Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51608 |
| ensemblid | ENSG00000239857.7 |
| hgncid | 21690 |
| symbol | GET4 |
| name | guided entry of tail-anchored proteins factor 4 |
| refseq_nuc | NM_015949.3 |
| refseq_prot | NP_057033.2 |
| ensembl_nuc | ENST00000265857.8 |
| ensembl_prot | ENSP00000265857.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 876554 |
| end | 896436 |
| strand | + |
| ver | v1.2 |
| region | chr7:876554-896436 |
| region5000 | chr7:871554-901436 |
| regionname0 | GET4_chr7_876554_896436 |
| regionname5000 | GET4_chr7_871554_901436 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 327 | 380 | 90 | 73 | 163 | 14 | 38 | 117 | GET4_chr7_871554_901436 | GET4 | MAAAA others(322): Show |
chr7 | 871554 | 901436 |
| a0002 | 0/0 | 327 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GET4_chr7_871554_901436 | GET4 | MAAAA others(322): Show |
chr7 | 871554 | 901436 |
| a0003 | 0/0 | 327 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | MAAAA others(322): Show |
chr7 | 871554 | 901436 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 981 | 237 | 53 | 44 | 107 | 8 | 24 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0002 | 0/0 | 981 | 86 | 5 | 12 | 55 | 4 | 10 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0003 | 0/0 | 981 | 19 | 6 | 10 | 0 | 1 | 2 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0004 | 0/0 | 981 | 9 | 9 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0005 | 0/0 | 981 | 5 | 3 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0006 | 0/0 | 981 | 5 | 4 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0008 | 0/0 | 981 | 3 | 0 | 2 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0009 | 0/1 | 981 | 3 | 0 | 0 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0010 | 0/0 | 981 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0011 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0012 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0013 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0014 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0015 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0016 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0017 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0019 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0020 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0001c0021 | 0/0 | 981 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0002c0007 | 0/0 | 981 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 | ||
| a0003c0018 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | ATGGC others(976): Show |
chr7 | 871554 | 901436 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2090 | 155 | 29 | 35 | 66 | 7 | 18 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0002 | 1/0 | 2090 | 37 | 9 | 5 | 16 | 1 | 5 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0003 | 0/0 | 2090 | 14 | 0 | 0 | 14 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0004 | 0/0 | 2090 | 6 | 5 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0005 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0008 | 0/0 | 2090 | 2 | 1 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0009 | 0/0 | 2090 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0010 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0012 | 0/0 | 2090 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0013 | 0/0 | 2090 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0014 | 0/0 | 2090 | 2 | 1 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0016 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0017 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0018 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0022 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0024 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0027 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0029 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0031 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0033 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0036 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0037 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0039 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0001t0041 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0001 | 0/0 | 2090 | 26 | 3 | 1 | 16 | 1 | 5 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0002 | 0/0 | 2090 | 38 | 2 | 9 | 23 | 0 | 4 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0003 | 0/0 | 2090 | 8 | 0 | 0 | 8 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0005 | 0/0 | 2090 | 4 | 0 | 1 | 0 | 3 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0006 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0007 | 0/0 | 2090 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0015 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0019 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0020 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0021 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0030 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0035 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0002t0038 | 0/0 | 2090 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0003t0001 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0003t0002 | 0/0 | 2090 | 14 | 2 | 9 | 0 | 1 | 2 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0003t0006 | 0/0 | 2090 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0003t0010 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0003t0034 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0004t0002 | 0/0 | 2090 | 6 | 6 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0004t0004 | 0/0 | 2090 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0005t0001 | 0/0 | 2090 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0005t0011 | 0/0 | 2090 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0005t0040 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0006t0002 | 0/0 | 2090 | 4 | 4 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0006t0023 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0008t0001 | 0/0 | 2090 | 3 | 0 | 2 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0009t0001 | 0/1 | 2090 | 3 | 0 | 0 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0010t0025 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0010t0026 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0010t0028 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0011t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0012t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0013t0032 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0014t0001 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0015t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0016t0001 | 0/0 | 2090 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0017t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0019t0001 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0020t0001 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0001c0021t0002 | 0/0 | 2090 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0002c0007t0001 | 0/0 | 2090 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| a0003c0018t0002 | 0/0 | 2090 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | AGAAG others(2085): Show |
chr7 | 871554 | 901436 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 0 | 3 | 4 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 4 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0016 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0002 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0003g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0013g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0013g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0014g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0017g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0018g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0022g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0024g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0027g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0029g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0033g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0036g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0037g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0039g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0005g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0005g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0015g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0019g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0020g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0021g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0030g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0035g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0002t0038g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0006g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0003t0034g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0004t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0004t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0004t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0004t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0004t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0004t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0004t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0005t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0005t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0005t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0005t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0005t0040g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0006t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0006t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0006t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0006t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0006t0023g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0008t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0008t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0009t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0009t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0009t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0010t0025g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0010t0026g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0010t0028g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0011t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0012t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0013t0032g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0014t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0015t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0016t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0017t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0019t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0020t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0001c0021t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0002c0007t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| a0003c0018t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | GBR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0246 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00280 | hp2 | a0001 | c0009 | t0001 | g0249 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0027 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0097 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00597 | hp2 | a0001 | c0001 | t0022 | g0208 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00621 | hp1 | a0001 | c0001 | t0016 | g0003 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00642 | hp2 | a0001 | c0002 | t0005 | g0027 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0046 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0046 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01081 | hp1 | a0001 | c0003 | t0002 | g0245 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01081 | hp2 | a0001 | c0006 | t0023 | g0241 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01106 | hp2 | a0001 | c0020 | t0001 | g0105 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01168 | hp2 | a0001 | c0008 | t0001 | g0251 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0252 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0163 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01243 | hp2 | a0001 | c0001 | t0014 | g0058 | AMR | PUR | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0250 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01261 | hp1 | a0001 | c0003 | t0034 | g0262 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01346 | hp2 | a0001 | c0008 | t0001 | g0248 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01496 | hp1 | a0001 | c0002 | t0006 | g0054 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01515 | hp1 | a0001 | c0002 | t0005 | g0028 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01517 | hp2 | a0001 | c0002 | t0005 | g0028 | EUR | IBS | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01891 | hp1 | a0001 | c0005 | t0040 | g0240 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0258 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0100 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01943 | hp1 | a0003 | c0018 | t0002 | g0010 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0259 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0261 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0268 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02004 | hp2 | a0001 | c0003 | t0002 | g0260 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0161 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0159 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02083 | hp2 | a0001 | c0002 | t0035 | g0103 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02132 | hp1 | a0001 | c0002 | t0015 | g0121 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0098 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0169 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02148 | hp1 | a0001 | c0003 | t0002 | g0266 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02148 | hp2 | a0001 | c0019 | t0001 | g0112 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02257 | hp1 | a0001 | c0001 | t0029 | g0173 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02258 | hp1 | a0001 | c0005 | t0011 | g0265 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02258 | hp2 | a0001 | c0021 | t0002 | g0083 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02280 | hp2 | a0001 | c0001 | t0024 | g0167 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02451 | hp2 | a0001 | c0006 | t0002 | g0264 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02615 | hp1 | a0001 | c0017 | t0002 | g0053 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0044 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02647 | hp2 | a0001 | c0003 | t0010 | g0150 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02698 | hp2 | a0001 | c0003 | t0002 | g0224 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0059 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02717 | hp2 | a0001 | c0003 | t0006 | g0044 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02723 | hp1 | a0001 | c0014 | t0001 | g0257 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02723 | hp2 | a0001 | c0010 | t0025 | g0057 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0107 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02896 | hp2 | a0001 | c0006 | t0002 | g0253 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02922 | hp1 | a0001 | c0012 | t0002 | g0019 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02965 | hp1 | a0001 | c0001 | t0036 | g0024 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02965 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0233 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03098 | hp2 | a0001 | c0010 | t0028 | g0055 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03130 | hp1 | a0001 | c0010 | t0026 | g0056 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03195 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03209 | hp2 | a0001 | c0003 | t0002 | g0151 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03225 | hp2 | a0001 | c0004 | t0002 | g0237 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03239 | hp1 | a0001 | c0009 | t0001 | g0243 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03453 | hp1 | a0001 | c0011 | t0002 | g0049 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0172 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03486 | hp2 | a0001 | c0004 | t0004 | g0235 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0088 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0086 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03516 | hp1 | a0001 | c0004 | t0004 | g0232 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03540 | hp2 | a0001 | c0006 | t0002 | g0242 | AFR | GWD | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03579 | hp1 | a0001 | c0005 | t0011 | g0254 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03654 | hp2 | a0001 | c0001 | t0037 | g0195 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03834 | hp1 | a0001 | c0008 | t0001 | g0247 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04115 | hp2 | a0001 | c0002 | t0038 | g0090 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0117 | SAS | BEB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0230 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | STU | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18522 | hp1 | a0001 | c0015 | t0002 | g0084 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | CHB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18948 | hp1 | a0001 | c0001 | t0013 | g0170 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18951 | hp1 | a0001 | c0001 | t0041 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18952 | hp2 | a0001 | c0001 | t0031 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18954 | hp1 | a0002 | c0007 | t0001 | g0020 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18954 | hp2 | a0001 | c0002 | t0020 | g0085 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18980 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18994 | hp1 | a0001 | c0002 | t0007 | g0143 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19010 | hp1 | a0001 | c0001 | t0018 | g0064 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19011 | hp2 | a0001 | c0002 | t0021 | g0113 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0234 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0114 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0115 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19067 | hp1 | a0002 | c0007 | t0001 | g0020 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19067 | hp2 | a0001 | c0001 | t0013 | g0176 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19070 | hp2 | a0002 | c0007 | t0001 | g0020 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19079 | hp2 | a0001 | c0002 | t0019 | g0094 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19081 | hp2 | a0001 | c0002 | t0030 | g0010 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19088 | hp1 | a0001 | c0016 | t0001 | g0031 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19088 | hp2 | a0001 | c0002 | t0007 | g0137 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19090 | hp1 | a0001 | c0001 | t0039 | g0007 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0050 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ASW | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0108 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | GIH | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | GIH | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02486 | hp1 | a0001 | c0006 | t0002 | g0263 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02559 | hp1 | a0001 | c0004 | t0004 | g0236 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG03471 | hp2 | a0001 | c0013 | t0032 | g0019 | AFR | MSL | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| HG06807 | hp2 | a0001 | c0001 | t0027 | g0238 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA21309 | hp1 | a0001 | c0001 | t0033 | g0078 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | LWK | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| homoSapiens | chm13v2 | a0001 | c0009 | t0001 | g0244 | REF | REF | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | GET4_chr7_871554_901436 | GET4 | chr7 | 871554 | 901436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:876717 | G | C | 1 | a0002 | 3 | NA18954.hp1 NA19067.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.72G>C | p.Gln24His | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/9 | 164/2090 | 72/984 | 24/327 | chr7 | 876717 | |||
| chr7:892322 | C | T | 1 | a0003 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.650C>T | p.Thr217Met | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/9 | 742/2090 | 650/984 | 217/327 | chr7 | 892322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:876699 | C | T | 1 | a0001c0021 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.54C>T | p.Arg18Arg | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/9 | 146/2090 | 54/984 | 18/327 | chr7 | 876699 | |||
| chr7:886080 | G | A | 4 | a0001c0003 a0001c0008 a0001c0009 others(1): Show |
25 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(22): Show |
synonymous_variant | LOW | c.180G>A | p.Thr60Thr | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/9 | 272/2090 | 180/984 | 60/327 | chr7 | 886080 | |||
| chr7:886119 | C | T | 1 | a0001c0020 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.219C>T | p.Phe73Phe | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/9 | 311/2090 | 219/984 | 73/327 | chr7 | 886119 | |||
| chr7:890971 | G | A | 4 | a0001c0005 a0001c0006 a0001c0008 others(1): Show |
15 | HG00280.hp2 HG01081.hp2 HG01168.hp2 others(12): Show |
synonymous_variant | LOW | c.510G>A | p.Ala170Ala | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/9 | 602/2090 | 510/984 | 170/327 | chr7 | 890971 | |||
| chr7:891052 | C | T | 7 | a0001c0002 a0001c0015 a0001c0016 others(4): Show |
92 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
synonymous_variant | LOW | c.591C>T | p.Ala197Ala | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/9 | 683/2090 | 591/984 | 197/327 | chr7 | 891052 | |||
| chr7:892317 | C | T | 1 | a0001c0019 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.645C>T | p.Val215Val | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/9 | 737/2090 | 645/984 | 215/327 | chr7 | 892317 | |||
| chr7:892323 | G | A | 6 | a0001c0005 a0001c0006 a0001c0008 others(3): Show |
18 | HG01081.hp2 HG01168.hp2 HG01175.hp1 others(15): Show |
synonymous_variant | LOW | c.651G>A | p.Thr217Thr | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/9 | 743/2090 | 651/984 | 217/327 | chr7 | 892323 | |||
| chr7:893904 | C | G | 2 | a0001c0006 a0001c0014 |
6 | HG01081.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.828C>G | p.Leu276Leu | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/9 | 920/2090 | 828/984 | 276/327 | chr7 | 893904 | |||
| chr7:893958 | C | T | 1 | a0001c0004 | 9 | HG02559.hp1 HG02965.hp2 HG02970.hp1 others(6): Show |
synonymous_variant | LOW | c.882C>T | p.Tyr294Tyr | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/9 | 974/2090 | 882/984 | 294/327 | chr7 | 893958 | |||
| chr7:895362 | C | T | 3 | a0001c0013 a0001c0017 a0001c0021 |
3 | HG02258.hp2 HG02615.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.924C>T | p.Ser308Ser | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1016/2090 | 924/984 | 308/327 | chr7 | 895362 | |||
| chr7:895398 | C | T | 1 | a0001c0016 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.960C>T | p.Asp320Asp | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1052/2090 | 960/984 | 320/327 | chr7 | 895398 | |||
| chr7:895401 | C | T | 1 | a0001c0012 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.963C>T | p.Gly321Gly | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1055/2090 | 963/984 | 321/327 | chr7 | 895401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:876599 | C | G | 1 | a0001c0001t0014 | 2 | HG01243.hp2 HG02717.hp1 |
5_prime_UTR_variant | MODIFIER | c.-47C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/9 | 47 | chr7 | 876599 | ||||||
| chr7:895446 | C | T | 2 | a0001c0001t0013 a0001c0001t0041 |
3 | NA18948.hp1 NA18951.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*24C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 24 | chr7 | 895446 | ||||||
| chr7:895449 | C | T | 1 | a0001c0005t0040 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 27 | chr7 | 895449 | ||||||
| chr7:895450 | G | A | 2 | a0001c0002t0007 a0001c0002t0015 |
3 | HG02132.hp1 NA18994.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*28G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 28 | chr7 | 895450 | ||||||
| chr7:895459 | C | T | 1 | a0001c0001t0039 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 37 | chr7 | 895459 | ||||||
| chr7:895483 | G | A | 1 | a0001c0001t0016 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 61 | chr7 | 895483 | ||||||
| chr7:895569 | C | T | 2 | a0001c0001t0004 a0001c0004t0004 |
9 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 147 | chr7 | 895569 | ||||||
| chr7:895583 | G | A | 7 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0018 others(4): Show |
27 | HG00558.hp1 HG02027.hp2 HG02071.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*161G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 161 | chr7 | 895583 | ||||||
| chr7:895584 | C | T | 1 | a0001c0002t0038 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*162C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 162 | chr7 | 895584 | ||||||
| chr7:895585 | G | A | 1 | a0001c0001t0022 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 163 | chr7 | 895585 | ||||||
| chr7:895627 | C | T | 1 | a0001c0001t0037 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 205 | chr7 | 895627 | ||||||
| chr7:895640 | C | T | 1 | a0001c0001t0036 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*218C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 218 | chr7 | 895640 | ||||||
| chr7:895669 | A | G | 1 | a0001c0002t0035 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 247 | chr7 | 895669 | ||||||
| chr7:895748 | A | T | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*326A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 326 | chr7 | 895748 | ||||||
| chr7:895757 | G | A | 1 | a0001c0006t0023 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 335 | chr7 | 895757 | ||||||
| chr7:895792 | G | A | 1 | a0001c0001t0024 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 370 | chr7 | 895792 | ||||||
| chr7:895795 | C | T | 1 | a0001c0002t0021 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 373 | chr7 | 895795 | ||||||
| chr7:895836 | C | A | 2 | a0001c0010t0025 a0001c0010t0026 |
2 | HG02723.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 414 | chr7 | 895836 | ||||||
| chr7:895883 | G | C | 3 | a0001c0001t0027 a0001c0010t0025 a0001c0010t0028 |
3 | HG02723.hp2 HG03098.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*461G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 461 | chr7 | 895883 | ||||||
| chr7:895907 | T | C | 1 | a0001c0001t0029 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 485 | chr7 | 895907 | ||||||
| chr7:895942 | G | A | 1 | a0001c0002t0007 | 2 | NA18994.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*520G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 520 | chr7 | 895942 | ||||||
| chr7:895989 | C | T | 1 | a0001c0003t0034 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 567 | chr7 | 895989 | ||||||
| chr7:895997 | G | C | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*575G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 575 | chr7 | 895997 | ||||||
| chr7:896052 | G | A | 1 | a0001c0002t0030 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*630G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 630 | chr7 | 896052 | ||||||
| chr7:896072 | C | T | 2 | a0001c0001t0005 a0001c0002t0005 |
5 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*650C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 650 | chr7 | 896072 | ||||||
| chr7:896125 | T | C | 1 | a0001c0001t0017 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 703 | chr7 | 896125 | ||||||
| chr7:896146 | A | G | 1 | a0001c0005t0011 | 2 | HG02258.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*724A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 724 | chr7 | 896146 | ||||||
| chr7:896147 | A | G | 2 | a0001c0001t0010 a0001c0003t0010 |
2 | HG02647.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*725A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 725 | chr7 | 896147 | ||||||
| chr7:896168 | T | C | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(25): Show |
234 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*746T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 746 | chr7 | 896168 | ||||||
| chr7:896169 | G | A | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*747G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 747 | chr7 | 896169 | ||||||
| chr7:896182 | G | A | 1 | a0001c0001t0031 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 760 | chr7 | 896182 | ||||||
| chr7:896270 | G | A | 2 | a0001c0002t0006 a0001c0003t0006 |
3 | HG01496.hp1 HG02647.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*848G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 848 | chr7 | 896270 | ||||||
| chr7:896270 | G | C | 1 | a0001c0013t0032 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*848G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 848 | chr7 | 896270 | ||||||
| chr7:896273 | G | T | 1 | a0001c0001t0029 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 851 | chr7 | 896273 | ||||||
| chr7:896293 | A | G | 1 | a0001c0001t0009 | 2 | HG02071.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*871A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 871 | chr7 | 896293 | ||||||
| chr7:896312 | A | G | 4 | a0001c0001t0033 a0001c0010t0025 a0001c0010t0026 others(1): Show |
4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*890A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 890 | chr7 | 896312 | ||||||
| chr7:896354 | C | T | 1 | a0001c0001t0008 | 2 | HG01192.hp1 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*932C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 932 | chr7 | 896354 | ||||||
| chr7:896405 | C | T | 1 | a0001c0002t0019 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*983C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 983 | chr7 | 896405 | ||||||
| chr7:896430 | A | G | 2 | a0001c0002t0006 a0001c0003t0006 |
3 | HG01496.hp1 HG02647.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1008A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1008 | chr7 | 896430 | ||||||
| chr7:896433 | G | A | 1 | a0001c0001t0018 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1011G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 9/9 | 1011 | chr7 | 896433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:876841 | C | CCGCCGCC others(12): Show |
1 | a0001c0002t0002g0047 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.155+51_155+69dupCC others(17): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 876841 | ||||||
| chr7:876847 | C | T | 1 | a0001c0002t0001g0269 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.155+47C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 876847 | |||||||
| chr7:876897 | C | G | 31 | a0001c0001t0001g0024 a0001c0001t0001g0255 a0001c0001t0001g0256 others(28): Show |
33 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.155+97C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 876897 | |||||||
| chr7:876978 | C | A | 1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.155+178C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 876978 | |||||||
| chr7:877041 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(261): Show |
345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.155+241T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877041 | |||||||
| chr7:877044 | T | C | 3 | a0001c0001t0002g0051 a0001c0003t0002g0050 a0001c0011t0002g0049 |
3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+244T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877044 | |||||||
| chr7:877045 | G | T | 3 | a0001c0001t0002g0051 a0001c0003t0002g0050 a0001c0011t0002g0049 |
3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+245G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877045 | |||||||
| chr7:877046 | CG | C | 3 | a0001c0001t0002g0051 a0001c0003t0002g0050 a0001c0011t0002g0049 |
3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+247delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877046 | |||||||
| chr7:877048 | T | C | 3 | a0001c0001t0002g0051 a0001c0003t0002g0050 a0001c0011t0002g0049 |
3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+248T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877048 | |||||||
| chr7:877049 | T | C | 3 | a0001c0001t0002g0051 a0001c0003t0002g0050 a0001c0011t0002g0049 |
3 | HG03453.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.155+249T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877049 | |||||||
| chr7:877054 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0239 |
5 | HG01255.hp1 HG01256.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.155+254C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877054 | |||||||
| chr7:877071 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.155+271C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877071 | |||||||
| chr7:877105 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA19009.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.155+305A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877105 | |||||||
| chr7:877151 | C | T | 1 | a0001c0003t0006g0044 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.155+351C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877151 | |||||||
| chr7:877179 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(111): Show |
163 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.155+379C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877179 | |||||||
| chr7:877202 | GCT | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(258): Show |
341 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.155+421_155+422del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 877202 | ||||||
| chr7:877205 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.155+405C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877205 | |||||||
| chr7:877225 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(78): Show |
110 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.155+425C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877225 | |||||||
| chr7:877271 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(95): Show |
141 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.155+471C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877271 | |||||||
| chr7:877300 | GC | G | 10 | a0001c0001t0002g0008 a0001c0001t0004g0231 a0001c0002t0002g0144 others(7): Show |
13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.155+506delC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 877300 | ||||||
| chr7:877301 | C | T | 1 | a0001c0002t0002g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.155+501C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877301 | |||||||
| chr7:877404 | G | A | 1 | a0001c0001t0004g0034 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.155+604G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877404 | |||||||
| chr7:877472 | C | T | 1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.155+672C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877472 | |||||||
| chr7:877498 | A | T | 2 | a0001c0001t0002g0039 a0002c0007t0001g0020 |
5 | NA18954.hp1 NA18971.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.155+698A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877498 | |||||||
| chr7:877547 | C | T | 57 | a0001c0001t0033g0078 a0001c0002t0001g0029 a0001c0002t0001g0030 others(54): Show |
64 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.155+747C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877547 | |||||||
| chr7:877589 | G | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(112): Show |
164 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.155+789G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877589 | |||||||
| chr7:877591 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(112): Show |
164 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.155+791C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877591 | |||||||
| chr7:877657 | C | T | 11 | a0001c0002t0001g0031 a0001c0002t0001g0116 a0001c0002t0001g0118 others(8): Show |
11 | HG02056.hp2 HG02074.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.155+857C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877657 | |||||||
| chr7:877694 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.155+894G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877694 | |||||||
| chr7:877697 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.155+897C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877697 | |||||||
| chr7:877715 | C | A | 59 | a0001c0001t0033g0078 a0001c0002t0001g0029 a0001c0002t0001g0030 others(56): Show |
66 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.155+915C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877715 | |||||||
| chr7:877761 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(102): Show |
153 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.155+961C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877761 | |||||||
| chr7:877826 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.155+1026C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877826 | |||||||
| chr7:877849 | C | G | 1 | a0001c0002t0001g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.155+1049C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877849 | |||||||
| chr7:877894 | C | T | 1 | a0001c0003t0002g0268 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.155+1094C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877894 | |||||||
| chr7:877916 | C | T | 31 | a0001c0001t0001g0024 a0001c0001t0001g0255 a0001c0001t0001g0256 others(28): Show |
33 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.155+1116C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 877916 | |||||||
| chr7:878002 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0186 a0001c0001t0001g0187 others(3): Show |
7 | HG00733.hp2 HG00738.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+1202C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878002 | |||||||
| chr7:878037 | T | A | 1 | a0001c0001t0004g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.155+1237T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878037 | |||||||
| chr7:878096 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.155+1296C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878096 | |||||||
| chr7:878169 | G | C | 1 | a0001c0001t0033g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155+1369G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878169 | |||||||
| chr7:878191 | G | A | 50 | a0001c0001t0033g0078 a0001c0002t0001g0029 a0001c0002t0001g0031 others(47): Show |
56 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.155+1391G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878191 | |||||||
| chr7:878210 | G | A | 2 | a0001c0002t0005g0027 a0001c0002t0005g0028 |
4 | HG00323.hp1 HG00642.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+1410G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878210 | |||||||
| chr7:878214 | C | G | 1 | a0001c0001t0002g0026 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.155+1414C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878214 | |||||||
| chr7:878574 | C | CT | 91 | a0001c0001t0001g0077 a0001c0001t0001g0123 a0001c0001t0001g0179 others(88): Show |
100 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.155+1791dupT | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878574 | ||||||
| chr7:878574 | C | CTT | 8 | a0001c0001t0001g0267 a0001c0002t0001g0029 a0001c0002t0001g0140 others(5): Show |
8 | HG03139.hp2 NA18953.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.155+1790_155+1791d others(4): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878574 | ||||||
| chr7:878612 | C | T | 1 | a0001c0002t0035g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.155+1812C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878612 | |||||||
| chr7:878615 | C | T | 27 | a0001c0001t0001g0123 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+1815C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878615 | |||||||
| chr7:878659 | A | G | 1 | a0001c0002t0035g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.155+1859A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878659 | |||||||
| chr7:878747 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.155+1947A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878747 | |||||||
| chr7:878773 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG02572.hp1 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155+1973G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878773 | |||||||
| chr7:878867 | C | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(109): Show |
161 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.155+2067C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878867 | |||||||
| chr7:878895 | TA | T | 3 | a0001c0010t0025g0057 a0001c0010t0026g0056 a0001c0010t0028g0055 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.155+2096delA | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878895 | |||||||
| chr7:878976 | A | AC | 70 | a0001c0001t0001g0267 a0001c0001t0033g0078 a0001c0002t0001g0029 others(67): Show |
77 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.155+2185dupC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878976 | ||||||
| chr7:878976 | AC | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(136): Show |
190 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.155+2185delC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 878976 | ||||||
| chr7:878983 | C | CG | 7 | a0001c0003t0002g0258 a0001c0003t0002g0259 a0001c0003t0002g0260 others(4): Show |
7 | HG01261.hp1 HG01928.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+2183_155+2184i others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 878983 | |||||||
| chr7:879036 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.155+2236G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879036 | |||||||
| chr7:879045 | G | A | 1 | a0001c0001t0003g0063 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.155+2245G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879045 | |||||||
| chr7:879108 | C | G | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.155+2308C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879108 | |||||||
| chr7:879126 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.155+2326T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879126 | |||||||
| chr7:879177 | T | G | 1 | a0001c0017t0002g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155+2377T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879177 | |||||||
| chr7:879242 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0002g0190 |
2 | HG01975.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.155+2442G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879242 | |||||||
| chr7:879317 | C | T | 2 | a0001c0001t0002g0178 a0001c0001t0002g0183 |
2 | NA19063.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.155+2517C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879317 | |||||||
| chr7:879360 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.155+2560T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879360 | |||||||
| chr7:879391 | A | G | 1 | a0001c0002t0002g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.155+2591A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879391 | |||||||
| chr7:879426 | C | G | 1 | a0001c0002t0005g0028 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.155+2626C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879426 | |||||||
| chr7:879496 | C | T | 3 | a0001c0010t0025g0057 a0001c0010t0026g0056 a0001c0010t0028g0055 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.155+2696C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879496 | |||||||
| chr7:879543 | G | A | 1 | a0001c0002t0015g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.155+2743G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879543 | |||||||
| chr7:879725 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0145 |
3 | HG00735.hp2 HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.155+2925G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879725 | |||||||
| chr7:879797 | C | T | 3 | a0001c0002t0002g0011 a0001c0002t0002g0099 a0001c0002t0002g0100 |
6 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+2997C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879797 | |||||||
| chr7:879871 | G | A | 1 | a0001c0001t0018g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.155+3071G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 879871 | |||||||
| chr7:880012 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.155+3212C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880012 | |||||||
| chr7:880095 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.155+3295A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880095 | |||||||
| chr7:880198 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.155+3398G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880198 | |||||||
| chr7:880324 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.155+3524A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880324 | |||||||
| chr7:880362 | C | T | 1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.155+3562C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880362 | |||||||
| chr7:880390 | C | T | 1 | a0001c0003t0010g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.155+3590C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880390 | |||||||
| chr7:880393 | C | T | 27 | a0001c0001t0001g0123 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+3593C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880393 | |||||||
| chr7:880432 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.155+3632C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880432 | |||||||
| chr7:880458 | G | A | 7 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 others(4): Show |
8 | HG02615.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.155+3658G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880458 | |||||||
| chr7:880575 | G | A | 3 | a0001c0001t0001g0223 a0001c0003t0002g0224 a0001c0003t0002g0230 |
3 | HG02602.hp2 HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.155+3775G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880575 | |||||||
| chr7:880609 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.155+3809G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880609 | |||||||
| chr7:880617 | A | C | 1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.155+3817A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880617 | |||||||
| chr7:880664 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(110): Show |
162 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.155+3864C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880664 | |||||||
| chr7:880665 | G | A | 1 | a0001c0002t0002g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.155+3865G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880665 | |||||||
| chr7:880746 | G | A | 4 | a0001c0002t0001g0101 a0001c0002t0003g0081 a0001c0002t0003g0082 others(1): Show |
4 | NA18946.hp2 NA18950.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+3946G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880746 | |||||||
| chr7:880775 | C | G | 27 | a0001c0001t0001g0123 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+3975C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880775 | |||||||
| chr7:880781 | A | G | 27 | a0001c0001t0001g0123 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+3981A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880781 | |||||||
| chr7:880840 | C | T | 49 | a0001c0002t0001g0029 a0001c0002t0001g0031 a0001c0002t0001g0080 others(46): Show |
55 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.155+4040C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880840 | |||||||
| chr7:880876 | G | A | 1 | a0001c0017t0002g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.155+4076G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880876 | |||||||
| chr7:880911 | C | T | 27 | a0001c0001t0001g0123 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.155+4111C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 880911 | |||||||
| chr7:881054 | G | A | 1 | a0001c0003t0006g0044 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.155+4254G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881054 | |||||||
| chr7:881131 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155+4331C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881131 | |||||||
| chr7:881205 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.155+4405G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881205 | |||||||
| chr7:881362 | C | T | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.155+4562C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881362 | |||||||
| chr7:881363 | G | A | 2 | a0001c0003t0002g0151 a0001c0003t0010g0150 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.155+4563G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881363 | |||||||
| chr7:881438 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.156-4618C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881438 | |||||||
| chr7:881688 | G | A | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-4368G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881688 | |||||||
| chr7:881707 | C | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
148 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.156-4349C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881707 | |||||||
| chr7:881754 | C | G | 30 | a0001c0001t0001g0123 a0001c0001t0014g0058 a0001c0001t0014g0059 others(27): Show |
32 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.156-4302C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881754 | |||||||
| chr7:881771 | A | G | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-4285A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881771 | |||||||
| chr7:881774 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(53): Show |
84 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.156-4282G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881774 | |||||||
| chr7:881798 | A | G | 1 | a0001c0002t0003g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.156-4258A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881798 | |||||||
| chr7:881990 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.156-4066T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 881990 | |||||||
| chr7:882007 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(261): Show |
345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.156-4049T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882007 | |||||||
| chr7:882030 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.156-4026T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882030 | |||||||
| chr7:882035 | C | T | 4 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-4021C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882035 | |||||||
| chr7:882154 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.156-3902T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882154 | |||||||
| chr7:882219 | T | C | 1 | a0001c0002t0020g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.156-3837T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882219 | |||||||
| chr7:882253 | C | G | 1 | a0001c0001t0013g0176 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.156-3803C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882253 | |||||||
| chr7:882355 | G | A | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-3701G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882355 | |||||||
| chr7:882460 | C | T | 3 | a0001c0005t0011g0254 a0001c0005t0011g0265 a0001c0006t0002g0253 |
3 | HG02258.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.156-3596C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882460 | |||||||
| chr7:882577 | A | AGGGATGG others(30): Show |
5 | a0001c0001t0009g0159 a0001c0010t0025g0057 a0001c0010t0026g0056 others(2): Show |
5 | HG02071.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-3385_156-3349d others(39): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 882577 | ||||||
| chr7:882577 | A | G | 43 | a0001c0001t0001g0123 a0001c0001t0014g0058 a0001c0001t0014g0059 others(40): Show |
45 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.156-3479A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882577 | |||||||
| chr7:882577 | AGGGATGG others(30): Show |
A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0051 a0001c0001t0004g0231 others(8): Show |
14 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.156-3385_156-3349d others(39): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 882577 | ||||||
| chr7:882582 | T | A | 4 | a0001c0002t0003g0114 a0001c0002t0003g0115 a0001c0002t0021g0113 others(1): Show |
4 | HG02148.hp2 NA19011.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-3474T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882582 | |||||||
| chr7:882622 | C | T | 2 | a0001c0003t0001g0152 a0001c0003t0002g0050 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.156-3434C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882622 | |||||||
| chr7:882651 | G | A | 2 | a0001c0002t0002g0032 a0001c0002t0002g0141 |
3 | NA18979.hp2 NA19055.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.156-3405G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882651 | |||||||
| chr7:882699 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0076 |
7 | NA18943.hp2 NA18944.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-3357G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882699 | |||||||
| chr7:882825 | G | C | 1 | a0001c0010t0028g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.156-3231G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882825 | |||||||
| chr7:882840 | C | G | 27 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-3216C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882840 | |||||||
| chr7:882874 | A | G | 30 | a0001c0001t0001g0123 a0001c0001t0014g0058 a0001c0001t0014g0059 others(27): Show |
32 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.156-3182A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882874 | |||||||
| chr7:882876 | A | C | 1 | a0001c0005t0011g0254 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.156-3180A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882876 | |||||||
| chr7:882905 | G | C | 2 | a0001c0001t0001g0182 a0001c0001t0002g0181 |
2 | HG01167.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.156-3151G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882905 | |||||||
| chr7:882910 | CCT | C | 17 | a0001c0003t0002g0046 a0001c0003t0002g0245 a0001c0003t0002g0246 others(14): Show |
18 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.156-3145_156-3144d others(4): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882910 | |||||||
| chr7:882921 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
358 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.156-3135A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 882921 | |||||||
| chr7:883194 | G | T | 3 | a0001c0005t0011g0254 a0001c0005t0011g0265 a0001c0006t0002g0253 |
3 | HG02258.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.156-2862G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883194 | |||||||
| chr7:883222 | C | G | 27 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-2834C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883222 | |||||||
| chr7:883240 | G | A | 5 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0211 others(2): Show |
5 | HG02080.hp2 NA18992.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-2816G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883240 | |||||||
| chr7:883444 | A | G | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.156-2612A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883444 | |||||||
| chr7:883563 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.156-2493A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883563 | |||||||
| chr7:883643 | T | C | 34 | a0001c0001t0001g0007 a0001c0001t0001g0123 a0001c0001t0001g0191 others(31): Show |
39 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.156-2413T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883643 | |||||||
| chr7:883930 | C | T | 4 | a0001c0006t0002g0242 a0001c0006t0002g0263 a0001c0006t0002g0264 others(1): Show |
4 | HG01081.hp2 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-2126C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883930 | |||||||
| chr7:883981 | G | A | 4 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-2075G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 883981 | |||||||
| chr7:884020 | C | T | 1 | a0001c0006t0002g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.156-2036C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884020 | |||||||
| chr7:884025 | G | A | 9 | a0001c0001t0002g0008 a0001c0001t0004g0231 a0001c0004t0002g0008 others(6): Show |
12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.156-2031G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884025 | |||||||
| chr7:884123 | C | T | 1 | a0001c0001t0033g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.156-1933C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884123 | |||||||
| chr7:884162 | G | A | 7 | a0001c0005t0011g0254 a0001c0005t0011g0265 a0001c0006t0002g0242 others(4): Show |
7 | HG01081.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.156-1894G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884162 | |||||||
| chr7:884218 | G | A | 29 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0002t0001g0075 others(26): Show |
31 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.156-1838G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884218 | |||||||
| chr7:884233 | G | A | 1 | a0001c0010t0028g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.156-1823G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884233 | |||||||
| chr7:884298 | G | A | 27 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-1758G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884298 | |||||||
| chr7:884343 | C | T | 2 | a0001c0003t0001g0152 a0001c0003t0002g0050 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.156-1713C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884343 | |||||||
| chr7:884424 | C | T | 27 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.156-1632C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884424 | |||||||
| chr7:884479 | C | T | 1 | a0001c0001t0018g0064 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.156-1577C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884479 | |||||||
| chr7:884495 | C | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(42): Show |
70 | HG00558.hp2 HG00639.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.156-1561C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884495 | |||||||
| chr7:884508 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.156-1548T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884508 | |||||||
| chr7:884512 | C | G | 1 | a0001c0003t0010g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.156-1544C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884512 | |||||||
| chr7:884547 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.156-1509G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884547 | |||||||
| chr7:884557 | G | T | 28 | a0001c0001t0002g0175 a0001c0002t0001g0075 a0001c0002t0001g0125 others(25): Show |
30 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.156-1499G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884557 | |||||||
| chr7:884593 | C | T | 1 | a0001c0014t0001g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.156-1463C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884593 | |||||||
| chr7:884625 | C | T | 1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.156-1431C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884625 | |||||||
| chr7:884709 | G | A | 1 | a0001c0003t0002g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.156-1347G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884709 | |||||||
| chr7:884791 | T | C | 1 | a0001c0002t0002g0124 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.156-1265T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884791 | |||||||
| chr7:884800 | T | A | 1 | a0001c0002t0019g0094 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.156-1256T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884800 | |||||||
| chr7:884813 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.156-1243C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884813 | |||||||
| chr7:884979 | A | G | 10 | a0001c0001t0002g0008 a0001c0001t0004g0231 a0001c0001t0027g0238 others(7): Show |
13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.156-1077A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 884979 | |||||||
| chr7:885133 | A | T | 1 | a0001c0002t0002g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.156-923A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885133 | |||||||
| chr7:885154 | G | T | 1 | a0001c0003t0034g0262 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.156-902G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885154 | |||||||
| chr7:885166 | C | G | 4 | a0001c0001t0002g0042 a0001c0002t0001g0030 a0001c0002t0001g0106 others(1): Show |
6 | HG02615.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.156-890C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885166 | |||||||
| chr7:885257 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.156-799C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885257 | |||||||
| chr7:885278 | C | T | 1 | a0002c0007t0001g0020 | 3 | NA18954.hp1 NA19067.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.156-778C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885278 | |||||||
| chr7:885347 | C | T | 2 | a0001c0002t0005g0027 a0001c0002t0005g0028 |
4 | HG00323.hp1 HG00642.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-709C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885347 | |||||||
| chr7:885382 | A | G | 9 | a0001c0001t0001g0267 a0001c0005t0011g0254 a0001c0005t0011g0265 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.156-674A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885382 | |||||||
| chr7:885395 | C | T | 53 | a0001c0001t0001g0225 a0001c0002t0001g0029 a0001c0002t0001g0031 others(50): Show |
59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.156-661C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885395 | |||||||
| chr7:885417 | C | T | 8 | a0001c0001t0002g0003 a0001c0001t0002g0155 a0001c0001t0002g0178 others(5): Show |
14 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.156-639C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885417 | |||||||
| chr7:885421 | A | AC | 11 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0156 others(8): Show |
11 | HG01243.hp1 HG01978.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.156-631dupC | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 885421 | ||||||
| chr7:885425 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.156-631C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885425 | |||||||
| chr7:885426 | G | A | 1 | a0001c0001t0037g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.156-630G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885426 | |||||||
| chr7:885434 | G | T | 4 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-622G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885434 | |||||||
| chr7:885507 | G | A | 1 | a0001c0004t0004g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.156-549G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885507 | |||||||
| chr7:885548 | G | A | 1 | a0001c0001t0002g0026 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.156-508G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885548 | |||||||
| chr7:885717 | C | G | 59 | a0001c0001t0001g0225 a0001c0001t0033g0078 a0001c0002t0001g0029 others(56): Show |
66 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.156-339C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885717 | |||||||
| chr7:885911 | G | A | 1 | a0001c0003t0002g0046 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.156-145G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 885911 | |||||||
| chr7:885997 | C | CG | 6 | a0001c0001t0001g0074 a0001c0001t0002g0051 a0001c0002t0002g0100 others(3): Show |
6 | HG01175.hp1 HG01928.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-54dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 885997 | ||||||
| chr7:886007 | C | CG | 8 | a0001c0001t0001g0061 a0001c0001t0002g0180 a0001c0001t0002g0181 others(5): Show |
8 | HG00544.hp1 HG00735.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-47dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr7 | 886007 | ||||||
| chr7:886011 | G | C | 9 | a0001c0001t0001g0267 a0001c0005t0011g0254 a0001c0005t0011g0265 others(6): Show |
9 | HG01081.hp2 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.156-45G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 886011 | |||||||
| chr7:886049 | G | C | 1 | a0001c0010t0028g0055 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.156-7G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 1/8 | chr7 | 886049 | |||||||
| chr7:886135 | GTAAGCCG others(54): Show |
G | 1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.234+3_234+63delAAG others(58): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr7 | 886135 | ||||||
| chr7:886159 | A | G | 29 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0002t0001g0075 others(26): Show |
30 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.234+25A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886159 | |||||||
| chr7:886229 | C | T | 54 | a0001c0001t0001g0225 a0001c0002t0001g0029 a0001c0002t0001g0031 others(51): Show |
60 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.234+95C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886229 | |||||||
| chr7:886312 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(165): Show |
223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.234+178A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886312 | |||||||
| chr7:886330 | G | A | 19 | a0001c0003t0002g0046 a0001c0003t0002g0224 a0001c0003t0002g0230 others(16): Show |
20 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.234+196G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886330 | |||||||
| chr7:886355 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0002g0181 |
2 | HG01167.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.235-214G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886355 | |||||||
| chr7:886424 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0002g0181 |
2 | HG01167.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.235-145G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886424 | |||||||
| chr7:886440 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(135): Show |
191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.235-129G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886440 | |||||||
| chr7:886468 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0154 a0001c0001t0001g0156 others(2): Show |
8 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.235-101C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886468 | |||||||
| chr7:886472 | C | T | 2 | a0001c0002t0002g0079 a0001c0002t0002g0093 |
2 | HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.235-97C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886472 | |||||||
| chr7:886503 | T | C | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.235-66T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 2/8 | chr7 | 886503 | |||||||
| chr7:886669 | ACCCCGGG others(30): Show |
A | 1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.316+27_316+63delAC others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 886669 | ||||||
| chr7:886731 | G | A | 2 | a0001c0002t0002g0079 a0001c0002t0002g0093 |
2 | HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.316+81G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 886731 | |||||||
| chr7:886785 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.316+135G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 886785 | |||||||
| chr7:886838 | C | G | 1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.316+188C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 886838 | |||||||
| chr7:887026 | A | G | 29 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0002t0001g0075 others(26): Show |
31 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.317-344A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887026 | |||||||
| chr7:887042 | C | T | 1 | a0001c0002t0002g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.317-328C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887042 | |||||||
| chr7:887154 | G | GCGTC | 27 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.317-210_317-207dup others(4): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr7 | 887154 | ||||||
| chr7:887220 | G | A | 4 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-150G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887220 | |||||||
| chr7:887333 | C | G | 1 | a0001c0001t0001g0015 | 4 | HG00323.hp2 HG00642.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-37C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887333 | |||||||
| chr7:887334 | G | A | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.317-36G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 3/8 | chr7 | 887334 | |||||||
| chr7:887640 | C | T | 1 | a0001c0001t0001g0013 | 4 | HG02886.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+121C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887640 | |||||||
| chr7:887643 | G | A | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.466+124G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887643 | |||||||
| chr7:887661 | C | G | 27 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.466+142C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887661 | |||||||
| chr7:887681 | G | A | 1 | a0001c0002t0002g0126 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.466+162G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887681 | |||||||
| chr7:887727 | C | T | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.466+208C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887727 | |||||||
| chr7:887731 | C | T | 1 | a0001c0001t0029g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.466+212C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887731 | |||||||
| chr7:887734 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.466+215C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887734 | |||||||
| chr7:887791 | G | C | 9 | a0001c0001t0002g0008 a0001c0001t0004g0231 a0001c0004t0002g0008 others(6): Show |
12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.466+272G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887791 | |||||||
| chr7:887801 | C | T | 10 | a0001c0001t0002g0008 a0001c0001t0004g0231 a0001c0001t0027g0238 others(7): Show |
13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.466+282C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887801 | |||||||
| chr7:887831 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
6 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+312T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887831 | |||||||
| chr7:887836 | C | T | 3 | a0001c0010t0025g0057 a0001c0010t0026g0056 a0001c0010t0028g0055 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.466+317C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887836 | |||||||
| chr7:887901 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0239 a0001c0020t0001g0105 |
6 | HG01106.hp2 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+382G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 887901 | |||||||
| chr7:888010 | ATTGAGTG others(33): Show |
A | 1 | a0001c0009t0001g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.466+492_466+531del others(40): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888010 | |||||||
| chr7:888026 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.466+507G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888026 | |||||||
| chr7:888058 | C | T | 1 | a0001c0001t0003g0073 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.466+539C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888058 | |||||||
| chr7:888125 | G | A | 21 | a0001c0003t0002g0046 a0001c0003t0002g0151 a0001c0003t0002g0224 others(18): Show |
22 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.466+606G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888125 | |||||||
| chr7:888150 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.466+631T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888150 | |||||||
| chr7:888290 | T | C | 31 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0002t0001g0075 others(28): Show |
34 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.466+771T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888290 | |||||||
| chr7:888446 | C | A | 1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+927C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888446 | |||||||
| chr7:888485 | T | C | 1 | a0001c0019t0001g0112 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.466+966T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888485 | |||||||
| chr7:888553 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.466+1034G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888553 | |||||||
| chr7:888583 | C | T | 4 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0006g0044 others(1): Show |
5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+1064C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888583 | |||||||
| chr7:888710 | C | G | 3 | a0001c0010t0025g0057 a0001c0010t0026g0056 a0001c0010t0028g0055 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.466+1191C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888710 | |||||||
| chr7:888740 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(250): Show |
332 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(329): Show |
intron_variant | MODIFIER | c.466+1221T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888740 | |||||||
| chr7:888743 | G | A | 1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+1224G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888743 | |||||||
| chr7:888781 | G | A | 1 | a0001c0001t0008g0163 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.466+1262G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888781 | |||||||
| chr7:888887 | G | A | 4 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0003g0098 others(1): Show |
4 | HG02040.hp2 HG02135.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+1368G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888887 | |||||||
| chr7:888967 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.466+1448G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888967 | |||||||
| chr7:888999 | C | T | 54 | a0001c0001t0001g0225 a0001c0002t0001g0029 a0001c0002t0001g0031 others(51): Show |
60 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.466+1480C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 888999 | |||||||
| chr7:889026 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.466+1507T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889026 | |||||||
| chr7:889053 | T | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 |
4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+1534T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889053 | |||||||
| chr7:889074 | T | C | 1 | a0001c0002t0002g0142 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.466+1555T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889074 | |||||||
| chr7:889089 | G | A | 2 | a0001c0002t0006g0054 a0001c0017t0002g0053 |
2 | HG01496.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.466+1570G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889089 | |||||||
| chr7:889244 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(126): Show |
178 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.467-1684C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889244 | |||||||
| chr7:889268 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.467-1660C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889268 | |||||||
| chr7:889275 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.467-1653G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889275 | |||||||
| chr7:889282 | C | G | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.467-1646C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889282 | |||||||
| chr7:889301 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-1627A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889301 | |||||||
| chr7:889421 | C | T | 3 | a0001c0010t0025g0057 a0001c0010t0026g0056 a0001c0010t0028g0055 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.467-1507C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889421 | |||||||
| chr7:889486 | C | T | 59 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(56): Show |
66 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.467-1442C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889486 | |||||||
| chr7:889503 | A | G | 3 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0006g0044 |
4 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1425A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889503 | |||||||
| chr7:889574 | C | T | 4 | a0001c0003t0002g0050 a0001c0010t0025g0057 a0001c0010t0026g0056 others(1): Show |
4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1354C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889574 | |||||||
| chr7:889666 | TAGGACGG others(260): Show |
T | 1 | a0001c0001t0014g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.467-1246_467-980de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889666 | ||||||
| chr7:889666 | TAGGACGG others(300): Show |
T | 3 | a0001c0001t0014g0059 a0001c0003t0006g0044 a0001c0011t0002g0049 |
4 | HG02647.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-1246_467-940de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889666 | ||||||
| chr7:889699 | C | CG | 3 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 |
5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1226dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889699 | ||||||
| chr7:889703 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 |
5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1225C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889703 | |||||||
| chr7:889708 | GAGCGGAG others(205): Show |
G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 |
5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1219_467-1008d others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889708 | |||||||
| chr7:889720 | T | C | 4 | a0001c0004t0002g0234 a0001c0005t0011g0254 a0001c0005t0011g0265 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1208T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889720 | |||||||
| chr7:889720 | T | TGCGAGCG others(608): Show |
1 | a0001c0001t0001g0071 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.467-1199_467-1198i others(617): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889720 | ||||||
| chr7:889726 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.467-1202C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889726 | |||||||
| chr7:889733 | T | C | 2 | a0001c0001t0001g0071 a0001c0004t0002g0234 |
2 | NA18983.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.467-1195T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889733 | |||||||
| chr7:889742 | G | C | 1 | a0001c0005t0040g0240 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.467-1186G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889742 | |||||||
| chr7:889743 | T | C | 3 | a0001c0001t0001g0076 a0001c0002t0002g0079 a0001c0002t0002g0093 |
3 | HG02896.hp1 HG03579.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.467-1185T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889743 | |||||||
| chr7:889743 | T | TCTGGGAG others(33): Show |
4 | a0001c0002t0002g0133 a0001c0002t0006g0054 a0001c0015t0002g0084 others(1): Show |
4 | HG01496.hp1 HG02148.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1166_467-1165i others(42): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889743 | ||||||
| chr7:889743 | T | TCTGGGAG others(73): Show |
12 | a0001c0002t0001g0125 a0001c0002t0001g0131 a0001c0002t0002g0032 others(9): Show |
14 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-1166_467-1165i others(82): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889743 | ||||||
| chr7:889762 | C | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(28): Show |
52 | HG00558.hp2 HG02027.hp2 HG02071.hp2 others(49): Show |
intron_variant | MODIFIER | c.467-1166C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889762 | |||||||
| chr7:889763 | G | A | 81 | a0001c0001t0001g0072 a0001c0001t0002g0008 a0001c0001t0002g0026 others(78): Show |
92 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.467-1165G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889763 | |||||||
| chr7:889773 | T | C | 8 | a0001c0001t0001g0071 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG01081.hp1 HG01261.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-1155T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889773 | |||||||
| chr7:889773 | T | TAGGACGG others(33): Show |
4 | a0001c0003t0002g0046 a0001c0003t0002g0246 a0001c0005t0001g0252 others(1): Show |
5 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-1127_467-1126i others(42): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889773 | ||||||
| chr7:889773 | TAGGACGG others(153): Show |
T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(95): Show |
140 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.467-1145_467-986de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889773 | ||||||
| chr7:889773 | TAGGACGG others(193): Show |
T | 1 | a0001c0001t0001g0036 | 2 | HG01261.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.467-1145_467-946de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889773 | ||||||
| chr7:889783 | C | CCTGGGAG others(633): Show |
1 | a0001c0003t0010g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.467-1127_467-1126i others(642): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889783 | ||||||
| chr7:889783 | C | CCTGGGAG others(433): Show |
1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.467-1127_467-1126i others(442): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889783 | ||||||
| chr7:889783 | C | T | 28 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0153 others(25): Show |
33 | HG00544.hp1 HG00733.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.467-1145C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889783 | |||||||
| chr7:889794 | A | AGGGAGCG others(233): Show |
1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-1127_467-1126i others(242): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889794 | ||||||
| chr7:889802 | A | AGAGCGGG others(513): Show |
1 | a0001c0001t0001g0060 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.467-1106_467-1105i others(522): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889802 | ||||||
| chr7:889802 | A | AGAGCGGG others(513): Show |
1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.467-1106_467-1105i others(522): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889802 | ||||||
| chr7:889802 | A | AGAGCGGG others(72): Show |
11 | a0001c0002t0001g0125 a0001c0002t0001g0131 a0001c0002t0002g0032 others(8): Show |
13 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-1067_467-1066i others(81): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889802 | ||||||
| chr7:889802 | A | C | 110 | a0001c0001t0001g0013 a0001c0001t0001g0071 a0001c0001t0001g0153 others(107): Show |
121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.467-1126A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889802 | |||||||
| chr7:889802 | A | T | 3 | a0001c0005t0011g0254 a0001c0005t0011g0265 a0001c0006t0002g0253 |
3 | HG02258.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-1126A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889802 | |||||||
| chr7:889806 | C | T | 5 | a0001c0005t0040g0240 a0001c0006t0002g0242 a0001c0006t0002g0263 others(2): Show |
5 | HG01081.hp2 HG01891.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1122C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889806 | |||||||
| chr7:889813 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0071 a0001c0001t0001g0229 others(29): Show |
33 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.467-1115T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889813 | |||||||
| chr7:889813 | T | TAGGACGG others(433): Show |
1 | a0001c0001t0001g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.467-1106_467-1105i others(442): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889813 | ||||||
| chr7:889813 | T | TAGGACGG others(513): Show |
1 | a0001c0001t0001g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.467-1076_467-1075i others(522): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889813 | ||||||
| chr7:889819 | G | GGGGCCTG others(112): Show |
2 | a0001c0002t0002g0127 a0001c0002t0002g0144 |
2 | NA18947.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.467-1106_467-1105i others(121): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889819 | ||||||
| chr7:889819 | G | GGGGCCTG others(1267): Show |
1 | a0001c0002t0002g0138 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.467-1106_467-1105i others(1276): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889819 | ||||||
| chr7:889823 | T | C | 105 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(102): Show |
132 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.467-1105T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889823 | |||||||
| chr7:889842 | C | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(20): Show |
42 | HG00558.hp2 HG02027.hp2 HG02071.hp2 others(39): Show |
intron_variant | MODIFIER | c.467-1086C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889842 | |||||||
| chr7:889846 | C | T | 1 | a0001c0017t0002g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-1082C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889846 | |||||||
| chr7:889853 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0024 others(39): Show |
47 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.467-1075T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889853 | |||||||
| chr7:889853 | TAGGACGG others(113): Show |
T | 5 | a0001c0001t0001g0215 a0001c0002t0002g0047 a0001c0010t0025g0057 others(2): Show |
5 | HG00733.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-1006_467-887de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889853 | ||||||
| chr7:889858 | CG | C | 4 | a0001c0002t0001g0101 a0001c0002t0003g0081 a0001c0002t0003g0082 others(1): Show |
4 | NA18946.hp2 NA18950.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-1066delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889858 | ||||||
| chr7:889859 | G | C | 1 | a0001c0004t0002g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.467-1069G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889859 | |||||||
| chr7:889859 | G | GGGGTCTG others(1227): Show |
2 | a0001c0002t0002g0136 a0001c0002t0002g0142 |
2 | HG00621.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.467-1047_467-1046i others(1236): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889859 | ||||||
| chr7:889882 | C | A | 13 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 others(10): Show |
14 | HG02615.hp2 HG02895.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-1046C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889882 | |||||||
| chr7:889882 | C | CGAGCGGG others(112): Show |
1 | a0001c0002t0002g0133 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.467-1027_467-1026i others(121): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889882 | ||||||
| chr7:889882 | C | T | 11 | a0001c0002t0001g0125 a0001c0002t0001g0131 a0001c0002t0002g0032 others(8): Show |
13 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-1046C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889882 | |||||||
| chr7:889893 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(64): Show |
91 | HG00280.hp1 HG00280.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.467-1035T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889893 | |||||||
| chr7:889893 | T | TAGGACGG others(33): Show |
1 | a0001c0001t0001g0223 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.467-1007_467-1006i others(42): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889893 | ||||||
| chr7:889893 | T | TAGGACGG others(232): Show |
1 | a0001c0015t0002g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467-1027_467-1026i others(241): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889893 | ||||||
| chr7:889893 | T | TAGGACGG others(303): Show |
1 | a0001c0019t0001g0112 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.467-1027_467-1026i others(312): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889893 | ||||||
| chr7:889898 | CG | C | 5 | a0001c0001t0001g0158 a0001c0001t0037g0195 a0001c0002t0002g0079 others(2): Show |
5 | HG01496.hp1 HG01891.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-1026delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889898 | ||||||
| chr7:889899 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.467-1029G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889899 | |||||||
| chr7:889899 | G | GGGTCTGG others(31): Show |
1 | a0001c0004t0002g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.467-1027_467-1026i others(40): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889899 | ||||||
| chr7:889903 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-1025T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889903 | |||||||
| chr7:889903 | T | TCTGGGAG others(509): Show |
2 | a0001c0005t0011g0254 a0001c0006t0002g0253 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-1007_467-1006i others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889903 | ||||||
| chr7:889915 | GGGAGCGA others(191): Show |
G | 1 | a0001c0001t0002g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.467-1010_467-813de others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889915 | ||||||
| chr7:889922 | A | AGAGCGGG others(832): Show |
1 | a0001c0004t0004g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.467-996_467-995ins others(839): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889922 | ||||||
| chr7:889922 | A | AGAGCGGG others(353): Show |
1 | a0001c0004t0004g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467-996_467-995ins others(360): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889922 | ||||||
| chr7:889922 | A | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.467-1006A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889922 | |||||||
| chr7:889922 | A | T | 22 | a0001c0001t0003g0063 a0001c0002t0001g0101 a0001c0002t0001g0125 others(19): Show |
24 | HG00544.hp1 HG02056.hp1 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-1006A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889922 | |||||||
| chr7:889926 | C | CGGGTGTT others(351): Show |
1 | a0001c0017t0002g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-996_467-995ins others(358): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889926 | ||||||
| chr7:889926 | C | CGGGTGTT others(351): Show |
1 | a0001c0002t0002g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.467-996_467-995ins others(358): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889926 | ||||||
| chr7:889926 | C | T | 2 | a0001c0002t0002g0138 a0001c0019t0001g0112 |
2 | HG02148.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.467-1002C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889926 | |||||||
| chr7:889927 | G | A | 1 | a0001c0019t0001g0112 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.467-1001G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889927 | |||||||
| chr7:889933 | C | T | 92 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0060 others(89): Show |
106 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.467-995C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889933 | |||||||
| chr7:889938 | CG | C | 59 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0001g0158 others(56): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.467-986delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889938 | ||||||
| chr7:889939 | G | GGGTCTGG others(31): Show |
4 | a0001c0005t0040g0240 a0001c0006t0002g0242 a0001c0006t0002g0263 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-987_467-986ins others(38): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889939 | ||||||
| chr7:889943 | T | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 others(12): Show |
19 | HG00544.hp1 HG01106.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.467-985T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889943 | |||||||
| chr7:889943 | T | TCTGGGAG others(467): Show |
1 | a0001c0009t0001g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.467-927_467-926ins others(474): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889943 | ||||||
| chr7:889943 | T | TCTGGGAG others(33): Show |
1 | a0001c0002t0007g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.467-967_467-966ins others(40): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889943 | ||||||
| chr7:889951 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 |
5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-977T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889951 | |||||||
| chr7:889960 | C | CGCGAGCG others(313): Show |
1 | a0001c0001t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(320): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889960 | ||||||
| chr7:889960 | C | T | 1 | a0001c0002t0002g0104 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.467-968C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889960 | |||||||
| chr7:889962 | C | A | 5 | a0001c0001t0001g0239 a0001c0001t0002g0008 a0001c0002t0002g0136 others(2): Show |
6 | HG00621.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-966C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889962 | |||||||
| chr7:889962 | C | T | 8 | a0001c0002t0002g0079 a0001c0002t0002g0093 a0001c0002t0002g0127 others(5): Show |
8 | HG01175.hp1 HG01496.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-966C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889962 | |||||||
| chr7:889962 | CGAGCGGG others(430): Show |
C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0037g0195 |
3 | HG01891.hp2 HG02976.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.467-955_467-519del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889962 | ||||||
| chr7:889963 | G | A | 1 | a0001c0001t0014g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.467-965G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889963 | |||||||
| chr7:889966 | C | T | 3 | a0001c0001t0001g0204 a0001c0002t0002g0136 a0001c0002t0002g0142 |
3 | HG00621.hp2 HG03942.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.467-962C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889966 | |||||||
| chr7:889970 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.467-958T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889970 | |||||||
| chr7:889973 | C | CAGGACGG others(513): Show |
1 | a0001c0003t0002g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(520): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889973 | ||||||
| chr7:889973 | C | CAGGACGG others(551): Show |
1 | a0001c0001t0027g0238 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.467-927_467-926ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889973 | ||||||
| chr7:889973 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(186): Show |
245 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.467-955C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889973 | |||||||
| chr7:889978 | CG | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0062 others(3): Show |
9 | HG01081.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-946delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889978 | ||||||
| chr7:889979 | G | GGGGCCTG others(671): Show |
1 | a0001c0001t0036g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(678): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGCCTG others(631): Show |
1 | a0001c0001t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGCCTG others(631): Show |
1 | a0001c0001t0001g0009 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGCCTG others(511): Show |
1 | a0001c0001t0003g0005 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGCCTG others(511): Show |
1 | a0001c0001t0003g0005 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.467-946_467-945ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(591): Show |
2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(512): Show |
1 | a0001c0002t0001g0075 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(519): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(551): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0076 a0001c0001t0003g0005 others(1): Show |
8 | HG02071.hp2 HG02129.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(631): Show |
1 | a0001c0001t0001g0004 | 2 | NA18946.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.467-916_467-915ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(591): Show |
1 | a0001c0001t0001g0004 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(551): Show |
2 | a0001c0001t0001g0065 a0001c0001t0003g0017 |
2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(551): Show |
2 | a0001c0001t0003g0017 a0001c0001t0003g0219 |
2 | HG02027.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(631): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0074 |
5 | NA18612.hp2 NA18984.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(591): Show |
2 | a0001c0001t0003g0063 a0001c0001t0018g0064 |
2 | NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(551): Show |
1 | a0001c0001t0001g0006 | 5 | NA18944.hp2 NA18967.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(551): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(4): Show |
9 | HG00558.hp2 HG02135.hp2 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-916_467-915ins others(558): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(511): Show |
1 | a0001c0001t0001g0070 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(550): Show |
1 | a0001c0004t0004g0232 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(557): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(591): Show |
1 | a0001c0001t0002g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.467-916_467-915ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(630): Show |
1 | a0001c0004t0002g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(637): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(590): Show |
1 | a0001c0001t0002g0008 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.467-916_467-915ins others(597): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(550): Show |
2 | a0001c0001t0004g0231 a0001c0004t0002g0008 |
3 | HG02257.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(557): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(550): Show |
3 | a0001c0004t0002g0008 a0001c0004t0002g0237 a0001c0014t0001g0257 |
3 | HG02723.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.467-916_467-915ins others(557): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGGTCTG others(592): Show |
1 | a0001c0001t0001g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.467-927_467-926ins others(599): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889979 | G | GGGTCTGG others(150): Show |
2 | a0001c0005t0001g0252 a0001c0008t0001g0247 |
2 | HG01175.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.467-947_467-946ins others(157): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889979 | ||||||
| chr7:889980 | G | GGGTCTGG others(116): Show |
1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-927_467-926ins others(123): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889980 | ||||||
| chr7:889983 | T | C | 7 | a0001c0001t0014g0058 a0001c0002t0001g0101 a0001c0002t0002g0127 others(4): Show |
7 | HG01243.hp2 NA18946.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-945T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889983 | |||||||
| chr7:889983 | T | TCTGGGAG others(348): Show |
2 | a0001c0005t0001g0250 a0001c0008t0001g0251 |
2 | HG01168.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.467-927_467-926ins others(355): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 889983 | ||||||
| chr7:889997 | G | C | 2 | a0001c0001t0004g0146 a0001c0001t0004g0147 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.467-931G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 889997 | |||||||
| chr7:890000 | C | T | 1 | a0001c0002t0001g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.467-928C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890000 | |||||||
| chr7:890002 | C | A | 8 | a0001c0002t0002g0047 a0001c0002t0002g0104 a0001c0002t0002g0107 others(5): Show |
8 | HG02148.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-926C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890002 | |||||||
| chr7:890002 | C | T | 49 | a0001c0002t0001g0029 a0001c0002t0001g0031 a0001c0002t0001g0080 others(46): Show |
55 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.467-926C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890002 | |||||||
| chr7:890002 | CGAGCGGG others(390): Show |
C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0209 |
5 | HG02886.hp2 HG02895.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-906_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890002 | ||||||
| chr7:890003 | G | A | 4 | a0001c0001t0014g0059 a0001c0002t0006g0054 a0001c0003t0006g0044 others(1): Show |
5 | HG01496.hp1 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-925G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890003 | |||||||
| chr7:890006 | C | T | 2 | a0001c0002t0002g0104 a0001c0015t0002g0084 |
2 | NA18522.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.467-922C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890006 | |||||||
| chr7:890013 | T | C | 31 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0227 others(28): Show |
33 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.467-915T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890013 | |||||||
| chr7:890013 | TAGGACGG others(395): Show |
T | 1 | a0001c0002t0002g0104 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.467-914_467-513del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890013 | |||||||
| chr7:890018 | CG | C | 8 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0072 others(5): Show |
8 | HG00621.hp2 HG02148.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-906delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890018 | ||||||
| chr7:890019 | G | GGGGCCTG others(511): Show |
1 | a0001c0001t0002g0026 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.467-906_467-905ins others(518): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGGTCTG others(631): Show |
1 | a0001c0001t0001g0069 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.467-876_467-875ins others(638): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGGTCTG others(591): Show |
1 | a0001c0001t0001g0077 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.467-876_467-875ins others(598): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGGTCTG others(271): Show |
1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-876_467-875ins others(278): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGGTCTG others(310): Show |
1 | a0001c0005t0011g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.467-836_467-835ins others(317): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGGTCTG others(111): Show |
1 | a0001c0001t0001g0061 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.467-866_467-749dup others(118): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGGTCTG others(1346): Show |
1 | a0001c0002t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.467-887_467-886ins others(1353): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGGTCTG others(1346): Show |
1 | a0001c0002t0002g0128 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.467-887_467-886ins others(1353): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGTCTGG others(269): Show |
1 | a0001c0009t0001g0249 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.467-907_467-906ins others(276): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890019 | G | GGGTCTGG others(308): Show |
1 | a0001c0008t0001g0248 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-907_467-906ins others(315): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890019 | ||||||
| chr7:890023 | T | C | 15 | a0001c0001t0002g0008 a0001c0001t0004g0231 a0001c0001t0014g0059 others(12): Show |
19 | HG01346.hp2 HG01496.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.467-905T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890023 | |||||||
| chr7:890041 | G | A | 1 | a0001c0002t0021g0113 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.467-887G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890041 | |||||||
| chr7:890042 | C | A | 2 | a0001c0002t0002g0138 a0001c0017t0002g0053 |
2 | HG02615.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.467-886C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890042 | |||||||
| chr7:890042 | C | T | 17 | a0001c0002t0001g0125 a0001c0002t0001g0129 a0001c0002t0001g0131 others(14): Show |
18 | HG00544.hp1 HG01081.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-886C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890042 | |||||||
| chr7:890043 | G | A | 7 | a0001c0002t0001g0031 a0001c0002t0001g0116 a0001c0002t0001g0118 others(4): Show |
7 | HG02056.hp2 HG02074.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-885G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890043 | |||||||
| chr7:890053 | T | C | 27 | a0001c0002t0002g0107 a0001c0003t0002g0046 a0001c0003t0002g0224 others(24): Show |
28 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.467-875T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890053 | |||||||
| chr7:890058 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.467-870C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890058 | |||||||
| chr7:890063 | T | C | 55 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(52): Show |
62 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.467-865T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890063 | |||||||
| chr7:890081 | G | GGGGGTAG others(5): Show |
1 | a0001c0001t0001g0071 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.467-847_467-846ins others(12): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890081 | |||||||
| chr7:890082 | C | A | 5 | a0001c0002t0002g0107 a0001c0002t0002g0142 a0001c0015t0002g0084 others(2): Show |
5 | HG02148.hp2 HG02615.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-846C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890082 | |||||||
| chr7:890082 | C | T | 16 | a0001c0001t0001g0071 a0001c0001t0001g0222 a0001c0002t0001g0101 others(13): Show |
17 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(14): Show |
intron_variant | MODIFIER | c.467-846C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890082 | |||||||
| chr7:890093 | T | C | 31 | a0001c0002t0001g0101 a0001c0002t0002g0079 a0001c0002t0002g0093 others(28): Show |
32 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.467-835T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890093 | |||||||
| chr7:890098 | C | CG | 93 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0068 others(90): Show |
107 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.467-827dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGCCT others(352): Show |
3 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 |
4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-827_467-826ins others(359): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGCCT others(2022): Show |
1 | a0001c0002t0002g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.467-827_467-826ins others(2029): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGCCT others(2022): Show |
1 | a0001c0002t0002g0124 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(2029): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGCCT others(2022): Show |
1 | a0001c0002t0001g0135 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(2029): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGTCT others(234): Show |
1 | a0001c0002t0003g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(241): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGTCT others(312): Show |
4 | a0001c0002t0001g0031 a0001c0002t0001g0118 a0001c0002t0001g0119 others(1): Show |
4 | HG02056.hp2 NA18747.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-827_467-826ins others(319): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGTCT others(312): Show |
3 | a0001c0002t0002g0086 a0001c0002t0002g0088 a0001c0002t0035g0103 |
3 | HG02083.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.467-827_467-826ins others(319): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGTCT others(312): Show |
1 | a0001c0002t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.467-827_467-826ins others(319): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGTCT others(588): Show |
1 | a0001c0002t0002g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.467-827_467-826ins others(595): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890098 | C | CGGGGTCT others(1148): Show |
1 | a0001c0002t0007g0137 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.467-827_467-826ins others(1155): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890098 | ||||||
| chr7:890102 | T | C | 22 | a0001c0001t0014g0058 a0001c0002t0001g0129 a0001c0002t0021g0113 others(19): Show |
24 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.467-826T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890102 | |||||||
| chr7:890121 | C | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(110): Show |
156 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.467-807C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890121 | |||||||
| chr7:890121 | C | T | 8 | a0001c0002t0001g0140 a0001c0002t0002g0079 a0001c0002t0002g0093 others(5): Show |
8 | HG01496.hp1 HG02148.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.467-807C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890121 | |||||||
| chr7:890122 | G | A | 2 | a0001c0010t0025g0057 a0001c0010t0026g0056 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.467-806G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890122 | |||||||
| chr7:890132 | T | C | 28 | a0001c0002t0002g0079 a0001c0002t0002g0093 a0001c0002t0002g0117 others(25): Show |
29 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.467-796T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890132 | |||||||
| chr7:890134 | G | GGACGGGG others(231): Show |
1 | a0001c0001t0003g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(238): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890134 | ||||||
| chr7:890137 | C | CG | 84 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 others(81): Show |
96 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.467-788dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(1030): Show |
1 | a0001c0002t0002g0130 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1037): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(1109): Show |
1 | a0001c0002t0001g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1116): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(1030): Show |
1 | a0001c0002t0002g0132 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1037): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(1029): Show |
1 | a0001c0002t0002g0133 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1036): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(1029): Show |
4 | a0001c0002t0001g0125 a0001c0002t0002g0033 a0001c0002t0007g0143 others(1): Show |
5 | HG00544.hp1 HG02132.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-788_467-787ins others(1036): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(1823): Show |
1 | a0001c0002t0002g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.467-788_467-787ins others(1830): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(1822): Show |
1 | a0001c0002t0002g0122 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.467-788_467-787ins others(1829): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890137 | C | CGGGGTCT others(989): Show |
1 | a0001c0002t0002g0126 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.467-788_467-787ins others(996): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890137 | ||||||
| chr7:890141 | T | C | 19 | a0001c0002t0001g0135 a0001c0002t0002g0124 a0001c0002t0002g0139 others(16): Show |
20 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.467-787T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890141 | |||||||
| chr7:890160 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0002g0178 a0001c0015t0002g0084 |
4 | HG01261.hp2 HG02273.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-768C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890160 | |||||||
| chr7:890160 | C | T | 48 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(45): Show |
55 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.467-768C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890160 | |||||||
| chr7:890160 | CGAGCGGG others(232): Show |
C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(96): Show |
141 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.467-748_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890160 | ||||||
| chr7:890171 | T | C | 59 | a0001c0002t0001g0029 a0001c0002t0001g0080 a0001c0002t0001g0089 others(56): Show |
66 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.467-757T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890171 | |||||||
| chr7:890176 | C | CG | 74 | a0001c0001t0001g0024 a0001c0001t0014g0058 a0001c0001t0014g0059 others(71): Show |
82 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.467-749dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGCCT others(34): Show |
2 | a0001c0003t0002g0246 a0001c0003t0002g0258 |
2 | HG00280.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.467-749_467-748ins others(41): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGCCT others(74): Show |
1 | a0001c0003t0002g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.467-749_467-748ins others(81): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(748): Show |
1 | a0001c0002t0002g0138 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(755): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(1387): Show |
1 | a0001c0002t0001g0129 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1394): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(113): Show |
1 | a0001c0006t0002g0253 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(120): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(273): Show |
1 | a0001c0005t0011g0254 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.467-749_467-748ins others(280): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(1902): Show |
1 | a0001c0002t0002g0032 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1909): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(1902): Show |
1 | a0001c0002t0002g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1909): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(1228): Show |
2 | a0001c0002t0002g0127 a0001c0002t0002g0144 |
2 | NA18947.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.467-749_467-748ins others(1235): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(1902): Show |
1 | a0001c0002t0002g0032 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.467-749_467-748ins others(1909): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890176 | C | CGGGGTCT others(311): Show |
3 | a0001c0002t0001g0101 a0001c0002t0003g0082 a0001c0002t0003g0111 |
3 | NA18950.hp2 NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.467-749_467-748ins others(318): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890176 | ||||||
| chr7:890180 | T | C | 22 | a0001c0002t0001g0129 a0001c0002t0001g0140 a0001c0002t0002g0122 others(19): Show |
23 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.467-748T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890180 | |||||||
| chr7:890180 | T | TCTGGGAG others(389): Show |
1 | a0001c0002t0006g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.467-719_467-718ins others(396): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890180 | ||||||
| chr7:890199 | C | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 |
5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-729C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890199 | |||||||
| chr7:890199 | C | T | 9 | a0001c0002t0002g0047 a0001c0002t0002g0107 a0001c0005t0040g0240 others(6): Show |
9 | HG01891.hp1 HG02148.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-729C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890199 | |||||||
| chr7:890199 | CGAGCGGG others(193): Show |
C | 2 | a0001c0001t0001g0036 a0001c0001t0002g0178 |
3 | HG01261.hp2 HG02273.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.467-709_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890199 | ||||||
| chr7:890203 | C | T | 3 | a0001c0002t0002g0107 a0001c0017t0002g0053 a0001c0019t0001g0112 |
3 | HG02148.hp2 HG02615.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.467-725C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890203 | |||||||
| chr7:890210 | T | C | 43 | a0001c0002t0001g0101 a0001c0002t0001g0135 a0001c0002t0002g0032 others(40): Show |
45 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.467-718T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890210 | |||||||
| chr7:890210 | T | TAGGACGG others(1780): Show |
1 | a0001c0006t0023g0241 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(1787): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890210 | ||||||
| chr7:890215 | CG | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0077 a0001c0001t0001g0197 others(4): Show |
9 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.467-709delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890215 | ||||||
| chr7:890216 | G | GGGTCTGG others(388): Show |
3 | a0001c0002t0001g0116 a0001c0002t0001g0120 a0001c0002t0003g0115 |
3 | HG02074.hp1 NA18953.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.467-710_467-709ins others(395): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | ||||||
| chr7:890216 | G | GGGTCTGG others(389): Show |
1 | a0001c0002t0002g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.467-710_467-709ins others(396): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | ||||||
| chr7:890216 | G | GGGTCTGG others(388): Show |
9 | a0001c0002t0001g0029 a0001c0002t0001g0095 a0001c0002t0001g0096 others(6): Show |
9 | HG00558.hp1 HG02040.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-710_467-709ins others(395): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | ||||||
| chr7:890216 | G | GGGTCTGG others(388): Show |
15 | a0001c0002t0001g0080 a0001c0002t0001g0089 a0001c0002t0001g0102 others(12): Show |
20 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.467-710_467-709ins others(395): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | ||||||
| chr7:890216 | G | GGGTCTGG others(468): Show |
1 | a0001c0002t0001g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.467-710_467-709ins others(475): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | ||||||
| chr7:890216 | G | GGGTCTGG others(111): Show |
1 | a0001c0015t0002g0084 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.467-710_467-709ins others(118): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | ||||||
| chr7:890216 | G | GGGTCTGG others(389): Show |
1 | a0001c0002t0003g0114 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.467-710_467-709ins others(396): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890216 | ||||||
| chr7:890220 | T | C | 48 | a0001c0002t0001g0029 a0001c0002t0001g0080 a0001c0002t0001g0089 others(45): Show |
55 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.467-708T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890220 | |||||||
| chr7:890220 | T | TCTGGGAG others(190): Show |
1 | a0001c0021t0002g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(197): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890220 | T | TCTGGGAG others(29): Show |
1 | a0001c0017t0002g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-679_467-678ins others(36): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890220 | T | TCTGGGAG others(349): Show |
1 | a0001c0002t0021g0113 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(356): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890220 | T | TCTGGGAG others(71): Show |
1 | a0001c0002t0003g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.467-690_467-689ins others(78): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890220 | T | TCTGGGAG others(72): Show |
1 | a0001c0002t0002g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.467-690_467-689ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890220 | T | TCTGGGAG others(349): Show |
3 | a0001c0002t0002g0079 a0001c0002t0002g0093 a0001c0002t0002g0117 |
3 | HG02896.hp1 HG03579.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.467-690_467-689ins others(356): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890220 | T | TCTGGGAG others(72): Show |
8 | a0001c0002t0001g0031 a0001c0002t0001g0087 a0001c0002t0001g0118 others(5): Show |
8 | HG01361.hp1 HG02056.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-690_467-689ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890220 | T | TCTGGGAG others(72): Show |
3 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 |
4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-690_467-689ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890220 | ||||||
| chr7:890239 | C | T | 5 | a0001c0002t0002g0136 a0001c0002t0002g0142 a0001c0010t0025g0057 others(2): Show |
5 | HG00621.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-689C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890239 | |||||||
| chr7:890239 | CGAGCGGG others(153): Show |
C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0210 |
5 | HG01106.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-669_467-510del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890239 | ||||||
| chr7:890250 | T | C | 106 | a0001c0001t0001g0024 a0001c0001t0001g0072 a0001c0001t0001g0226 others(103): Show |
118 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.467-678T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890250 | |||||||
| chr7:890250 | T | TAGGACGG others(1106): Show |
1 | a0001c0005t0040g0240 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.467-670_467-669ins others(1113): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890250 | ||||||
| chr7:890250 | T | TAGGACGG others(150): Show |
1 | a0001c0001t0001g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.467-670_467-669ins others(157): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890250 | ||||||
| chr7:890255 | CGGGGTCT others(114): Show |
C | 2 | a0001c0003t0006g0044 a0001c0011t0002g0049 |
3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.467-669_467-549del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890255 | ||||||
| chr7:890260 | T | C | 13 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0002t0002g0107 others(10): Show |
13 | HG01243.hp2 HG01261.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-668T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890260 | |||||||
| chr7:890277 | C | CGCGAGCG others(192): Show |
1 | a0001c0004t0004g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467-650_467-649ins others(199): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890277 | ||||||
| chr7:890277 | C | CGCGAGCG others(192): Show |
1 | a0001c0004t0004g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.467-650_467-649ins others(199): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890277 | ||||||
| chr7:890277 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(35): Show |
61 | HG00558.hp2 HG00639.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.467-651C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890277 | |||||||
| chr7:890277 | CGTGAGCG others(113): Show |
C | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.467-638_467-519del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890277 | ||||||
| chr7:890279 | T | C | 93 | a0001c0001t0001g0077 a0001c0001t0003g0005 a0001c0002t0001g0029 others(90): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.467-649T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890279 | |||||||
| chr7:890279 | T | TGAGCGGG others(152): Show |
1 | a0001c0005t0001g0250 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.467-612_467-611ins others(159): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(827): Show |
1 | a0001c0002t0015g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(787): Show |
2 | a0001c0002t0007g0137 a0001c0002t0007g0143 |
2 | NA18994.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.467-639_467-638ins others(794): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(667): Show |
1 | a0001c0002t0002g0136 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.467-639_467-638ins others(674): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(667): Show |
1 | a0001c0002t0001g0140 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.467-639_467-638ins others(674): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(667): Show |
4 | a0001c0002t0001g0129 a0001c0002t0002g0127 a0001c0002t0002g0128 others(1): Show |
4 | NA18947.hp2 NA18982.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-639_467-638ins others(674): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(827): Show |
1 | a0001c0002t0002g0130 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(827): Show |
1 | a0001c0002t0001g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(827): Show |
3 | a0001c0002t0002g0033 a0001c0002t0002g0126 a0001c0002t0002g0132 |
3 | NA18939.hp2 NA19068.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.467-639_467-638ins others(834): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890279 | T | TGAGCGGG others(787): Show |
3 | a0001c0002t0001g0125 a0001c0002t0002g0033 a0001c0002t0002g0133 |
3 | HG00544.hp1 NA18962.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.467-639_467-638ins others(794): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890279 | ||||||
| chr7:890290 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(24): Show |
45 | HG00558.hp2 HG00639.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.467-638C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890290 | |||||||
| chr7:890300 | T | C | 1 | a0001c0002t0002g0142 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.467-628T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890300 | |||||||
| chr7:890317 | C | G | 1 | a0001c0008t0001g0251 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.467-611C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890317 | |||||||
| chr7:890317 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.467-611C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890317 | |||||||
| chr7:890319 | C | A | 4 | a0001c0002t0002g0047 a0001c0010t0025g0057 a0001c0010t0026g0056 others(1): Show |
4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-609C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890319 | |||||||
| chr7:890319 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.467-609C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890319 | |||||||
| chr7:890320 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0108 |
3 | HG02895.hp1 NA20752.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.467-608G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890320 | |||||||
| chr7:890323 | C | T | 4 | a0001c0002t0002g0047 a0001c0010t0025g0057 a0001c0010t0026g0056 others(1): Show |
4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-605C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890323 | |||||||
| chr7:890329 | TCAGGACG others(78): Show |
T | 4 | a0001c0002t0002g0047 a0001c0010t0025g0057 a0001c0010t0026g0056 others(1): Show |
4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-597_467-513del others(85): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890329 | ||||||
| chr7:890330 | C | T | 6 | a0001c0001t0001g0077 a0001c0002t0002g0142 a0001c0003t0001g0152 others(3): Show |
6 | HG02647.hp2 HG03209.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-598C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890330 | |||||||
| chr7:890335 | CG | C | 5 | a0001c0003t0002g0050 a0001c0006t0002g0242 a0001c0006t0002g0263 others(2): Show |
5 | HG01168.hp2 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-589delG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890335 | ||||||
| chr7:890340 | T | C | 1 | a0001c0008t0001g0251 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.467-588T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890340 | |||||||
| chr7:890357 | T | C | 36 | a0001c0001t0001g0077 a0001c0002t0002g0122 a0001c0002t0002g0134 others(33): Show |
37 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.467-571T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890357 | |||||||
| chr7:890359 | C | A | 2 | a0001c0003t0002g0050 a0001c0003t0002g0151 |
2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.467-569C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890359 | |||||||
| chr7:890359 | C | CGAGCGGG others(193): Show |
1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-559_467-558ins others(200): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890359 | ||||||
| chr7:890359 | C | T | 1 | a0001c0008t0001g0248 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-569C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890359 | |||||||
| chr7:890370 | C | T | 5 | a0001c0002t0002g0142 a0001c0003t0001g0152 a0001c0003t0002g0050 others(2): Show |
5 | HG02647.hp2 HG03209.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-558C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890370 | |||||||
| chr7:890397 | T | C | 32 | a0001c0002t0002g0142 a0001c0003t0001g0152 a0001c0003t0002g0046 others(29): Show |
34 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.467-531T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890397 | |||||||
| chr7:890397 | T | G | 1 | a0001c0008t0001g0248 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-531T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890397 | |||||||
| chr7:890399 | T | A | 2 | a0001c0005t0011g0254 a0001c0006t0002g0253 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-529T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890399 | |||||||
| chr7:890399 | T | C | 108 | a0001c0001t0001g0077 a0001c0001t0014g0058 a0001c0001t0014g0059 others(105): Show |
119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.467-529T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890399 | |||||||
| chr7:890403 | C | T | 2 | a0001c0005t0011g0254 a0001c0006t0002g0253 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.467-525C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890403 | |||||||
| chr7:890410 | T | C | 17 | a0001c0001t0001g0077 a0001c0002t0001g0129 a0001c0002t0002g0122 others(14): Show |
17 | HG00280.hp2 HG01168.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.467-518T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890410 | |||||||
| chr7:890415 | C | CG | 14 | a0001c0001t0001g0077 a0001c0003t0002g0046 a0001c0003t0002g0224 others(11): Show |
15 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-510dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGCCTG others(307): Show |
1 | a0001c0008t0001g0248 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-493_467-492ins others(314): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(28): Show |
1 | a0001c0002t0006g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(2055): Show |
1 | a0001c0006t0002g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(2062): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(2055): Show |
2 | a0001c0006t0002g0242 a0001c0006t0002g0264 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.467-510_467-509ins others(2062): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(68): Show |
1 | a0001c0005t0001g0250 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(75): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(228): Show |
2 | a0001c0008t0001g0251 a0001c0009t0001g0243 |
2 | HG01168.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.467-510_467-509ins others(235): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(427): Show |
1 | a0001c0008t0001g0247 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(434): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(1096): Show |
1 | a0001c0002t0002g0142 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(1103): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(387): Show |
2 | a0001c0005t0001g0252 a0001c0009t0001g0249 |
2 | HG00280.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.467-510_467-509ins others(394): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(302): Show |
1 | a0001c0002t0002g0127 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(309): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(302): Show |
1 | a0001c0002t0002g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(309): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(108): Show |
52 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(49): Show |
59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.467-510_467-509ins others(115): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(302): Show |
20 | a0001c0002t0001g0125 a0001c0002t0001g0129 a0001c0002t0001g0131 others(17): Show |
22 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.467-510_467-509ins others(309): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(268): Show |
1 | a0001c0005t0011g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(275): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(307): Show |
1 | a0001c0006t0023g0241 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(314): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(68): Show |
1 | a0001c0017t0002g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467-510_467-509ins others(75): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(342): Show |
2 | a0001c0002t0002g0122 a0001c0002t0002g0134 |
2 | NA18612.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.467-510_467-509ins others(349): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | CGGGGTCT others(146): Show |
1 | a0001c0019t0001g0112 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.467-510_467-509ins others(153): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890415 | ||||||
| chr7:890415 | C | T | 4 | a0001c0002t0002g0047 a0001c0010t0025g0057 a0001c0010t0026g0056 others(1): Show |
4 | HG02723.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-513C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890415 | |||||||
| chr7:890419 | C | T | 13 | a0001c0003t0002g0046 a0001c0003t0002g0224 a0001c0003t0002g0230 others(10): Show |
14 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-509C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890419 | |||||||
| chr7:890436 | T | C | 14 | a0001c0001t0002g0048 a0001c0003t0002g0046 a0001c0003t0002g0224 others(11): Show |
15 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-492T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890436 | |||||||
| chr7:890438 | T | C | 13 | a0001c0003t0002g0046 a0001c0003t0002g0224 a0001c0003t0002g0230 others(10): Show |
14 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.467-490T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890438 | |||||||
| chr7:890449 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(114): Show |
165 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.467-479T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890449 | |||||||
| chr7:890449 | T | TAGGACGG others(72): Show |
4 | a0001c0003t0002g0046 a0001c0003t0002g0245 a0001c0003t0002g0246 others(1): Show |
5 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-471_467-470ins others(79): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890449 | ||||||
| chr7:890449 | T | TAGGACGG others(112): Show |
8 | a0001c0003t0002g0224 a0001c0003t0002g0230 a0001c0003t0002g0259 others(5): Show |
8 | HG01261.hp1 HG01981.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.467-471_467-470ins others(119): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr7 | 890449 | ||||||
| chr7:890603 | T | C | 1 | a0001c0001t0002g0026 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.467-325T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890603 | |||||||
| chr7:890610 | T | A | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.467-318T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890610 | |||||||
| chr7:890711 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.467-217C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890711 | |||||||
| chr7:890727 | C | T | 2 | a0001c0001t0014g0058 a0001c0001t0014g0059 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.467-201C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 4/8 | chr7 | 890727 | |||||||
| chr7:891143 | C | A | 3 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 |
4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.605+77C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891143 | |||||||
| chr7:891183 | C | T | 1 | a0001c0001t0010g0172 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.605+117C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891183 | |||||||
| chr7:891212 | C | G | 1 | a0001c0001t0029g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.605+146C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891212 | |||||||
| chr7:891304 | G | A | 1 | a0001c0002t0002g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.605+238G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891304 | |||||||
| chr7:891327 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.605+261C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891327 | |||||||
| chr7:891367 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0022g0208 |
2 | HG00597.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.605+301G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891367 | |||||||
| chr7:891384 | A | G | 4 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0006g0044 others(1): Show |
5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.605+318A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891384 | |||||||
| chr7:891490 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.605+424G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891490 | |||||||
| chr7:891501 | C | T | 1 | a0001c0003t0002g0260 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.605+435C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891501 | |||||||
| chr7:891530 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.605+464G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891530 | |||||||
| chr7:891675 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.606-603C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891675 | |||||||
| chr7:891750 | C | T | 1 | a0001c0002t0001g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.606-528C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891750 | |||||||
| chr7:891766 | G | A | 1 | a0001c0002t0001g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.606-512G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891766 | |||||||
| chr7:891785 | G | C | 7 | a0001c0005t0001g0250 a0001c0005t0001g0252 a0001c0008t0001g0247 others(4): Show |
7 | HG00280.hp2 HG01168.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.606-493G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891785 | |||||||
| chr7:891804 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.606-474C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891804 | |||||||
| chr7:891814 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.606-464G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891814 | |||||||
| chr7:891815 | C | T | 1 | a0001c0002t0002g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.606-463C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891815 | |||||||
| chr7:891816 | T | C | 6 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0002t0006g0054 others(3): Show |
7 | HG01243.hp2 HG01496.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.606-462T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891816 | |||||||
| chr7:891846 | CAG | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 |
4 | HG02615.hp2 HG02895.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-431_606-430del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891846 | |||||||
| chr7:891867 | A | G | 8 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(5): Show |
10 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.606-411A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891867 | |||||||
| chr7:891888 | C | G | 1 | a0001c0002t0003g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.606-390C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891888 | |||||||
| chr7:891930 | G | C | 1 | a0001c0001t0003g0063 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.606-348G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891930 | |||||||
| chr7:891939 | C | T | 1 | a0001c0001t0001g0013 | 4 | HG02886.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-339C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891939 | |||||||
| chr7:891967 | G | C | 4 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0006g0044 others(1): Show |
5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-311G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891967 | |||||||
| chr7:891980 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.606-298G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 891980 | |||||||
| chr7:892010 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0014g0058 a0001c0001t0014g0059 others(4): Show |
11 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.606-268G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892010 | |||||||
| chr7:892023 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(64): Show |
100 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.606-255G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892023 | |||||||
| chr7:892132 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0212 |
2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.606-146G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892132 | |||||||
| chr7:892169 | A | G | 8 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(5): Show |
10 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.606-109A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892169 | |||||||
| chr7:892206 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.606-72G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892206 | |||||||
| chr7:892224 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.606-54G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892224 | |||||||
| chr7:892227 | CAGA | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0041 |
6 | HG01256.hp2 HG01258.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.606-48_606-46delAA others(1): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | 892227 | ||||||
| chr7:892239 | C | T | 1 | a0001c0003t0002g0046 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.606-39C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892239 | |||||||
| chr7:892253 | A | C | 1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.606-25A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892253 | |||||||
| chr7:892254 | C | A | 1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.606-24C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 5/8 | chr7 | 892254 | |||||||
| chr7:892465 | T | C | 4 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0006g0044 others(1): Show |
5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+47T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892465 | |||||||
| chr7:892564 | G | A | 1 | a0001c0002t0002g0138 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.746+146G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892564 | |||||||
| chr7:892593 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.746+175G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892593 | |||||||
| chr7:892620 | C | T | 13 | a0001c0003t0002g0046 a0001c0003t0002g0224 a0001c0003t0002g0230 others(10): Show |
14 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.746+202C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892620 | |||||||
| chr7:892631 | GTGGGTGT others(17): Show |
G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(102): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.746+217_746+240del others(24): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 892631 | ||||||
| chr7:892633 | G | A | 1 | a0001c0001t0029g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.746+215G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892633 | |||||||
| chr7:892657 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.746+239G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892657 | |||||||
| chr7:892673 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.746+255G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892673 | |||||||
| chr7:892794 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.746+376C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892794 | |||||||
| chr7:892819 | C | T | 24 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0002g0003 others(21): Show |
33 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.746+401C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892819 | |||||||
| chr7:892858 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.746+440G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892858 | |||||||
| chr7:892882 | G | C | 10 | a0001c0002t0001g0031 a0001c0002t0001g0116 a0001c0002t0001g0118 others(7): Show |
10 | HG02056.hp2 HG02074.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.746+464G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892882 | |||||||
| chr7:892889 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.746+471C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892889 | |||||||
| chr7:892937 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG02572.hp1 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.746+519G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892937 | |||||||
| chr7:892983 | A | C | 1 | a0001c0002t0035g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.746+565A>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892983 | |||||||
| chr7:892983 | A | G | 4 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0006g0044 others(1): Show |
5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+565A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892983 | |||||||
| chr7:892984 | AGT | A | 3 | a0001c0001t0002g0039 a0001c0001t0002g0165 a0002c0007t0001g0020 |
6 | NA18944.hp1 NA18954.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.746+569_746+570del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 892984 | ||||||
| chr7:892993 | G | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(262): Show |
346 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.746+575G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 892993 | |||||||
| chr7:893020 | G | GTT | 4 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0006g0044 others(1): Show |
5 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.746+602_746+603ins others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893020 | |||||||
| chr7:893022 | G | T | 39 | a0001c0002t0001g0029 a0001c0002t0001g0031 a0001c0002t0001g0092 others(36): Show |
42 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.746+604G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893022 | |||||||
| chr7:893047 | GTT | G | 24 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0002g0003 others(21): Show |
33 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.746+630_746+631del others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893047 | |||||||
| chr7:893055 | TGGGCGTG others(28): Show |
T | 1 | a0001c0001t0001g0216 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.746+648_747-640del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893055 | ||||||
| chr7:893059 | CGTG | C | 4 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.746+648_746+650del others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893059 | ||||||
| chr7:893077 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.746+659C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893077 | |||||||
| chr7:893090 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-650C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893090 | |||||||
| chr7:893094 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747-646C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893094 | |||||||
| chr7:893101 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-639A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893101 | |||||||
| chr7:893113 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0207 |
2 | HG03225.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.747-627A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893113 | |||||||
| chr7:893129 | CGTG | C | 52 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(49): Show |
59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.747-607_747-605del others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893129 | ||||||
| chr7:893158 | A | G | 28 | a0001c0002t0001g0075 a0001c0002t0001g0119 a0001c0002t0001g0125 others(25): Show |
30 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.747-582A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893158 | |||||||
| chr7:893172 | T | G | 2 | a0001c0002t0002g0086 a0001c0002t0002g0088 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.747-568T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893172 | |||||||
| chr7:893172 | T | TTGCAGGT others(28): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0212 |
2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.747-548_747-514dup others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893172 | ||||||
| chr7:893172 | TTGCAGGT others(98): Show |
T | 1 | a0001c0001t0002g0026 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.747-513_747-409del | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893172 | ||||||
| chr7:893190 | C | T | 1 | a0001c0001t0008g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.747-550C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893190 | |||||||
| chr7:893192 | C | T | 1 | a0001c0008t0001g0251 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.747-548C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893192 | |||||||
| chr7:893196 | C | T | 1 | a0001c0003t0002g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.747-544C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893196 | |||||||
| chr7:893198 | CGGTGGTG others(28): Show |
C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0002g0048 others(4): Show |
8 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.747-513_747-479del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893198 | ||||||
| chr7:893233 | T | C | 4 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 others(1): Show |
5 | HG02258.hp2 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.747-507T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893233 | |||||||
| chr7:893233 | T | TGGTGGTG others(28): Show |
4 | a0001c0005t0011g0254 a0001c0005t0011g0265 a0001c0006t0002g0253 others(1): Show |
4 | HG02258.hp1 HG02896.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.747-437_747-403dup others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893233 | ||||||
| chr7:893233 | TGGTGGTG others(28): Show |
T | 3 | a0001c0002t0001g0089 a0001c0003t0006g0044 a0001c0011t0002g0049 |
4 | HG02647.hp1 HG02717.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-437_747-403del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893233 | ||||||
| chr7:893268 | C | CGGTGGTG others(494): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.747-178_747-177ins others(501): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893268 | ||||||
| chr7:893268 | C | CGGTGGTG others(28): Show |
1 | a0001c0001t0001g0206 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.747-444_747-443ins others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893268 | ||||||
| chr7:893268 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.747-472C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893268 | |||||||
| chr7:893301 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.747-439C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893301 | |||||||
| chr7:893302 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.747-438G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893302 | |||||||
| chr7:893330 | C | T | 2 | a0001c0003t0006g0044 a0001c0011t0002g0049 |
3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747-410C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893330 | |||||||
| chr7:893331 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0014g0058 a0001c0001t0014g0059 |
3 | HG01243.hp2 HG02717.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.747-409G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893331 | |||||||
| chr7:893332 | C | T | 2 | a0001c0003t0006g0044 a0001c0011t0002g0049 |
3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747-408C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893332 | |||||||
| chr7:893332 | CGGGCGTG others(28): Show |
C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0213 a0001c0001t0001g0220 |
4 | HG01255.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.747-397_747-363del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893332 | ||||||
| chr7:893336 | CGTG | C | 4 | a0001c0001t0001g0009 a0001c0001t0002g0175 a0001c0001t0010g0172 others(1): Show |
4 | HG02280.hp2 HG03041.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.747-395_747-393del others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893336 | ||||||
| chr7:893338 | T | C | 6 | a0001c0001t0001g0206 a0001c0002t0001g0030 a0001c0002t0001g0106 others(3): Show |
7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-402T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893338 | |||||||
| chr7:893346 | G | A | 4 | a0001c0001t0004g0034 a0001c0001t0004g0146 a0001c0001t0004g0147 others(1): Show |
5 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.747-394G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893346 | |||||||
| chr7:893346 | G | T | 6 | a0001c0001t0001g0206 a0001c0002t0001g0030 a0001c0002t0001g0106 others(3): Show |
7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-394G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893346 | |||||||
| chr7:893347 | T | G | 6 | a0001c0001t0001g0206 a0001c0002t0001g0030 a0001c0002t0001g0106 others(3): Show |
7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-393T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893347 | |||||||
| chr7:893347 | T | TTGCAGGT others(28): Show |
47 | a0001c0002t0001g0029 a0001c0002t0001g0031 a0001c0002t0001g0087 others(44): Show |
53 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.747-376_747-375ins others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893347 | ||||||
| chr7:893347 | TTGCAGGT others(25): Show |
T | 1 | a0001c0002t0038g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.747-375_747-344del others(32): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893347 | ||||||
| chr7:893353 | G | A | 27 | a0001c0002t0001g0075 a0001c0002t0001g0125 a0001c0002t0001g0129 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.747-387G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893353 | |||||||
| chr7:893365 | T | C | 8 | a0001c0001t0001g0206 a0001c0002t0001g0030 a0001c0002t0001g0106 others(5): Show |
10 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.747-375T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893365 | |||||||
| chr7:893367 | T | C | 6 | a0001c0001t0001g0206 a0001c0002t0001g0030 a0001c0002t0001g0106 others(3): Show |
7 | HG02148.hp2 HG02258.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.747-373T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893367 | |||||||
| chr7:893371 | C | CGCG | 2 | a0001c0003t0006g0044 a0001c0011t0002g0049 |
3 | HG02647.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.747-368_747-367ins others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893371 | ||||||
| chr7:893376 | T | TG | 5 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 others(2): Show |
6 | HG02148.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-363dupG | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893376 | ||||||
| chr7:893379 | G | GGT | 5 | a0001c0002t0001g0030 a0001c0002t0001g0106 a0001c0002t0001g0108 others(2): Show |
6 | HG02148.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.747-361_747-360ins others(2): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893379 | |||||||
| chr7:893399 | T | C | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-341T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893399 | |||||||
| chr7:893434 | C | T | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-306C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893434 | |||||||
| chr7:893435 | A | G | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-305A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893435 | |||||||
| chr7:893439 | A | G | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-301A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893439 | |||||||
| chr7:893463 | C | T | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-277C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893463 | |||||||
| chr7:893467 | C | T | 55 | a0001c0001t0002g0008 a0001c0001t0002g0205 a0001c0001t0004g0231 others(52): Show |
64 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.747-273C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893467 | |||||||
| chr7:893476 | T | G | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-264T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893476 | |||||||
| chr7:893478 | GTGCAGGT others(25): Show |
G | 44 | a0001c0002t0001g0029 a0001c0002t0001g0031 a0001c0002t0001g0087 others(41): Show |
50 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.747-242_747-211del others(32): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893478 | ||||||
| chr7:893485 | TGAGTGTT others(27): Show |
T | 1 | a0001c0002t0020g0085 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.747-253_747-220del others(34): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893485 | ||||||
| chr7:893493 | G | A | 12 | a0001c0003t0002g0046 a0001c0003t0002g0224 a0001c0003t0002g0230 others(9): Show |
13 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.747-247G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893493 | |||||||
| chr7:893499 | G | A | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-241G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893499 | |||||||
| chr7:893503 | ATGGTGGT others(25): Show |
A | 2 | a0001c0002t0001g0080 a0001c0002t0001g0089 |
2 | HG02602.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.747-229_747-198del others(32): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893503 | ||||||
| chr7:893510 | TTGCAGGT others(28): Show |
T | 1 | a0001c0001t0001g0012 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.747-212_747-178del others(35): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893510 | ||||||
| chr7:893516 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.747-224G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893516 | |||||||
| chr7:893528 | T | C | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-212T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893528 | |||||||
| chr7:893530 | T | C | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-210T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893530 | |||||||
| chr7:893531 | A | G | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-209A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893531 | |||||||
| chr7:893531 | AGGCGTGG others(92): Show |
A | 1 | a0001c0021t0002g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.747-175_747-77delT others(98): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893531 | ||||||
| chr7:893534 | C | T | 3 | a0001c0001t0001g0072 a0001c0002t0038g0090 a0001c0019t0001g0112 |
3 | HG02148.hp2 HG03225.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.747-206C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893534 | |||||||
| chr7:893535 | G | T | 9 | a0001c0001t0002g0008 a0001c0001t0004g0231 a0001c0004t0002g0008 others(6): Show |
12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.747-205G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893535 | |||||||
| chr7:893536 | T | C | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-204T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893536 | |||||||
| chr7:893543 | G | T | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-197G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893543 | |||||||
| chr7:893563 | C | T | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-177C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893563 | |||||||
| chr7:893596 | A | G | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-144A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893596 | |||||||
| chr7:893597 | T | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(193): Show |
246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.747-143T>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893597 | |||||||
| chr7:893598 | G | A | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-142G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893598 | |||||||
| chr7:893601 | C | CACG | 25 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0002g0003 others(22): Show |
34 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.747-139_747-138ins others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893601 | |||||||
| chr7:893603 | C | CGGT | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(244): Show |
323 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.747-135_747-133dup others(3): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893603 | ||||||
| chr7:893603 | C | CGGTGGTG others(98): Show |
1 | a0001c0001t0001g0072 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.747-133_747-132ins others(105): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | 893603 | ||||||
| chr7:893603 | C | T | 29 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0002g0003 others(26): Show |
38 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.747-137C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893603 | |||||||
| chr7:893608 | T | G | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-132T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893608 | |||||||
| chr7:893609 | G | T | 2 | a0001c0002t0038g0090 a0001c0019t0001g0112 |
2 | HG02148.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.747-131G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893609 | |||||||
| chr7:893655 | T | C | 5 | a0001c0001t0014g0058 a0001c0001t0014g0059 a0001c0003t0002g0151 others(2): Show |
6 | HG01243.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.747-85T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893655 | |||||||
| chr7:893710 | C | G | 1 | a0001c0003t0002g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.747-30C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893710 | |||||||
| chr7:893732 | T | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0002g0003 others(23): Show |
36 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
splice_region_variant&intron_variant | LOW | c.747-8T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 6/8 | chr7 | 893732 | |||||||
| chr7:893861 | G | C | 1 | a0001c0003t0002g0260 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.823-38G>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 7/8 | chr7 | 893861 | |||||||
| chr7:893984 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0002g0217 |
5 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.895+13G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 893984 | |||||||
| chr7:893997 | C | T | 1 | a0001c0004t0004g0235 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.895+26C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 893997 | |||||||
| chr7:894014 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.895+43C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894014 | |||||||
| chr7:894034 | T | C | 1 | a0001c0001t0013g0170 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.895+63T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894034 | |||||||
| chr7:894058 | C | T | 1 | a0001c0003t0002g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.895+87C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894058 | |||||||
| chr7:894112 | T | C | 2 | a0001c0003t0002g0050 a0001c0017t0002g0053 |
2 | HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.895+141T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894112 | |||||||
| chr7:894121 | A | ATTATTAG others(23): Show |
1 | a0001c0001t0002g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.895+151_895+180dup others(30): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 894121 | ||||||
| chr7:894121 | A | ATTATTAG others(53): Show |
1 | a0001c0003t0006g0044 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.895+180_895+181ins others(60): Show |
GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr7 | 894121 | ||||||
| chr7:894161 | C | T | 1 | a0001c0001t0029g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.895+190C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894161 | |||||||
| chr7:894181 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.895+210A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894181 | |||||||
| chr7:894209 | A | G | 1 | a0001c0021t0002g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.895+238A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894209 | |||||||
| chr7:894211 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.895+240T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894211 | |||||||
| chr7:894254 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.895+283C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894254 | |||||||
| chr7:894267 | G | A | 3 | a0001c0010t0025g0057 a0001c0010t0026g0056 a0001c0010t0028g0055 |
3 | HG02723.hp2 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.895+296G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894267 | |||||||
| chr7:894286 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.895+315G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894286 | |||||||
| chr7:894307 | C | T | 1 | a0001c0004t0002g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.895+336C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894307 | |||||||
| chr7:894321 | G | A | 1 | a0001c0003t0006g0044 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.895+350G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894321 | |||||||
| chr7:894343 | C | T | 1 | a0001c0003t0002g0268 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.895+372C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894343 | |||||||
| chr7:894357 | C | T | 27 | a0001c0001t0029g0173 a0001c0002t0001g0075 a0001c0002t0001g0125 others(24): Show |
29 | HG00544.hp1 HG00621.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.895+386C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894357 | |||||||
| chr7:894360 | G | A | 1 | a0001c0001t0002g0026 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.895+389G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894360 | |||||||
| chr7:894367 | C | T | 1 | a0001c0002t0001g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.895+396C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894367 | |||||||
| chr7:894394 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
244 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.895+423G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894394 | |||||||
| chr7:894435 | C | A | 3 | a0001c0002t0001g0095 a0001c0002t0001g0096 a0001c0002t0003g0098 |
3 | HG02040.hp2 HG02135.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.895+464C>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894435 | |||||||
| chr7:894441 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG00558.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.895+470G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894441 | |||||||
| chr7:894552 | C | T | 2 | a0001c0001t0001g0204 a0001c0002t0001g0110 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.895+581C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894552 | |||||||
| chr7:894558 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.895+587C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894558 | |||||||
| chr7:894561 | A | G | 2 | a0001c0010t0025g0057 a0001c0010t0028g0055 |
2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.895+590A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894561 | |||||||
| chr7:894630 | C | T | 1 | a0001c0003t0002g0224 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.895+659C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894630 | |||||||
| chr7:894649 | G | A | 1 | a0001c0002t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.895+678G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894649 | |||||||
| chr7:894670 | G | A | 1 | a0001c0001t0033g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.896-664G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894670 | |||||||
| chr7:894692 | G | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0073 |
8 | HG02071.hp2 HG02129.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.896-642G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894692 | |||||||
| chr7:894717 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.896-617G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894717 | |||||||
| chr7:894718 | T | G | 1 | a0001c0001t0033g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.896-616T>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894718 | |||||||
| chr7:894720 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.896-614G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894720 | |||||||
| chr7:894748 | G | A | 1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896-586G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894748 | |||||||
| chr7:894770 | C | T | 20 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0066 others(17): Show |
29 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.896-564C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894770 | |||||||
| chr7:894856 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(40): Show |
69 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.896-478A>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894856 | |||||||
| chr7:894868 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.896-466G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894868 | |||||||
| chr7:894892 | C | T | 22 | a0001c0002t0001g0125 a0001c0002t0001g0129 a0001c0002t0001g0131 others(19): Show |
24 | HG00544.hp1 HG00621.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.896-442C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894892 | |||||||
| chr7:894893 | G | T | 2 | a0001c0001t0012g0161 a0001c0001t0012g0168 |
2 | HG02055.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.896-441G>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894893 | |||||||
| chr7:894921 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.896-413C>G | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894921 | |||||||
| chr7:894938 | C | T | 2 | a0001c0003t0001g0152 a0001c0003t0002g0050 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.896-396C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894938 | |||||||
| chr7:894939 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.896-395G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894939 | |||||||
| chr7:894943 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.896-391T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894943 | |||||||
| chr7:894973 | A | T | 1 | a0001c0001t0027g0238 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.896-361A>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894973 | |||||||
| chr7:894985 | G | A | 2 | a0001c0002t0001g0030 a0001c0002t0001g0106 |
3 | HG02615.hp2 HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.896-349G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 894985 | |||||||
| chr7:895005 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.896-329T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895005 | |||||||
| chr7:895088 | C | T | 7 | a0001c0005t0001g0250 a0001c0005t0001g0252 a0001c0008t0001g0247 others(4): Show |
7 | HG00280.hp2 HG01168.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.896-246C>T | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895088 | |||||||
| chr7:895137 | T | C | 3 | a0001c0003t0001g0152 a0001c0003t0002g0050 a0001c0003t0010g0150 |
3 | HG02647.hp2 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.896-197T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895137 | |||||||
| chr7:895188 | T | C | 2 | a0001c0017t0002g0053 a0001c0021t0002g0083 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.896-146T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895188 | |||||||
| chr7:895197 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0003g0005 a0001c0001t0003g0073 others(1): Show |
10 | HG01891.hp2 HG02071.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.896-137G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895197 | |||||||
| chr7:895211 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.896-123T>C | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895211 | |||||||
| chr7:895267 | G | A | 1 | a0001c0003t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896-67G>A | GET4 | ENSG00000239857.7 | transcript | ENST00000265857.8 | protein_coding | 8/8 | chr7 | 895267 |