A | 27 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0057others(24): Show | 27 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1099-10022delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524910 | ||||||
| chr1:217524911
|
G | GA | 4 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041others(1): Show | 4 | HG01071.hp1 HG01358.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-10023_1099-10 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524911 | ||||||
| chr1:217524911
|
G | GGGGAGAG others(118): Show |
1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1099-10023_1099-10 others(131): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524911 | ||||||
| chr1:217524912
|
G | A | 1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1099-10023C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524912 | ||||||
| chr1:217524914
|
G | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1099-10025C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524914 | ||||||
| chr1:217524917
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-10028C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524917 | ||||||
| chr1:217524918
|
G | A | 33 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(30): Show | 33 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1099-10029C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524918 | ||||||
| chr1:217524918
|
G | GGGGGAGA others(35): Show |
1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-10030_1099-10 others(48): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524918 | ||||||
| chr1:217524918
|
GGGGGAGA others(7): Show |
G | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1099-10043_1099-10 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524918 | ||||||
| chr1:217524919
|
G | A | 2 | a0001c0001t0002g0118a0001c0001t0010g0134 | 2 | HG02735.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1099-10030C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524919 | ||||||
| chr1:217524919
|
G | GAGA | 38 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 38 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1099-10031_1099-10 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524919 | ||||||
| chr1:217524919
|
G | GGGA | 12 | a0001c0001t0001g0029a0001c0001t0001g0054a0001c0001t0001g0082others(9): Show | 12 | HG01175.hp2 HG01884.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099-10031_1099-10 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524919 | ||||||
| chr1:217524920
|
GGGA | G | 16 | a0001c0001t0002g0104a0001c0001t0006g0146a0001c0001t0006g0173others(13): Show | 16 | HG00597.hp1 HG00609.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099-10034_1099-10 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524920 | ||||||
| chr1:217524920
|
GGGAGAGG others(3): Show |
G | 2 | a0001c0001t0003g0009a0001c0001t0004g0130 | 2 | HG03225.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1099-10041_1099-10 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524920 | ||||||
| chr1:217524921
|
G | A | 1 | a0001c0001t0005g0051 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1099-10032C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524921 | ||||||
| chr1:217524922
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1099-10033C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524922 | ||||||
| chr1:217524923
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0001g0082a0001c0001t0002g0099others(10): Show | 13 | HG01175.hp2 HG01884.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-10034T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524923 | ||||||
| chr1:217524925
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0002g0121a0001c0001t0006g0180 | 3 | HG01243.hp2 HG03486.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1099-10036T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524925 | ||||||
| chr1:217524925
|
AG | A | 21 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0073others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1099-10037delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524925 | ||||||
| chr1:217524926
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-10037C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(551): Show |
1 | a0001c0001t0001g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(564): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(196): Show |
1 | a0001c0001t0001g0054 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(209): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(274): Show |
1 | a0001c0001t0006g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(287): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(334): Show |
1 | a0001c0007t0002g0147 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(347): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(346): Show |
1 | a0001c0001t0001g0022 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(359): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(370): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0049 | 2 | HG02145.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1099-10038_1099-10 others(383): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(406): Show |
1 | a0001c0001t0001g0024 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(419): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(412): Show |
1 | a0001c0001t0003g0048 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(425): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(430): Show |
1 | a0001c0001t0001g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(443): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(454): Show |
1 | a0001c0001t0003g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(467): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(502): Show |
2 | a0001c0001t0001g0034a0001c0001t0020g0160 | 2 | HG01515.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1099-10038_1099-10 others(515): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(520): Show |
1 | a0001c0001t0003g0039 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(533): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(538): Show |
1 | a0001c0001t0001g0018 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(551): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(556): Show |
1 | a0001c0001t0003g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(569): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524926
|
G | GGGAGAGG others(652): Show |
1 | a0001c0001t0026g0090 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1099-10038_1099-10 others(665): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524926 | ||||||
| chr1:217524927
|
G | GGGAGAGG others(82): Show |
1 | a0001c0001t0001g0060 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1099-10039_1099-10 others(95): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524927 | ||||||
| chr1:217524927
|
G | GGGAGAGG others(89): Show |
1 | a0001c0001t0001g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1099-10039_1099-10 others(102): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524927 | ||||||
| chr1:217524927
|
G | GGGAGAGG others(131): Show |
1 | a0001c0001t0001g0062 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1099-10039_1099-10 others(144): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524927 | ||||||
| chr1:217524927
|
G | GGGAGAGG others(138): Show |
1 | a0001c0001t0001g0063 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1099-10039_1099-10 others(151): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524927 | ||||||
| chr1:217524928
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0002g0124 | 2 | HG03688.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1099-10039C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524928 | ||||||
| chr1:217524929
|
GA | G | 14 | a0001c0001t0002g0104a0001c0001t0003g0059a0001c0001t0003g0077others(11): Show | 14 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-10041delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524929 | ||||||
| chr1:217524930
|
A | G | 15 | a0001c0001t0001g0028a0001c0001t0001g0082a0001c0001t0002g0099others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-10041T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524930 | ||||||
| chr1:217524931
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1099-10042C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524931 | ||||||
| chr1:217524932
|
A | G | 5 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0124others(2): Show | 5 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-10043T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524932 | ||||||
| chr1:217524932
|
AG | A | 49 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(46): Show | 49 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1099-10044delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524932 | ||||||
| chr1:217524933
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0002g0099 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-10044C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524933 | ||||||
| chr1:217524933
|
G | GA | 2 | a0001c0001t0001g0028a0001c0001t0003g0089 | 2 | HG00558.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1099-10045_1099-10 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524933 | ||||||
| chr1:217524933
|
G | GGGGAGA | 4 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0002g0168others(1): Show | 4 | HG00741.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-10050_1099-10 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524933 | ||||||
| chr1:217524933
|
G | GGGGAGAG others(17): Show |
1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1099-10045_1099-10 others(30): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524933 | ||||||
| chr1:217524933
|
G | GGGGAGAG others(336): Show |
1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1099-10045_1099-10 others(349): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524933 | ||||||
| chr1:217524936
|
GA | G | 17 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0003g0059others(14): Show | 17 | HG00597.hp1 HG00609.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1099-10048delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524936 | ||||||
| chr1:217524937
|
A | AGAGGGAG others(166): Show |
1 | a0001c0001t0002g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1099-10049_1099-10 others(179): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524937 | ||||||
| chr1:217524939
|
A | G | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1099-10050T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524939 | ||||||
| chr1:217524943
|
A | G | 11 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1099-10054T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524943 | ||||||
| chr1:217524944
|
G | C | 1 | a0002c0002t0013g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1099-10055C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524944 | ||||||
| chr1:217525069
|
T | C | 2 | a0001c0001t0002g0114a0001c0001t0002g0121 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1099-10180A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525069 | ||||||
| chr1:217525265
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0002g0157 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1099-10376A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525265 | ||||||
| chr1:217525266
|
A | G | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-10377T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525266 | ||||||
| chr1:217525391
|
ATCTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1099-10513_1099-10 others(17): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525391 | ||||||
| chr1:217525400
|
A | C | 1 | a0001c0001t0006g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1099-10511T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525400 | ||||||
| chr1:217525514
|
C | T | 5 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0033g0081others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-10625G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525514 | ||||||
| chr1:217525882
|
C | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-10993G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525882 | ||||||
| chr1:217525949
|
G | C | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-11060C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217525949 | ||||||
| chr1:217526022
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1099-11133G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526022 | ||||||
| chr1:217526026
|
G | T | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-11137C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526026 | ||||||
| chr1:217526106
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1099-11217G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526106 | ||||||
| chr1:217526123
|
G | GA | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-11235dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526123 | ||||||
| chr1:217526159
|
G | A | 5 | a0001c0001t0011g0141a0001c0001t0012g0088a0001c0001t0034g0027others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-11270C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526159 | ||||||
| chr1:217526306
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1099-11417T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526306 | ||||||
| chr1:217526364
|
T | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-11475A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526364 | ||||||
| chr1:217526461
|
A | C | 100 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(97): Show | 100 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1099-11572T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526461 | ||||||
| chr1:217526474
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-11585G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526474 | ||||||
| chr1:217526480
|
G | C | 1 | a0001c0001t0002g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1099-11591C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526480 | ||||||
| chr1:217526502
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0002g0099 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-11613T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526502 | ||||||
| chr1:217526657
|
C | T | 9 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-11768G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217526657 | ||||||
| chr1:217527053
|
G | GAATTATT others(30): Show |
4 | a0001c0001t0004g0152a0001c0001t0004g0179a0001c0001t0009g0178others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-12201_1099-12 others(43): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527053 | ||||||
| chr1:217527053
|
GAATTATT others(30): Show |
G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0159others(2): Show | 5 | HG01167.hp1 HG01361.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-12201_1099-12 others(43): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527053 | ||||||
| chr1:217527083
|
AATGATAT others(49): Show |
A | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1099-12250_1099-12 others(62): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527083 | ||||||
| chr1:217527225
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-12336G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527225 | ||||||
| chr1:217527361
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1099-12472A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527361 | ||||||
| chr1:217527414
|
G | T | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1099-12525C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527414 | ||||||
| chr1:217527463
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-12574G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527463 | ||||||
| chr1:217527478
|
A | AT | 6 | a0001c0001t0001g0038a0001c0001t0001g0061a0001c0001t0011g0166others(3): Show | 6 | HG01261.hp2 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-12590dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527478 | ||||||
| chr1:217527478
|
AT | A | 60 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(57): Show | 60 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1099-12590delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527478 | ||||||
| chr1:217527594
|
CAAACA | C | 2 | a0001c0001t0001g0044a0001c0001t0005g0033 | 2 | HG01256.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1099-12710_1099-12 others(11): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527594 | ||||||
| chr1:217527617
|
A | G | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1099-12728T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527617 | ||||||
| chr1:217527623
|
C | G | 17 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0114others(14): Show | 17 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1099-12734G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527623 | ||||||
| chr1:217527748
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121 | 3 | HG01243.hp2 HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-12859T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527748 | ||||||
| chr1:217527921
|
T | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-13032A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217527921 | ||||||
| chr1:217528147
|
G | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-13258C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528147 | ||||||
| chr1:217528168
|
C | T | 109 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(106): Show | 109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1099-13279G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528168 | ||||||
| chr1:217528245
|
C | T | 144 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(141): Show | 144 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.1099-13356G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528245 | ||||||
| chr1:217528288
|
T | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-13399A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528288 | ||||||
| chr1:217528336
|
T | C | 1 | a0001c0001t0011g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1099-13447A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528336 | ||||||
| chr1:217528821
|
C | T | 9 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-13932G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528821 | ||||||
| chr1:217528845
|
G | A | 1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1099-13956C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528845 | ||||||
| chr1:217528935
|
A | G | 10 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0006g0173others(7): Show | 10 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-14046T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528935 | ||||||
| chr1:217529073
|
T | C | 9 | a0001c0001t0004g0152a0001c0001t0004g0179a0001c0001t0009g0178others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-14184A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217529073 | ||||||
| chr1:217529076
|
C | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-14187G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217529076 | ||||||
| chr1:217529277
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099-14388G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217529277 | ||||||
| chr1:217529324
|
G | A | 34 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(31): Show | 34 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-14435C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217529324 | ||||||
| chr1:217529575
|
G | A | 9 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-14686C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217529575 | ||||||
| chr1:217529699
|
T | TGTTCCTC others(11): Show |
1 | a0001c0001t0003g0039 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1099-14828_1099-14 others(24): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217529699 | ||||||
| chr1:217529741
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-14852G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217529741 | ||||||
| chr1:217530634
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-15745A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217530634 | ||||||
| chr1:217530886
|
T | C | 1 | a0001c0001t0006g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1099-15997A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217530886 | ||||||
| chr1:217530911
|
T | C | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-16022A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217530911 | ||||||
| chr1:217531044
|
A | AAC | 51 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1099-16157_1099-16 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531044 | ||||||
| chr1:217531044
|
A | C | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1099-16155T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531044 | ||||||
| chr1:217531044
|
AAC | A | 15 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0004g0126others(12): Show | 15 | HG00597.hp1 HG00609.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1099-16157_1099-16 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531044 | ||||||
| chr1:217531044
|
AACAC | A | 10 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0004g0130others(7): Show | 10 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-16159_1099-16 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531044 | ||||||
| chr1:217531044
|
AACACAC | A | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-16161_1099-16 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531044 | ||||||
| chr1:217531076
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-16187T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531076 | ||||||
| chr1:217531076
|
AT | A | 96 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(93): Show | 96 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1099-16188delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531076 | ||||||
| chr1:217531077
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-16188A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531077 | ||||||
| chr1:217531079
|
T | A | 97 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(94): Show | 97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1099-16190A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531079 | ||||||
| chr1:217531328
|
G | A | 110 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(107): Show | 110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1099-16439C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531328 | ||||||
| chr1:217531523
|
C | T | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-16634G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531523 | ||||||
| chr1:217531768
|
A | G | 42 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(39): Show | 42 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1099-16879T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531768 | ||||||
| chr1:217531772
|
C | T | 27 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0024others(24): Show | 27 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1099-16883G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531772 | ||||||
| chr1:217531804
|
C | G | 99 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(96): Show | 99 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1099-16915G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531804 | ||||||
| chr1:217531809
|
A | G | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1099-16920T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531809 | ||||||
| chr1:217532231
|
G | A | 1 | a0001c0001t0014g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1099-17342C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532231 | ||||||
| chr1:217532605
|
G | A | 40 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-17716C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532605 | ||||||
| chr1:217532877
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0031g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1099-18002_1099-17 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532877 | ||||||
| chr1:217532886
|
GT | G | 5 | a0001c0001t0002g0118a0001c0001t0015g0175a0001c0001t0016g0083others(2): Show | 5 | HG02145.hp2 HG02735.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-17998delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532886 | ||||||
| chr1:217532886
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1099-18013_1099-17 others(22): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532886 | ||||||
| chr1:217532897
|
TTTG | T | 86 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(83): Show | 86 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1099-18011_1099-18 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532897 | ||||||
| chr1:217532898
|
TTG | T | 49 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0017others(46): Show | 49 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1099-18011_1099-18 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532898 | ||||||
| chr1:217532900
|
GT | G | 21 | a0001c0001t0001g0063a0001c0001t0002g0099a0001c0001t0002g0103others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1099-18012delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532900 | ||||||
| chr1:217532900
|
GTT | G | 12 | a0001c0001t0001g0082a0001c0001t0002g0121a0001c0001t0002g0148others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1099-18013_1099-18 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532900 | ||||||
| chr1:217532901
|
T | G | 48 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0017others(45): Show | 48 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1099-18012A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532901 | ||||||
| chr1:217532902
|
T | G | 86 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(83): Show | 86 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1099-18013A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532902 | ||||||
| chr1:217532906
|
T | G | 40 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-18017A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532906 | ||||||
| chr1:217532990
|
C | T | 11 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0002g0121others(8): Show | 11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-18101G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217532990 | ||||||
| chr1:217533089
|
TG | T | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-18201delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533089 | ||||||
| chr1:217533178
|
G | T | 9 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-18289C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533178 | ||||||
| chr1:217533234
|
C | T | 4 | a0001c0001t0002g0118a0001c0001t0003g0077a0001c0001t0007g0075others(1): Show | 4 | HG01884.hp1 HG02735.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-18345G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533234 | ||||||
| chr1:217533318
|
G | A | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-18429C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533318 | ||||||
| chr1:217533366
|
C | T | 97 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(94): Show | 97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1099-18477G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533366 | ||||||
| chr1:217533425
|
A | T | 1 | a0001c0001t0004g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099-18536T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533425 | ||||||
| chr1:217533831
|
C | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(36): Show | 39 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1099-18942G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533831 | ||||||
| chr1:217533942
|
A | G | 109 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(106): Show | 109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1099-19053T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533942 | ||||||
| chr1:217533976
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-19087C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533976 | ||||||
| chr1:217534073
|
G | A | 8 | a0001c0001t0006g0173a0001c0001t0022g0182a0001c0001t0022g0183others(5): Show | 8 | HG01891.hp2 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-19184C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534073 | ||||||
| chr1:217534131
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0007g0011a0001c0001t0007g0013others(1): Show | 4 | HG00738.hp1 HG01358.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-19242C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534131 | ||||||
| chr1:217534169
|
T | C | 1 | a0001c0001t0009g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1099-19280A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534169 | ||||||
| chr1:217534448
|
T | G | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1099-19559A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534448 | ||||||
| chr1:217534509
|
T | C | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1099-19620A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534509 | ||||||
| chr1:217534552
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-19663A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534552 | ||||||
| chr1:217534574
|
GA | G | 56 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0082others(53): Show | 56 | HG00597.hp1 HG00609.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1099-19686delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534574 | ||||||
| chr1:217534574
|
GAA | G | 19 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0045others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1099-19687_1099-19 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534574 | ||||||
| chr1:217534574
|
GAAA | G | 80 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(77): Show | 80 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1099-19688_1099-19 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534574 | ||||||
| chr1:217534882
|
T | C | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-19993A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217534882 | ||||||
| chr1:217535046
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1099-20157T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217535046 | ||||||
| chr1:217535191
|
C | G | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-20302G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217535191 | ||||||
| chr1:217535340
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-20451C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217535340 | ||||||
| chr1:217535381
|
T | C | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1099-20492A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217535381 | ||||||
| chr1:217535537
|
G | C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-20648C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217535537 | ||||||
| chr1:217535542
|
G | A | 9 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-20653C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217535542 | ||||||
| chr1:217535794
|
CTTGGAA | C | 4 | a0001c0001t0002g0118a0001c0001t0003g0077a0001c0001t0007g0075others(1): Show | 4 | HG01884.hp1 HG02735.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-20911_1099-20 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217535794 | ||||||
| chr1:217536242
|
A | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(38): Show | 41 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-21353T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217536242 | ||||||
| chr1:217536328
|
T | C | 2 | a0001c0001t0020g0109a0001c0001t0024g0003 | 2 | HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1099-21439A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217536328 | ||||||
| chr1:217536548
|
C | G | 40 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(37): Show | 40 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-21659G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217536548 | ||||||
| chr1:217536742
|
C | T | 1 | a0001c0001t0007g0075 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1099-21853G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217536742 | ||||||
| chr1:217536927
|
G | A | 3 | a0001c0001t0006g0173a0001c0001t0033g0081a0001c0001t0042g0174 | 3 | HG01891.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1099-22038C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217536927 | ||||||
| chr1:217537123
|
T | C | 1 | a0002c0002t0019g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1099-22234A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537123 | ||||||
| chr1:217537191
|
C | T | 9 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(6): Show | 9 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1099-22302G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537191 | ||||||
| chr1:217537209
|
CA | C | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-22321delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537209 | ||||||
| chr1:217537245
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1099-22356G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537245 | ||||||
| chr1:217537287
|
C | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-22398G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537287 | ||||||
| chr1:217537317
|
A | G | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-22428T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537317 | ||||||
| chr1:217537484
|
C | A | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-22595G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537484 | ||||||
| chr1:217537490
|
C | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0159others(2): Show | 5 | HG01167.hp1 HG01361.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-22601G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537490 | ||||||
| chr1:217537521
|
C | T | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-22632G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537521 | ||||||
| chr1:217537600
|
A | G | 109 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(106): Show | 109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1099-22711T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537600 | ||||||
| chr1:217537758
|
TC | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-22870delG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537758 | ||||||
| chr1:217537801
|
T | C | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0009g0098 | 3 | HG01884.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-22912A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537801 | ||||||
| chr1:217538189
|
G | C | 1 | a0001c0001t0002g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1099-23300C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217538189 | ||||||
| chr1:217538443
|
A | T | 172 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(169): Show | 172 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1099-23554T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217538443 | ||||||
| chr1:217538483
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1099-23594G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217538483 | ||||||
| chr1:217538528
|
C | T | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-23639G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217538528 | ||||||
| chr1:217538764
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(38): Show | 41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-23875G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217538764 | ||||||
| chr1:217538806
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0002g0103a0001c0001t0002g0137others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-23917T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217538806 | ||||||
| chr1:217539215
|
A | T | 1 | a0001c0001t0005g0050 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1099-24326T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539215 | ||||||
| chr1:217539261
|
G | GA | 10 | a0001c0001t0002g0104a0001c0001t0003g0009a0001c0001t0006g0146others(7): Show | 10 | HG00597.hp1 HG00609.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-24373dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539261 | ||||||
| chr1:217539272
|
G | A | 1 | a0001c0001t0031g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1099-24383C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539272 | ||||||
| chr1:217539529
|
A | G | 63 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(60): Show | 63 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1099-24640T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539529 | ||||||
| chr1:217539746
|
C | A | 1 | a0001c0001t0005g0043 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1099-24857G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539746 | ||||||
| chr1:217539833
|
T | C | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1099-24944A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539833 | ||||||
| chr1:217539908
|
G | GA | 118 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(115): Show | 118 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1099-25020dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539908 | ||||||
| chr1:217539987
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-25098C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217539987 | ||||||
| chr1:217540145
|
A | G | 3 | a0001c0001t0005g0085a0001c0001t0008g0096a0001c0001t0014g0084 | 3 | HG02809.hp2 HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1099-25256T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217540145 | ||||||
| chr1:217540154
|
T | C | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1099-25265A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217540154 | ||||||
| chr1:217540238
|
G | C | 2 | a0001c0001t0002g0114a0001c0001t0002g0121 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1099-25349C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217540238 | ||||||
| chr1:217540866
|
C | A | 1 | a0002c0002t0028g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1099-25977G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217540866 | ||||||
| chr1:217540932
|
AAT | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-26045_1099-26 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217540932 | ||||||
| chr1:217541002
|
C | T | 1 | a0001c0001t0009g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1099-26113G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217541002 | ||||||
| chr1:217541116
|
G | A | 35 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1099-26227C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217541116 | ||||||
| chr1:217541442
|
T | G | 13 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 13 | HG00738.hp1 HG01081.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-26553A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217541442 | ||||||
| chr1:217541796
|
C | A | 111 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(108): Show | 111 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1099-26907G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217541796 | ||||||
| chr1:217541918
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1099-27029A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217541918 | ||||||
| chr1:217541960
|
T | A | 1 | a0001c0001t0011g0166 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1099-27071A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217541960 | ||||||
| chr1:217542147
|
G | C | 1 | a0001c0001t0005g0020 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1099-27258C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542147 | ||||||
| chr1:217542222
|
A | G | 111 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(108): Show | 111 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1099-27333T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542222 | ||||||
| chr1:217542308
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0159 | 3 | HG01167.hp1 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1099-27419C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542308 | ||||||
| chr1:217542390
|
G | A | 16 | a0001c0001t0001g0057a0001c0001t0003g0009a0001c0001t0003g0021others(13): Show | 16 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099-27501C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542390 | ||||||
| chr1:217542518
|
C | T | 1 | a0001c0001t0012g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1099-27629G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542518 | ||||||
| chr1:217542536
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1099-27647A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542536 | ||||||
| chr1:217542597
|
G | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(38): Show | 41 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-27708C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542597 | ||||||
| chr1:217542600
|
G | C | 4 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0011g0138others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-27711C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542600 | ||||||
| chr1:217542747
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1099-27858G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542747 | ||||||
| chr1:217542800
|
A | G | 111 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(108): Show | 111 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1099-27911T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542800 | ||||||
| chr1:217542972
|
A | C | 15 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1099-28083T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217542972 | ||||||
| chr1:217543174
|
T | G | 5 | a0001c0001t0011g0141a0001c0001t0012g0088a0001c0001t0034g0027others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-28285A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543174 | ||||||
| chr1:217543268
|
CG | C | 14 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(11): Show | 14 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1099-28380delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543268 | ||||||
| chr1:217543269
|
G | GT | 63 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(60): Show | 63 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1099-28381dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543269 | ||||||
| chr1:217543269
|
G | GTT | 21 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0064others(18): Show | 21 | HG00597.hp2 HG00609.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1099-28382_1099-28 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543269 | ||||||
| chr1:217543269
|
G | T | 1 | a0001c0001t0015g0176 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1099-28380C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543269 | ||||||
| chr1:217543353
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-28464A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543353 | ||||||
| chr1:217543370
|
C | T | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-28481G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543370 | ||||||
| chr1:217543459
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-28570G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543459 | ||||||
| chr1:217543516
|
G | T | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-28627C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543516 | ||||||
| chr1:217543520
|
C | T | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(32): Show | 35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1099-28631G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543520 | ||||||
| chr1:217543535
|
T | C | 111 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(108): Show | 111 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1099-28646A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543535 | ||||||
| chr1:217543548
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-28659G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543548 | ||||||
| chr1:217543858
|
G | T | 35 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1099-28969C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543858 | ||||||
| chr1:217543934
|
A | C | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-29045T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543934 | ||||||
| chr1:217543952
|
T | C | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-29063A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543952 | ||||||
| chr1:217543970
|
A | G | 1 | a0001c0001t0002g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1099-29081T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543970 | ||||||
| chr1:217544032
|
A | T | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0006g0180 | 3 | HG02559.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-29143T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544032 | ||||||
| chr1:217544192
|
C | T | 1 | a0001c0001t0022g0183 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1099-29303G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544192 | ||||||
| chr1:217544246
|
T | C | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1099-29357A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544246 | ||||||
| chr1:217544258
|
G | A | 4 | a0001c0001t0002g0118a0001c0001t0003g0030a0001c0001t0009g0187others(1): Show | 4 | HG00741.hp1 HG02735.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-29369C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544258 | ||||||
| chr1:217544356
|
G | C | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1099-29467C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544356 | ||||||
| chr1:217544368
|
GAGCAACA others(2): Show |
G | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-29488_1099-29 others(15): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544368 | ||||||
| chr1:217544378
|
A | T | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-29489T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544378 | ||||||
| chr1:217544379
|
C | T | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-29490G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544379 | ||||||
| chr1:217544392
|
CA | C | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-29504delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544392 | ||||||
| chr1:217544672
|
G | C | 18 | a0001c0001t0001g0057a0001c0001t0003g0009a0001c0001t0003g0021others(15): Show | 18 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1099-29783C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544672 | ||||||
| chr1:217544788
|
T | C | 2 | a0001c0001t0003g0077a0001c0001t0040g0135 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1099-29899A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544788 | ||||||
| chr1:217544790
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-29901G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544790 | ||||||
| chr1:217544999
|
C | T | 9 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099-30110G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217544999 | ||||||
| chr1:217545154
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1099-30265G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545154 | ||||||
| chr1:217545346
|
C | T | 2 | a0002c0002t0013g0046a0002c0002t0030g0047 | 2 | NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1099-30457G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545346 | ||||||
| chr1:217545447
|
C | T | 34 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(31): Show | 34 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-30558G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545447 | ||||||
| chr1:217545479
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-30590G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545479 | ||||||
| chr1:217545503
|
A | G | 2 | a0001c0001t0016g0083a0001c0005t0009g0145 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1099-30614T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545503 | ||||||
| chr1:217545714
|
A | T | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1099-30825T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545714 | ||||||
| chr1:217545806
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1099-30917C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545806 | ||||||
| chr1:217545817
|
A | G | 19 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0003g0009others(16): Show | 19 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.1099-30928T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545817 | ||||||
| chr1:217545966
|
C | T | 2 | a0001c0001t0003g0077a0001c0001t0040g0135 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1099-31077G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217545966 | ||||||
| chr1:217546221
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0006g0180 | 3 | HG02559.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-31332G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217546221 | ||||||
| chr1:217546341
|
C | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1099-31452G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217546341 | ||||||
| chr1:217546730
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 13 | HG00738.hp1 HG01081.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-31841G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217546730 | ||||||
| chr1:217546789
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1099-31900T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217546789 | ||||||
| chr1:217547139
|
A | G | 141 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(138): Show | 141 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1099-32250T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547139 | ||||||
| chr1:217547165
|
C | T | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(32): Show | 35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1099-32276G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547165 | ||||||
| chr1:217547319
|
C | T | 18 | a0001c0001t0001g0057a0001c0001t0003g0009a0001c0001t0003g0021others(15): Show | 18 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1099-32430G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547319 | ||||||
| chr1:217547340
|
G | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(29): Show | 32 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.1099-32451C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547340 | ||||||
| chr1:217547347
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1099-32458G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547347 | ||||||
| chr1:217547349
|
C | CA | 76 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(73): Show | 76 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1099-32461dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547349 | ||||||
| chr1:217547377
|
C | T | 14 | a0001c0001t0001g0057a0001c0001t0003g0009a0001c0001t0003g0021others(11): Show | 14 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1099-32488G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547377 | ||||||
| chr1:217547746
|
T | C | 2 | a0001c0001t0007g0075a0001c0001t0009g0098 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-32857A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547746 | ||||||
| chr1:217547795
|
C | T | 1 | a0002c0002t0013g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1099-32906G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547795 | ||||||
| chr1:217547993
|
C | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(31): Show | 34 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-33104G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547993 | ||||||
| chr1:217548256
|
T | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(32): Show | 35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1099-33367A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217548256 | ||||||
| chr1:217548418
|
T | C | 12 | a0001c0001t0001g0057a0001c0001t0003g0009a0001c0001t0003g0021others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1099-33529A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217548418 | ||||||
| chr1:217548611
|
G | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-33722C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217548611 | ||||||
| chr1:217548820
|
A | G | 2 | a0001c0001t0002g0114a0001c0001t0002g0121 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1099-33931T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217548820 | ||||||
| chr1:217548936
|
G | T | 39 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(36): Show | 39 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1099-34047C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217548936 | ||||||
| chr1:217548987
|
T | C | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-34098A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217548987 | ||||||
| chr1:217549107
|
A | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(32): Show | 35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1099-34218T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549107 | ||||||
| chr1:217549127
|
G | C | 100 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(97): Show | 100 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1099-34238C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549127 | ||||||
| chr1:217549197
|
A | G | 5 | a0001c0001t0011g0141a0001c0001t0012g0088a0001c0001t0034g0027others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-34308T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549197 | ||||||
| chr1:217549282
|
A | AT | 15 | a0001c0001t0006g0100a0001c0001t0009g0178a0001c0001t0011g0141others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1099-34394dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549282 | ||||||
| chr1:217549409
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1099-34520A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549409 | ||||||
| chr1:217549423
|
G | C | 1 | a0001c0001t0021g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1099-34534C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549423 | ||||||
| chr1:217549548
|
C | CT | 39 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(36): Show | 39 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1099-34660_1099-34 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549548 | ||||||
| chr1:217549603
|
TAG | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-34716_1099-34 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549603 | ||||||
| chr1:217550047
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-35158T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217550047 | ||||||
| chr1:217550160
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-35271A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217550160 | ||||||
| chr1:217550585
|
G | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(33): Show | 36 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1099-35696C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217550585 | ||||||
| chr1:217550644
|
C | T | 2 | a0001c0001t0007g0075a0001c0001t0009g0098 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-35755G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217550644 | ||||||
| chr1:217550853
|
TTATAA | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-35969_1099-35 others(11): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217550853 | ||||||
| chr1:217550922
|
C | T | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(33): Show | 36 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1099-36033G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217550922 | ||||||
| chr1:217551252
|
A | G | 2 | a0001c0001t0002g0114a0001c0001t0002g0121 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1099-36363T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551252 | ||||||
| chr1:217551285
|
C | G | 1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1099-36396G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551285 | ||||||
| chr1:217551294
|
G | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-36405C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551294 | ||||||
| chr1:217551409
|
G | C | 1 | a0001c0001t0007g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1099-36520C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551409 | ||||||
| chr1:217551636
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0002g0099a0001c0001t0006g0180 | 3 | HG02559.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1099-36747G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551636 | ||||||
| chr1:217551678
|
TA | T | 2 | a0001c0001t0003g0077a0001c0001t0040g0135 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1099-36790delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551678 | ||||||
| chr1:217551784
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1099-36895A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551784 | ||||||
| chr1:217551851
|
T | C | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1099-36962A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217551851 | ||||||
| chr1:217552095
|
C | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(19): Show | 22 | HG00738.hp1 HG01081.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1099-37206G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217552095 | ||||||
| chr1:217552108
|
C | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1099-37219G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217552108 | ||||||
| chr1:217552252
|
T | C | 17 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0003g0009others(14): Show | 17 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099-37363A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217552252 | ||||||
| chr1:217552336
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-37447G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217552336 | ||||||
| chr1:217552560
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1099-37671G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217552560 | ||||||
| chr1:217552561
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1099-37672G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217552561 | ||||||
| chr1:217552716
|
G | C | 20 | a0001c0001t0001g0057a0001c0001t0003g0009a0001c0001t0003g0021others(17): Show | 20 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1099-37827C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217552716 | ||||||
| chr1:217553042
|
CAG | C | 8 | a0001c0001t0004g0111a0001c0001t0005g0085a0001c0001t0006g0107others(5): Show | 8 | HG01261.hp1 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-38155_1099-38 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217553042 | ||||||
| chr1:217553089
|
C | T | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-38200G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217553089 | ||||||
| chr1:217553812
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0171 | 2 | HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1099-38923G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217553812 | ||||||
| chr1:217553875
|
T | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0023others(32): Show | 35 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1099-38986A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217553875 | ||||||
| chr1:217554330
|
C | T | 15 | a0001c0001t0001g0057a0001c0001t0003g0009a0001c0001t0003g0021others(12): Show | 15 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.1099-39441G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217554330 | ||||||
| chr1:217554334
|
A | G | 28 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0002g0114others(25): Show | 28 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1099-39445T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217554334 | ||||||
| chr1:217554627
|
C | T | 1 | a0001c0001t0008g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1099-39738G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217554627 | ||||||
| chr1:217554709
|
T | A | 75 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(72): Show | 75 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1099-39820A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217554709 | ||||||
| chr1:217555012
|
A | G | 4 | a0001c0001t0007g0075a0001c0001t0009g0098a0001c0001t0022g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-40123T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555012 | ||||||
| chr1:217555186
|
C | T | 1 | a0001c0001t0014g0094 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1099-40297G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555186 | ||||||
| chr1:217555291
|
T | C | 4 | a0001c0001t0007g0075a0001c0001t0009g0098a0001c0001t0022g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-40402A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555291 | ||||||
| chr1:217555553
|
C | G | 1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1099-40664G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555553 | ||||||
| chr1:217555651
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1099-40762T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555651 | ||||||
| chr1:217555894
|
C | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0002g0139others(14): Show | 17 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099-41005G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555894 | ||||||
| chr1:217555929
|
T | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1099-41040A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555929 | ||||||
| chr1:217555999
|
T | C | 1 | a0001c0001t0036g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1099-41110A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217555999 | ||||||
| chr1:217556441
|
A | G | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-41552T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217556441 | ||||||
| chr1:217556754
|
T | C | 16 | a0001c0001t0001g0057a0001c0001t0002g0139a0001c0001t0003g0009others(13): Show | 16 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099-41865A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217556754 | ||||||
| chr1:217556786
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1099-41897T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217556786 | ||||||
| chr1:217556788
|
T | G | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1099-41899A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217556788 | ||||||
| chr1:217556831
|
G | A | 29 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1099-41942C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217556831 | ||||||
| chr1:217557098
|
CTT | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-42211_1099-42 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557098 | ||||||
| chr1:217557238
|
C | A | 1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1099-42349G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557238 | ||||||
| chr1:217557268
|
G | A | 2 | a0001c0001t0007g0075a0001c0001t0009g0098 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-42379C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557268 | ||||||
| chr1:217557321
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1099-42432A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557321 | ||||||
| chr1:217557409
|
C | CA | 6 | a0001c0001t0001g0041a0001c0001t0002g0168a0001c0001t0005g0050others(3): Show | 6 | HG00673.hp2 HG01433.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-42521dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557409 | ||||||
| chr1:217557409
|
CA | C | 27 | a0001c0001t0001g0057a0001c0001t0001g0066a0001c0001t0002g0118others(24): Show | 27 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1099-42521delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557409 | ||||||
| chr1:217557599
|
T | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0041 | 3 | HG01071.hp1 HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1099-42710A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557599 | ||||||
| chr1:217557770
|
C | A | 1 | a0001c0001t0027g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1099-42881G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557770 | ||||||
| chr1:217557815
|
T | G | 1 | a0001c0001t0002g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1099-42926A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557815 | ||||||
| chr1:217557982
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1099-43093C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217557982 | ||||||
| chr1:217558194
|
C | A | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-43305G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217558194 | ||||||
| chr1:217558463
|
C | G | 1 | a0001c0001t0002g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099-43574G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217558463 | ||||||
| chr1:217558536
|
C | T | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1099-43647G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217558536 | ||||||
| chr1:217558544
|
C | G | 1 | a0001c0001t0003g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1099-43655G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217558544 | ||||||
| chr1:217558591
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-43702G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217558591 | ||||||
| chr1:217558766
|
A | G | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-43877T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217558766 | ||||||
| chr1:217559082
|
T | C | 1 | a0001c0001t0031g0040 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1099-44193A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559082 | ||||||
| chr1:217559291
|
C | T | 2 | a0001c0001t0007g0075a0001c0001t0009g0098 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-44402G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559291 | ||||||
| chr1:217559313
|
A | G | 2 | a0001c0001t0022g0182a0001c0001t0025g0001 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1099-44424T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559313 | ||||||
| chr1:217559316
|
T | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-44427A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559316 | ||||||
| chr1:217559355
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1099-44466C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559355 | ||||||
| chr1:217559375
|
A | G | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-44486T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559375 | ||||||
| chr1:217559401
|
C | T | 2 | a0001c0001t0007g0075a0001c0001t0009g0098 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-44512G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559401 | ||||||
| chr1:217559465
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-44576C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559465 | ||||||
| chr1:217559524
|
G | A | 4 | a0001c0001t0007g0075a0001c0001t0009g0098a0001c0001t0022g0182others(1): Show | 4 | HG02486.hp2 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-44635C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559524 | ||||||
| chr1:217559747
|
T | A | 1 | a0001c0001t0003g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099-44858A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559747 | ||||||
| chr1:217559873
|
G | A | 15 | a0001c0001t0001g0057a0001c0001t0002g0139a0001c0001t0003g0009others(12): Show | 15 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.1099-44984C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559873 | ||||||
| chr1:217559873
|
G | GGA | 16 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(13): Show | 16 | HG00621.hp2 HG00673.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1099-44986_1099-44 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559873 | ||||||
| chr1:217559873
|
GGAGAGA | G | 10 | a0001c0001t0006g0173a0001c0001t0007g0075a0001c0001t0009g0098others(7): Show | 10 | HG01891.hp2 HG02486.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-44990_1099-44 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559873 | ||||||
| chr1:217559952
|
G | C | 17 | a0001c0001t0001g0057a0001c0001t0002g0118a0001c0001t0002g0139others(14): Show | 17 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099-45063C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559952 | ||||||
| chr1:217559998
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1099-45109C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217559998 | ||||||
| chr1:217560068
|
C | T | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-45179G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217560068 | ||||||
| chr1:217560189
|
G | C | 10 | a0001c0001t0006g0173a0001c0001t0007g0075a0001c0001t0009g0098others(7): Show | 10 | HG01891.hp2 HG02486.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-45300C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217560189 | ||||||
| chr1:217560281
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-45392C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217560281 | ||||||
| chr1:217560528
|
T | C | 27 | a0001c0001t0001g0057a0001c0001t0002g0118a0001c0001t0002g0139others(24): Show | 27 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1099-45639A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217560528 | ||||||
| chr1:217560660
|
G | T | 17 | a0001c0001t0001g0057a0001c0001t0002g0118a0001c0001t0002g0139others(14): Show | 17 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099-45771C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217560660 | ||||||
| chr1:217560769
|
G | A | 8 | a0001c0001t0006g0173a0001c0001t0007g0075a0001c0001t0009g0098others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-45880C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217560769 | ||||||
| chr1:217560849
|
G | C | 1 | a0001c0001t0040g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1099-45960C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217560849 | ||||||
| chr1:217561058
|
C | T | 4 | a0001c0001t0005g0085a0001c0001t0008g0096a0001c0001t0014g0084others(1): Show | 4 | HG02809.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-46169G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217561058 | ||||||
| chr1:217561267
|
C | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG00621.hp2 HG00673.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-46378G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217561267 | ||||||
| chr1:217561306
|
T | G | 8 | a0001c0001t0006g0173a0001c0001t0007g0075a0001c0001t0009g0098others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-46417A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217561306 | ||||||
| chr1:217561672
|
T | C | 10 | a0001c0001t0006g0173a0001c0001t0007g0075a0001c0001t0009g0098others(7): Show | 10 | HG01891.hp2 HG02486.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-46783A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217561672 | ||||||
| chr1:217561727
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1099-46838T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217561727 | ||||||
| chr1:217561755
|
T | G | 2 | a0001c0001t0007g0075a0001c0001t0009g0098 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1099-46866A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217561755 | ||||||
| chr1:217561917
|
G | C | 1 | a0001c0001t0009g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1099-47028C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217561917 | ||||||
| chr1:217562036
|
T | C | 17 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0002g0139others(14): Show | 17 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099-47147A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562036 | ||||||
| chr1:217562050
|
C | G | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-47161G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562050 | ||||||
| chr1:217562299
|
C | G | 5 | a0001c0001t0004g0111a0001c0001t0006g0107a0001c0001t0006g0136others(2): Show | 5 | HG01261.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-47410G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562299 | ||||||
| chr1:217562305
|
C | T | 2 | a0001c0001t0007g0076a0001c0001t0014g0094 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1099-47416G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562305 | ||||||
| chr1:217562306
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1099-47417C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562306 | ||||||
| chr1:217562409
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-47520G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562409 | ||||||
| chr1:217562437
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-47548C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562437 | ||||||
| chr1:217562438
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1099-47549T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562438 | ||||||
| chr1:217562462
|
T | C | 1 | a0003c0003t0037g0080 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1099-47573A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562462 | ||||||
| chr1:217562765
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1098+47556G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562765 | ||||||
| chr1:217562948
|
T | C | 5 | a0001c0001t0001g0044a0001c0001t0002g0099a0001c0001t0002g0104others(2): Show | 5 | HG01243.hp2 HG01256.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+47373A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217562948 | ||||||
| chr1:217563004
|
GT | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0002g0122others(30): Show | 33 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1098+47316delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217563004 | ||||||
| chr1:217563075
|
A | G | 33 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(30): Show | 33 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1098+47246T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217563075 | ||||||
| chr1:217563372
|
C | A | 2 | a0001c0001t0007g0075a0001c0001t0009g0098 | 2 | HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1098+46949G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217563372 | ||||||
| chr1:217563466
|
A | T | 1 | a0001c0001t0008g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1098+46855T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217563466 | ||||||
| chr1:217563771
|
G | A | 8 | a0001c0001t0006g0173a0001c0001t0007g0075a0001c0001t0009g0098others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+46550C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217563771 | ||||||
| chr1:217563787
|
A | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0025others(51): Show | 54 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1098+46534T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217563787 | ||||||
| chr1:217563868
|
A | G | 8 | a0001c0001t0006g0173a0001c0001t0007g0075a0001c0001t0009g0098others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+46453T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217563868 | ||||||
| chr1:217564043
|
T | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 13 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+46278A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564043 | ||||||
| chr1:217564045
|
GA | G | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0099others(24): Show | 27 | HG01081.hp1 HG01167.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1098+46275delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564045 | ||||||
| chr1:217564045
|
GAA | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+46274_1098+46 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564045 | ||||||
| chr1:217564045
|
GAAA | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0019others(30): Show | 33 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1098+46273_1098+46 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564045 | ||||||
| chr1:217564045
|
GAAAA | G | 62 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(59): Show | 62 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1098+46272_1098+46 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564045 | ||||||
| chr1:217564127
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1098+46194A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564127 | ||||||
| chr1:217564133
|
G | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+46188C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564133 | ||||||
| chr1:217564199
|
G | T | 171 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.1098+46122C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564199 | ||||||
| chr1:217564200
|
T | A | 98 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0022others(95): Show | 98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1098+46121A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564200 | ||||||
| chr1:217564214
|
G | A | 90 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0022others(87): Show | 90 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1098+46107C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564214 | ||||||
| chr1:217564287
|
C | T | 33 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(30): Show | 33 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.1098+46034G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564287 | ||||||
| chr1:217564413
|
C | T | 3 | a0001c0001t0002g0112a0001c0001t0007g0076a0001c0001t0014g0094 | 3 | HG01884.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1098+45908G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564413 | ||||||
| chr1:217564509
|
GT | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 14 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+45811delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564509 | ||||||
| chr1:217564856
|
A | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+45465T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564856 | ||||||
| chr1:217564881
|
G | A | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+45440C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564881 | ||||||
| chr1:217564966
|
CATT | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+45352_1098+45 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564966 | ||||||
| chr1:217564990
|
A | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+45331T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564990 | ||||||
| chr1:217565063
|
G | A | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1098+45258C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565063 | ||||||
| chr1:217565064
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1098+45257T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565064 | ||||||
| chr1:217565218
|
C | T | 11 | a0001c0001t0002g0099a0001c0001t0006g0173a0001c0001t0007g0075others(8): Show | 11 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+45103G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565218 | ||||||
| chr1:217565634
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1098+44687C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565634 | ||||||
| chr1:217565639
|
C | A | 11 | a0001c0001t0002g0099a0001c0001t0006g0173a0001c0001t0007g0075others(8): Show | 11 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+44682G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565639 | ||||||
| chr1:217565694
|
T | C | 37 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(34): Show | 37 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1098+44627A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565694 | ||||||
| chr1:217565737
|
C | G | 1 | a0001c0001t0002g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1098+44584G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565737 | ||||||
| chr1:217565756
|
TA | T | 74 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0025others(71): Show | 74 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1098+44564delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565756 | ||||||
| chr1:217565798
|
T | C | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+44523A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565798 | ||||||
| chr1:217565856
|
G | C | 74 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0025others(71): Show | 74 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1098+44465C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565856 | ||||||
| chr1:217565872
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1098+44449G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565872 | ||||||
| chr1:217565932
|
T | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 13 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.1098+44389A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565932 | ||||||
| chr1:217566050
|
G | A | 3 | a0001c0001t0009g0187a0001c0001t0022g0182a0003c0003t0010g0188 | 3 | HG02970.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+44271C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566050 | ||||||
| chr1:217566101
|
C | CA | 19 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(16): Show | 19 | HG00738.hp1 HG01243.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1098+44219dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | ||||||
| chr1:217566101
|
C | CAA | 9 | a0001c0001t0001g0034a0001c0001t0001g0082a0001c0001t0002g0114others(6): Show | 9 | HG00741.hp2 HG01433.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+44218_1098+44 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | ||||||
| chr1:217566101
|
CA | C | 47 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0026others(44): Show | 47 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1098+44219delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | ||||||
| chr1:217566101
|
CAA | C | 21 | a0001c0001t0001g0024a0001c0001t0001g0049a0001c0001t0001g0091others(18): Show | 21 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1098+44218_1098+44 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | ||||||
| chr1:217566101
|
CAAA | C | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+44217_1098+44 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | ||||||
| chr1:217566101
|
CAAAAAAA others(5): Show |
C | 14 | a0001c0001t0002g0132a0001c0001t0002g0159a0001c0001t0004g0111others(11): Show | 14 | HG01167.hp1 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+44208_1098+44 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | ||||||
| chr1:217566101
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0131 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1098+44207_1098+44 others(19): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | ||||||
| chr1:217566297
|
T | G | 1 | a0001c0001t0041g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1098+44024A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566297 | ||||||
| chr1:217566442
|
C | A | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+43879G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566442 | ||||||
| chr1:217566666
|
T | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+43655A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566666 | ||||||
| chr1:217566693
|
G | A | 1 | a0001c0001t0014g0032 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1098+43628C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566693 | ||||||
| chr1:217567006
|
G | A | 74 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0025others(71): Show | 74 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1098+43315C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567006 | ||||||
| chr1:217567034
|
T | C | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1098+43287A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567034 | ||||||
| chr1:217567045
|
G | GT | 48 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(45): Show | 48 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1098+43275_1098+43 others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567045 | ||||||
| chr1:217567045
|
G | GTT | 4 | a0001c0001t0001g0038a0001c0001t0002g0139a0001c0001t0040g0135others(1): Show | 4 | HG01358.hp1 HG02055.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+43275_1098+43 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567045 | ||||||
| chr1:217567045
|
G | GTTT | 16 | a0001c0001t0001g0019a0001c0001t0002g0122a0001c0001t0002g0123others(13): Show | 16 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1098+43275_1098+43 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567045 | ||||||
| chr1:217567045
|
G | GTTTT | 4 | a0001c0001t0001g0008a0001c0001t0002g0148a0001c0001t0002g0171others(1): Show | 4 | HG02523.hp2 HG02738.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+43275_1098+43 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567045 | ||||||
| chr1:217567045
|
GC | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 14 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+43275delG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567045 | ||||||
| chr1:217567046
|
C | T | 80 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0025others(77): Show | 80 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1098+43275G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567046 | ||||||
| chr1:217567046
|
CT | C | 5 | a0001c0001t0004g0111a0001c0001t0006g0107a0001c0001t0020g0109others(2): Show | 5 | HG01261.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+43274delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567046 | ||||||
| chr1:217567049
|
T | G | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 12 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1098+43272A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567049 | ||||||
| chr1:217567050
|
T | G | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1098+43271A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567050 | ||||||
| chr1:217567112
|
T | C | 1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1098+43209A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567112 | ||||||
| chr1:217567234
|
C | T | 2 | a0001c0001t0002g0104a0001c0001t0009g0105 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1098+43087G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567234 | ||||||
| chr1:217567253
|
T | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0026others(55): Show | 58 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1098+43068A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567253 | ||||||
| chr1:217567268
|
A | T | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1098+43053T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567268 | ||||||
| chr1:217567273
|
C | T | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+43048G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567273 | ||||||
| chr1:217567289
|
G | A | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1098+43032C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567289 | ||||||
| chr1:217567323
|
G | A | 6 | a0001c0001t0001g0044a0001c0001t0002g0104a0001c0001t0002g0121others(3): Show | 6 | HG01243.hp2 HG01256.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+42998C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567323 | ||||||
| chr1:217567838
|
C | T | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(32): Show | 35 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1098+42483G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567838 | ||||||
| chr1:217567844
|
T | C | 14 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0003g0009others(11): Show | 14 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+42477A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567844 | ||||||
| chr1:217567859
|
G | A | 4 | a0001c0001t0011g0166a0001c0001t0015g0175a0001c0001t0015g0176others(1): Show | 4 | HG02698.hp2 HG03669.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+42462C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567859 | ||||||
| chr1:217567871
|
A | C | 4 | a0001c0001t0001g0082a0001c0001t0023g0002a0003c0003t0010g0140others(1): Show | 4 | HG02622.hp1 HG03225.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+42450T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567871 | ||||||
| chr1:217567880
|
G | A | 15 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 15 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1098+42441C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567880 | ||||||
| chr1:217567975
|
A | G | 1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1098+42346T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567975 | ||||||
| chr1:217567978
|
A | G | 1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1098+42343T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567978 | ||||||
| chr1:217567979
|
C | T | 1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1098+42342G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567979 | ||||||
| chr1:217567986
|
G | A | 4 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(1): Show | 4 | HG02559.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+42335C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567986 | ||||||
| chr1:217567988
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1098+42333C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217567988 | ||||||
| chr1:217568116
|
CA | C | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+42204delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568116 | ||||||
| chr1:217568124
|
A | C | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+42197T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568124 | ||||||
| chr1:217568170
|
T | C | 7 | a0001c0001t0004g0152a0001c0001t0006g0100a0001c0001t0008g0096others(4): Show | 7 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+42151A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568170 | ||||||
| chr1:217568207
|
T | G | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 10 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+42114A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568207 | ||||||
| chr1:217568330
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1098+41991G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568330 | ||||||
| chr1:217568462
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1098+41859C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568462 | ||||||
| chr1:217568575
|
A | G | 4 | a0001c0001t0011g0166a0001c0001t0015g0175a0001c0001t0015g0176others(1): Show | 4 | HG02698.hp2 HG03669.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+41746T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568575 | ||||||
| chr1:217568657
|
T | C | 12 | a0001c0001t0001g0025a0001c0001t0002g0139a0001c0001t0003g0009others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+41664A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568657 | ||||||
| chr1:217568863
|
G | A | 1 | a0001c0001t0010g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1098+41458C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568863 | ||||||
| chr1:217568889
|
T | A | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1098+41432A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568889 | ||||||
| chr1:217568922
|
G | A | 5 | a0001c0001t0002g0099a0001c0001t0002g0171a0001c0001t0007g0075others(2): Show | 5 | HG02559.hp2 HG02896.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+41399C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217568922 | ||||||
| chr1:217569177
|
C | T | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+41144G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569177 | ||||||
| chr1:217569178
|
G | A | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+41143C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569178 | ||||||
| chr1:217569193
|
AG | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1098+41127delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569193 | ||||||
| chr1:217569266
|
A | T | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+41055T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569266 | ||||||
| chr1:217569449
|
C | CT | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+40871dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569449 | ||||||
| chr1:217569466
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1098+40855C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569466 | ||||||
| chr1:217569516
|
G | A | 1 | a0001c0001t0005g0043 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1098+40805C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569516 | ||||||
| chr1:217569524
|
G | A | 21 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+40797C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569524 | ||||||
| chr1:217569563
|
C | T | 1 | a0001c0001t0026g0090 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1098+40758G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569563 | ||||||
| chr1:217569564
|
A | G | 1 | a0001c0001t0026g0090 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1098+40757T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569564 | ||||||
| chr1:217569565
|
T | C | 1 | a0001c0001t0026g0090 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1098+40756A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569565 | ||||||
| chr1:217569588
|
G | A | 2 | a0002c0002t0013g0046a0002c0002t0030g0047 | 2 | NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1098+40733C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569588 | ||||||
| chr1:217569601
|
G | A | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+40720C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217569601 | ||||||
| chr1:217570154
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1098+40167G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570154 | ||||||
| chr1:217570261
|
G | A | 1 | a0001c0001t0009g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1098+40060C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570261 | ||||||
| chr1:217570277
|
A | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 12 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1098+40044T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570277 | ||||||
| chr1:217570323
|
G | A | 1 | a0004c0006t0001g0053 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1098+39998C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570323 | ||||||
| chr1:217570356
|
G | A | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1098+39965C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570356 | ||||||
| chr1:217570404
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+39917G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570404 | ||||||
| chr1:217570441
|
G | A | 1 | a0001c0001t0017g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1098+39880C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570441 | ||||||
| chr1:217570443
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+39878C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570443 | ||||||
| chr1:217570607
|
C | T | 100 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(97): Show | 100 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1098+39714G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570607 | ||||||
| chr1:217570736
|
C | T | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+39585G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570736 | ||||||
| chr1:217570894
|
G | A | 73 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0026others(70): Show | 73 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1098+39427C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217570894 | ||||||
| chr1:217571012
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1098+39309A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571012 | ||||||
| chr1:217571026
|
G | A | 1 | a0001c0001t0006g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1098+39295C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571026 | ||||||
| chr1:217571225
|
T | C | 1 | a0002c0002t0008g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1098+39096A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571225 | ||||||
| chr1:217571289
|
A | T | 1 | a0001c0005t0004g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1098+39032T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571289 | ||||||
| chr1:217571350
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1098+38971T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571350 | ||||||
| chr1:217571500
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+38821A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571500 | ||||||
| chr1:217571512
|
T | TAA | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+38807_1098+38 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571512 | ||||||
| chr1:217571512
|
TA | T | 51 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(48): Show | 51 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1098+38808delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571512 | ||||||
| chr1:217571513
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+38808T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571513 | ||||||
| chr1:217571642
|
G | A | 38 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(35): Show | 38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+38679C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571642 | ||||||
| chr1:217571661
|
A | C | 87 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(84): Show | 87 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1098+38660T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571661 | ||||||
| chr1:217571684
|
C | T | 14 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 14 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+38637G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571684 | ||||||
| chr1:217571703
|
C | CA | 49 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0025others(46): Show | 49 | HG00558.hp2 HG00673.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.1098+38617dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571703 | ||||||
| chr1:217571703
|
C | CAA | 24 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0054others(21): Show | 24 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.1098+38616_1098+38 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571703 | ||||||
| chr1:217571703
|
C | CAAA | 14 | a0001c0001t0002g0118a0001c0001t0002g0139a0001c0001t0003g0021others(11): Show | 14 | HG00597.hp1 HG00609.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+38615_1098+38 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571703 | ||||||
| chr1:217571710
|
A | C | 3 | a0001c0001t0023g0002a0003c0003t0010g0140a0003c0003t0010g0167 | 3 | HG02622.hp1 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1098+38611T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571710 | ||||||
| chr1:217571710
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0099 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1098+38600_1098+38 others(17): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571710 | ||||||
| chr1:217571720
|
A | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0091others(5): Show | 8 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+38601T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571720 | ||||||
| chr1:217571721
|
C | A | 55 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(52): Show | 55 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1098+38600G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571721 | ||||||
| chr1:217571809
|
C | T | 12 | a0001c0001t0002g0118a0001c0001t0002g0139a0001c0001t0003g0009others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+38512G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571809 | ||||||
| chr1:217571950
|
G | GAGGA | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 49 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1098+38367_1098+38 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571950 | ||||||
| chr1:217571950
|
GAGGA | G | 11 | a0001c0001t0006g0146a0001c0001t0006g0173a0001c0001t0009g0187others(8): Show | 11 | HG01891.hp2 HG02615.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+38367_1098+38 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571950 | ||||||
| chr1:217572000
|
A | AGAAG | 26 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0099others(23): Show | 26 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1098+38317_1098+38 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572000 | ||||||
| chr1:217572000
|
AGAAG | A | 13 | a0001c0001t0002g0118a0001c0001t0002g0139a0001c0001t0003g0009others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+38317_1098+38 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572000 | ||||||
| chr1:217572013
|
G | A | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+38308C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572013 | ||||||
| chr1:217572020
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1098+38301C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572020 | ||||||
| chr1:217572086
|
T | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+38235A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572086 | ||||||
| chr1:217572087
|
A | T | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+38234T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572087 | ||||||
| chr1:217572227
|
T | G | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+38094A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572227 | ||||||
| chr1:217572242
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+38079C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572242 | ||||||
| chr1:217572459
|
T | C | 1 | a0001c0001t0007g0004 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1098+37862A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572459 | ||||||
| chr1:217572909
|
G | A | 8 | a0001c0001t0006g0146a0001c0001t0006g0173a0001c0001t0022g0182others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+37412C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217572909 | ||||||
| chr1:217573460
|
G | A | 22 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+36861C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217573460 | ||||||
| chr1:217573499
|
A | G | 1 | a0001c0001t0009g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1098+36822T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217573499 | ||||||
| chr1:217573611
|
T | C | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+36710A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217573611 | ||||||
| chr1:217573671
|
A | T | 12 | a0001c0001t0004g0111a0001c0001t0005g0085a0001c0001t0006g0107others(9): Show | 12 | HG01243.hp1 HG01261.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+36650T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217573671 | ||||||
| chr1:217573850
|
C | T | 6 | a0001c0001t0001g0044a0001c0001t0002g0104a0001c0001t0002g0121others(3): Show | 6 | HG01243.hp2 HG01256.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+36471G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217573850 | ||||||
| chr1:217573953
|
G | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+36368C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217573953 | ||||||
| chr1:217574090
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+36231T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574090 | ||||||
| chr1:217574151
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1098+36170G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574151 | ||||||
| chr1:217574260
|
A | G | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+36061T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574260 | ||||||
| chr1:217574551
|
A | G | 1 | a0001c0001t0003g0052 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1098+35770T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574551 | ||||||
| chr1:217574623
|
A | C | 86 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0026others(83): Show | 86 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1098+35698T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574623 | ||||||
| chr1:217574629
|
A | G | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+35692T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574629 | ||||||
| chr1:217574755
|
T | C | 1 | a0001c0001t0008g0096 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1098+35566A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574755 | ||||||
| chr1:217574983
|
A | T | 39 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(36): Show | 39 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1098+35338T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217574983 | ||||||
| chr1:217575171
|
T | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+35150A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575171 | ||||||
| chr1:217575210
|
C | G | 1 | a0001c0001t0044g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1098+35111G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575210 | ||||||
| chr1:217575339
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1098+34982G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575339 | ||||||
| chr1:217575604
|
T | C | 12 | a0001c0001t0002g0118a0001c0001t0002g0139a0001c0001t0003g0009others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+34717A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575604 | ||||||
| chr1:217575826
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1098+34495A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575826 | ||||||
| chr1:217575856
|
A | G | 13 | a0001c0001t0002g0099a0001c0001t0006g0146a0001c0001t0006g0173others(10): Show | 13 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+34465T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575856 | ||||||
| chr1:217575940
|
T | A | 1 | a0001c0001t0014g0032 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1098+34381A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575940 | ||||||
| chr1:217575958
|
C | T | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+34363G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217575958 | ||||||
| chr1:217576219
|
T | C | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+34102A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217576219 | ||||||
| chr1:217576251
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1098+34070T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217576251 | ||||||
| chr1:217576513
|
C | T | 6 | a0001c0001t0002g0099a0001c0001t0002g0118a0001c0001t0007g0075others(3): Show | 6 | HG02486.hp2 HG02559.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+33808G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217576513 | ||||||
| chr1:217576894
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0007g0012 | 2 | HG01081.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1098+33427A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217576894 | ||||||
| chr1:217576906
|
A | T | 21 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+33415T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217576906 | ||||||
| chr1:217577133
|
A | G | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1098+33188T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577133 | ||||||
| chr1:217577326
|
T | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+32995A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577326 | ||||||
| chr1:217577354
|
T | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+32967A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577354 | ||||||
| chr1:217577439
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1098+32882A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577439 | ||||||
| chr1:217577575
|
C | T | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+32746G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577575 | ||||||
| chr1:217577736
|
C | CTTA | 2 | a0001c0001t0004g0127a0001c0001t0006g0128 | 2 | HG01106.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1098+32582_1098+32 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577736 | ||||||
| chr1:217577736
|
C | CTTT | 8 | a0001c0001t0006g0146a0001c0001t0006g0173a0001c0001t0022g0182others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+32584_1098+32 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577736 | ||||||
| chr1:217577739
|
A | T | 91 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(88): Show | 91 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1098+32582T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577739 | ||||||
| chr1:217577745
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+32576T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577745 | ||||||
| chr1:217577799
|
G | A | 8 | a0001c0001t0006g0146a0001c0001t0006g0173a0001c0001t0022g0182others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+32522C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577799 | ||||||
| chr1:217577872
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+32449G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577872 | ||||||
| chr1:217577905
|
C | A | 100 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(97): Show | 100 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1098+32416G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577905 | ||||||
| chr1:217577935
|
C | T | 38 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(35): Show | 38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+32386G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577935 | ||||||
| chr1:217578064
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+32257C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578064 | ||||||
| chr1:217578142
|
G | A | 14 | a0001c0001t0004g0111a0001c0001t0004g0179a0001c0001t0005g0033others(11): Show | 14 | HG01243.hp1 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+32179C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578142 | ||||||
| chr1:217578280
|
G | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1098+32041C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578280 | ||||||
| chr1:217578527
|
C | T | 1 | a0001c0001t0017g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1098+31794G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578527 | ||||||
| chr1:217578534
|
C | G | 23 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(20): Show | 23 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1098+31787G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578534 | ||||||
| chr1:217578647
|
G | A | 23 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(20): Show | 23 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1098+31674C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578647 | ||||||
| chr1:217578911
|
T | C | 4 | a0001c0001t0001g0057a0001c0001t0003g0058a0001c0001t0005g0069others(1): Show | 4 | HG00621.hp1 HG03831.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+31410A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578911 | ||||||
| chr1:217578972
|
A | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 14 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+31349T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217578972 | ||||||
| chr1:217579045
|
C | T | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+31276G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579045 | ||||||
| chr1:217579079
|
T | C | 22 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+31242A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579079 | ||||||
| chr1:217579128
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+31193C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579128 | ||||||
| chr1:217579151
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+31170C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579151 | ||||||
| chr1:217579234
|
A | C | 17 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0006g0146others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1098+31087T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579234 | ||||||
| chr1:217579373
|
G | GA | 39 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(36): Show | 39 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1098+30947dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579373 | ||||||
| chr1:217579434
|
A | G | 10 | a0001c0001t0006g0143a0001c0001t0009g0178a0001c0001t0011g0141others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1098+30887T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579434 | ||||||
| chr1:217579487
|
T | A | 12 | a0001c0001t0002g0118a0001c0001t0002g0139a0001c0001t0003g0009others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+30834A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579487 | ||||||
| chr1:217579489
|
C | G | 3 | a0001c0001t0001g0044a0001c0001t0002g0104a0001c0001t0009g0105 | 3 | HG01256.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1098+30832G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579489 | ||||||
| chr1:217579727
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+30594C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579727 | ||||||
| chr1:217579900
|
T | C | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+30421A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579900 | ||||||
| chr1:217580322
|
G | T | 12 | a0001c0001t0001g0025a0001c0001t0002g0139a0001c0001t0003g0009others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1098+29999C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580322 | ||||||
| chr1:217580356
|
T | C | 60 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(57): Show | 60 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1098+29965A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580356 | ||||||
| chr1:217580517
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1098+29804C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580517 | ||||||
| chr1:217580597
|
C | A | 2 | a0001c0001t0001g0017a0002c0002t0012g0007 | 2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1098+29724G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580597 | ||||||
| chr1:217580732
|
TAGAAAGG others(296): Show |
T | 110 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1098+29286_1098+29 others(6): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580732 | ||||||
| chr1:217580881
|
G | A | 2 | a0001c0001t0004g0152a0003c0003t0010g0151 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1098+29440C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580881 | ||||||
| chr1:217580886
|
T | TA | 6 | a0001c0001t0001g0044a0001c0001t0002g0104a0001c0001t0002g0121others(3): Show | 6 | HG01243.hp2 HG01256.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+29434dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580886 | ||||||
| chr1:217580925
|
G | A | 2 | a0001c0001t0005g0005a0001c0001t0036g0065 | 2 | NA18943.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1098+29396C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217580925 | ||||||
| chr1:217581015
|
C | CA | 32 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1098+29305dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581015 | ||||||
| chr1:217581327
|
G | A | 38 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(35): Show | 38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+28994C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581327 | ||||||
| chr1:217581389
|
A | C | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1098+28932T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581389 | ||||||
| chr1:217581441
|
T | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(26): Show | 29 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1098+28880A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581441 | ||||||
| chr1:217581547
|
T | C | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+28774A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581547 | ||||||
| chr1:217581551
|
T | A | 19 | a0001c0001t0001g0073a0001c0001t0002g0122a0001c0001t0002g0123others(16): Show | 19 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1098+28770A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581551 | ||||||
| chr1:217581560
|
C | T | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 10 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+28761G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581560 | ||||||
| chr1:217581617
|
C | G | 110 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1098+28704G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581617 | ||||||
| chr1:217581658
|
T | A | 1 | a0002c0002t0030g0047 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1098+28663A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581658 | ||||||
| chr1:217581689
|
T | G | 38 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(35): Show | 38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+28632A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581689 | ||||||
| chr1:217581824
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+28497C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581824 | ||||||
| chr1:217581827
|
T | C | 56 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(53): Show | 56 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1098+28494A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581827 | ||||||
| chr1:217581949
|
T | TG | 17 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0006g0146others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1098+28371dupC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581949 | ||||||
| chr1:217581983
|
C | G | 2 | a0001c0001t0001g0049a0001c0001t0003g0052 | 2 | NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1098+28338G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217581983 | ||||||
| chr1:217582026
|
G | A | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+28295C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217582026 | ||||||
| chr1:217582379
|
A | T | 1 | a0001c0001t0004g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1098+27942T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217582379 | ||||||
| chr1:217582682
|
A | C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1098+27639T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217582682 | ||||||
| chr1:217582798
|
A | T | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1098+27523T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217582798 | ||||||
| chr1:217582835
|
T | C | 22 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+27486A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217582835 | ||||||
| chr1:217582839
|
C | A | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(33): Show | 36 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1098+27482G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217582839 | ||||||
| chr1:217582934
|
G | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+27387C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217582934 | ||||||
| chr1:217583018
|
T | C | 1 | a0001c0001t0005g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1098+27303A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583018 | ||||||
| chr1:217583070
|
G | A | 51 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1098+27251C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583070 | ||||||
| chr1:217583085
|
T | C | 56 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(53): Show | 56 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1098+27236A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583085 | ||||||
| chr1:217583125
|
G | A | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+27196C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583125 | ||||||
| chr1:217583426
|
C | T | 54 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(51): Show | 54 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1098+26895G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583426 | ||||||
| chr1:217583564
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+26757G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583564 | ||||||
| chr1:217583567
|
T | A | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+26754A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583567 | ||||||
| chr1:217583570
|
C | CA | 26 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0034others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1098+26750dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583570 | ||||||
| chr1:217583570
|
CA | C | 23 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0002g0122others(20): Show | 23 | HG00099.hp2 HG00609.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1098+26750delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583570 | ||||||
| chr1:217583621
|
A | G | 110 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1098+26700T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583621 | ||||||
| chr1:217583639
|
A | C | 1 | a0001c0001t0004g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1098+26682T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583639 | ||||||
| chr1:217583746
|
T | C | 1 | a0001c0001t0004g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1098+26575A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583746 | ||||||
| chr1:217583793
|
A | T | 11 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+26528T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583793 | ||||||
| chr1:217583919
|
C | T | 1 | a0001c0001t0014g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1098+26402G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217583919 | ||||||
| chr1:217584035
|
T | C | 5 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+26286A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584035 | ||||||
| chr1:217584073
|
G | T | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+26248C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584073 | ||||||
| chr1:217584222
|
C | G | 110 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1098+26099G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584222 | ||||||
| chr1:217584223
|
C | T | 1 | a0001c0001t0011g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1098+26098G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584223 | ||||||
| chr1:217584226
|
G | A | 10 | a0001c0001t0006g0143a0001c0001t0009g0178a0001c0001t0011g0141others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1098+26095C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584226 | ||||||
| chr1:217584261
|
G | A | 48 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(45): Show | 48 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1098+26060C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584261 | ||||||
| chr1:217584263
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1098+26058G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584263 | ||||||
| chr1:217584264
|
G | A | 2 | a0001c0001t0018g0185a0001c0001t0018g0186 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1098+26057C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584264 | ||||||
| chr1:217584342
|
AAAATATA others(3): Show |
A | 1 | a0001c0001t0011g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1098+25969_1098+25 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584342 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(40): Show |
1 | a0001c0001t0003g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(53): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(35): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0025 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(30): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(34): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(21): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0038a0001c0001t0003g0058 | 2 | HG01358.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(27): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0026g0090 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(33): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(22): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0003g0039others(2): Show | 5 | HG00558.hp1 HG00621.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(35): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0003g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(37): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(13): Show |
7 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0054others(4): Show | 7 | HG00621.hp1 HG01071.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(26): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(15): Show |
3 | a0001c0001t0001g0064a0001c0001t0002g0117a0001c0001t0002g0161 | 3 | HG00597.hp2 NA19077.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(28): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(17): Show |
2 | a0001c0001t0002g0150a0001c0001t0015g0153 | 2 | HG01261.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(30): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(21): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(14): Show |
5 | a0001c0001t0001g0049a0001c0001t0003g0052a0001c0001t0005g0050others(2): Show | 5 | HG00673.hp2 HG01993.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(27): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(16): Show |
4 | a0001c0001t0001g0068a0001c0001t0002g0169a0001c0001t0010g0134others(1): Show | 4 | HG02040.hp2 HG02970.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(29): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0024 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(37): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0066 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(26): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0005g0043a0001c0001t0005g0095 | 2 | HG02148.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(28): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(10): Show |
4 | a0001c0001t0027g0093a0001c0001t0033g0081a0001c0001t0041g0181others(1): Show | 4 | HG01891.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(23): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(12): Show |
2 | a0001c0001t0001g0026a0001c0001t0001g0037 | 2 | HG03491.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(25): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(14): Show |
6 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG00558.hp2 HG01496.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(27): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0006g0173a0001c0001t0022g0183 | 2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(22): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0007g0004 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(26): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(8): Show |
9 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0006g0146others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1098+25976_1098+25 others(21): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0007g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(20): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0024g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1098+25976_1098+25 others(18): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
A | T | 2 | a0001c0004t0008g0119a0001c0005t0004g0144 | 2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1098+25977T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584344
|
AATATATA others(3): Show |
A | 37 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0099others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1098+25967_1098+25 others(16): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584344 | ||||||
| chr1:217584346
|
T | A | 3 | a0001c0001t0002g0118a0001c0001t0005g0074a0001c0001t0007g0014 | 3 | HG00099.hp1 HG02735.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1098+25975A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584346 | ||||||
| chr1:217584348
|
T | A | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1098+25973A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584348 | ||||||
| chr1:217584362
|
T | C | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+25959A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584362 | ||||||
| chr1:217584364
|
T | C | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+25957A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584364 | ||||||
| chr1:217584364
|
T | TACAC | 11 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0006g0146others(8): Show | 11 | HG01884.hp2 HG02280.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+25953_1098+25 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584364 | ||||||
| chr1:217584364
|
T | TACACAC | 6 | a0001c0001t0006g0173a0001c0001t0022g0183a0001c0001t0027g0093others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+25951_1098+25 others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584364 | ||||||
| chr1:217584364
|
T | TATATATA others(29): Show |
1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+25956_1098+25 others(42): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584364 | ||||||
| chr1:217584366
|
C | T | 46 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 46 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1098+25955G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584366 | ||||||
| chr1:217584487
|
C | T | 17 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0006g0146others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1098+25834G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584487 | ||||||
| chr1:217584519
|
A | T | 3 | a0001c0001t0002g0118a0001c0001t0009g0187a0003c0003t0010g0188 | 3 | HG02735.hp1 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+25802T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584519 | ||||||
| chr1:217584894
|
C | T | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+25427G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217584894 | ||||||
| chr1:217585168
|
T | C | 1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1098+25153A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585168 | ||||||
| chr1:217585202
|
A | G | 11 | a0001c0001t0001g0025a0001c0001t0003g0009a0001c0001t0003g0021others(8): Show | 11 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1098+25119T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585202 | ||||||
| chr1:217585375
|
C | T | 8 | a0001c0001t0002g0139a0001c0001t0003g0009a0001c0001t0003g0021others(5): Show | 8 | HG00597.hp1 HG00609.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+24946G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585375 | ||||||
| chr1:217585385
|
G | A | 36 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(33): Show | 36 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1098+24936C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585385 | ||||||
| chr1:217585463
|
A | T | 1 | a0001c0001t0006g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1098+24858T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585463 | ||||||
| chr1:217585515
|
T | G | 110 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(107): Show | 110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1098+24806A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585515 | ||||||
| chr1:217585841
|
A | ATATAGCC others(49): Show |
1 | a0001c0001t0001g0066 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1098+24479_1098+24 others(62): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585841 | ||||||
| chr1:217585841
|
A | G | 1 | a0003c0003t0010g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1098+24480T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585841 | ||||||
| chr1:217585899
|
T | A | 71 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(68): Show | 71 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1098+24422A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585899 | ||||||
| chr1:217585991
|
T | A | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 49 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1098+24330A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585991 | ||||||
| chr1:217586281
|
A | G | 5 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+24040T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586281 | ||||||
| chr1:217586357
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1098+23964A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586357 | ||||||
| chr1:217586365
|
CT | C | 35 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0114others(32): Show | 35 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1098+23955delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586365 | ||||||
| chr1:217586468
|
C | A | 1 | a0001c0001t0009g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1098+23853G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586468 | ||||||
| chr1:217586472
|
C | A | 1 | a0001c0001t0036g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1098+23849G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586472 | ||||||
| chr1:217586491
|
A | C | 5 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+23830T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586491 | ||||||
| chr1:217586541
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+23780G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586541 | ||||||
| chr1:217586592
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+23729G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586592 | ||||||
| chr1:217586874
|
C | T | 1 | a0001c0001t0029g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1098+23447G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586874 | ||||||
| chr1:217586922
|
A | C | 109 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(106): Show | 109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1098+23399T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586922 | ||||||
| chr1:217586946
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+23375G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217586946 | ||||||
| chr1:217587074
|
C | G | 109 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(106): Show | 109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1098+23247G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587074 | ||||||
| chr1:217587383
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+22938G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587383 | ||||||
| chr1:217587461
|
G | C | 10 | a0001c0001t0002g0103a0001c0001t0006g0146a0001c0001t0007g0076others(7): Show | 10 | HG01884.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+22860C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587461 | ||||||
| chr1:217587479
|
C | T | 53 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(50): Show | 53 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1098+22842G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587479 | ||||||
| chr1:217587543
|
C | G | 58 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(55): Show | 58 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1098+22778G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587543 | ||||||
| chr1:217587805
|
C | T | 5 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+22516G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587805 | ||||||
| chr1:217587851
|
A | G | 59 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(56): Show | 59 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1098+22470T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587851 | ||||||
| chr1:217587862
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+22459A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587862 | ||||||
| chr1:217587867
|
G | A | 4 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(1): Show | 4 | HG02559.hp2 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+22454C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587867 | ||||||
| chr1:217588062
|
G | A | 1 | a0001c0001t0015g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1098+22259C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217588062 | ||||||
| chr1:217588330
|
C | G | 1 | a0003c0003t0010g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1098+21991G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217588330 | ||||||
| chr1:217588466
|
A | C | 1 | a0001c0001t0002g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1098+21855T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217588466 | ||||||
| chr1:217588526
|
A | T | 15 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0006g0146others(12): Show | 15 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1098+21795T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217588526 | ||||||
| chr1:217588840
|
A | C | 38 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(35): Show | 38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+21481T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217588840 | ||||||
| chr1:217588841
|
G | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+21480C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217588841 | ||||||
| chr1:217588949
|
C | T | 8 | a0001c0001t0001g0024a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098+21372G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217588949 | ||||||
| chr1:217589278
|
C | T | 37 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0104others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1098+21043G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589278 | ||||||
| chr1:217589317
|
G | C | 3 | a0001c0001t0016g0083a0001c0005t0004g0144a0001c0005t0009g0145 | 3 | HG01433.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1098+21004C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589317 | ||||||
| chr1:217589414
|
G | C | 13 | a0001c0001t0002g0104a0001c0001t0002g0139a0001c0001t0003g0009others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+20907C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589414 | ||||||
| chr1:217589439
|
G | C | 14 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0006g0146others(11): Show | 14 | HG01884.hp2 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+20882C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589439 | ||||||
| chr1:217589577
|
A | T | 59 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(56): Show | 59 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1098+20744T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589577 | ||||||
| chr1:217589615
|
TA | T | 13 | a0001c0001t0002g0104a0001c0001t0002g0139a0001c0001t0003g0009others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+20705delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589615 | ||||||
| chr1:217589791
|
A | G | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+20530T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589791 | ||||||
| chr1:217589983
|
T | G | 3 | a0001c0001t0002g0118a0001c0001t0009g0187a0003c0003t0010g0188 | 3 | HG02735.hp1 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+20338A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217589983 | ||||||
| chr1:217590022
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1098+20299C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590022 | ||||||
| chr1:217590024
|
C | CT | 10 | a0001c0001t0004g0152a0001c0001t0005g0033a0001c0001t0005g0085others(7): Show | 10 | HG01243.hp1 HG01496.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+20296dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590024 | ||||||
| chr1:217590024
|
C | CTT | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+20295_1098+20 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590024 | ||||||
| chr1:217590219
|
A | G | 4 | a0001c0001t0011g0166a0001c0001t0015g0175a0001c0001t0015g0176others(1): Show | 4 | HG02698.hp2 HG03669.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+20102T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590219 | ||||||
| chr1:217590358
|
T | A | 1 | a0001c0001t0004g0126 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1098+19963A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590358 | ||||||
| chr1:217590382
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+19939G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590382 | ||||||
| chr1:217590871
|
G | A | 25 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 25 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1098+19450C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590871 | ||||||
| chr1:217590950
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1098+19371A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590950 | ||||||
| chr1:217590988
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1098+19333C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217590988 | ||||||
| chr1:217591256
|
A | G | 7 | a0001c0001t0003g0077a0001c0001t0006g0173a0001c0001t0022g0183others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+19065T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591256 | ||||||
| chr1:217591360
|
C | T | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+18961G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591360 | ||||||
| chr1:217591430
|
C | G | 44 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(41): Show | 44 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1098+18891G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591430 | ||||||
| chr1:217591475
|
A | G | 132 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1098+18846T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591475 | ||||||
| chr1:217591478
|
G | A | 1 | a0001c0001t0006g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1098+18843C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591478 | ||||||
| chr1:217591582
|
T | C | 43 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(40): Show | 43 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1098+18739A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591582 | ||||||
| chr1:217591679
|
T | G | 1 | a0001c0001t0044g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1098+18642A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591679 | ||||||
| chr1:217591698
|
T | C | 3 | a0001c0001t0002g0112a0001c0001t0007g0076a0001c0001t0014g0094 | 3 | HG01884.hp2 HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1098+18623A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591698 | ||||||
| chr1:217591899
|
A | G | 1 | a0002c0002t0039g0162 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1098+18422T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591899 | ||||||
| chr1:217591962
|
G | T | 2 | a0001c0001t0004g0111a0001c0001t0006g0107 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1098+18359C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591962 | ||||||
| chr1:217592008
|
CA | C | 132 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1098+18312delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592008 | ||||||
| chr1:217592034
|
TAAAG | T | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+18283_1098+18 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592034 | ||||||
| chr1:217592094
|
C | T | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1098+18227G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592094 | ||||||
| chr1:217592107
|
T | C | 132 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1098+18214A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592107 | ||||||
| chr1:217592241
|
A | G | 5 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+18080T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592241 | ||||||
| chr1:217592342
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1098+17979G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592342 | ||||||
| chr1:217592373
|
G | T | 1 | a0001c0001t0021g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1098+17948C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592373 | ||||||
| chr1:217592389
|
C | T | 1 | a0001c0001t0003g0039 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1098+17932G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592389 | ||||||
| chr1:217592410
|
A | G | 143 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1098+17911T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592410 | ||||||
| chr1:217592418
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+17903T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592418 | ||||||
| chr1:217592597
|
C | T | 1 | a0004c0006t0001g0053 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1098+17724G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592597 | ||||||
| chr1:217592681
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1098+17640A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592681 | ||||||
| chr1:217592728
|
C | A | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+17593G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592728 | ||||||
| chr1:217592742
|
A | G | 45 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(42): Show | 45 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1098+17579T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592742 | ||||||
| chr1:217592768
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1098+17553T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592768 | ||||||
| chr1:217592815
|
A | C | 1 | a0001c0001t0003g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1098+17506T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592815 | ||||||
| chr1:217592905
|
G | A | 13 | a0001c0001t0002g0104a0001c0001t0002g0139a0001c0001t0003g0009others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+17416C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592905 | ||||||
| chr1:217593468
|
A | C | 38 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(35): Show | 38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+16853T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593468 | ||||||
| chr1:217593657
|
G | T | 2 | a0002c0002t0013g0046a0002c0002t0030g0047 | 2 | NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1098+16664C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593657 | ||||||
| chr1:217593705
|
T | A | 14 | a0001c0001t0001g0025a0001c0001t0002g0104a0001c0001t0002g0139others(11): Show | 14 | HG00597.hp1 HG00609.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+16616A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593705 | ||||||
| chr1:217593735
|
CTA | C | 2 | a0001c0001t0004g0152a0003c0003t0010g0151 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1098+16584_1098+16 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593735 | ||||||
| chr1:217593767
|
T | C | 122 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.1098+16554A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593767 | ||||||
| chr1:217593836
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+16485C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593836 | ||||||
| chr1:217593925
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+16396T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593925 | ||||||
| chr1:217593972
|
G | T | 2 | a0001c0001t0044g0115a0002c0002t0019g0172 | 2 | HG01081.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1098+16349C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217593972 | ||||||
| chr1:217594173
|
G | T | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1098+16148C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594173 | ||||||
| chr1:217594281
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+16040T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594281 | ||||||
| chr1:217594356
|
A | G | 43 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(40): Show | 43 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1098+15965T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594356 | ||||||
| chr1:217594493
|
G | T | 22 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+15828C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594493 | ||||||
| chr1:217594626
|
T | C | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+15695A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594626 | ||||||
| chr1:217594799
|
A | G | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1098+15522T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594799 | ||||||
| chr1:217594852
|
T | C | 1 | a0001c0001t0003g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1098+15469A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594852 | ||||||
| chr1:217594917
|
G | A | 5 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+15404C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217594917 | ||||||
| chr1:217595103
|
G | A | 43 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(40): Show | 43 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1098+15218C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595103 | ||||||
| chr1:217595113
|
T | C | 22 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+15208A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595113 | ||||||
| chr1:217595128
|
T | C | 1 | a0002c0002t0012g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1098+15193A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595128 | ||||||
| chr1:217595331
|
T | C | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1098+14990A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595331 | ||||||
| chr1:217595389
|
A | G | 2 | a0001c0001t0002g0137a0001c0001t0006g0136 | 2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1098+14932T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595389 | ||||||
| chr1:217595507
|
C | CT | 22 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1098+14813dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595507 | ||||||
| chr1:217595509
|
T | C | 1 | a0001c0001t0006g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1098+14812A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595509 | ||||||
| chr1:217595541
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1098+14780G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595541 | ||||||
| chr1:217595617
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1098+14704T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595617 | ||||||
| chr1:217595647
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+14674C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595647 | ||||||
| chr1:217595759
|
C | T | 21 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0002g0122others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1098+14562G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595759 | ||||||
| chr1:217595763
|
G | A | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1098+14558C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595763 | ||||||
| chr1:217595783
|
A | T | 10 | a0001c0001t0002g0103a0001c0001t0002g0112a0001c0001t0006g0146others(7): Show | 10 | HG01884.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+14538T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595783 | ||||||
| chr1:217595795
|
C | T | 7 | a0001c0001t0004g0152a0001c0001t0006g0100a0001c0001t0008g0096others(4): Show | 7 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1098+14526G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595795 | ||||||
| chr1:217595938
|
A | T | 74 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1098+14383T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217595938 | ||||||
| chr1:217596166
|
CACTT | C | 9 | a0001c0001t0002g0137a0001c0001t0004g0152a0001c0001t0006g0100others(6): Show | 9 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+14151_1098+14 others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596166 | ||||||
| chr1:217596174
|
G | A | 44 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(41): Show | 44 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1098+14147C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596174 | ||||||
| chr1:217596342
|
T | G | 143 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.1098+13979A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596342 | ||||||
| chr1:217596452
|
A | G | 39 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0036others(36): Show | 39 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1098+13869T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596452 | ||||||
| chr1:217596484
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1098+13837A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596484 | ||||||
| chr1:217596515
|
A | G | 5 | a0001c0001t0002g0099a0001c0001t0007g0075a0001c0001t0009g0098others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+13806T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596515 | ||||||
| chr1:217596716
|
C | T | 154 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1098+13605G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596716 | ||||||
| chr1:217596891
|
C | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 32 | HG00099.hp1 HG00738.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1098+13430G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596891 | ||||||
| chr1:217597084
|
T | A | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1098+13237A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597084 | ||||||
| chr1:217597095
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1098+13226G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597095 | ||||||
| chr1:217597150
|
C | A | 3 | a0001c0001t0002g0121a0001c0001t0002g0131a0001c0001t0002g0132 | 3 | HG01243.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1098+13171G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597150 | ||||||
| chr1:217597163
|
CA | C | 14 | a0001c0001t0006g0133a0001c0001t0006g0173a0001c0001t0006g0180others(11): Show | 14 | HG00597.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+13157delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597163 | ||||||
| chr1:217597294
|
C | T | 1 | a0001c0001t0009g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1098+13027G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597294 | ||||||
| chr1:217597317
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1098+13004C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597317 | ||||||
| chr1:217597344
|
T | TA | 5 | a0001c0001t0001g0041a0001c0001t0003g0059a0001c0001t0005g0051others(2): Show | 5 | HG01175.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+12976dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597344 | ||||||
| chr1:217597532
|
T | C | 5 | a0001c0001t0003g0030a0001c0001t0007g0004a0002c0002t0013g0046others(2): Show | 5 | HG00597.hp1 HG00741.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+12789A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597532 | ||||||
| chr1:217597587
|
A | G | 3 | a0001c0001t0002g0114a0001c0001t0009g0187a0003c0003t0010g0188 | 3 | HG02970.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+12734T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597587 | ||||||
| chr1:217597876
|
C | G | 3 | a0001c0001t0002g0103a0001c0001t0008g0096a0001c0004t0008g0097 | 3 | HG01243.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1098+12445G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217597876 | ||||||
| chr1:217598077
|
C | T | 1 | a0001c0001t0036g0065 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1098+12244G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598077 | ||||||
| chr1:217598255
|
G | A | 1 | a0001c0001t0017g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1098+12066C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598255 | ||||||
| chr1:217598387
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG00597.hp2 HG01496.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+11934G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598387 | ||||||
| chr1:217598445
|
T | TA | 18 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(15): Show | 18 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1098+11875dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598445 | ||||||
| chr1:217598453
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1098+11868T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598453 | ||||||
| chr1:217598454
|
T | A | 2 | a0001c0001t0002g0114a0001c0001t0040g0135 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1098+11867A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598454 | ||||||
| chr1:217598625
|
C | G | 14 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(11): Show | 14 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+11696G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598625 | ||||||
| chr1:217598627
|
G | A | 13 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1098+11694C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598627 | ||||||
| chr1:217598929
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1098+11392G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598929 | ||||||
| chr1:217598981
|
G | A | 1 | a0001c0001t0033g0081 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1098+11340C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598981 | ||||||
| chr1:217599197
|
A | C | 13 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1098+11124T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217599197 | ||||||
| chr1:217599215
|
C | T | 1 | a0001c0001t0011g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1098+11106G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217599215 | ||||||
| chr1:217599838
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1098+10483A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217599838 | ||||||
| chr1:217599991
|
A | G | 5 | a0001c0001t0002g0121a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG01109.hp1 HG01243.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+10330T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217599991 | ||||||
| chr1:217600005
|
T | G | 2 | a0001c0005t0004g0144a0001c0005t0009g0145 | 2 | HG01433.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1098+10316A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600005 | ||||||
| chr1:217600065
|
C | T | 16 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(13): Show | 16 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+10256G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600065 | ||||||
| chr1:217600121
|
G | T | 17 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(14): Show | 17 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1098+10200C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600121 | ||||||
| chr1:217600282
|
T | C | 3 | a0001c0001t0012g0031a0001c0001t0014g0032a0001c0001t0034g0027 | 3 | HG02280.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1098+10039A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600282 | ||||||
| chr1:217600292
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+10029A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600292 | ||||||
| chr1:217600384
|
T | C | 1 | a0001c0001t0017g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1098+9937A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600384 | ||||||
| chr1:217600554
|
C | T | 1 | a0001c0001t0004g0120 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1098+9767G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600554 | ||||||
| chr1:217600728
|
TA | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0030others(3): Show | 6 | HG00597.hp1 HG00741.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+9592delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600728 | ||||||
| chr1:217600730
|
A | T | 1 | a0001c0001t0003g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1098+9591T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217600730 | ||||||
| chr1:217601286
|
C | T | 2 | a0001c0005t0004g0144a0001c0005t0009g0145 | 2 | HG01433.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1098+9035G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601286 | ||||||
| chr1:217601287
|
A | G | 97 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(94): Show | 97 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.1098+9034T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601287 | ||||||
| chr1:217601428
|
C | CA | 24 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(21): Show | 24 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1098+8892dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601428 | ||||||
| chr1:217601582
|
C | T | 14 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(11): Show | 14 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+8739G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601582 | ||||||
| chr1:217601660
|
A | T | 93 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(90): Show | 93 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.1098+8661T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601660 | ||||||
| chr1:217601758
|
T | C | 1 | a0001c0001t0012g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1098+8563A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601758 | ||||||
| chr1:217601803
|
T | G | 6 | a0001c0001t0002g0148a0001c0001t0002g0161a0001c0001t0002g0164others(3): Show | 6 | HG02040.hp1 HG02155.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+8518A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601803 | ||||||
| chr1:217601834
|
C | T | 8 | a0001c0001t0006g0173a0001c0001t0006g0180a0001c0001t0009g0187others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+8487G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601834 | ||||||
| chr1:217601882
|
T | C | 4 | a0001c0001t0001g0049a0001c0001t0003g0052a0001c0001t0005g0050others(1): Show | 4 | HG00673.hp2 NA18983.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+8439A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601882 | ||||||
| chr1:217601960
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0003g0058 | 2 | NA18962.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1098+8361G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601960 | ||||||
| chr1:217602339
|
A | T | 46 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(43): Show | 46 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.1098+7982T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217602339 | ||||||
| chr1:217602650
|
G | T | 1 | a0001c0007t0002g0147 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1098+7671C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217602650 | ||||||
| chr1:217602660
|
T | C | 1 | a0001c0004t0008g0097 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1098+7661A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217602660 | ||||||
| chr1:217602848
|
A | G | 37 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(34): Show | 37 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1098+7473T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217602848 | ||||||
| chr1:217603014
|
T | A | 1 | a0001c0004t0008g0119 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1098+7307A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217603014 | ||||||
| chr1:217603224
|
C | T | 47 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(44): Show | 47 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1098+7097G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217603224 | ||||||
| chr1:217603605
|
A | AATTT | 2 | a0001c0001t0008g0096a0001c0004t0008g0097 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1098+6712_1098+671 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217603605 | ||||||
| chr1:217603612
|
T | G | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1098+6709A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217603612 | ||||||
| chr1:217603724
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1098+6597C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217603724 | ||||||
| chr1:217603821
|
C | T | 16 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(13): Show | 16 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+6500G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217603821 | ||||||
| chr1:217603901
|
G | T | 16 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(13): Show | 16 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098+6420C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217603901 | ||||||
| chr1:217604051
|
A | G | 2 | a0001c0001t0004g0152a0003c0003t0010g0151 | 2 | HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1098+6270T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217604051 | ||||||
| chr1:217604268
|
T | A | 2 | a0001c0005t0004g0144a0001c0005t0009g0145 | 2 | HG01433.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1098+6053A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217604268 | ||||||
| chr1:217604367
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1098+5954A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217604367 | ||||||
| chr1:217604548
|
G | A | 18 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(15): Show | 18 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1098+5773C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217604548 | ||||||
| chr1:217604599
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1098+5722T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217604599 | ||||||
| chr1:217604750
|
G | A | 14 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(11): Show | 14 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+5571C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217604750 | ||||||
| chr1:217604854
|
T | C | 34 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(31): Show | 34 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1098+5467A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217604854 | ||||||
| chr1:217605023
|
C | CAAAAT | 4 | a0001c0001t0007g0078a0001c0001t0007g0079a0001c0001t0033g0081others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+5293_1098+529 others(9): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217605023 | ||||||
| chr1:217605066
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+5255A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217605066 | ||||||
| chr1:217605360
|
CA | C | 3 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098 | 3 | HG02559.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1098+4960delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217605360 | ||||||
| chr1:217605828
|
C | A | 187 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0016others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(184): Show |
intron_variant | MODIFIER | c.1098+4493G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217605828 | ||||||
| chr1:217606030
|
T | C | 2 | a0001c0001t0014g0094a0001c0001t0027g0093 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1098+4291A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217606030 | ||||||
| chr1:217606377
|
G | A | 1 | a0001c0001t0029g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1098+3944C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217606377 | ||||||
| chr1:217606418
|
C | T | 1 | a0001c0001t0032g0056 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1098+3903G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217606418 | ||||||
| chr1:217606748
|
A | C | 92 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(89): Show | 92 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.1098+3573T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217606748 | ||||||
| chr1:217606748
|
A | T | 4 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098others(1): Show | 4 | HG01168.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+3573T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217606748 | ||||||
| chr1:217607130
|
A | G | 96 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(93): Show | 96 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(93): Show |
intron_variant | MODIFIER | c.1098+3191T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217607130 | ||||||
| chr1:217607336
|
C | T | 2 | a0001c0001t0002g0104a0001c0001t0009g0105 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1098+2985G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217607336 | ||||||
| chr1:217607372
|
G | T | 2 | a0001c0005t0004g0144a0001c0005t0009g0145 | 2 | HG01433.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1098+2949C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217607372 | ||||||
| chr1:217607514
|
G | A | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1098+2807C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217607514 | ||||||
| chr1:217607604
|
G | T | 1 | a0003c0003t0010g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1098+2717C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217607604 | ||||||
| chr1:217607834
|
C | G | 1 | a0001c0001t0007g0014 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1098+2487G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217607834 | ||||||
| chr1:217607946
|
A | C | 17 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(14): Show | 17 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1098+2375T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217607946 | ||||||
| chr1:217608006
|
A | T | 1 | a0001c0001t0034g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1098+2315T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217608006 | ||||||
| chr1:217608216
|
GA | G | 47 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(44): Show | 47 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1098+2104delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217608216 | ||||||
| chr1:217608482
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+1839A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217608482 | ||||||
| chr1:217608638
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1098+1683A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217608638 | ||||||
| chr1:217608931
|
T | C | 96 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(93): Show | 96 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(93): Show |
intron_variant | MODIFIER | c.1098+1390A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217608931 | ||||||
| chr1:217608962
|
T | C | 1 | a0001c0001t0004g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1098+1359A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217608962 | ||||||
| chr1:217609043
|
CAATT | C | 10 | a0001c0001t0002g0171a0001c0001t0004g0179a0001c0001t0006g0143others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1098+1274_1098+127 others(8): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217609043 | ||||||
| chr1:217609372
|
A | C | 3 | a0001c0001t0002g0114a0001c0001t0017g0116a0001c0001t0044g0115 | 3 | HG01433.hp1 HG03453.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1098+949T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217609372 | ||||||
| chr1:217609394
|
T | C | 2 | a0001c0001t0002g0139a0001c0001t0002g0168 | 2 | HG01952.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1098+927A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217609394 | ||||||
| chr1:217609552
|
A | AG | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1098+768_1098+769i others(3): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217609552 | ||||||
| chr1:217610465
|
G | A | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1019-65C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 4/9 | chr1 | 217610465 | ||||||
| chr1:217610468
|
C | T | 47 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(44): Show | 47 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1019-68G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 4/9 | chr1 | 217610468 | ||||||
| chr1:217610726
|
G | C | 1 | a0001c0001t0016g0086 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1018+163C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 4/9 | chr1 | 217610726 | ||||||
| chr1:217610750
|
A | G | 13 | a0001c0001t0002g0114a0001c0001t0002g0171a0001c0001t0004g0179others(10): Show | 13 | HG01081.hp1 HG01433.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1018+139T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 4/9 | chr1 | 217610750 | ||||||
| chr1:217611089
|
A | AC | 13 | a0001c0001t0006g0173a0001c0001t0006g0180a0001c0001t0009g0187others(10): Show | 13 | HG01081.hp1 HG01891.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.836-19dupG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217611089 | ||||||
| chr1:217611387
|
GCTTCA | G | 47 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(44): Show | 47 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.836-321_836-317del others(5): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217611387 | ||||||
| chr1:217611815
|
G | A | 1 | a0001c0001t0024g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.836-744C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217611815 | ||||||
| chr1:217611902
|
A | G | 1 | a0001c0001t0022g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.836-831T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217611902 | ||||||
| chr1:217612023
|
A | T | 1 | a0002c0002t0013g0055 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.836-952T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217612023 | ||||||
| chr1:217612168
|
G | A | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.836-1097C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217612168 | ||||||
| chr1:217612322
|
T | C | 4 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098others(1): Show | 4 | HG01168.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-1251A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217612322 | ||||||
| chr1:217612549
|
C | A | 95 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(92): Show | 95 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.836-1478G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217612549 | ||||||
| chr1:217612612
|
T | A | 4 | a0001c0001t0005g0085a0001c0001t0012g0088a0001c0001t0014g0084others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.835+1529A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217612612 | ||||||
| chr1:217612934
|
G | A | 5 | a0001c0001t0002g0137a0001c0001t0006g0133a0001c0001t0006g0136others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.835+1207C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217612934 | ||||||
| chr1:217612980
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.835+1161G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217612980 | ||||||
| chr1:217613411
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.835+730A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217613411 | ||||||
| chr1:217613456
|
G | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0169 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.835+685C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217613456 | ||||||
| chr1:217613513
|
G | A | 43 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0034others(40): Show | 43 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.835+628C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217613513 | ||||||
| chr1:217613796
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0005g0043 | 2 | HG01256.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.835+345A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217613796 | ||||||
| chr1:217613828
|
C | T | 2 | a0001c0001t0004g0127a0001c0001t0006g0128 | 2 | HG01106.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.835+313G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217613828 | ||||||
| chr1:217613998
|
C | T | 3 | a0001c0001t0003g0077a0001c0001t0007g0075a0001c0001t0007g0076 | 3 | HG01884.hp1 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.835+143G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217613998 | ||||||
| chr1:217614034
|
G | T | 1 | a0001c0001t0003g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.835+107C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 3/9 | chr1 | 217614034 | ||||||
| chr1:217614256
|
C | T | 1 | a0001c0001t0004g0120 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.774-54G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614256 | ||||||
| chr1:217614388
|
T | G | 3 | a0001c0001t0002g0114a0001c0001t0017g0116a0001c0001t0044g0115 | 3 | HG01433.hp1 HG03453.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.774-186A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614388 | ||||||
| chr1:217614474
|
C | A | 1 | a0001c0001t0003g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.774-272G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614474 | ||||||
| chr1:217614474
|
C | T | 47 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(44): Show | 47 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.774-272G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614474 | ||||||
| chr1:217614521
|
T | C | 95 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(92): Show | 95 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.774-319A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614521 | ||||||
| chr1:217614690
|
T | G | 2 | a0001c0001t0018g0185a0001c0001t0018g0186 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.774-488A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614690 | ||||||
| chr1:217614716
|
G | GA | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.774-515dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614716 | ||||||
| chr1:217614719
|
T | A | 84 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(81): Show | 84 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.774-517A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614719 | ||||||
| chr1:217614733
|
C | T | 1 | a0001c0001t0004g0120 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.774-531G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614733 | ||||||
| chr1:217614774
|
CA | C | 12 | a0001c0001t0001g0026a0001c0001t0002g0169a0001c0001t0004g0120others(9): Show | 12 | HG01891.hp2 HG01993.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.774-573delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614774 | ||||||
| chr1:217614788
|
A | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0082others(29): Show | 32 | HG00738.hp1 HG01081.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.774-586T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614788 | ||||||
| chr1:217614791
|
T | A | 3 | a0001c0001t0002g0129a0001c0001t0004g0127a0001c0001t0006g0128 | 3 | HG00741.hp2 HG01106.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.774-589A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614791 | ||||||
| chr1:217614852
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.774-650T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614852 | ||||||
| chr1:217615021
|
T | C | 4 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098others(1): Show | 4 | HG01168.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.774-819A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217615021 | ||||||
| chr1:217615256
|
C | T | 1 | a0002c0002t0012g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.774-1054G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217615256 | ||||||
| chr1:217615342
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.774-1140A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217615342 | ||||||
| chr1:217615945
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.774-1743C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217615945 | ||||||
| chr1:217615950
|
A | C | 1 | a0001c0004t0008g0119 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.774-1748T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217615950 | ||||||
| chr1:217616102
|
T | C | 3 | a0001c0001t0002g0114a0001c0001t0017g0116a0001c0001t0044g0115 | 3 | HG01433.hp1 HG03453.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.774-1900A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217616102 | ||||||
| chr1:217616309
|
A | C | 96 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(93): Show | 96 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(93): Show |
intron_variant | MODIFIER | c.774-2107T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217616309 | ||||||
| chr1:217616462
|
G | A | 3 | a0001c0001t0006g0165a0001c0001t0011g0166a0003c0003t0010g0167 | 3 | HG02622.hp1 HG03710.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.774-2260C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217616462 | ||||||
| chr1:217616698
|
C | A | 1 | a0001c0001t0017g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.774-2496G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217616698 | ||||||
| chr1:217616699
|
G | C | 2 | a0001c0001t0017g0116a0001c0001t0044g0115 | 2 | HG01433.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.774-2497C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217616699 | ||||||
| chr1:217616764
|
T | C | 2 | a0001c0001t0017g0116a0001c0001t0044g0115 | 2 | HG01433.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.774-2562A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217616764 | ||||||
| chr1:217617022
|
ACAAAATA others(1): Show |
A | 163 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0028others(160): Show | 163 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.773+2753_773+2760d others(10): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617022 | ||||||
| chr1:217617147
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.773+2636T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617147 | ||||||
| chr1:217617240
|
T | C | 1 | a0001c0001t0017g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.773+2543A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617240 | ||||||
| chr1:217617449
|
T | C | 10 | a0001c0001t0002g0104a0001c0001t0002g0112a0001c0001t0004g0102others(7): Show | 10 | HG01261.hp1 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.773+2334A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617449 | ||||||
| chr1:217617641
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.773+2142G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617641 | ||||||
| chr1:217617654
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.773+2129G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617654 | ||||||
| chr1:217617684
|
G | C | 13 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.773+2099C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617684 | ||||||
| chr1:217617685
|
C | A | 13 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.773+2098G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617685 | ||||||
| chr1:217617911
|
T | C | 1 | a0001c0001t0004g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.773+1872A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217617911 | ||||||
| chr1:217618221
|
CT | C | 47 | a0001c0001t0001g0045a0001c0001t0002g0137a0001c0001t0002g0139others(44): Show | 47 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.773+1561delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618221 | ||||||
| chr1:217618377
|
T | C | 2 | a0001c0001t0002g0139a0001c0001t0002g0168 | 2 | HG01952.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.773+1406A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618377 | ||||||
| chr1:217618380
|
C | G | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.773+1403G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618380 | ||||||
| chr1:217618485
|
G | A | 1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.773+1298C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618485 | ||||||
| chr1:217618493
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.773+1290G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618493 | ||||||
| chr1:217618781
|
G | A | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.773+1002C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618781 | ||||||
| chr1:217618807
|
A | G | 47 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(44): Show | 47 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.773+976T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618807 | ||||||
| chr1:217618814
|
T | A | 2 | a0002c0002t0013g0046a0002c0002t0030g0047 | 2 | NA18983.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.773+969A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618814 | ||||||
| chr1:217618816
|
C | T | 17 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(14): Show | 17 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.773+967G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618816 | ||||||
| chr1:217618848
|
A | G | 3 | a0001c0001t0002g0103a0001c0001t0008g0096a0001c0004t0008g0097 | 3 | HG01243.hp1 HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.773+935T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618848 | ||||||
| chr1:217618963
|
G | GA | 20 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.773+819dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618963 | ||||||
| chr1:217618968
|
A | T | 8 | a0001c0001t0006g0173a0001c0001t0006g0180a0001c0001t0009g0187others(5): Show | 8 | HG01891.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.773+815T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618968 | ||||||
| chr1:217619022
|
A | C | 1 | a0002c0002t0019g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.773+761T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217619022 | ||||||
| chr1:217619199
|
A | G | 1 | a0001c0001t0004g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.773+584T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217619199 | ||||||
| chr1:217619236
|
GT | G | 17 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(14): Show | 17 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.773+546delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217619236 | ||||||
| chr1:217619753
|
A | G | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.773+30T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217619753 | ||||||
| chr1:217620596
|
T | TTAA | 40 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(37): Show | 40 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.57-100_57-98dupTTA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217620596 | ||||||
| chr1:217620801
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.57-302G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217620801 | ||||||
| chr1:217621011
|
G | A | 1 | a0001c0001t0025g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.57-512C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217621011 | ||||||
| chr1:217621511
|
T | G | 1 | a0001c0001t0003g0052 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.57-1012A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217621511 | ||||||
| chr1:217621822
|
A | T | 1 | a0001c0001t0002g0171 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.57-1323T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217621822 | ||||||
| chr1:217622095
|
G | A | 1 | a0003c0003t0010g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.57-1596C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622095 | ||||||
| chr1:217622246
|
CA | C | 46 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(43): Show | 46 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.57-1748delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622246 | ||||||
| chr1:217622475
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.57-1976T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622475 | ||||||
| chr1:217622549
|
T | A | 46 | a0001c0001t0002g0137a0001c0001t0002g0139a0001c0001t0002g0148others(43): Show | 46 | HG00099.hp2 HG00738.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.57-2050A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622549 | ||||||
| chr1:217622566
|
C | T | 15 | a0001c0001t0001g0082a0001c0001t0003g0077a0001c0001t0005g0085others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.57-2067G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622566 | ||||||
| chr1:217622601
|
T | C | 4 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098others(1): Show | 4 | HG01168.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.57-2102A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622601 | ||||||
| chr1:217622700
|
T | C | 1 | a0001c0001t0012g0088 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57-2201A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622700 | ||||||
| chr1:217622719
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.57-2220A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622719 | ||||||
| chr1:217622868
|
A | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57-2369T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622868 | ||||||
| chr1:217622957
|
G | A | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.57-2458C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622957 | ||||||
| chr1:217622976
|
T | C | 1 | a0001c0001t0003g0048 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.57-2477A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217622976 | ||||||
| chr1:217623309
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57-2810A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623309 | ||||||
| chr1:217623321
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57-2822G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623321 | ||||||
| chr1:217623380
|
T | A | 12 | a0001c0001t0002g0171a0001c0001t0004g0179a0001c0001t0006g0143others(9): Show | 12 | HG01081.hp1 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.57-2881A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623380 | ||||||
| chr1:217623601
|
A | G | 1 | a0001c0001t0006g0146 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.57-3102T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623601 | ||||||
| chr1:217623614
|
T | TTTTTAGG others(56): Show |
1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-3116_57-3115ins others(63): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623614 | ||||||
| chr1:217623797
|
G | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-3298C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623797 | ||||||
| chr1:217623857
|
G | A | 1 | a0001c0001t0017g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.57-3358C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623857 | ||||||
| chr1:217623992
|
A | C | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-3493T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217623992 | ||||||
| chr1:217624233
|
A | G | 1 | a0002c0002t0012g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.57-3734T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624233 | ||||||
| chr1:217624234
|
T | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-3735A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624234 | ||||||
| chr1:217624285
|
A | C | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-3786T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624285 | ||||||
| chr1:217624288
|
C | G | 6 | a0001c0001t0006g0180a0001c0001t0009g0187a0001c0001t0022g0182others(3): Show | 6 | HG02970.hp2 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.57-3789G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624288 | ||||||
| chr1:217624289
|
G | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-3790C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624289 | ||||||
| chr1:217624312
|
G | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-3813C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624312 | ||||||
| chr1:217624344
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0003g0052a0001c0001t0005g0050others(1): Show | 4 | HG00673.hp2 NA18983.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-3845G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624344 | ||||||
| chr1:217624347
|
G | C | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.57-3848C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624347 | ||||||
| chr1:217624451
|
A | T | 1 | a0001c0001t0003g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.57-3952T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624451 | ||||||
| chr1:217624452
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.57-3953C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624452 | ||||||
| chr1:217624491
|
C | T | 37 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(34): Show | 37 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.57-3992G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624491 | ||||||
| chr1:217624606
|
T | G | 27 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0057others(24): Show | 27 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.57-4107A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624606 | ||||||
| chr1:217624907
|
T | A | 1 | a0001c0001t0005g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.57-4408A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217624907 | ||||||
| chr1:217625011
|
A | G | 13 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0112others(10): Show | 13 | HG01243.hp1 HG01261.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.57-4512T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625011 | ||||||
| chr1:217625088
|
T | C | 17 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(14): Show | 17 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.57-4589A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625088 | ||||||
| chr1:217625519
|
C | T | 1 | a0001c0001t0005g0005 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57-5020G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625519 | ||||||
| chr1:217625533
|
A | C | 2 | a0001c0005t0004g0144a0001c0005t0009g0145 | 2 | HG01433.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.57-5034T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625533 | ||||||
| chr1:217625703
|
G | C | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-5204C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625703 | ||||||
| chr1:217625704
|
C | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57-5205G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625704 | ||||||
| chr1:217625817
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.56+5099A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625817 | ||||||
| chr1:217625820
|
T | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+5096A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625820 | ||||||
| chr1:217625958
|
T | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4958A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217625958 | ||||||
| chr1:217626159
|
G | C | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4757C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626159 | ||||||
| chr1:217626160
|
C | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4756G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626160 | ||||||
| chr1:217626279
|
A | G | 3 | a0001c0001t0002g0114a0001c0001t0017g0116a0001c0001t0044g0115 | 3 | HG01433.hp1 HG03453.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.56+4637T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626279 | ||||||
| chr1:217626366
|
T | G | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.56+4550A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626366 | ||||||
| chr1:217626522
|
G | C | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4394C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626522 | ||||||
| chr1:217626523
|
C | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4393G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626523 | ||||||
| chr1:217626699
|
A | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4217T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626699 | ||||||
| chr1:217626700
|
G | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4216C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626700 | ||||||
| chr1:217626705
|
T | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+4211A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626705 | ||||||
| chr1:217626787
|
C | T | 1 | a0001c0001t0023g0002 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.56+4129G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626787 | ||||||
| chr1:217626818
|
A | T | 89 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(86): Show | 89 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.56+4098T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626818 | ||||||
| chr1:217626858
|
T | C | 3 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098 | 3 | HG02559.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.56+4058A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626858 | ||||||
| chr1:217626985
|
G | GA | 16 | a0001c0001t0001g0082a0001c0001t0003g0077a0001c0001t0005g0085others(13): Show | 16 | HG00597.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.56+3930dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217626985 | ||||||
| chr1:217627021
|
T | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+3895A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627021 | ||||||
| chr1:217627230
|
A | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+3686T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627230 | ||||||
| chr1:217627288
|
T | C | 1 | a0001c0001t0004g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.56+3628A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627288 | ||||||
| chr1:217627290
|
C | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+3626G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627290 | ||||||
| chr1:217627291
|
T | C | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+3625A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627291 | ||||||
| chr1:217627308
|
T | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+3608A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627308 | ||||||
| chr1:217627383
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.56+3533A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627383 | ||||||
| chr1:217627620
|
C | A | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.56+3296G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627620 | ||||||
| chr1:217627667
|
C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.56+3249G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627667 | ||||||
| chr1:217627804
|
T | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+3112A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627804 | ||||||
| chr1:217627928
|
CAAAAA | C | 3 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098 | 3 | HG02559.hp2 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.56+2983_56+2987del others(5): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627928 | ||||||
| chr1:217627982
|
T | C | 4 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098others(1): Show | 4 | HG01168.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+2934A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217627982 | ||||||
| chr1:217628008
|
A | G | 96 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(93): Show | 96 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(93): Show |
intron_variant | MODIFIER | c.56+2908T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628008 | ||||||
| chr1:217628068
|
T | G | 2 | a0001c0001t0018g0185a0001c0001t0018g0186 | 2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.56+2848A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628068 | ||||||
| chr1:217628093
|
T | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0003g0089others(1): Show | 4 | HG00558.hp1 HG02135.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.56+2823A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628093 | ||||||
| chr1:217628367
|
T | C | 17 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(14): Show | 17 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+2549A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628367 | ||||||
| chr1:217628409
|
GA | G | 4 | a0001c0001t0002g0099a0001c0001t0006g0100a0001c0001t0009g0098others(1): Show | 4 | HG01168.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+2506delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628409 | ||||||
| chr1:217628659
|
T | A | 3 | a0001c0001t0023g0002a0001c0001t0024g0003a0001c0001t0025g0001 | 3 | HG01891.hp1 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.56+2257A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628659 | ||||||
| chr1:217628682
|
TA | T | 26 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0121others(23): Show | 26 | HG00099.hp2 HG00609.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.56+2233delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628682 | ||||||
| chr1:217628703
|
A | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+2213T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628703 | ||||||
| chr1:217628717
|
C | G | 2 | a0001c0001t0008g0096a0001c0004t0008g0097 | 2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.56+2199G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628717 | ||||||
| chr1:217628931
|
G | T | 1 | a0001c0001t0002g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.56+1985C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628931 | ||||||
| chr1:217628942
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0006g0136 | 2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.56+1974G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628942 | ||||||
| chr1:217629138
|
G | C | 2 | a0001c0001t0023g0002a0001c0001t0024g0003 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.56+1778C>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629138 | ||||||
| chr1:217629164
|
T | A | 2 | a0001c0001t0014g0094a0001c0001t0027g0093 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.56+1752A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629164 | ||||||
| chr1:217629207
|
AATTTTTA others(6): Show |
A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+1696_56+1708del others(13): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629207 | ||||||
| chr1:217629209
|
TTTTTACA others(5): Show |
T | 19 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(16): Show | 19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.56+1695_56+1706del others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629209 | ||||||
| chr1:217629219
|
CCAGATAG others(5): Show |
C | 3 | a0001c0001t0006g0133a0001c0001t0010g0134a0001c0001t0040g0135 | 3 | HG02055.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.56+1685_56+1696del others(12): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629219 | ||||||
| chr1:217629223
|
A | G | 1 | a0001c0001t0007g0004 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.56+1693T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629223 | ||||||
| chr1:217629224
|
T | C | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.56+1692A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629224 | ||||||
| chr1:217629225
|
A | T | 20 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.56+1691T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629225 | ||||||
| chr1:217629226
|
GTCATACA | G | 19 | a0001c0001t0002g0114a0001c0001t0002g0117a0001c0001t0002g0118others(16): Show | 19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.56+1683_56+1689del others(7): Show |
GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629226 | ||||||
| chr1:217629230
|
T | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+1686A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629230 | ||||||
| chr1:217629233
|
A | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+1683T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629233 | ||||||
| chr1:217629533
|
A | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+1383T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629533 | ||||||
| chr1:217629540
|
T | C | 1 | a0001c0001t0005g0095 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.56+1376A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629540 | ||||||
| chr1:217629548
|
T | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+1368A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629548 | ||||||
| chr1:217629903
|
T | C | 2 | a0001c0001t0009g0187a0003c0003t0010g0188 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.56+1013A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629903 | ||||||
| chr1:217629908
|
G | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+1008C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629908 | ||||||
| chr1:217629910
|
T | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+1006A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629910 | ||||||
| chr1:217629945
|
T | G | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+971A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629945 | ||||||
| chr1:217630264
|
G | T | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+652C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217630264 | ||||||
| chr1:217630530
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.56+386T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217630530 | ||||||
| chr1:217630653
|
C | T | 3 | a0001c0001t0002g0114a0001c0001t0017g0116a0001c0001t0044g0115 | 3 | HG01433.hp1 HG03453.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.56+263G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217630653 | ||||||
| chr1:217630737
|
G | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+179C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217630737 | ||||||
| chr1:217630758
|
C | A | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+158G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217630758 | ||||||
| chr1:217630759
|
A | C | 1 | a0001c0001t0004g0113 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.56+157T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217630759 | ||||||
| chr1:217630866
|
G | T | 17 | a0001c0001t0002g0099a0001c0001t0002g0103a0001c0001t0002g0104others(14): Show | 17 | HG01168.hp2 HG01243.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.56+50C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217630866 |