Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MFGAA others(523): Show |
chr1 | 217421992 | 217636090 |
| a0002 | 0/0 | 528 | 10 | 0 | 1 | 5 | 0 | 4 | 3 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | MFGAA others(523): Show |
chr1 | 217421992 | 217636090 |
| a0003 | 0/0 | 528 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | MFGAA others(523): Show |
chr1 | 217421992 | 217636090 |
| a0004 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | MFGAA others(523): Show |
chr1 | 217421992 | 217636090 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1584 | 166 | 66 | 34 | 36 | 6 | 22 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | ATGTT others(1579): Show |
chr1 | 217421992 | 217636090 | ||
| a0001c0004 | 0/0 | 1584 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | ATGTT others(1579): Show |
chr1 | 217421992 | 217636090 | ||
| a0001c0005 | 0/0 | 1584 | 2 | 1 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | ATGTT others(1579): Show |
chr1 | 217421992 | 217636090 | ||
| a0001c0007 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | ATGTT others(1579): Show |
chr1 | 217421992 | 217636090 | ||
| a0002c0002 | 0/0 | 1584 | 10 | 0 | 1 | 5 | 0 | 4 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | ATGTT others(1579): Show |
chr1 | 217421992 | 217636090 | ||
| a0003c0003 | 0/0 | 1584 | 5 | 5 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | ATGTT others(1579): Show |
chr1 | 217421992 | 217636090 | ||
| a0004c0006 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | ATGTT others(1579): Show |
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 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0002 | 0/1 | 5859 | 29 | 10 | 6 | 8 | 1 | 3 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0003 | 0/0 | 5860 | 12 | 1 | 2 | 7 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5855): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0004 | 0/0 | 5855 | 11 | 5 | 2 | 2 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0005 | 0/0 | 5855 | 11 | 2 | 2 | 5 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0006 | 0/0 | 5853 | 10 | 8 | 1 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5848): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0007 | 0/0 | 5853 | 9 | 4 | 4 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5848): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0008 | 0/0 | 5859 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0009 | 0/0 | 5855 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0010 | 0/0 | 5859 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0011 | 0/0 | 5860 | 4 | 1 | 1 | 0 | 1 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5855): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0012 | 0/0 | 5859 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0014 | 0/0 | 5856 | 3 | 3 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5851): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0015 | 0/0 | 5855 | 3 | 0 | 1 | 0 | 0 | 2 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0016 | 0/0 | 5855 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0017 | 0/0 | 5859 | 2 | 0 | 2 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0018 | 0/0 | 5859 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0020 | 0/0 | 5856 | 2 | 1 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5851): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0021 | 0/0 | 5856 | 2 | 1 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5851): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0022 | 0/0 | 5856 | 2 | 2 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5851): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0023 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5853): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0024 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0025 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5853): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0026 | 0/0 | 5859 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0027 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5853): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0029 | 0/0 | 5860 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5855): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0031 | 0/0 | 5859 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0032 | 0/0 | 5859 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0033 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0034 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0035 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0036 | 0/0 | 5855 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0038 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0040 | 0/0 | 5836 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5831): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0041 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5849): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0042 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0043 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0001t0044 | 0/0 | 5844 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5839): Show |
chr1 | 217421992 | 217636090 |
| a0001c0004t0008 | 0/0 | 5859 | 3 | 0 | 3 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0001c0005t0004 | 0/0 | 5855 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0005t0009 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5850): Show |
chr1 | 217421992 | 217636090 |
| a0001c0007t0002 | 0/0 | 5859 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0002c0002t0008 | 0/0 | 5859 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0002c0002t0012 | 0/0 | 5859 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0002c0002t0013 | 0/0 | 5859 | 3 | 0 | 0 | 3 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0002c0002t0019 | 0/0 | 5859 | 2 | 0 | 1 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0002c0002t0028 | 0/0 | 5858 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5853): Show |
chr1 | 217421992 | 217636090 |
| a0002c0002t0030 | 0/0 | 5860 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5855): Show |
chr1 | 217421992 | 217636090 |
| a0002c0002t0039 | 0/0 | 5860 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5855): Show |
chr1 | 217421992 | 217636090 |
| a0003c0003t0010 | 0/0 | 5859 | 4 | 4 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| a0003c0003t0037 | 0/0 | 5860 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5855): Show |
chr1 | 217421992 | 217636090 |
| a0004c0006t0001 | 0/0 | 5859 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | GTCGG others(5854): Show |
chr1 | 217421992 | 217636090 |
| actghapid | grch38/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 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0023 | 1/0 | 1 | 0 | 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 |
| a0001c0001t0001g0058 | 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 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0090 | 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 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0002g0162 | 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 |
| a0001c0001t0003g0020 | 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 |
| a0001c0001t0003g0057 | 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 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0004g0161 | 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 |
| a0001c0001t0005g0019 | 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 |
| a0001c0001t0006g0140 | 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 |
| a0001c0001t0006g0144 | 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 |
| a0001c0001t0006g0174 | 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 |
| a0001c0001t0010g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0011g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0011g0147 | 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 |
| a0001c0001t0015g0151 | 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 |
| a0001c0001t0020g0158 | 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 |
| a0001c0001t0026g0091 | 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 |
| a0001c0001t0040g0164 | 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 |
| a0001c0001t0042g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0001t0043g0139 | 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 |
| a0001c0005t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0005t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0001c0007t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0002c0002t0008g0154 | 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 |
| a0002c0002t0019g0153 | 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 |
| a0002c0002t0039g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0003c0003t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| a0003c0003t0010g0149 | 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 | g0135 | 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 | g0062 | 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 | g0156 | 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 | g0021 | AMR | PUR | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0157 | 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 | g0152 | 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 | g0151 | 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 | g0145 | 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 | g0141 | AMR | CLM | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0060 | 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 | g0158 | 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 | g0173 | 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 | g0063 | 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 | g0147 | 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 | g0142 | AFR | ACB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02055 | hp2 | a0001 | c0001 | t0040 | g0164 | 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 | g0022 | 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 | g0061 | 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 | g0162 | EAS | CDX | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0140 | 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 | g0146 | 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 | g0015 | 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 | g0174 | 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 | g0148 | 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 | g0160 | SAS | PJL | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | 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 | g0149 | 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 | g0163 | 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 | g0133 | 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 | g0155 | 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 | g0143 | 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 | g0161 | 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 | g0139 | 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 | g0017 | 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 | g0154 | SAS | STU | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG03704 | hp1 | a0002 | c0002 | t0019 | g0153 | 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 | g0020 | SAS | BEB | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0016 | 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 | g0091 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0064 | 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 | g0136 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0058 | 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 | g0057 | 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 | g0144 | AFR | LWK | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19043 | hp2 | a0003 | c0003 | t0010 | g0137 | AFR | LWK | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0019 | 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 | g0134 | 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 | g0138 | 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 | g0150 | 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 | a0001 | c0001 | t0002 | g0117 | REF | REF | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0023 | REF | REF | GPATCH2_chr1_217421992_217636090 | GPATCH2 | chr1 | 217421992 | 217636090 |
| view | 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 |
| view | 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 |
| view | 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 | a0001c0001t0015 a0001c0001t0035 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0034 a0001c0001t0043 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0002c0002t0013 a0002c0002t0030 |
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 | a0001c0001t0009 a0001c0001t0016 a0001c0005t0009 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0008 a0001c0001t0012 a0001c0004t0008 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0029 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0040 |
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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(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 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0020 others(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 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(27): Show |
95 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(92): 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 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0025 |
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 |
| view | 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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0033g0081 a0001c0001t0041g0181 a0001c0001t0042g0173 |
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 | a0001c0001t0014g0084 a0001c0001t0021g0177 |
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 | a0001c0001t0033g0081 a0001c0001t0041g0181 a0001c0001t0042g0173 |
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 | a0001c0001t0009g0098 a0001c0001t0009g0105 a0001c0001t0009g0178 others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0006g0143 | 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 | a0001c0001t0011g0138 | 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 | a0003c0003t0010g0137 a0003c0003t0010g0149 a0003c0003t0010g0167 |
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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0007g0011 a0001c0001t0007g0013 |
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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0003c0003t0010g0188 a0003c0003t0037g0080 |
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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0004g0150 a0001c0001t0010g0163 |
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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0127 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 |
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 | a0003c0003t0010g0137 a0003c0003t0010g0149 a0003c0003t0010g0167 others(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 | a0003c0003t0010g0188 a0003c0003t0037g0080 |
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 | a0001c0001t0002g0112 a0001c0001t0011g0138 |
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 | a0001c0001t0002g0099 a0001c0001t0002g0104 |
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 | a0001c0001t0001g0038 a0001c0001t0014g0084 a0001c0001t0033g0081 others(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 | a0001c0001t0021g0177 a0001c0001t0038g0110 a0001c0005t0004g0141 others(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 | a0001c0001t0001g0025 a0002c0002t0013g0087 |
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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0018g0186 a0001c0001t0023g0002 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0003c0003t0010g0137 a0003c0003t0010g0149 a0003c0003t0010g0167 |
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 | a0001c0001t0043g0139 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0099 a0001c0001t0002g0104 others(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 | a0001c0001t0033g0081 a0001c0001t0041g0181 a0001c0001t0042g0173 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0025g0001 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0063 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0033g0081 a0001c0001t0041g0181 a0001c0001t0042g0173 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0004g0150 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0004g0150 a0001c0001t0006g0100 a0001c0001t0006g0107 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0002g0134 a0001c0001t0002g0171 a0001c0001t0018g0185 others(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 | a0001c0001t0006g0140 a0001c0001t0006g0174 a0001c0001t0006g0180 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0008g0096 a0001c0001t0012g0088 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0018 a0001c0001t0014g0084 a0001c0001t0021g0177 others(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 | a0001c0001t0001g0018 a0001c0001t0014g0084 a0001c0001t0021g0177 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 |
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 | a0001c0005t0004g0141 | 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 | a0001c0001t0001g0018 a0001c0001t0014g0084 a0001c0001t0021g0177 others(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 | a0001c0001t0006g0140 | 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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0005g0019 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0002g0114 a0001c0001t0003g0077 |
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 | a0001c0001t0014g0084 a0001c0001t0021g0177 a0001c0001t0033g0081 others(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 | a0001c0001t0002g0156 | 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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0044g0115 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0044g0115 |
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 | a0001c0001t0005g0019 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0014g0084 a0001c0001t0021g0177 a0001c0001t0033g0081 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0044g0115 |
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 | a0001c0001t0002g0104 a0001c0001t0002g0112 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0010g0163 others(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 | a0001c0001t0006g0133 a0001c0001t0007g0075 |
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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0044g0115 |
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 | a0001c0001t0006g0174 | 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 | a0001c0001t0001g0018 a0001c0001t0014g0084 a0001c0001t0021g0177 others(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 | a0001c0001t0006g0140 a0001c0001t0006g0174 a0001c0001t0006g0180 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0044g0115 |
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 | a0001c0001t0004g0113 a0001c0001t0004g0120 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | a0001c0001t0001g0018 a0001c0005t0004g0141 |
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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0127 others(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 | a0001c0001t0001g0010 a0001c0001t0002g0169 a0001c0001t0011g0135 others(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 | a0001c0001t0033g0081 a0001c0001t0041g0181 a0001c0001t0042g0173 |
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 | a0001c0001t0004g0150 a0001c0001t0010g0163 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0004g0113 others(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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | a0001c0001t0014g0084 a0001c0001t0021g0177 |
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 | a0001c0001t0005g0069 a0001c0001t0005g0071 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0002g0118 a0001c0001t0002g0184 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0025g0001 others(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 | a0001c0001t0006g0140 a0001c0001t0006g0180 a0001c0001t0007g0078 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0025g0001 others(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 | a0001c0001t0033g0081 a0001c0001t0041g0181 a0001c0001t0042g0173 |
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 | a0003c0003t0010g0137 a0003c0003t0010g0149 a0003c0003t0010g0167 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0025g0001 others(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 | a0001c0001t0005g0095 a0001c0001t0022g0182 a0001c0001t0022g0183 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0014g0084 a0001c0001t0021g0177 a0001c0001t0033g0081 others(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 | a0003c0003t0010g0137 a0003c0003t0010g0149 a0003c0003t0010g0167 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0025g0001 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0025g0001 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0044g0115 |
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 | a0001c0001t0033g0081 a0001c0001t0041g0181 a0001c0001t0042g0173 |
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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0044g0115 |
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 | a0001c0001t0034g0027 a0001c0001t0043g0139 |
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 | a0001c0001t0006g0100 a0001c0001t0006g0107 a0001c0001t0006g0128 others(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 | a0001c0001t0004g0150 a0001c0001t0010g0163 |
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 | a0001c0001t0001g0090 | 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 | a0001c0001t0022g0182 a0001c0001t0022g0183 a0001c0001t0025g0001 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0020g0158 a0001c0001t0032g0056 |
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 | a0001c0001t0001g0018 a0001c0001t0002g0114 a0001c0001t0002g0121 others(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 | a0001c0001t0002g0114 a0001c0001t0025g0001 |
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 | a0001c0001t0022g0182 a0001c0001t0040g0164 a0001c0001t0044g0115 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0009g0178 others(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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0002c0002t0013g0046 a0002c0002t0013g0055 a0002c0002t0030g0047 |
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 | a0001c0001t0004g0161 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0009g0178 others(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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0009g0178 others(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 | a0001c0001t0006g0174 a0001c0001t0009g0187 a0001c0001t0014g0094 others(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 | a0001c0001t0004g0150 a0001c0001t0009g0178 |
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 | a0001c0001t0011g0138 | 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 | a0001c0001t0006g0174 a0001c0001t0009g0187 a0001c0001t0014g0094 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0006g0174 a0001c0001t0027g0093 a0001c0001t0033g0081 others(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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0004g0161 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1278-3712A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217453049 | |||||||
| chr1:217453324 | T | C | 1 | a0001c0001t0006g0144 | 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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0002g0157 | 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 | a0001c0001t0006g0174 a0001c0001t0009g0187 a0001c0001t0014g0094 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0006g0174 a0001c0001t0033g0081 a0001c0001t0042g0173 |
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 | |||||||
| chr1:217454545 | C | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | 90 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0026 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1278-5252dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 8/9 | chr1 | 217454588 | |||||||
| chr1:217454588 | C | CAA | 55 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0009g0178 others(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 | a0001c0001t0006g0174 a0001c0001t0009g0187 a0001c0001t0016g0086 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0006g0174 a0001c0001t0027g0093 a0001c0001t0033g0081 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0159 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0006g0174 a0001c0001t0009g0187 a0001c0001t0016g0086 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0006g0107 a0001c0001t0006g0133 a0001c0001t0006g0144 |
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 | a0001c0001t0006g0107 a0001c0001t0006g0133 a0001c0001t0006g0144 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0150 a0001c0001t0009g0178 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0002g0156 a0001c0001t0006g0165 a0001c0001t0007g0004 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0001g0018 a0001c0001t0038g0110 a0003c0003t0010g0137 others(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 | a0001c0001t0009g0187 a0001c0001t0016g0086 |
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 | a0001c0001t0006g0174 a0001c0001t0033g0081 a0001c0001t0042g0173 |
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 | a0002c0002t0008g0154 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0057 |
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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0007g0079 a0001c0001t0018g0185 a0001c0001t0018g0186 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0005t0004g0141 | 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 | a0001c0001t0038g0110 a0003c0003t0010g0137 a0003c0003t0010g0149 others(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 | a0001c0001t0004g0130 a0001c0001t0009g0187 a0001c0001t0016g0086 |
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 | a0001c0001t0001g0018 a0001c0001t0006g0174 a0001c0001t0014g0094 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | |||||||
| chr1:217463094 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0038g0110 a0001c0001t0040g0164 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0001g0018 a0001c0001t0025g0001 a0001c0001t0038g0110 others(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 | a0001c0001t0001g0018 a0001c0001t0002g0122 a0001c0001t0002g0159 others(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 | a0001c0001t0003g0006 a0001c0001t0003g0052 a0001c0001t0005g0050 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0002g0099 others(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 | a0001c0001t0016g0086 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0006g0174 a0001c0001t0009g0187 a0001c0001t0014g0094 others(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 | a0001c0001t0002g0156 a0001c0001t0006g0165 a0001c0001t0007g0004 others(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 | a0001c0001t0001g0010 a0001c0001t0003g0009 a0001c0001t0003g0072 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0004g0102 a0001c0001t0004g0111 a0001c0001t0006g0140 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0015g0175 a0001c0001t0015g0176 |
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 | a0001c0001t0008g0096 a0001c0001t0012g0088 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0022g0182 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0006g0107 a0001c0001t0006g0144 |
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 | a0001c0001t0006g0107 a0001c0001t0006g0133 a0001c0001t0006g0144 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0131 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0022g0182 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0002g0104 a0001c0001t0002g0112 a0001c0001t0009g0105 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0002c0002t0039g0160 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0007t0002g0145 a0002c0002t0019g0153 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0003c0003t0010g0137 others(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 | a0001c0001t0001g0036 a0001c0001t0002g0156 a0001c0001t0006g0165 others(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 | a0001c0001t0010g0163 | 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 | a0001c0001t0005g0050 a0001c0001t0005g0051 |
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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0092 a0001c0001t0005g0019 a0002c0002t0013g0046 others(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 | a0001c0001t0005g0005 a0001c0001t0018g0185 a0001c0001t0018g0186 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0026 others(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 | 20 | a0001c0001t0001g0054 a0001c0001t0002g0129 a0001c0001t0002g0168 others(17): Show |
20 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(17): 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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0025 others(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 | a0001c0001t0002g0156 a0001c0001t0003g0057 a0001c0001t0005g0019 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0063 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0044 a0001c0001t0021g0177 a0002c0002t0013g0055 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0062 others(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 | a0003c0003t0010g0137 a0003c0003t0010g0149 a0003c0003t0010g0167 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0006g0107 a0001c0001t0006g0133 a0001c0001t0006g0144 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0009g0098 a0001c0001t0014g0084 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0040g0164 others(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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0006g0174 a0001c0001t0009g0187 a0001c0001t0016g0086 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0003c0003t0010g0137 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0073 a0001c0001t0007g0014 a0001c0001t0022g0182 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0025 others(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 | a0001c0001t0004g0130 a0001c0001t0008g0096 a0001c0001t0009g0187 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0057 a0001c0001t0025g0001 |
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 | a0001c0001t0006g0174 a0001c0001t0027g0093 a0001c0001t0033g0081 others(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 | a0001c0001t0003g0020 | 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 | a0001c0001t0016g0083 a0001c0005t0004g0141 a0001c0005t0009g0142 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0025g0001 others(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 | a0001c0001t0014g0094 a0001c0001t0021g0106 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0025g0001 others(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 | a0001c0001t0025g0001 a0001c0001t0038g0110 |
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 | a0001c0001t0018g0185 a0001c0001t0018g0186 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0063 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0004g0161 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0009g0187 a0001c0001t0012g0031 a0001c0001t0016g0086 |
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 | a0001c0001t0004g0111 a0001c0001t0006g0140 a0001c0001t0007g0078 others(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 | a0001c0001t0012g0088 a0001c0004t0008g0108 a0001c0004t0008g0119 |
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 | a0001c0001t0002g0104 a0001c0001t0002g0112 a0001c0001t0004g0150 others(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 | a0001c0001t0001g0092 a0001c0001t0005g0019 a0002c0002t0028g0070 |
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 | a0002c0002t0013g0046 a0002c0002t0013g0055 a0002c0002t0013g0087 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0021 others(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 | a0001c0001t0006g0174 a0001c0001t0027g0093 a0001c0001t0033g0081 others(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 | a0001c0001t0001g0090 a0001c0001t0003g0039 a0001c0001t0003g0089 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0009g0098 a0001c0001t0014g0084 a0001c0001t0023g0002 |
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 | a0001c0001t0006g0133 | 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 | a0003c0003t0010g0137 a0003c0003t0010g0149 a0003c0003t0010g0167 |
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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0040g0164 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0011g0135 |
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 | a0001c0001t0025g0001 a0001c0001t0038g0110 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0146 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 others(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 | a0001c0001t0009g0098 a0001c0001t0014g0084 a0001c0001t0023g0002 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0002g0159 a0001c0001t0003g0006 a0001c0001t0003g0052 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0006g0180 a0001c0001t0034g0027 a0001c0001t0043g0139 others(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 | a0001c0001t0044g0115 a0002c0002t0012g0007 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0010 a0001c0001t0002g0156 a0001c0001t0006g0165 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0010 a0001c0001t0002g0156 a0001c0001t0006g0165 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0057 |
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 | a0001c0001t0001g0058 a0001c0001t0005g0051 a0001c0001t0006g0174 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0002g0104 a0001c0001t0002g0112 a0001c0001t0009g0105 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0004g0161 | 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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0040g0164 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0001g0010 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0018 a0001c0001t0004g0130 a0001c0001t0038g0110 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0015g0151 | 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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0073 a0002c0002t0019g0172 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0045 a0001c0001t0035g0035 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0082 others(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 | a0001c0001t0022g0182 a0001c0001t0022g0183 |
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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0004g0161 a0001c0001t0005g0095 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0018 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0092 others(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 | a0001c0001t0006g0174 a0001c0001t0027g0093 a0001c0001t0033g0081 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0040g0164 | 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 | 32 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0066 others(29): Show |
32 | HG00099.hp1 HG00673.hp2 HG01071.hp2 others(29): 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0006g0174 a0001c0001t0027g0093 a0001c0001t0033g0081 others(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 | a0001c0001t0005g0043 a0001c0001t0007g0014 |
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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0118 others(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 | |||||||
| chr1:217499293 | T | A | 4 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0006g0180 a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | 9 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0118 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167-1339delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217499733 | |||||||
| chr1:217499774 | C | T | 1 | a0001c0001t0040g0164 | 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 | a0001c0001t0006g0180 a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0004g0150 a0001c0001t0004g0179 a0001c0001t0009g0178 others(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 | 115 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(112): Show |
115 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(112): 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0118 others(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 | a0002c0002t0013g0046 a0002c0002t0030g0047 |
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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0006g0180 a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): 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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): 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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 |
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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0004g0111 a0001c0001t0006g0107 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0002g0155 | 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): 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 | a0001c0001t0001g0017 | 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 | 113 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(110): Show |
113 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(110): 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0004g0111 a0001c0001t0006g0107 a0001c0001t0021g0106 others(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 | a0001c0001t0002g0125 a0001c0001t0004g0161 |
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 | a0001c0001t0002g0103 a0001c0001t0002g0112 a0001c0001t0006g0140 others(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 | 97 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): 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 | 50 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(47): Show |
50 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(47): 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 | a0001c0001t0015g0151 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0004g0130 a0001c0001t0008g0096 |
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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1166+8129G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 6/9 | chr1 | 217506693 | |||||||
| chr1:217506738 | A | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0002g0159 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | 97 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0009g0187 a0001c0001t0016g0086 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0157 others(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 | a0001c0001t0015g0151 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0006g0143 | 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 | 90 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(87): Show |
90 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(87): 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 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0159 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0002g0156 others(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 | a0001c0001t0001g0008 a0002c0002t0012g0007 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0118 others(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 | a0001c0001t0010g0163 | 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 | 108 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(105): Show |
108 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): 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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0003g0059 a0001c0001t0011g0147 a0001c0001t0029g0042 |
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 | a0001c0001t0003g0006 a0001c0001t0003g0048 |
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 | a0002c0002t0039g0160 | 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | 97 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0045 others(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 | a0001c0001t0011g0166 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | 97 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): 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 | 99 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(96): Show |
99 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(96): 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 | a0001c0001t0006g0174 a0001c0001t0007g0013 a0001c0001t0022g0183 others(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 | 99 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(96): Show |
99 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1099-711G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217515600 | |||||||
| chr1:217515614 | C | T | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0001g0054 a0001c0001t0003g0039 a0001c0001t0006g0174 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | 112 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(109): Show |
112 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1099-1339delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217516227 | |||||||
| chr1:217516231 | T | A | 2 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(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 | a0001c0001t0006g0140 | 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0003g0059 a0001c0001t0011g0147 |
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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0004g0152 | 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0006g0143 | 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 | a0001c0001t0006g0143 | 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0002g0159 | 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 | a0001c0001t0011g0135 | 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 | a0001c0007t0002g0145 | 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | 97 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): 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 | a0001c0001t0005g0085 a0001c0001t0008g0096 |
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 | 97 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0002g0157 | 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 | a0001c0001t0002g0118 a0001c0001t0003g0077 a0001c0001t0007g0075 others(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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0004g0150 a0001c0001t0004g0179 a0001c0001t0009g0178 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0002g0131 others(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 | a0001c0001t0014g0084 a0001c0001t0023g0002 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0090 a0001c0001t0002g0146 others(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 | 48 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(45): Show |
48 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(45): 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 | a0001c0001t0002g0104 a0001c0001t0002g0146 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0029 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0028 others(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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0004g0102 a0001c0004t0008g0119 |
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 | a0001c0001t0004g0102 a0001c0004t0008g0119 |
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 | a0001c0001t0040g0164 | 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 | 57 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(54): Show |
57 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(54): 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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0001g0060 | 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 | a0001c0001t0002g0118 a0001c0001t0004g0130 a0001c0001t0004g0150 others(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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | 54 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(51): Show |
54 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1099-8235T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523124 | |||||||
| chr1:217523175 | A | T | 63 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(60): Show |
63 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(60): 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 | 39 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(36): Show |
39 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(36): 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 | a0001c0001t0003g0006 a0001c0001t0003g0039 a0001c0001t0003g0048 |
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 | a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0016 a0001c0001t0044g0115 a0002c0002t0012g0007 |
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 | a0001c0001t0001g0016 a0001c0001t0044g0115 a0002c0002t0012g0007 |
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 | a0001c0001t0006g0174 a0001c0001t0033g0081 a0001c0001t0041g0181 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0136 | 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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | 39 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(36): Show |
39 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1099-8918dupG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217523806 | |||||||
| chr1:217523829 | G | A | 10 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0004g0152 | 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 | a0001c0001t0004g0127 a0001c0001t0006g0128 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0118 others(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 | 105 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(102): Show |
105 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(102): 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0002g0118 a0001c0001t0004g0130 |
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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0002g0157 | 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0004g0152 a0001c0001t0020g0158 |
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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0024 a0001c0001t0003g0006 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0024 a0001c0001t0003g0006 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0024 a0001c0001t0003g0006 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0024 a0001c0001t0003g0006 a0001c0001t0003g0039 others(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 | 159 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(156): Show |
159 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(156): 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0002g0155 | 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 | a0001c0001t0015g0151 | 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 | a0001c0001t0002g0136 | 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 | a0001c0001t0003g0052 a0001c0001t0005g0095 |
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 | a0001c0001t0002g0159 a0001c0001t0005g0019 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0067 |
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 | a0001c0001t0001g0066 a0001c0001t0035g0035 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0003g0072 others(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 | a0001c0001t0001g0068 a0001c0001t0002g0162 a0001c0001t0003g0057 |
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 | a0001c0001t0001g0026 a0001c0001t0007g0004 |
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 | 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 | a0002c0002t0008g0154 | 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 | a0001c0001t0002g0157 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0157 | 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 | a0001c0001t0011g0166 a0001c0001t0015g0176 a0001c0001t0021g0177 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0090 a0001c0001t0002g0146 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0090 a0001c0001t0002g0146 others(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 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0004g0152 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0157 a0001c0001t0005g0033 a0001c0001t0010g0163 others(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 | a0001c0001t0003g0009 a0001c0001t0004g0130 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0118 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0004g0152 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0004g0161 | 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 | a0001c0001t0002g0146 | 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 | a0002c0002t0019g0153 | 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 | a0001c0001t0002g0099 a0001c0001t0006g0174 a0001c0001t0022g0183 others(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 | a0001c0001t0011g0138 a0001c0001t0012g0088 |
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 | a0001c0001t0043g0139 a0001c0004t0008g0097 |
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 | a0003c0003t0010g0149 | 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 | a0001c0001t0002g0099 a0001c0001t0006g0174 a0001c0001t0022g0183 others(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 | a0001c0001t0009g0187 a0001c0001t0017g0101 |
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 | a0001c0001t0002g0099 a0001c0001t0003g0059 a0001c0001t0006g0174 others(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 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0002g0099 a0001c0001t0006g0174 a0001c0001t0022g0183 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0082 others(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 | 30 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0037 others(27): Show |
30 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(27): 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 | a0001c0001t0002g0104 a0001c0001t0006g0143 a0001c0001t0009g0105 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0082 others(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 | 68 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(65): Show |
68 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(65): 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 | a0001c0001t0010g0163 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0099 a0001c0001t0004g0130 a0001c0001t0006g0174 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0036 others(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 | a0001c0001t0005g0033 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0118 a0001c0001t0002g0157 |
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 | 31 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0037 others(28): Show |
31 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(28): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0148 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | 29 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0037 others(26): Show |
29 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(26): 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0121 a0001c0001t0002g0131 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0011g0147 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0041 others(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 | a0001c0001t0010g0163 | 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 | 66 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(63): Show |
66 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(63): 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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(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 | a0001c0001t0017g0116 a0001c0001t0032g0056 |
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 | 26 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0058 others(23): Show |
26 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099-10022delC | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217524910 | |||||||
| chr1:217524911 | G | GA | 4 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0041 others(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 | a0001c0001t0010g0163 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | 32 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(29): Show |
32 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(29): 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 | a0001c0001t0002g0118 a0001c0001t0010g0163 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0104 a0001c0001t0006g0143 a0001c0001t0006g0174 others(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 | a0001c0001t0003g0009 a0001c0001t0004g0130 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0001g0028 a0001c0001t0002g0121 a0001c0001t0006g0180 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0044 a0001c0001t0001g0073 others(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 | a0001c0001t0006g0144 | 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 | a0001c0007t0002g0145 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0049 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0034 a0001c0001t0020g0158 |
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 | a0001c0001t0001g0017 | 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 | a0001c0001t0026g0091 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0028 a0001c0001t0002g0124 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0059 a0001c0001t0003g0077 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0082 a0001c0001t0002g0099 others(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 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0124 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 |
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 | a0001c0001t0001g0028 a0001c0001t0003g0089 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0002g0168 others(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(336): Show |
1 | a0001c0001t0010g0163 | 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0003g0059 others(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 | a0001c0001t0002g0148 | 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 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0121 |
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 | a0001c0001t0001g0018 a0001c0001t0002g0155 |
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 | a0001c0001t0001g0090 | 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0033g0081 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0040g0164 | 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0011g0138 a0001c0001t0012g0088 a0001c0001t0034g0027 others(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 | a0001c0001t0040g0164 | 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 | 99 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(96): Show |
99 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(96): 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0004g0150 a0001c0001t0004g0179 a0001c0001t0009g0178 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0157 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0060 a0001c0001t0011g0166 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0044 a0001c0001t0005g0033 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0114 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 |
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 | a0001c0001t0040g0164 | 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 | 108 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(105): Show |
108 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1099-13279G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217528168 | |||||||
| chr1:217528245 | C | T | 143 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(140): Show |
143 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(140): 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0011g0135 | 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | |||||||
| chr1:217528935 | A | G | 10 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0006g0174 others(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 | a0001c0001t0004g0150 a0001c0001t0004g0179 a0001c0001t0009g0178 others(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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0155 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0006g0144 | 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0004g0126 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0004g0130 others(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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | 95 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(92): Show |
95 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(92): 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 | 96 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(93): Show |
96 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1099-16190A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217531079 | |||||||
| chr1:217531328 | G | A | 109 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(106): Show |
109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): 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 | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(38): Show |
41 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(38): 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0024 others(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 | 98 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(95): Show |
98 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(95): 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 | a0001c0001t0006g0143 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0002g0118 a0001c0001t0015g0175 a0001c0001t0016g0083 others(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 | |||||||
| chr1:217532897 | TTTG | T | 86 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0064 a0001c0001t0002g0099 a0001c0001t0002g0103 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0121 a0001c0001t0002g0146 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0002g0121 others(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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0002g0118 a0001c0001t0003g0077 a0001c0001t0007g0075 others(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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-18429C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217533318 | |||||||
| chr1:217533366 | C | T | 96 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(93): Show |
96 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(93): 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 | a0001c0001t0004g0161 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | 108 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(105): Show |
108 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): 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 | a0001c0001t0006g0174 a0001c0001t0022g0182 a0001c0001t0022g0183 others(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 | a0001c0001t0001g0010 a0001c0001t0007g0011 a0001c0001t0007g0013 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0045 others(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 | 79 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(76): Show |
79 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(76): 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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0002g0118 a0001c0001t0003g0077 a0001c0001t0007g0075 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0020g0109 a0001c0001t0024g0003 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0006g0174 a0001c0001t0033g0081 a0001c0001t0042g0173 |
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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0040g0164 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0157 others(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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | 108 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(105): Show |
108 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1099-22711T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537600 | |||||||
| chr1:217537758 | TC | T | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1099-22870delG | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217537758 | |||||||
| chr1:217537801 | T | C | 3 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | 171 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(168): Show |
171 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(168): 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(37): Show |
40 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(37): 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 | a0001c0001t0001g0018 a0001c0001t0002g0103 a0001c0001t0002g0134 others(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 | a0001c0001t0002g0104 a0001c0001t0003g0009 a0001c0001t0006g0143 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | 117 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0021 others(114): Show |
117 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(114): 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 | a0001c0001t0005g0085 a0001c0001t0008g0096 a0001c0001t0014g0084 |
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 | a0001c0001t0002g0114 a0001c0001t0002g0121 |
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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | 110 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(107): Show |
110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): 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 | a0001c0001t0005g0019 | 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 | 110 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(107): Show |
110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0157 |
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 | a0001c0001t0001g0058 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0011g0135 others(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 | 110 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(107): Show |
110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): 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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0011g0138 a0001c0001t0012g0088 a0001c0001t0034g0027 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | 62 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0025 others(59): Show |
62 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.1099-28381dupA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543269 | |||||||
| chr1:217543269 | G | GTT | 21 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | 34 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(31): Show |
34 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-28631G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217543520 | |||||||
| chr1:217543535 | T | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(107): Show |
110 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(107): 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0006g0180 |
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 | a0001c0001t0002g0118 a0001c0001t0003g0030 a0001c0001t0009g0187 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0003g0077 a0001c0001t0040g0164 |
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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0002c0002t0013g0046 a0002c0002t0030g0047 |
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 | 33 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(30): Show |
33 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(30): 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 | a0001c0001t0016g0083 a0001c0005t0009g0142 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0003g0009 others(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 | a0001c0001t0003g0077 a0001c0001t0040g0164 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0006g0180 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | 140 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(137): Show |
140 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1099-32250T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547139 | |||||||
| chr1:217547165 | C | T | 34 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(31): Show |
34 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(31): 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 | a0001c0001t0001g0058 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 75 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(72): Show |
75 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1099-32461dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547349 | |||||||
| chr1:217547377 | C | T | 14 | a0001c0001t0001g0058 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | 33 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(30): Show |
33 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1099-33104G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217547993 | |||||||
| chr1:217548256 | T | C | 34 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(31): Show |
34 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(31): 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 | a0001c0001t0001g0058 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0114 a0001c0001t0002g0121 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | 34 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(31): Show |
34 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-34218T>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217549107 | |||||||
| chr1:217549127 | G | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(96): Show |
99 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(96): 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 | a0001c0001t0011g0138 a0001c0001t0012g0088 a0001c0001t0034g0027 others(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 | a0001c0001t0006g0100 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | 38 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(35): Show |
38 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(35): 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | 35 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(32): Show |
35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): 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 | a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | 35 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(32): Show |
35 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(32): 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 | a0001c0001t0002g0114 a0001c0001t0002g0121 |
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 | a0001c0001t0010g0163 | 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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0082 a0001c0001t0002g0099 a0001c0001t0006g0180 |
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 | a0001c0001t0003g0077 a0001c0001t0040g0164 |
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 | a0001c0001t0006g0143 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0003g0009 others(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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0001g0058 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0004g0111 a0001c0001t0005g0085 a0001c0001t0006g0107 others(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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0134 a0001c0001t0002g0171 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0002g0114 others(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 | 74 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(71): Show |
74 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(71): 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 | a0001c0001t0007g0075 a0001c0001t0009g0098 a0001c0001t0022g0182 others(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 | a0001c0001t0007g0075 a0001c0001t0009g0098 a0001c0001t0022g0182 others(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 | a0001c0001t0002g0157 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0002g0136 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0001g0058 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | 28 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(25): Show |
28 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(25): 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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0001g0041 a0001c0001t0002g0168 a0001c0001t0005g0050 others(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 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0002g0118 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0041 |
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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0022g0182 a0001c0001t0025g0001 |
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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0007g0075 a0001c0001t0009g0098 a0001c0001t0022g0182 others(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 | a0001c0001t0001g0058 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0006g0174 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0058 a0001c0001t0002g0118 a0001c0001t0002g0136 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0006g0174 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0058 a0001c0001t0002g0118 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0058 a0001c0001t0002g0118 a0001c0001t0002g0136 others(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 | a0001c0001t0006g0174 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0040g0164 | 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 | a0001c0001t0005g0085 a0001c0001t0008g0096 a0001c0001t0014g0084 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0006g0174 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0006g0174 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0002g0136 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0004g0111 a0001c0001t0006g0107 a0001c0001t0006g0133 others(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 | a0001c0001t0007g0076 a0001c0001t0014g0094 |
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 | a0001c0001t0001g0044 a0001c0001t0002g0099 a0001c0001t0002g0104 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0002g0122 others(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 | 32 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(29): Show |
32 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(29): 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 | a0001c0001t0007g0075 a0001c0001t0009g0098 |
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 | a0001c0001t0006g0174 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0025 others(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 | a0001c0001t0006g0174 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0099 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0018 others(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 | 61 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(58): Show |
61 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(58): 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 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0002g0122 others(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 | 170 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.1098+46122C>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564199 | |||||||
| chr1:217564200 | T | A | 97 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0021 others(94): Show |
97 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1098+46121A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564200 | |||||||
| chr1:217564214 | G | A | 89 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0021 others(86): Show |
89 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1098+46107C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217564214 | |||||||
| chr1:217564287 | C | T | 32 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(29): Show |
32 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(29): 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 | a0001c0001t0002g0112 a0001c0001t0007g0076 a0001c0001t0014g0094 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0002g0122 others(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 | a0001c0001t0006g0143 | 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 | a0001c0001t0002g0099 a0001c0001t0006g0174 a0001c0001t0007g0075 others(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 | a0001c0001t0002g0099 a0001c0001t0006g0174 a0001c0001t0007g0075 others(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 | 36 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(33): Show |
36 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(33): 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 | a0001c0001t0002g0134 | 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 | 73 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0025 others(70): Show |
73 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1098+44564delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217565756 | |||||||
| chr1:217565798 | T | C | 2 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | 73 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0025 others(70): Show |
73 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(70): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0009g0187 a0001c0001t0022g0182 a0003c0003t0010g0188 |
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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0082 a0001c0001t0002g0114 others(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 | 46 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0026 others(43): Show |
46 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1098+44219delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217566101 | |||||||
| chr1:217566101 | CAA | C | 21 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0090 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0002g0132 a0001c0001t0002g0157 a0001c0001t0004g0111 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0002g0122 others(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 | 73 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0025 others(70): Show |
73 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(70): 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 | 47 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(44): Show |
47 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(44): 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 | a0001c0001t0001g0038 a0001c0001t0002g0136 a0001c0001t0040g0164 others(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 | a0001c0001t0001g0018 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0008 a0001c0001t0002g0146 a0001c0001t0002g0171 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | 79 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0025 others(76): Show |
79 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(76): 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 | a0001c0001t0004g0111 a0001c0001t0006g0107 a0001c0001t0020g0109 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0104 a0001c0001t0009g0105 |
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 | 57 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0026 others(54): Show |
57 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(54): 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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0001g0044 a0001c0001t0002g0104 a0001c0001t0002g0121 others(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 | 34 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(31): Show |
34 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(31): 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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0011g0166 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0001g0082 a0001c0001t0023g0002 a0003c0003t0010g0137 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0004g0150 a0001c0001t0006g0100 a0001c0001t0008g0096 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0011g0166 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0001g0025 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0010g0163 | 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 | a0001c0001t0002g0099 a0001c0001t0002g0171 a0001c0001t0007g0075 others(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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0026g0091 | 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 | a0001c0001t0026g0091 | 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 | a0001c0001t0026g0091 | 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 | a0002c0002t0013g0046 a0002c0002t0030g0047 |
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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | 99 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(96): Show |
99 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(96): 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 | 72 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(69): Show |
72 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(69): 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0006g0144 | 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 | a0002c0002t0008g0154 | 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 | a0001c0005t0004g0141 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | 50 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(47): Show |
50 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(47): 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 | 37 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(34): Show |
37 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1098+38679C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571642 | |||||||
| chr1:217571661 | A | C | 86 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(83): Show |
86 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(83): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | 48 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0025 others(45): Show |
48 | HG00558.hp2 HG00673.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1098+38617dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217571703 | |||||||
| chr1:217571703 | C | CAA | 24 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0054 others(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 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0003g0020 others(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 | a0001c0001t0023g0002 a0003c0003t0010g0137 a0003c0003t0010g0167 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0090 others(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 | 54 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(51): Show |
54 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(51): 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 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | 48 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(45): Show |
48 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(45): 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 | a0001c0001t0006g0143 a0001c0001t0006g0174 a0001c0001t0009g0187 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0099 others(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 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0006g0143 a0001c0001t0006g0174 a0001c0001t0022g0182 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0004g0111 a0001c0001t0005g0085 a0001c0001t0006g0107 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0104 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | 85 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0026 others(82): Show |
85 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(82): 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 | 38 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(35): Show |
38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): 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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0099 a0001c0001t0006g0143 a0001c0001t0006g0174 others(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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0002g0099 a0001c0001t0002g0118 a0001c0001t0007g0075 others(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 | a0001c0001t0001g0045 a0001c0001t0007g0012 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0006g0143 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0002g0134 | 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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0004g0127 a0001c0001t0006g0128 |
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 | a0001c0001t0006g0143 a0001c0001t0006g0174 a0001c0001t0022g0182 others(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 | 90 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(87): Show |
90 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(87): 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 | a0001c0001t0006g0143 a0001c0001t0006g0174 a0001c0001t0022g0182 others(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 | 99 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(96): Show |
99 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1098+32416G>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217577905 | |||||||
| chr1:217577935 | C | T | 37 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(34): Show |
37 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(34): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0004g0111 a0001c0001t0004g0179 a0001c0001t0005g0033 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0057 a0001c0001t0005g0069 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0112 a0001c0001t0006g0143 others(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 | 38 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(35): Show |
38 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+30947dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217579373 | |||||||
| chr1:217579434 | A | G | 10 | a0001c0001t0006g0140 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | a0001c0001t0002g0118 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0044 a0001c0001t0002g0104 a0001c0001t0009g0105 |
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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0001g0025 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | 59 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(56): Show |
59 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(56): 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 | a0001c0001t0001g0016 a0002c0002t0012g0007 |
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 | 109 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(106): Show |
109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): 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 | a0001c0001t0004g0150 a0003c0003t0010g0149 |
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 | a0001c0001t0001g0044 a0001c0001t0002g0104 a0001c0001t0002g0121 others(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 | a0001c0001t0005g0005 a0001c0001t0036g0065 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | 37 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(34): Show |
37 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(34): 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0073 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | 109 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(106): Show |
109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): 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 | 37 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(34): Show |
37 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(34): 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 | 55 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(52): Show |
55 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(52): 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 | a0001c0001t0002g0103 a0001c0001t0002g0112 a0001c0001t0006g0143 others(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 | a0001c0001t0001g0049 a0001c0001t0003g0052 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | 35 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(32): Show |
35 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(32): 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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 55 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(52): Show |
55 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(52): 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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | 109 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(106): Show |
109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): 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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | 109 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(106): Show |
109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): 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 | a0001c0001t0011g0135 | 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 | a0001c0001t0006g0140 a0001c0001t0009g0178 a0001c0001t0011g0138 others(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 | 47 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(44): Show |
47 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(44): 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 | a0001c0001t0018g0185 a0001c0001t0018g0186 |
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 | a0001c0001t0011g0147 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0038 a0001c0001t0003g0057 |
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 | a0001c0001t0026g0091 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0054 others(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 |
2 | a0001c0001t0001g0062 a0001c0001t0002g0159 |
2 | HG00597.hp2 NA19077.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 | a0001c0001t0002g0148 a0001c0001t0015g0151 |
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 | a0001c0001t0001g0049 a0001c0001t0003g0052 a0001c0001t0005g0050 others(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 | a0001c0001t0001g0068 a0001c0001t0002g0169 a0001c0001t0010g0163 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0095 |
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 | a0001c0001t0027g0093 a0001c0001t0033g0081 a0001c0001t0041g0181 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0037 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0063 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 |
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 | a0001c0001t0002g0103 a0001c0001t0002g0112 a0001c0001t0006g0143 others(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 | a0001c0004t0008g0119 a0001c0005t0004g0141 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0099 others(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 | a0001c0001t0002g0118 a0001c0001t0005g0074 a0001c0001t0007g0014 |
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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0002g0103 a0001c0001t0002g0112 a0001c0001t0006g0143 others(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 | a0001c0001t0006g0174 a0001c0001t0022g0183 a0001c0001t0027g0093 others(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 | 45 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(42): Show |
45 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(42): 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 | a0001c0001t0002g0103 a0001c0001t0002g0112 a0001c0001t0006g0143 others(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 | a0001c0001t0002g0118 a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0001g0025 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | a0001c0001t0002g0136 a0001c0001t0003g0009 a0001c0001t0003g0020 others(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 | 35 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(32): Show |
35 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(32): 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 | 109 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(106): Show |
109 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(106): 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 | a0003c0003t0010g0137 | 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 | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(67): Show |
70 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1098+24422A>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217585899 | |||||||
| chr1:217585991 | T | A | 48 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(45): Show |
48 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(45): 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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0114 others(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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | 108 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(105): Show |
108 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): 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 | 108 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(105): Show |
108 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(105): 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 | a0001c0001t0002g0103 a0001c0001t0006g0143 a0001c0001t0007g0076 others(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 | 52 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(49): Show |
52 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1098+22842G>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217587479 | |||||||
| chr1:217587543 | C | G | 57 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(54): Show |
57 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(54): 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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | 58 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(55): Show |
58 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(55): 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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | a0001c0001t0015g0151 | 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 | a0003c0003t0010g0137 | 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 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0006g0143 others(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 | 37 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(34): Show |
37 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(34): 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 | a0001c0001t0001g0024 a0001c0001t0001g0090 a0001c0001t0001g0092 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0104 others(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 | a0001c0001t0016g0083 a0001c0005t0004g0141 a0001c0005t0009g0142 |
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 | a0001c0001t0002g0104 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0006g0143 others(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 | 58 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(55): Show |
58 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(55): 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 | a0001c0001t0002g0104 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0002g0118 a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0004g0150 a0001c0001t0005g0033 a0001c0001t0005g0085 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0011g0166 a0001c0001t0015g0175 a0001c0001t0015g0176 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0003g0077 a0001c0001t0006g0174 a0001c0001t0022g0183 others(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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | 43 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(40): Show |
43 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1098+18891G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217591430 | |||||||
| chr1:217591475 | A | G | 131 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(128): 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 | 42 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(39): Show |
42 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(39): 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 | a0001c0001t0002g0112 a0001c0001t0007g0076 a0001c0001t0014g0094 |
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 | a0002c0002t0039g0160 | 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 | a0001c0001t0004g0111 a0001c0001t0006g0107 |
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 | 131 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.1098+18312delT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217592008 | |||||||
| chr1:217592034 | TAAAG | T | 2 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | 131 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(128): 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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | 142 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(139): 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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | 44 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(41): Show |
44 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(41): 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 | a0001c0001t0002g0156 | 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 | a0001c0001t0002g0104 a0001c0001t0002g0136 a0001c0001t0003g0009 others(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 | 37 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(34): Show |
37 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(34): 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 | a0002c0002t0013g0046 a0002c0002t0030g0047 |
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 | a0001c0001t0001g0025 a0001c0001t0002g0104 a0001c0001t0002g0136 others(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 | a0001c0001t0004g0150 a0003c0003t0010g0149 |
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 | 121 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(118): 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 | a0001c0001t0044g0115 a0002c0002t0019g0172 |
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 | 42 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(39): Show |
42 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(39): 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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | 42 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(39): Show |
42 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(39): 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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0002g0134 a0001c0001t0006g0133 |
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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0002g0155 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0002g0122 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0112 a0001c0001t0006g0143 others(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 | a0001c0001t0004g0150 a0001c0001t0006g0100 a0001c0001t0008g0096 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0002g0134 a0001c0001t0004g0150 a0001c0001t0006g0100 others(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 | 43 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0037 others(40): Show |
43 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1098+14147C>T | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596174 | |||||||
| chr1:217596342 | T | G | 142 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(139): Show |
142 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.1098+13979A>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217596342 | |||||||
| chr1:217596452 | A | G | 38 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0036 others(35): Show |
38 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(35): 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 | a0001c0001t0002g0099 a0001c0001t0007g0075 a0001c0001t0009g0098 others(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 | 153 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(150): 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 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0121 a0001c0001t0002g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0006g0144 a0001c0001t0006g0174 a0001c0001t0006g0180 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0041 a0001c0001t0003g0059 a0001c0001t0005g0051 others(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 | a0001c0001t0003g0030 a0001c0001t0007g0004 a0002c0002t0013g0046 others(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 | a0001c0001t0002g0114 a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0002g0103 a0001c0001t0008g0096 a0001c0004t0008g0097 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(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 | 17 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(14): Show |
17 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1098+11875dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217598445 | |||||||
| chr1:217598453 | A | T | 1 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0114 a0001c0001t0040g0164 |
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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0011g0147 | 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 | a0001c0001t0002g0121 a0001c0001t0002g0131 a0001c0001t0002g0132 others(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 | a0001c0005t0004g0141 a0001c0005t0009g0142 |
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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | 16 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(13): Show |
16 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(13): 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 | a0001c0001t0012g0031 a0001c0001t0014g0032 a0001c0001t0034g0027 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0003g0030 others(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 | a0001c0005t0004g0141 a0001c0005t0009g0142 |
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 | 96 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(93): Show |
96 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.1098+9034T>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601287 | |||||||
| chr1:217601428 | C | CA | 23 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(20): Show |
23 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1098+8892dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 5/9 | chr1 | 217601428 | |||||||
| chr1:217601582 | C | T | 14 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | 92 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(89): Show |
92 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(89): 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 | a0001c0001t0002g0146 a0001c0001t0002g0159 a0001c0001t0002g0162 others(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 | a0001c0001t0006g0174 a0001c0001t0006g0180 a0001c0001t0009g0187 others(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 | a0001c0001t0001g0049 a0001c0001t0003g0052 a0001c0001t0005g0050 others(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 | a0001c0001t0001g0058 a0001c0001t0003g0057 |
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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | a0001c0007t0002g0145 | 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 | 36 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(33): Show |
36 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(33): 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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | a0001c0001t0008g0096 a0001c0004t0008g0097 |
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 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0004g0150 a0003c0003t0010g0149 |
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 | a0001c0005t0004g0141 a0001c0005t0009g0142 |
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 | 17 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(14): Show |
17 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(14): 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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | 33 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(30): Show |
33 | HG00609.hp2 HG00738.hp1 HG00741.hp2 others(30): 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 | a0001c0001t0007g0078 a0001c0001t0007g0079 a0001c0001t0033g0081 others(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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 |
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 | |||||||
| chr1:217606030 | T | C | 2 | a0001c0001t0014g0094 a0001c0001t0027g0093 |
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 | 91 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(88): Show |
91 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(88): 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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 others(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 | 95 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(92): Show |
95 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(92): 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 | a0001c0001t0002g0104 a0001c0001t0009g0105 |
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 | a0001c0005t0004g0141 a0001c0005t0009g0142 |
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 | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): 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 | a0003c0003t0010g0137 | 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 | 16 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(13): Show |
16 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(13): 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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | 95 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(92): Show |
95 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(92): 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 | a0001c0001t0002g0171 a0001c0001t0004g0179 a0001c0001t0006g0140 others(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 | a0001c0001t0002g0114 a0001c0001t0017g0116 a0001c0001t0044g0115 |
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 | a0001c0001t0002g0136 a0001c0001t0002g0168 |
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 | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): 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 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0171 a0001c0001t0004g0179 others(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 | a0001c0001t0006g0174 a0001c0001t0006g0180 a0001c0001t0009g0187 others(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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 others(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 | 94 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(91): Show |
94 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(91): 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 | a0001c0001t0005g0085 a0001c0001t0012g0088 a0001c0001t0014g0084 others(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 | a0001c0001t0002g0134 a0001c0001t0006g0133 a0001c0001t0006g0144 others(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 | a0001c0001t0002g0148 a0001c0001t0002g0169 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0044 a0001c0001t0005g0043 |
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 | a0001c0001t0004g0127 a0001c0001t0006g0128 |
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 | a0001c0001t0003g0077 a0001c0001t0007g0075 a0001c0001t0007g0076 |
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 | a0001c0001t0002g0114 a0001c0001t0017g0116 a0001c0001t0044g0115 |
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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | 94 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(91): Show |
94 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(91): 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 | a0001c0001t0018g0185 a0001c0001t0018g0186 |
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 | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.774-515dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217614716 | |||||||
| chr1:217614719 | T | A | 83 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(80): Show |
83 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(80): 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 | a0001c0001t0001g0026 a0001c0001t0002g0169 a0001c0001t0004g0120 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0082 others(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 | a0001c0001t0002g0129 a0001c0001t0004g0127 a0001c0001t0006g0128 |
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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 others(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 | a0001c0001t0002g0146 | 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 | a0001c0001t0002g0114 a0001c0001t0017g0116 a0001c0001t0044g0115 |
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 | 95 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(92): Show |
95 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(92): 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 | a0001c0001t0006g0165 a0001c0001t0011g0166 a0003c0003t0010g0167 |
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 | a0001c0001t0017g0116 a0001c0001t0044g0115 |
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 | a0001c0001t0017g0116 a0001c0001t0044g0115 |
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 | 162 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0028 others(159): Show |
162 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(159): 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 | a0001c0001t0002g0104 a0001c0001t0002g0112 a0001c0001t0004g0102 others(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 | a0001c0001t0002g0146 | 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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | a0001c0001t0001g0045 a0001c0001t0002g0134 a0001c0001t0002g0136 others(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 | a0001c0001t0002g0136 a0001c0001t0002g0168 |
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 | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.773+1403G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618380 | |||||||
| 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 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | a0002c0002t0013g0046 a0002c0002t0030g0047 |
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 | 16 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(13): Show |
16 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(13): 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 | a0001c0001t0002g0103 a0001c0001t0008g0096 a0001c0004t0008g0097 |
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 | 19 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.773+819dupT | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217618963 | |||||||
| chr1:217618968 | A | T | 8 | a0001c0001t0006g0174 a0001c0001t0006g0180 a0001c0001t0009g0187 others(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 | 16 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(13): Show |
16 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.773+546delA | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 2/9 | chr1 | 217619236 | |||||||
| chr1:217619753 | A | G | 3 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | 39 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(36): Show |
39 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(36): 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 | a0003c0003t0010g0137 | 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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0146 others(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 | a0001c0001t0001g0082 a0001c0001t0003g0077 a0001c0001t0005g0085 others(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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 others(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 | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): 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 | a0001c0001t0002g0171 a0001c0001t0004g0179 a0001c0001t0006g0140 others(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 | a0001c0001t0006g0143 | 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 | a0001c0001t0006g0180 a0001c0001t0009g0187 a0001c0001t0022g0182 others(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 | a0001c0001t0001g0049 a0001c0001t0003g0052 a0001c0001t0005g0050 others(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 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | 36 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(33): Show |
36 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(33): 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 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0058 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0104 a0001c0001t0002g0112 others(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 | 16 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(13): Show |
16 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(13): 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 | a0001c0005t0004g0141 a0001c0005t0009g0142 |
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 | a0001c0001t0002g0114 a0001c0001t0017g0116 a0001c0001t0044g0115 |
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 | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): 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 | 88 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(85): Show |
88 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(85): 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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 |
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 | a0001c0001t0001g0082 a0001c0001t0003g0077 a0001c0001t0005g0085 others(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 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 |
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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 others(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 | 95 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(92): Show |
95 | HG00099.hp2 HG00609.hp2 HG00738.hp2 others(92): 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 | a0001c0001t0018g0185 a0001c0001t0018g0186 |
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 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0003g0089 others(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 | 16 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(13): Show |
16 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(13): 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 | a0001c0001t0002g0099 a0001c0001t0006g0100 a0001c0001t0009g0098 others(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 | a0001c0001t0023g0002 a0001c0001t0024g0003 a0001c0001t0025g0001 |
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 | 25 | a0001c0001t0002g0118 a0001c0001t0002g0121 a0001c0001t0002g0122 others(22): Show |
25 | HG00099.hp2 HG00609.hp2 HG00741.hp2 others(22): 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 | a0001c0001t0008g0096 a0001c0004t0008g0097 |
2 | HG01243.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.56+2199G>C | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217628717 | |||||||
| chr1:217628942 | C | T | 2 | a0001c0001t0002g0134 a0001c0001t0006g0133 |
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 | a0001c0001t0023g0002 a0001c0001t0024g0003 |
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 | a0001c0001t0014g0094 a0001c0001t0027g0093 |
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 | 18 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(15): Show |
18 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(15): 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 | a0001c0001t0006g0144 a0001c0001t0010g0163 a0001c0001t0040g0164 |
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 | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.56+1692A>G | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629224 | |||||||
| chr1:217629225 | A | T | 19 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(16): Show |
19 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.56+1691T>A | GPATCH2 | ENSG00000092978.11 | transcript | ENST00000366935.8 | protein_coding | 1/9 | chr1 | 217629225 | |||||||
| chr1:217629226 | GTCATACA | G | 18 | a0001c0001t0002g0114 a0001c0001t0002g0118 a0001c0001t0002g0121 others(15): Show |
18 | HG00609.hp2 HG00741.hp2 HG01106.hp2 others(15): 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 | a0001c0001t0009g0187 a0003c0003t0010g0188 |
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 | a0001c0001t0002g0114 a0001c0001t0017g0116 a0001c0001t0044g0115 |
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 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0104 others(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 |