Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9837 |
| ensemblid | ENSG00000101003.12 |
| hgncid | 28980 |
| symbol | GINS1 |
| name | GINS complex subunit 1 |
| refseq_nuc | NM_021067.5 |
| refseq_prot | NP_066545.3 |
| ensembl_nuc | ENST00000262460.5 |
| ensembl_prot | ENSP00000262460.4 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 25407673 |
| end | 25448563 |
| strand | + |
| ver | v1.2 |
| region | chr20:25407673-25448563 |
| region5000 | chr20:25402673-25453563 |
| regionname0 | GINS1_chr20_25407673_25448563 |
| regionname5000 | GINS1_chr20_25402673_25453563 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 196 | 295 | 83 | 49 | 127 | 6 | 28 | 91 | GINS1_chr20_25402673_25453563 | GINS1 | MFCEK others(191): Show |
chr20 | 25402673 | 25453563 |
| a0002 | 0/0 | 196 | 64 | 11 | 27 | 2 | 10 | 14 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | MFCEK others(191): Show |
chr20 | 25402673 | 25453563 |
| a0003 | 0/0 | 190 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | MELIR others(185): Show |
chr20 | 25402673 | 25453563 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 588 | 295 | 83 | 49 | 127 | 6 | 28 | GINS1_chr20_25402673_25453563 | GINS1 | ATGTT others(583): Show |
chr20 | 25402673 | 25453563 | ||
| a0002c0002 | 0/0 | 588 | 64 | 11 | 27 | 2 | 10 | 14 | GINS1_chr20_25402673_25453563 | GINS1 | ATGTT others(583): Show |
chr20 | 25402673 | 25453563 | ||
| a0003c0003 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTGTT others(583): Show |
chr20 | 25402673 | 25453563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3310 | 175 | 22 | 30 | 101 | 4 | 17 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0002 | 1/0 | 3311 | 82 | 36 | 14 | 22 | 1 | 8 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3306): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0003 | 0/0 | 3310 | 5 | 5 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0004 | 0/0 | 3310 | 5 | 2 | 2 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0005 | 0/0 | 3310 | 4 | 4 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0006 | 0/0 | 3310 | 4 | 2 | 1 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0007 | 0/0 | 3310 | 3 | 0 | 0 | 3 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0008 | 0/0 | 3310 | 2 | 2 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0009 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3619): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0010 | 0/0 | 3625 | 2 | 2 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3620): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0011 | 0/0 | 3311 | 2 | 2 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3306): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0012 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3306): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0013 | 0/0 | 3311 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3306): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0014 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3306): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0015 | 0/0 | 3311 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3306): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0016 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0017 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0018 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0019 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0001c0001t0020 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| a0002c0002t0002 | 0/0 | 3311 | 64 | 11 | 27 | 2 | 10 | 14 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3306): Show |
chr20 | 25402673 | 25453563 |
| a0003c0003t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | GTTCG others(3305): Show |
chr20 | 25402673 | 25453563 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0008g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0012g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0013g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0014g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0015g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0018g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0019g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0001c0001t0020g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0117 | EUR | GBR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0131 | EUR | FIN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0093 | EUR | FIN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0133 | EUR | FIN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0130 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG00741 | hp2 | a0001 | c0001 | t0015 | g0148 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0070 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0091 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0047 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0069 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0119 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0128 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0022 | EUR | IBS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0092 | EUR | IBS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0147 | EUR | IBS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0068 | EUR | IBS | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0109 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0313 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0121 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0023 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0017 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0124 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CDX | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0080 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0146 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02717 | hp2 | a0001 | c0001 | t0017 | g0163 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0094 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0115 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02970 | hp2 | a0001 | c0001 | t0016 | g0009 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0040 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0066 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0332 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0039 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0114 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0312 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0157 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0105 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0318 | AFR | ESN | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0136 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03927 | hp1 | a0001 | c0001 | t0019 | g0274 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0106 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04115 | hp2 | a0001 | c0001 | t0020 | g0156 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0135 | SAS | STU | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | YRI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0108 | AFR | YRI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0210 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | LWK | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | LWK | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | LWK | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19079 | hp1 | a0001 | c0001 | t0018 | g0270 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0333 | AFR | YRI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ASW | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | ASW | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0073 | EUR | TSI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0103 | EUR | TSI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0139 | EUR | TSI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | GIH | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | ACB | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | USA | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | USA | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | USA | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | LWK | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0292 | REF | REF | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0204 | REF | REF | GINS1_chr20_25402673_25453563 | GINS1 | chr20 | 25402673 | 25453563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:25407821 | A | G | 1 | a0003 | 1 | HG02083.hp2 | start_lost | HIGH | c.1A>G | p.Met1? | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/7 | 149/3311 | 1/591 | 1/196 | chr20 | 25407821 | |||
| chr20:25418154 | G | A | 1 | a0002 | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
missense_variant | MODERATE | c.289G>A | p.Val97Ile | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/7 | 437/3311 | 289/591 | 97/196 | chr20 | 25418154 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:25407720 | T | A | 1 | a0001c0001t0012 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/7 | 101 | chr20 | 25407720 | ||||||
| chr20:25407799 | G | T | 1 | a0001c0001t0011 | 2 | HG02976.hp2 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-22G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/7 | 22 | chr20 | 25407799 | ||||||
| chr20:25407800 | C | T | 1 | a0001c0001t0011 | 2 | HG02976.hp2 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-21C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/7 | 21 | chr20 | 25407800 | ||||||
| chr20:25446006 | A | C | 1 | a0001c0001t0020 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 15 | chr20 | 25446006 | ||||||
| chr20:25446056 | C | T | 1 | a0001c0001t0019 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*65C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 65 | chr20 | 25446056 | ||||||
| chr20:25446057 | CA | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*67delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 67 | chr20 | 25446057 | ||||||
| chr20:25446332 | G | A | 11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(8): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 341 | chr20 | 25446332 | ||||||
| chr20:25446388 | T | TTACAGTG others(307): Show |
1 | a0001c0001t0009 | 2 | HG02559.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*412_*413insTTTTTT others(308): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 413 | INFO_REALIGN_3_PRIME | chr20 | 25446388 | |||||
| chr20:25446388 | T | TTACAGTG others(308): Show |
1 | a0001c0001t0010 | 2 | HG02145.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*412_*413insTTTTTT others(309): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 413 | INFO_REALIGN_3_PRIME | chr20 | 25446388 | |||||
| chr20:25446445 | G | T | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 454 | chr20 | 25446445 | ||||||
| chr20:25446935 | C | A | 1 | a0001c0001t0016 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 944 | chr20 | 25446935 | ||||||
| chr20:25446977 | A | G | 1 | a0001c0001t0015 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*986A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 986 | chr20 | 25446977 | ||||||
| chr20:25447018 | T | G | 3 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0013 |
8 | HG01255.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1027T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1027 | chr20 | 25447018 | ||||||
| chr20:25447106 | C | T | 1 | a0001c0001t0006 | 4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1115C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1115 | chr20 | 25447106 | ||||||
| chr20:25447186 | C | T | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1195C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1195 | chr20 | 25447186 | ||||||
| chr20:25447189 | G | A | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1198 | chr20 | 25447189 | ||||||
| chr20:25447190 | C | G | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1199C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1199 | chr20 | 25447190 | ||||||
| chr20:25447191 | C | A | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1200C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1200 | chr20 | 25447191 | ||||||
| chr20:25447193 | C | A | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1202C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1202 | chr20 | 25447193 | ||||||
| chr20:25447194 | C | T | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1203C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1203 | chr20 | 25447194 | ||||||
| chr20:25447198 | C | T | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1207C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1207 | chr20 | 25447198 | ||||||
| chr20:25447199 | C | A | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1208C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1208 | chr20 | 25447199 | ||||||
| chr20:25447200 | T | C | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1209T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1209 | chr20 | 25447200 | ||||||
| chr20:25447201 | G | T | 1 | a0001c0001t0018 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1210G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1210 | chr20 | 25447201 | ||||||
| chr20:25447326 | G | A | 2 | a0001c0001t0012 a0001c0001t0014 |
2 | HG01884.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1335G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1335 | chr20 | 25447326 | ||||||
| chr20:25447625 | T | C | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1634T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1634 | chr20 | 25447625 | ||||||
| chr20:25447641 | T | C | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(3): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1650T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1650 | chr20 | 25447641 | ||||||
| chr20:25447675 | G | A | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1684G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 1684 | chr20 | 25447675 | ||||||
| chr20:25447999 | T | C | 2 | a0001c0001t0009 a0001c0001t0010 |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2008T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 2008 | chr20 | 25447999 | ||||||
| chr20:25448023 | C | T | 1 | a0001c0001t0007 | 3 | NA18946.hp2 NA18967.hp1 NA18994.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2032C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 2032 | chr20 | 25448023 | ||||||
| chr20:25448150 | T | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2159T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 2159 | chr20 | 25448150 | ||||||
| chr20:25448316 | A | G | 1 | a0001c0001t0008 | 2 | HG03098.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2325A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 2325 | chr20 | 25448316 | ||||||
| chr20:25448454 | G | A | 2 | a0001c0001t0005 a0001c0001t0017 |
5 | HG02145.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2463G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 7/7 | 2463 | chr20 | 25448454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:25407928 | C | G | 4 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(1): Show |
4 | HG00639.hp1 HG00741.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+33C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25407928 | |||||||
| chr20:25408081 | G | A | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+186G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408081 | |||||||
| chr20:25408198 | A | G | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.75+303A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408198 | |||||||
| chr20:25408267 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.75+372A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408267 | |||||||
| chr20:25408275 | G | T | 1 | a0001c0001t0002g0331 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.75+380G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408275 | |||||||
| chr20:25408420 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.75+525G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408420 | |||||||
| chr20:25408478 | ATAT | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+587_75+589delTA others(1): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr20 | 25408478 | ||||||
| chr20:25408517 | A | C | 1 | a0001c0001t0001g0330 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.75+622A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408517 | |||||||
| chr20:25408518 | G | A | 1 | a0001c0001t0001g0330 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.75+623G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408518 | |||||||
| chr20:25408694 | A | G | 13 | a0001c0001t0002g0317 a0001c0001t0002g0318 a0001c0001t0002g0319 others(10): Show |
13 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+799A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25408694 | |||||||
| chr20:25408931 | CAG | C | 3 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG01943.hp2 HG01952.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.75+1038_75+1039del others(2): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr20 | 25408931 | ||||||
| chr20:25409080 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.75+1185G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409080 | |||||||
| chr20:25409120 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
7 | HG01081.hp2 HG03579.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1225G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409120 | |||||||
| chr20:25409177 | A | T | 2 | a0001c0001t0012g0313 a0001c0001t0014g0312 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+1282A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409177 | |||||||
| chr20:25409281 | G | A | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.75+1386G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409281 | |||||||
| chr20:25409475 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.75+1580C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409475 | |||||||
| chr20:25409648 | T | C | 151 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(148): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.75+1753T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409648 | |||||||
| chr20:25409736 | T | A | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1841T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409736 | |||||||
| chr20:25409955 | T | C | 2 | a0001c0001t0012g0313 a0001c0001t0014g0312 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+2060T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25409955 | |||||||
| chr20:25410212 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.75+2317G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410212 | |||||||
| chr20:25410295 | C | T | 1 | a0001c0001t0015g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.75+2400C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410295 | |||||||
| chr20:25410330 | G | A | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.75+2435G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410330 | |||||||
| chr20:25410562 | CTTTTT | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0166 a0001c0001t0001g0167 |
4 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+2671_75+2675del others(5): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr20 | 25410562 | ||||||
| chr20:25410593 | G | A | 1 | a0002c0002t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.75+2698G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410593 | |||||||
| chr20:25410657 | G | C | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+2762G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410657 | |||||||
| chr20:25410669 | C | T | 4 | a0001c0001t0008g0332 a0001c0001t0008g0333 a0002c0002t0002g0146 others(1): Show |
4 | HG01516.hp1 HG02602.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+2774C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410669 | |||||||
| chr20:25410814 | C | A | 1 | a0002c0002t0002g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.75+2919C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410814 | |||||||
| chr20:25410843 | G | A | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-2947G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410843 | |||||||
| chr20:25410852 | C | T | 4 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 others(1): Show |
4 | HG02165.hp2 NA18944.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-2938C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410852 | |||||||
| chr20:25410858 | C | T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | NA19002.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.76-2932C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410858 | |||||||
| chr20:25410966 | T | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(48): Show |
59 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.76-2824T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410966 | |||||||
| chr20:25410986 | A | C | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-2804A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25410986 | |||||||
| chr20:25411023 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.76-2767C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25411023 | |||||||
| chr20:25411037 | G | GGA | 7 | a0001c0001t0001g0003 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
9 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-2751_76-2750dup others(2): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr20 | 25411037 | ||||||
| chr20:25411257 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
9 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-2533A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25411257 | |||||||
| chr20:25411261 | T | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-2529T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25411261 | |||||||
| chr20:25411333 | C | T | 177 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.76-2457C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25411333 | |||||||
| chr20:25411491 | C | G | 7 | a0001c0001t0002g0008 a0001c0001t0002g0140 a0001c0001t0002g0141 others(4): Show |
8 | HG00099.hp1 HG00642.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-2299C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25411491 | |||||||
| chr20:25411748 | A | G | 151 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(148): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.76-2042A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25411748 | |||||||
| chr20:25411893 | A | G | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.76-1897A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25411893 | |||||||
| chr20:25411943 | CA | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(117): Show |
131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.76-1833delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr20 | 25411943 | ||||||
| chr20:25412216 | C | A | 1 | a0001c0001t0001g0330 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.76-1574C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412216 | |||||||
| chr20:25412218 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0294 a0001c0001t0001g0295 others(8): Show |
12 | HG00544.hp2 HG01070.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-1572A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412218 | |||||||
| chr20:25412282 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(278): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.76-1508A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412282 | |||||||
| chr20:25412338 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.76-1452G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412338 | |||||||
| chr20:25412398 | AC | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.76-1391delC | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412398 | |||||||
| chr20:25412400 | A | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.76-1390A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412400 | |||||||
| chr20:25412415 | C | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.76-1375C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412415 | |||||||
| chr20:25412435 | A | T | 1 | a0001c0001t0001g0330 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.76-1355A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412435 | |||||||
| chr20:25412450 | G | A | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.76-1340G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412450 | |||||||
| chr20:25412481 | G | A | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.76-1309G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412481 | |||||||
| chr20:25412606 | T | A | 1 | a0001c0001t0001g0330 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.76-1184T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412606 | |||||||
| chr20:25412650 | A | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-1140A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412650 | |||||||
| chr20:25412778 | A | G | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.76-1012A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25412778 | |||||||
| chr20:25413056 | AT | A | 23 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0002g0035 others(20): Show |
23 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.76-718delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr20 | 25413056 | ||||||
| chr20:25413123 | G | A | 1 | a0002c0002t0002g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.76-667G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413123 | |||||||
| chr20:25413188 | A | T | 1 | a0001c0001t0002g0329 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-602A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413188 | |||||||
| chr20:25413245 | C | T | 1 | a0001c0001t0015g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.76-545C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413245 | |||||||
| chr20:25413362 | A | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-428A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413362 | |||||||
| chr20:25413363 | T | C | 5 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(2): Show |
5 | HG00741.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-427T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413363 | |||||||
| chr20:25413415 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.76-375G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413415 | |||||||
| chr20:25413443 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.76-347T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413443 | |||||||
| chr20:25413585 | T | G | 1 | a0001c0001t0001g0330 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.76-205T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 1/6 | chr20 | 25413585 | |||||||
| chr20:25413930 | G | T | 1 | a0001c0001t0006g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.140+76G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25413930 | |||||||
| chr20:25413966 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.140+112C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25413966 | |||||||
| chr20:25414005 | C | T | 5 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(2): Show |
5 | HG00741.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+151C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414005 | |||||||
| chr20:25414021 | C | G | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+167C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414021 | |||||||
| chr20:25414126 | G | A | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+272G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414126 | |||||||
| chr20:25414168 | G | A | 5 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+314G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414168 | |||||||
| chr20:25414189 | C | CA | 69 | a0001c0001t0001g0025 a0001c0001t0001g0181 a0001c0001t0001g0182 others(66): Show |
71 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.140+358dupA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25414189 | ||||||
| chr20:25414189 | C | CAA | 53 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(50): Show |
61 | HG00544.hp1 HG01081.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.140+357_140+358dup others(2): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25414189 | ||||||
| chr20:25414189 | C | CAAA | 6 | a0001c0001t0001g0174 a0001c0001t0002g0036 a0001c0001t0002g0041 others(3): Show |
6 | HG02027.hp2 HG03225.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+356_140+358dup others(3): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25414189 | ||||||
| chr20:25414189 | C | CAAAA | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.140+355_140+358dup others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25414189 | ||||||
| chr20:25414189 | CA | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0020 others(31): Show |
37 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.140+358delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25414189 | ||||||
| chr20:25414265 | T | A | 1 | a0001c0001t0001g0330 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.140+411T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414265 | |||||||
| chr20:25414286 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.140+432C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414286 | |||||||
| chr20:25414439 | G | A | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+585G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414439 | |||||||
| chr20:25414561 | G | A | 51 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(48): Show |
59 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.140+707G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414561 | |||||||
| chr20:25414892 | T | C | 168 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(165): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.140+1038T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414892 | |||||||
| chr20:25414939 | A | G | 5 | a0001c0001t0004g0009 a0001c0001t0004g0161 a0001c0001t0004g0162 others(2): Show |
5 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+1085A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414939 | |||||||
| chr20:25414941 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(80): Show |
91 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.140+1087A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25414941 | |||||||
| chr20:25415000 | C | T | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.140+1146C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415000 | |||||||
| chr20:25415083 | C | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+1229C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415083 | |||||||
| chr20:25415154 | T | C | 1 | a0002c0002t0002g0112 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.140+1300T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415154 | |||||||
| chr20:25415229 | G | A | 3 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG01943.hp2 HG01952.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.140+1375G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415229 | |||||||
| chr20:25415242 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.140+1388G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415242 | |||||||
| chr20:25415316 | G | C | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+1462G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415316 | |||||||
| chr20:25415402 | C | T | 4 | a0002c0002t0002g0138 a0002c0002t0002g0139 a0002c0002t0002g0146 others(1): Show |
4 | HG01516.hp1 HG02602.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+1548C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415402 | |||||||
| chr20:25415475 | G | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0137 |
3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.140+1621G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415475 | |||||||
| chr20:25415531 | C | T | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-1573C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415531 | |||||||
| chr20:25415685 | C | CA | 18 | a0001c0001t0001g0186 a0001c0001t0001g0233 a0001c0001t0001g0234 others(15): Show |
18 | HG01993.hp1 HG02145.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.141-1399dupA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25415685 | ||||||
| chr20:25415685 | C | CAA | 7 | a0001c0001t0004g0009 a0001c0001t0004g0157 a0001c0001t0004g0161 others(4): Show |
7 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-1400_141-1399d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25415685 | ||||||
| chr20:25415685 | CA | C | 17 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(14): Show |
17 | HG01109.hp2 HG01975.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.141-1399delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr20 | 25415685 | ||||||
| chr20:25415706 | G | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | NA18941.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.141-1398G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415706 | |||||||
| chr20:25415861 | T | G | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG00741.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-1243T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25415861 | |||||||
| chr20:25416102 | T | A | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.141-1002T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416102 | |||||||
| chr20:25416335 | G | C | 1 | a0001c0001t0009g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.141-769G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416335 | |||||||
| chr20:25416380 | C | T | 5 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-724C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416380 | |||||||
| chr20:25416389 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.141-715A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416389 | |||||||
| chr20:25416418 | T | A | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.141-686T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416418 | |||||||
| chr20:25416521 | A | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.141-583A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416521 | |||||||
| chr20:25416621 | G | C | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.141-483G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416621 | |||||||
| chr20:25416636 | A | C | 27 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(24): Show |
35 | HG00544.hp1 HG01255.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.141-468A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416636 | |||||||
| chr20:25416749 | T | A | 26 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(23): Show |
34 | HG00544.hp1 HG01255.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.141-355T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416749 | |||||||
| chr20:25416751 | A | G | 5 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-353A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 2/6 | chr20 | 25416751 | |||||||
| chr20:25417269 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.239+67A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417269 | |||||||
| chr20:25417344 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239+142T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417344 | |||||||
| chr20:25417593 | T | C | 1 | a0001c0001t0009g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239+391T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417593 | |||||||
| chr20:25417594 | G | T | 1 | a0001c0001t0012g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.239+392G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417594 | |||||||
| chr20:25417603 | C | T | 2 | a0002c0002t0002g0067 a0002c0002t0002g0108 |
2 | HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.239+401C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417603 | |||||||
| chr20:25417794 | T | C | 29 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(26): Show |
37 | HG00544.hp1 HG01255.hp1 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.240-311T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417794 | |||||||
| chr20:25417933 | C | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-172C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417933 | |||||||
| chr20:25417973 | T | C | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-132T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25417973 | |||||||
| chr20:25418020 | G | A | 1 | a0002c0002t0002g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.240-85G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25418020 | |||||||
| chr20:25418051 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.240-54A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 3/6 | chr20 | 25418051 | |||||||
| chr20:25418240 | G | C | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.330+45G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25418240 | |||||||
| chr20:25418548 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.330+353C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25418548 | |||||||
| chr20:25418770 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.330+575A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25418770 | |||||||
| chr20:25418983 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.330+788G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25418983 | |||||||
| chr20:25419289 | T | G | 8 | a0001c0001t0002g0007 a0001c0001t0002g0086 a0001c0001t0002g0087 others(5): Show |
9 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.330+1094T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419289 | |||||||
| chr20:25419343 | G | GA | 128 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(125): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.330+1160dupA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25419343 | ||||||
| chr20:25419350 | A | AC | 5 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(2): Show |
5 | HG00741.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.330+1155_330+1156i others(3): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419350 | |||||||
| chr20:25419371 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.330+1176T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419371 | |||||||
| chr20:25419383 | T | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(17): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+1188T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419383 | |||||||
| chr20:25419518 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(21): Show |
27 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.330+1323C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419518 | |||||||
| chr20:25419535 | G | A | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.330+1340G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419535 | |||||||
| chr20:25419601 | A | G | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+1406A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419601 | |||||||
| chr20:25419604 | T | C | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.330+1409T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419604 | |||||||
| chr20:25419684 | A | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+1489A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419684 | |||||||
| chr20:25419731 | C | G | 1 | a0002c0002t0002g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.330+1536C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419731 | |||||||
| chr20:25419818 | A | G | 2 | a0001c0001t0011g0039 a0001c0001t0011g0040 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.330+1623A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419818 | |||||||
| chr20:25419851 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0025 others(194): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.330+1656A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419851 | |||||||
| chr20:25419872 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02132.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.330+1677G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25419872 | |||||||
| chr20:25420144 | A | T | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.330+1949A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420144 | |||||||
| chr20:25420154 | G | T | 6 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0282 others(3): Show |
6 | HG00558.hp1 HG00609.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.330+1959G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420154 | |||||||
| chr20:25420216 | C | A | 1 | a0001c0001t0013g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.330+2021C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420216 | |||||||
| chr20:25420237 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.330+2042G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420237 | |||||||
| chr20:25420286 | A | G | 1 | a0002c0002t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.330+2091A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420286 | |||||||
| chr20:25420367 | G | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0025 others(194): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.330+2172G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420367 | |||||||
| chr20:25420567 | A | G | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.330+2372A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420567 | |||||||
| chr20:25420599 | G | A | 89 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0081 others(86): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.330+2404G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420599 | |||||||
| chr20:25420746 | C | T | 1 | a0002c0002t0002g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.330+2551C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420746 | |||||||
| chr20:25420752 | G | C | 1 | a0002c0002t0002g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.330+2557G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420752 | |||||||
| chr20:25420781 | CA | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
94 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.330+2601delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25420781 | ||||||
| chr20:25420781 | CAA | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0025 others(189): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.330+2600_330+2601d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25420781 | ||||||
| chr20:25420835 | C | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.330+2640C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420835 | |||||||
| chr20:25420851 | A | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.330+2656A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420851 | |||||||
| chr20:25420939 | C | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.330+2744C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25420939 | |||||||
| chr20:25421059 | A | G | 1 | a0001c0001t0014g0312 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.330+2864A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421059 | |||||||
| chr20:25421126 | T | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(17): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.330+2931T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421126 | |||||||
| chr20:25421175 | C | G | 1 | a0001c0001t0001g0302 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.330+2980C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421175 | |||||||
| chr20:25421191 | A | G | 39 | a0002c0002t0002g0034 a0002c0002t0002g0066 a0002c0002t0002g0085 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.330+2996A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421191 | |||||||
| chr20:25421226 | A | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(185): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.330+3031A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421226 | |||||||
| chr20:25421451 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.330+3256A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421451 | |||||||
| chr20:25421735 | C | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.331-3476C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421735 | |||||||
| chr20:25421771 | A | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-3440A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421771 | |||||||
| chr20:25421882 | G | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-3329G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421882 | |||||||
| chr20:25421946 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.331-3265A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25421946 | |||||||
| chr20:25422016 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0294 a0001c0001t0001g0295 others(4): Show |
8 | HG01070.hp1 HG01978.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-3195G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422016 | |||||||
| chr20:25422142 | A | G | 90 | a0001c0001t0001g0213 a0001c0001t0002g0007 a0001c0001t0002g0008 others(87): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.331-3069A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422142 | |||||||
| chr20:25422174 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.331-3037A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422174 | |||||||
| chr20:25422203 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.331-3008C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422203 | |||||||
| chr20:25422270 | C | T | 1 | a0002c0002t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.331-2941C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422270 | |||||||
| chr20:25422332 | G | A | 5 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.331-2879G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422332 | |||||||
| chr20:25422464 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.331-2747G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422464 | |||||||
| chr20:25422516 | T | C | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-2695T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422516 | |||||||
| chr20:25422662 | A | G | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-2549A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422662 | |||||||
| chr20:25422706 | T | G | 1 | a0001c0001t0002g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.331-2505T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422706 | |||||||
| chr20:25422812 | T | C | 1 | a0002c0002t0002g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.331-2399T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422812 | |||||||
| chr20:25422814 | T | C | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-2397T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422814 | |||||||
| chr20:25422838 | G | A | 5 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(2): Show |
5 | HG01515.hp1 HG01975.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.331-2373G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422838 | |||||||
| chr20:25422862 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.331-2349C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25422862 | |||||||
| chr20:25423113 | G | GT | 11 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.331-2088dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423113 | ||||||
| chr20:25423172 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.331-2039T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423172 | |||||||
| chr20:25423257 | G | T | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.331-1954G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423257 | |||||||
| chr20:25423391 | A | C | 177 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.331-1820A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423391 | |||||||
| chr20:25423392 | G | A | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.331-1819G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423392 | |||||||
| chr20:25423452 | C | CT | 6 | a0001c0001t0001g0149 a0001c0001t0001g0184 a0001c0001t0001g0207 others(3): Show |
6 | HG01123.hp2 HG01943.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.331-1725dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTT | 6 | a0001c0001t0001g0031 a0001c0001t0001g0172 a0001c0001t0001g0211 others(3): Show |
6 | HG01069.hp2 HG01081.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.331-1726_331-1725d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0032 others(3): Show |
8 | HG00140.hp2 HG01106.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-1727_331-1725d others(5): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(1): Show |
13 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0229 others(10): Show |
15 | HG02300.hp2 HG02523.hp1 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.331-1755_331-1754i others(10): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(2): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0235 a0001c0001t0001g0236 others(21): Show |
28 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.331-1755_331-1754i others(11): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(3): Show |
19 | a0001c0001t0001g0010 a0001c0001t0001g0166 a0001c0001t0001g0167 others(16): Show |
20 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.331-1755_331-1754i others(12): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(4): Show |
9 | a0001c0001t0001g0234 a0001c0001t0001g0275 a0001c0001t0001g0276 others(6): Show |
9 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-1755_331-1754i others(13): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(5): Show |
3 | a0001c0001t0001g0278 a0001c0001t0001g0285 a0001c0001t0001g0336 |
3 | HG01346.hp2 NA18956.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.331-1755_331-1754i others(14): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(6): Show |
1 | a0001c0001t0001g0337 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.331-1755_331-1754i others(15): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(7): Show |
1 | a0001c0001t0001g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.331-1755_331-1754i others(16): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | C | CTTTTCTT others(11): Show |
1 | a0001c0001t0001g0280 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.331-1755_331-1754i others(20): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CT | C | 18 | a0001c0001t0001g0020 a0001c0001t0001g0192 a0001c0001t0001g0193 others(15): Show |
18 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.331-1725delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTT | C | 12 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00423.hp2 HG01884.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.331-1726_331-1725d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTT | C | 8 | a0001c0001t0002g0316 a0001c0001t0002g0318 a0001c0001t0002g0329 others(5): Show |
8 | HG01109.hp1 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-1730_331-1725d others(8): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT | C | 101 | a0001c0001t0001g0335 a0001c0001t0002g0007 a0001c0001t0002g0008 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.331-1731_331-1725d others(9): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT others(1): Show |
C | 48 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(45): Show |
56 | HG00544.hp1 HG01109.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.331-1732_331-1725d others(10): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0002g0063 a0001c0001t0005g0158 a0001c0001t0006g0021 others(5): Show |
8 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-1733_331-1725d others(11): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0010g0017 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.331-1734_331-1725d others(12): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0188 a0001c0001t0009g0018 a0001c0001t0010g0016 |
3 | HG02129.hp1 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.331-1735_331-1725d others(13): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0009g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.331-1736_331-1725d others(14): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0169 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.331-1737_331-1725d others(15): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423452 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0015g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.331-1738_331-1725d others(16): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423452 | ||||||
| chr20:25423456 | T | TC | 7 | a0001c0001t0001g0014 a0001c0001t0001g0294 a0001c0001t0001g0295 others(4): Show |
8 | HG01070.hp1 HG01978.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.331-1755_331-1754i others(3): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423456 | |||||||
| chr20:25423462 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.331-1749T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423462 | |||||||
| chr20:25423464 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.331-1747T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423464 | |||||||
| chr20:25423578 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-1633C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423578 | |||||||
| chr20:25423612 | C | CT | 8 | a0001c0001t0001g0206 a0001c0001t0001g0241 a0001c0001t0001g0242 others(5): Show |
8 | HG00621.hp2 HG00673.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.331-1582dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423612 | ||||||
| chr20:25423612 | CT | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.331-1582delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr20 | 25423612 | ||||||
| chr20:25423627 | TTTC | T | 140 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(137): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.331-1583_331-1581d others(5): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423627 | |||||||
| chr20:25423628 | TTC | T | 25 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(22): Show |
25 | HG01167.hp1 HG01361.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.331-1582_331-1581d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423628 | |||||||
| chr20:25423755 | T | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(278): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.331-1456T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423755 | |||||||
| chr20:25423806 | G | A | 2 | a0001c0001t0010g0016 a0001c0001t0010g0017 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.331-1405G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423806 | |||||||
| chr20:25423905 | T | C | 177 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.331-1306T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423905 | |||||||
| chr20:25423910 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-1301G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423910 | |||||||
| chr20:25423941 | A | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.331-1270A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25423941 | |||||||
| chr20:25424006 | A | C | 1 | a0001c0001t0002g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.331-1205A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424006 | |||||||
| chr20:25424274 | C | G | 1 | a0001c0001t0001g0230 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.331-937C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424274 | |||||||
| chr20:25424442 | T | A | 335 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(332): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.331-769T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424442 | |||||||
| chr20:25424450 | T | A | 177 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.331-761T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424450 | |||||||
| chr20:25424482 | A | G | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.331-729A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424482 | |||||||
| chr20:25424550 | A | C | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.331-661A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424550 | |||||||
| chr20:25424585 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0290 |
3 | HG02257.hp1 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.331-626T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424585 | |||||||
| chr20:25424589 | C | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.331-622C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424589 | |||||||
| chr20:25424833 | C | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(278): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.331-378C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424833 | |||||||
| chr20:25424974 | G | C | 1 | a0001c0001t0011g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.331-237G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25424974 | |||||||
| chr20:25425142 | G | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.331-69G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 4/6 | chr20 | 25425142 | |||||||
| chr20:25425405 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.447+78A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25425405 | |||||||
| chr20:25425485 | G | A | 2 | a0001c0001t0003g0151 a0001c0001t0003g0152 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.447+158G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25425485 | |||||||
| chr20:25425614 | T | TA | 5 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG00423.hp2 HG00609.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+291dupA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25425614 | ||||||
| chr20:25425728 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.447+401A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25425728 | |||||||
| chr20:25425730 | G | C | 168 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(165): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.447+403G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25425730 | |||||||
| chr20:25426021 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.447+694C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426021 | |||||||
| chr20:25426126 | CTTTT | C | 16 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0002g0070 others(13): Show |
16 | HG00323.hp1 HG01081.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.447+801_447+804del others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25426126 | ||||||
| chr20:25426148 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.447+821G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426148 | |||||||
| chr20:25426363 | A | G | 5 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+1036A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426363 | |||||||
| chr20:25426473 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.447+1146A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426473 | |||||||
| chr20:25426523 | AT | A | 14 | a0001c0001t0001g0227 a0001c0001t0001g0233 a0001c0001t0001g0243 others(11): Show |
14 | HG00423.hp1 HG01993.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.447+1206delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25426523 | ||||||
| chr20:25426602 | C | T | 1 | a0002c0002t0002g0103 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.447+1275C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426602 | |||||||
| chr20:25426603 | G | A | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.447+1276G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426603 | |||||||
| chr20:25426611 | C | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+1284C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426611 | |||||||
| chr20:25426612 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.447+1285G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426612 | |||||||
| chr20:25426641 | T | C | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.447+1314T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426641 | |||||||
| chr20:25426755 | G | C | 177 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.447+1428G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426755 | |||||||
| chr20:25426794 | C | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.447+1467C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426794 | |||||||
| chr20:25426912 | C | T | 2 | a0001c0001t0012g0313 a0001c0001t0014g0312 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.447+1585C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426912 | |||||||
| chr20:25426949 | C | T | 168 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(165): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.447+1622C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25426949 | |||||||
| chr20:25427259 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.447+1932C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25427259 | |||||||
| chr20:25427388 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
9 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+2061C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25427388 | |||||||
| chr20:25427627 | A | G | 1 | a0001c0001t0006g0022 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.447+2300A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25427627 | |||||||
| chr20:25427754 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.447+2427A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25427754 | |||||||
| chr20:25427869 | A | AT | 141 | a0001c0001t0001g0010 a0001c0001t0001g0191 a0001c0001t0001g0215 others(138): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.447+2561dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25427869 | ||||||
| chr20:25427958 | G | C | 1 | a0001c0001t0001g0280 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.447+2631G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25427958 | |||||||
| chr20:25428007 | G | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+2680G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428007 | |||||||
| chr20:25428118 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.447+2791C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428118 | |||||||
| chr20:25428162 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+2835C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428162 | |||||||
| chr20:25428163 | G | A | 1 | a0002c0002t0002g0080 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.447+2836G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428163 | |||||||
| chr20:25428365 | C | G | 33 | a0001c0001t0001g0020 a0001c0001t0001g0182 a0001c0001t0001g0185 others(30): Show |
33 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.447+3038C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428365 | |||||||
| chr20:25428397 | C | CT | 96 | a0001c0001t0001g0150 a0001c0001t0001g0207 a0001c0001t0001g0213 others(93): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.447+3094dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428397 | ||||||
| chr20:25428397 | C | CTT | 26 | a0001c0001t0001g0298 a0001c0001t0002g0006 a0001c0001t0002g0042 others(23): Show |
27 | HG01099.hp2 HG01106.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.447+3093_447+3094d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428397 | ||||||
| chr20:25428397 | C | CTTT | 12 | a0001c0001t0002g0043 a0001c0001t0002g0317 a0001c0001t0002g0319 others(9): Show |
12 | HG01109.hp1 HG01255.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.447+3092_447+3094d others(5): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428397 | ||||||
| chr20:25428397 | CT | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0166 others(17): Show |
22 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.447+3094delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428397 | ||||||
| chr20:25428397 | CTT | C | 7 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.447+3093_447+3094d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428397 | ||||||
| chr20:25428397 | CTTTTTTT others(3): Show |
C | 14 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(11): Show |
21 | HG00544.hp1 HG02027.hp2 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.447+3085_447+3094d others(12): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428397 | ||||||
| chr20:25428430 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+3103G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428430 | |||||||
| chr20:25428472 | C | T | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+3145C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428472 | |||||||
| chr20:25428496 | T | C | 1 | a0001c0001t0002g0331 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.447+3169T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428496 | |||||||
| chr20:25428506 | C | G | 18 | a0001c0001t0002g0008 a0001c0001t0002g0081 a0001c0001t0002g0082 others(15): Show |
19 | HG00099.hp1 HG00642.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.447+3179C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428506 | |||||||
| chr20:25428555 | C | T | 2 | a0001c0001t0012g0313 a0001c0001t0014g0312 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.447+3228C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428555 | |||||||
| chr20:25428557 | C | T | 16 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(13): Show |
16 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.447+3230C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428557 | |||||||
| chr20:25428587 | G | A | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+3260G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428587 | |||||||
| chr20:25428605 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.447+3278C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428605 | |||||||
| chr20:25428629 | CTCCTAAC others(6): Show |
C | 1 | a0001c0001t0001g0298 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.447+3303_447+3315d others(15): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428629 | |||||||
| chr20:25428651 | A | G | 3 | a0002c0002t0002g0066 a0002c0002t0002g0107 a0002c0002t0002g0135 |
3 | HG02738.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.447+3324A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428651 | |||||||
| chr20:25428655 | C | T | 1 | a0001c0001t0002g0329 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.447+3328C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428655 | |||||||
| chr20:25428683 | T | C | 2 | a0001c0001t0010g0016 a0001c0001t0010g0017 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.447+3356T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428683 | |||||||
| chr20:25428699 | C | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.447+3372C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428699 | |||||||
| chr20:25428794 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.447+3467G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428794 | |||||||
| chr20:25428826 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.447+3499T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428826 | |||||||
| chr20:25428908 | G | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0100 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.447+3581G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428908 | |||||||
| chr20:25428969 | C | CT | 15 | a0001c0001t0001g0184 a0001c0001t0001g0188 a0001c0001t0001g0196 others(12): Show |
15 | HG00597.hp1 HG00621.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.447+3679dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0308 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.447+3657_447+3679d others(25): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0190 |
2 | NA18968.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.447+3642C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428969 | |||||||
| chr20:25428969 | CT | C | 8 | a0001c0001t0001g0195 a0001c0001t0001g0212 a0001c0001t0001g0213 others(5): Show |
8 | HG00438.hp1 HG02083.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.447+3679delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT | C | 6 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0008g0332 others(3): Show |
6 | HG01515.hp1 HG01975.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+3673_447+3679d others(9): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0004g0161 a0001c0001t0005g0159 a0001c0001t0005g0160 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.447+3672_447+3679d others(10): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(2): Show |
C | 13 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(10): Show |
13 | HG01167.hp1 HG01361.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.447+3671_447+3679d others(11): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0005g0158 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.447+3670_447+3679d others(12): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0262 |
2 | NA18980.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.447+3668_447+3679d others(14): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0247 a0001c0001t0001g0281 |
3 | HG00099.hp2 NA18967.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.447+3667_447+3679d others(15): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(7): Show |
C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(71): Show |
83 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.447+3666_447+3679d others(16): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(8): Show |
C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
28 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.447+3665_447+3679d others(17): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(11): Show |
C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+3662_447+3679d others(20): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(20): Show |
C | 140 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(137): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.447+3653_447+3679d others(29): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428969 | CTTTTTTT others(21): Show |
C | 1 | a0001c0001t0002g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.447+3652_447+3679d others(30): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25428969 | ||||||
| chr20:25428975 | T | C | 1 | a0001c0001t0008g0333 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.447+3648T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428975 | |||||||
| chr20:25428978 | T | C | 1 | a0001c0001t0008g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.447+3651T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25428978 | |||||||
| chr20:25429150 | G | A | 89 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0081 others(86): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.447+3823G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429150 | |||||||
| chr20:25429172 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.447+3845T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429172 | |||||||
| chr20:25429215 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0035 a0001c0001t0002g0061 |
4 | NA18939.hp1 NA18966.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+3888C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429215 | |||||||
| chr20:25429232 | C | T | 2 | a0002c0002t0002g0104 a0002c0002t0002g0123 |
2 | HG02257.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.447+3905C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429232 | |||||||
| chr20:25429285 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.447+3958G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429285 | |||||||
| chr20:25429345 | A | G | 1 | a0001c0001t0012g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.447+4018A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429345 | |||||||
| chr20:25429575 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0002g0318 |
2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.447+4248G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429575 | |||||||
| chr20:25429584 | AACT | A | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+4258_447+4260d others(5): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429584 | |||||||
| chr20:25429623 | G | A | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.447+4296G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429623 | |||||||
| chr20:25429630 | G | A | 1 | a0002c0002t0002g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.447+4303G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429630 | |||||||
| chr20:25429631 | T | C | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+4304T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429631 | |||||||
| chr20:25429696 | ATTAG | A | 14 | a0001c0001t0002g0008 a0001c0001t0002g0083 a0001c0001t0002g0084 others(11): Show |
15 | HG00099.hp1 HG00642.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.447+4372_447+4375d others(6): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25429696 | ||||||
| chr20:25429972 | G | C | 1 | a0001c0001t0013g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.447+4645G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429972 | |||||||
| chr20:25429973 | C | A | 1 | a0001c0001t0013g0047 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.447+4646C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25429973 | |||||||
| chr20:25430029 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.447+4702C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430029 | |||||||
| chr20:25430170 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.447+4843C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430170 | |||||||
| chr20:25430190 | C | T | 1 | a0001c0001t0015g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.447+4863C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430190 | |||||||
| chr20:25430191 | G | A | 6 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(3): Show |
6 | HG02083.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+4864G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430191 | |||||||
| chr20:25430209 | C | A | 1 | a0002c0002t0002g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.447+4882C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430209 | |||||||
| chr20:25430267 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.447+4940C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430267 | |||||||
| chr20:25430450 | A | T | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.447+5123A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430450 | |||||||
| chr20:25430470 | T | C | 1 | a0002c0002t0002g0101 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.447+5143T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430470 | |||||||
| chr20:25430691 | C | T | 1 | a0001c0001t0011g0040 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.447+5364C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25430691 | |||||||
| chr20:25431056 | A | T | 26 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0081 others(23): Show |
28 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.447+5729A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431056 | |||||||
| chr20:25431081 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.447+5754C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431081 | |||||||
| chr20:25431115 | A | G | 141 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.447+5788A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431115 | |||||||
| chr20:25431130 | A | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+5803A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431130 | |||||||
| chr20:25431180 | T | C | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.447+5853T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431180 | |||||||
| chr20:25431281 | T | C | 2 | a0001c0001t0002g0097 a0001c0001t0002g0100 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.447+5954T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431281 | |||||||
| chr20:25431406 | A | C | 1 | a0001c0001t0005g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.447+6079A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431406 | |||||||
| chr20:25431406 | A | G | 4 | a0002c0002t0002g0138 a0002c0002t0002g0139 a0002c0002t0002g0146 others(1): Show |
4 | HG01516.hp1 HG02602.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+6079A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431406 | |||||||
| chr20:25431499 | C | T | 168 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(165): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.447+6172C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431499 | |||||||
| chr20:25431575 | C | CT | 9 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0002g0110 others(6): Show |
9 | HG02145.hp1 HG02559.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+6261dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25431575 | ||||||
| chr20:25431575 | CT | C | 11 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(8): Show |
11 | HG01109.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.447+6261delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25431575 | ||||||
| chr20:25431656 | C | T | 1 | a0002c0002t0002g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.447+6329C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431656 | |||||||
| chr20:25431666 | G | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.447+6339G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431666 | |||||||
| chr20:25431904 | A | G | 39 | a0002c0002t0002g0034 a0002c0002t0002g0066 a0002c0002t0002g0085 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.447+6577A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431904 | |||||||
| chr20:25431936 | C | T | 13 | a0001c0001t0001g0233 a0001c0001t0001g0241 a0001c0001t0001g0244 others(10): Show |
13 | HG00673.hp2 HG01993.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.447+6609C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25431936 | |||||||
| chr20:25432062 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+6735G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432062 | |||||||
| chr20:25432161 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0329 |
2 | HG01109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.447+6834C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432161 | |||||||
| chr20:25432200 | G | T | 1 | a0001c0001t0009g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.447+6873G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432200 | |||||||
| chr20:25432371 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.447+7044C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432371 | |||||||
| chr20:25432385 | C | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | NA18612.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.447+7058C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432385 | |||||||
| chr20:25432389 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.447+7062G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432389 | |||||||
| chr20:25432525 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.447+7198G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432525 | |||||||
| chr20:25432664 | G | A | 4 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(1): Show |
4 | HG00639.hp1 HG00741.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+7337G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432664 | |||||||
| chr20:25432855 | T | C | 1 | a0001c0001t0008g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.447+7528T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432855 | |||||||
| chr20:25432863 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.447+7536T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25432863 | |||||||
| chr20:25433268 | T | G | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.447+7941T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25433268 | |||||||
| chr20:25433474 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.447+8147A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25433474 | |||||||
| chr20:25433477 | A | G | 1 | a0001c0001t0004g0165 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.447+8150A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25433477 | |||||||
| chr20:25433516 | CCATATCA others(652): Show |
C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0248 |
2 | NA18952.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.448-8183_448-7525d others(2): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25433516 | ||||||
| chr20:25433600 | A | AT | 6 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(3): Show |
6 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-8097dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25433600 | ||||||
| chr20:25433618 | C | T | 1 | a0002c0002t0002g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.448-8084C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25433618 | |||||||
| chr20:25433671 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-8031G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25433671 | |||||||
| chr20:25433783 | C | T | 168 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(165): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.448-7919C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25433783 | |||||||
| chr20:25433903 | T | G | 151 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(148): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.448-7799T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25433903 | |||||||
| chr20:25434128 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.448-7574A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434128 | |||||||
| chr20:25434168 | C | T | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-7534C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434168 | |||||||
| chr20:25434237 | C | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.448-7465C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434237 | |||||||
| chr20:25434287 | C | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-7415C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434287 | |||||||
| chr20:25434288 | G | C | 151 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(148): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.448-7414G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434288 | |||||||
| chr20:25434419 | G | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-7283G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434419 | |||||||
| chr20:25434443 | T | TTTTTC | 151 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(148): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.448-7254_448-7250d others(7): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25434443 | ||||||
| chr20:25434462 | G | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.448-7240G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434462 | |||||||
| chr20:25434496 | G | A | 3 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 |
3 | HG02165.hp2 NA18944.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.448-7206G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434496 | |||||||
| chr20:25434588 | G | A | 177 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(174): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.448-7114G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434588 | |||||||
| chr20:25434596 | A | G | 14 | a0001c0001t0002g0064 a0001c0001t0002g0317 a0001c0001t0002g0318 others(11): Show |
14 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.448-7106A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434596 | |||||||
| chr20:25434620 | C | T | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-7082C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434620 | |||||||
| chr20:25434702 | C | T | 4 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | NA18983.hp2 NA18994.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-7000C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434702 | |||||||
| chr20:25434882 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.448-6820G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434882 | |||||||
| chr20:25434979 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.448-6723T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25434979 | |||||||
| chr20:25435092 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.448-6610T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435092 | |||||||
| chr20:25435227 | T | G | 1 | a0001c0001t0009g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.448-6475T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435227 | |||||||
| chr20:25435378 | A | G | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-6324A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435378 | |||||||
| chr20:25435623 | T | C | 1 | a0002c0002t0002g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.448-6079T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435623 | |||||||
| chr20:25435739 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(192): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.448-5963C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435739 | |||||||
| chr20:25435764 | C | CA | 70 | a0001c0001t0001g0028 a0001c0001t0001g0170 a0001c0001t0001g0171 others(67): Show |
71 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.448-5914dupA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25435764 | ||||||
| chr20:25435781 | A | C | 7 | a0001c0001t0001g0277 a0001c0001t0006g0021 a0001c0001t0006g0022 others(4): Show |
7 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.448-5921A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435781 | |||||||
| chr20:25435782 | A | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(152): Show |
164 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.448-5920A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435782 | |||||||
| chr20:25435783 | A | C | 15 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0195 others(12): Show |
15 | HG00597.hp1 HG02027.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.448-5919A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435783 | |||||||
| chr20:25435787 | AAC | A | 8 | a0001c0001t0001g0277 a0001c0001t0006g0021 a0001c0001t0006g0022 others(5): Show |
8 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.448-5914_448-5913d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435787 | |||||||
| chr20:25435788 | AC | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(153): Show |
165 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.448-5912delC | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25435788 | ||||||
| chr20:25435789 | C | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(169): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.448-5913C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25435789 | |||||||
| chr20:25435810 | C | CT | 11 | a0001c0001t0002g0097 a0001c0001t0002g0100 a0001c0001t0002g0143 others(8): Show |
11 | HG01175.hp1 HG01258.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.448-5872dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25435810 | ||||||
| chr20:25435810 | CTTTTTTT | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(240): Show |
263 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.448-5878_448-5872d others(9): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25435810 | ||||||
| chr20:25435897 | CCA | C | 6 | a0001c0001t0001g0185 a0001c0001t0001g0265 a0001c0001t0001g0271 others(3): Show |
6 | HG00621.hp1 HG02040.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-5803_448-5802d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25435897 | ||||||
| chr20:25435979 | A | AT | 6 | a0001c0001t0002g0051 a0001c0001t0002g0064 a0001c0001t0002g0318 others(3): Show |
6 | HG01106.hp2 HG01175.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-5707dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25435979 | ||||||
| chr20:25435979 | AT | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(187): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.448-5707delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25435979 | ||||||
| chr20:25436074 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | NA18612.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.448-5628C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436074 | |||||||
| chr20:25436103 | G | A | 1 | a0001c0001t0011g0040 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.448-5599G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436103 | |||||||
| chr20:25436137 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0166 a0001c0001t0001g0167 |
4 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-5565A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436137 | |||||||
| chr20:25436153 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.448-5549A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436153 | |||||||
| chr20:25436306 | T | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(192): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.448-5396T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436306 | |||||||
| chr20:25436400 | T | A | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.448-5302T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436400 | |||||||
| chr20:25436494 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0286 |
3 | HG03490.hp1 HG03834.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.448-5208G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436494 | |||||||
| chr20:25436949 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0290 |
3 | HG02257.hp1 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.448-4753C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436949 | |||||||
| chr20:25436956 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.448-4746T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25436956 | |||||||
| chr20:25437150 | G | C | 1 | a0001c0001t0002g0006 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.448-4552G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437150 | |||||||
| chr20:25437227 | A | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.448-4475A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437227 | |||||||
| chr20:25437230 | C | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-4472C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437230 | |||||||
| chr20:25437230 | C | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(10): Show |
13 | HG00597.hp1 HG01109.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.448-4472C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437230 | |||||||
| chr20:25437294 | C | T | 1 | a0002c0002t0002g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.448-4408C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437294 | |||||||
| chr20:25437524 | C | A | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.448-4178C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437524 | |||||||
| chr20:25437549 | TG | T | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-4152delG | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437549 | |||||||
| chr20:25437553 | C | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG00544.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.448-4149C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437553 | |||||||
| chr20:25437554 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(17): Show |
23 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.448-4148G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437554 | |||||||
| chr20:25437846 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(156): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.448-3856C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437846 | |||||||
| chr20:25437870 | G | A | 2 | a0001c0001t0002g0038 a0001c0001t0002g0331 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.448-3832G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437870 | |||||||
| chr20:25437987 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.448-3715C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25437987 | |||||||
| chr20:25438045 | T | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(192): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.448-3657T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438045 | |||||||
| chr20:25438115 | G | A | 2 | a0001c0001t0011g0039 a0001c0001t0011g0040 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.448-3587G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438115 | |||||||
| chr20:25438119 | C | CA | 6 | a0001c0001t0001g0255 a0001c0001t0001g0260 a0001c0001t0001g0303 others(3): Show |
6 | HG01070.hp1 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-3565dupA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438119 | ||||||
| chr20:25438119 | C | CAA | 151 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
161 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.448-3566_448-3565d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438119 | ||||||
| chr20:25438119 | C | CAAA | 31 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(28): Show |
31 | HG01109.hp2 HG01167.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.448-3567_448-3565d others(5): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438119 | ||||||
| chr20:25438119 | CA | C | 15 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(12): Show |
22 | HG00544.hp1 HG02027.hp2 HG02896.hp1 others(19): Show |
intron_variant | MODIFIER | c.448-3565delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438119 | ||||||
| chr20:25438119 | CAA | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
9 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-3566_448-3565d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438119 | ||||||
| chr20:25438301 | C | T | 2 | a0001c0001t0001g0334 a0001c0001t0001g0337 |
2 | HG00741.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.448-3401C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438301 | |||||||
| chr20:25438313 | C | T | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.448-3389C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438313 | |||||||
| chr20:25438373 | A | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.448-3329A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438373 | |||||||
| chr20:25438512 | C | CT | 19 | a0001c0001t0002g0083 a0001c0001t0002g0088 a0001c0001t0002g0100 others(16): Show |
19 | HG00323.hp1 HG01106.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.448-3164dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438512 | ||||||
| chr20:25438512 | CT | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(187): Show |
210 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.448-3164delT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438512 | ||||||
| chr20:25438512 | CTT | C | 15 | a0001c0001t0001g0149 a0001c0001t0001g0166 a0001c0001t0001g0173 others(12): Show |
15 | HG00140.hp2 HG01069.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.448-3165_448-3164d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25438512 | ||||||
| chr20:25438583 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.448-3119C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438583 | |||||||
| chr20:25438728 | C | T | 50 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(47): Show |
58 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.448-2974C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438728 | |||||||
| chr20:25438950 | G | A | 5 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-2752G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25438950 | |||||||
| chr20:25439158 | G | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.448-2544G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439158 | |||||||
| chr20:25439329 | G | C | 1 | a0001c0001t0020g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.448-2373G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439329 | |||||||
| chr20:25439440 | A | G | 5 | a0002c0002t0002g0130 a0002c0002t0002g0131 a0002c0002t0002g0132 others(2): Show |
5 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-2262A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439440 | |||||||
| chr20:25439441 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(192): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.448-2261A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439441 | |||||||
| chr20:25439527 | G | A | 1 | a0002c0002t0002g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.448-2175G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439527 | |||||||
| chr20:25439576 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.448-2126C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439576 | |||||||
| chr20:25439601 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.448-2101T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439601 | |||||||
| chr20:25439724 | C | T | 1 | a0001c0001t0009g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.448-1978C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439724 | |||||||
| chr20:25439818 | C | T | 1 | a0002c0002t0002g0118 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.448-1884C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25439818 | |||||||
| chr20:25439994 | CA | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(171): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.448-1693delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25439994 | ||||||
| chr20:25440057 | G | A | 1 | a0002c0002t0002g0128 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.448-1645G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440057 | |||||||
| chr20:25440092 | G | C | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.448-1610G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440092 | |||||||
| chr20:25440094 | T | C | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.448-1608T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440094 | |||||||
| chr20:25440124 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.448-1578C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440124 | |||||||
| chr20:25440152 | C | T | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-1550C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440152 | |||||||
| chr20:25440528 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.448-1174C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440528 | |||||||
| chr20:25440575 | C | T | 2 | a0001c0001t0009g0018 a0001c0001t0009g0019 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.448-1127C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440575 | |||||||
| chr20:25440810 | C | CA | 26 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0182 others(23): Show |
26 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.448-870dupA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25440810 | ||||||
| chr20:25440810 | C | CAA | 6 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
6 | HG02280.hp1 HG02451.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-871_448-870dup others(2): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25440810 | ||||||
| chr20:25440810 | CA | C | 49 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(46): Show |
57 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.448-870delA | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25440810 | ||||||
| chr20:25440810 | CAAAAAAA | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0168 a0001c0001t0001g0171 others(2): Show |
7 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.448-876_448-870del others(7): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25440810 | ||||||
| chr20:25440810 | CAAAAAAA others(3): Show |
C | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.448-879_448-870del others(10): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25440810 | ||||||
| chr20:25440810 | CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG00741.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.448-881_448-870del others(12): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25440810 | ||||||
| chr20:25440827 | A | G | 1 | a0001c0001t0012g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.448-875A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440827 | |||||||
| chr20:25440829 | A | G | 6 | a0001c0001t0002g0064 a0001c0001t0008g0332 a0001c0001t0008g0333 others(3): Show |
6 | HG02559.hp2 HG02896.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-873A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440829 | |||||||
| chr20:25440835 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.448-867A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440835 | |||||||
| chr20:25440837 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.448-865G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440837 | |||||||
| chr20:25440890 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 |
3 | NA18962.hp1 NA18971.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.448-812C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25440890 | |||||||
| chr20:25441012 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(192): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.448-690C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25441012 | |||||||
| chr20:25441044 | A | G | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.448-658A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25441044 | |||||||
| chr20:25441091 | C | T | 2 | a0001c0001t0010g0016 a0001c0001t0010g0017 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.448-611C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25441091 | |||||||
| chr20:25441291 | C | T | 1 | a0002c0002t0002g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.448-411C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25441291 | |||||||
| chr20:25441333 | T | C | 1 | a0001c0001t0009g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.448-369T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25441333 | |||||||
| chr20:25441351 | T | C | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.448-351T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25441351 | |||||||
| chr20:25441430 | A | AG | 7 | a0001c0001t0004g0009 a0001c0001t0004g0157 a0001c0001t0004g0161 others(4): Show |
7 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.448-268dupG | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr20 | 25441430 | ||||||
| chr20:25441505 | C | T | 2 | a0001c0001t0011g0039 a0001c0001t0011g0040 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.448-197C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 5/6 | chr20 | 25441505 | |||||||
| chr20:25441847 | A | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(79): Show |
90 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.522+71A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25441847 | |||||||
| chr20:25441897 | A | C | 1 | a0002c0002t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.522+121A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25441897 | |||||||
| chr20:25442036 | A | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.522+260A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442036 | |||||||
| chr20:25442325 | C | CATCT | 9 | a0001c0001t0002g0314 a0001c0001t0009g0018 a0001c0001t0010g0016 others(6): Show |
9 | HG00639.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.522+562_522+565dup others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442325 | ||||||
| chr20:25442325 | CATCT | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(10): Show |
13 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.522+562_522+565del others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442325 | ||||||
| chr20:25442330 | A | ATCTG | 3 | a0001c0001t0006g0022 a0001c0001t0006g0023 a0001c0001t0006g0024 |
3 | HG01515.hp1 HG01975.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.522+557_522+558ins others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442330 | ||||||
| chr20:25442334 | A | G | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+558A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442334 | |||||||
| chr20:25442338 | A | ATCTG | 5 | a0001c0001t0015g0148 a0002c0002t0002g0073 a0002c0002t0002g0096 others(2): Show |
5 | HG00323.hp2 HG00639.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.522+594_522+597dup others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442338 | ||||||
| chr20:25442338 | A | ATCTGTCT others(17): Show |
1 | a0001c0001t0008g0333 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.522+574_522+597dup others(24): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442338 | ||||||
| chr20:25442338 | A | G | 6 | a0001c0001t0002g0036 a0001c0001t0005g0160 a0001c0001t0006g0021 others(3): Show |
6 | HG01515.hp1 HG01975.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+562A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442338 | |||||||
| chr20:25442338 | ATCTG | A | 41 | a0001c0001t0001g0011 a0001c0001t0001g0184 a0001c0001t0001g0188 others(38): Show |
43 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.522+594_522+597del others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442338 | ||||||
| chr20:25442338 | ATCTGTCT others(1): Show |
A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(132): Show |
146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.522+590_522+597del others(8): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442338 | ||||||
| chr20:25442338 | ATCTGTCT others(5): Show |
A | 1 | a0001c0001t0001g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.522+586_522+597del others(12): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442338 | ||||||
| chr20:25442342 | G | A | 1 | a0001c0001t0009g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.522+566G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442342 | |||||||
| chr20:25442370 | G | A | 40 | a0001c0001t0001g0011 a0001c0001t0001g0184 a0001c0001t0001g0188 others(37): Show |
41 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.522+594G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442370 | |||||||
| chr20:25442370 | G | GTCTA | 10 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.522+610_522+613dup others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442370 | ||||||
| chr20:25442374 | A | G | 3 | a0001c0001t0002g0046 a0001c0001t0011g0039 a0001c0001t0011g0040 |
3 | HG02976.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.522+598A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442374 | |||||||
| chr20:25442521 | A | G | 2 | a0001c0001t0008g0332 a0001c0001t0008g0333 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.522+745A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442521 | |||||||
| chr20:25442559 | A | C | 1 | a0002c0002t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.522+783A>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442559 | |||||||
| chr20:25442596 | CTAT | C | 7 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.522+834_522+836del others(3): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442596 | ||||||
| chr20:25442608 | TTA | T | 57 | a0001c0001t0001g0025 a0001c0001t0001g0181 a0001c0001t0001g0211 others(54): Show |
65 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.522+834_522+835del others(2): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442608 | ||||||
| chr20:25442610 | A | T | 9 | a0001c0001t0002g0084 a0001c0001t0002g0097 a0001c0001t0002g0100 others(6): Show |
9 | HG01123.hp1 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.522+834A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442610 | |||||||
| chr20:25442610 | ATT | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(180): Show |
195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.522+848_522+849del others(2): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25442610 | ||||||
| chr20:25442613 | T | A | 12 | a0001c0001t0011g0039 a0001c0001t0011g0040 a0002c0002t0002g0070 others(9): Show |
12 | HG00323.hp1 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.522+837T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442613 | |||||||
| chr20:25442615 | T | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(20): Show |
26 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.522+839T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442615 | |||||||
| chr20:25442666 | G | A | 2 | a0001c0001t0012g0313 a0001c0001t0014g0312 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.522+890G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442666 | |||||||
| chr20:25442902 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(182): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.522+1126G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442902 | |||||||
| chr20:25442968 | A | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+1192A>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25442968 | |||||||
| chr20:25443071 | G | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.522+1295G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25443071 | |||||||
| chr20:25443149 | G | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(80): Show |
91 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.522+1373G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25443149 | |||||||
| chr20:25443185 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0013g0047 |
2 | HG01255.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.522+1409T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25443185 | |||||||
| chr20:25443322 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.522+1546T>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25443322 | |||||||
| chr20:25443424 | C | T | 4 | a0001c0001t0009g0018 a0001c0001t0009g0019 a0001c0001t0010g0016 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+1648C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25443424 | |||||||
| chr20:25443476 | C | CT | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(177): Show |
191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.522+1719dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443476 | ||||||
| chr20:25443476 | C | CTT | 6 | a0001c0001t0001g0205 a0001c0001t0001g0232 a0001c0001t0001g0233 others(3): Show |
6 | HG02965.hp2 HG03831.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+1718_522+1719d others(4): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443476 | ||||||
| chr20:25443623 | C | T | 1 | a0002c0002t0002g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.522+1847C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25443623 | |||||||
| chr20:25443980 | T | TATCTATC others(4): Show |
1 | a0001c0001t0002g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.523-1943_523-1942i others(13): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25443980 | |||||||
| chr20:25443980 | T | TTATC | 13 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 others(10): Show |
13 | HG00423.hp1 HG01516.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.523-1907_523-1904d others(6): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443980 | ||||||
| chr20:25443980 | T | TTATCTAT others(1): Show |
90 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.523-1911_523-1904d others(10): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443980 | ||||||
| chr20:25443980 | T | TTATCTAT others(5): Show |
120 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0013 others(117): Show |
126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.523-1915_523-1904d others(14): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443980 | ||||||
| chr20:25443980 | T | TTATCTAT others(9): Show |
50 | a0001c0001t0001g0025 a0001c0001t0001g0178 a0001c0001t0001g0181 others(47): Show |
51 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.523-1919_523-1904d others(18): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443980 | ||||||
| chr20:25443980 | T | TTATCTAT others(13): Show |
17 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0202 others(14): Show |
17 | HG00609.hp1 HG01109.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.523-1923_523-1904d others(22): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443980 | ||||||
| chr20:25443980 | T | TTATCTAT others(17): Show |
5 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0289 others(2): Show |
5 | HG01496.hp1 HG01943.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-1927_523-1904d others(26): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443980 | ||||||
| chr20:25443980 | TTATC | T | 33 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(30): Show |
41 | HG00544.hp1 HG01255.hp1 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.523-1907_523-1904d others(6): Show |
GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25443980 | ||||||
| chr20:25444031 | A | G | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG00741.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.523-1892A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444031 | |||||||
| chr20:25444032 | G | A | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG00741.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.523-1891G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444032 | |||||||
| chr20:25444072 | C | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(156): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.523-1851C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444072 | |||||||
| chr20:25444077 | T | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(182): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.523-1846T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444077 | |||||||
| chr20:25444078 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.523-1845C>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444078 | |||||||
| chr20:25444203 | C | T | 2 | a0001c0001t0003g0153 a0001c0001t0003g0154 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.523-1720C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444203 | |||||||
| chr20:25444442 | A | G | 7 | a0001c0001t0004g0009 a0001c0001t0004g0157 a0001c0001t0004g0161 others(4): Show |
7 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.523-1481A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444442 | |||||||
| chr20:25444546 | T | G | 2 | a0001c0001t0002g0315 a0001c0001t0002g0316 |
2 | HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.523-1377T>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444546 | |||||||
| chr20:25444580 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.523-1343C>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444580 | |||||||
| chr20:25444916 | G | C | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-1007G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25444916 | |||||||
| chr20:25445092 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.523-831T>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445092 | |||||||
| chr20:25445172 | A | G | 56 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0182 others(53): Show |
57 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.523-751A>G | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445172 | |||||||
| chr20:25445246 | G | T | 1 | a0001c0001t0001g0220 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.523-677G>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445246 | |||||||
| chr20:25445307 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(192): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.523-616G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445307 | |||||||
| chr20:25445332 | C | T | 17 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 others(14): Show |
17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.523-591C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445332 | |||||||
| chr20:25445339 | G | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG01516.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.523-584G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445339 | |||||||
| chr20:25445348 | A | AT | 17 | a0001c0001t0001g0205 a0001c0001t0001g0242 a0001c0001t0001g0265 others(14): Show |
17 | HG00673.hp1 HG01192.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.523-559dupT | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr20 | 25445348 | ||||||
| chr20:25445442 | G | A | 5 | a0002c0002t0002g0069 a0002c0002t0002g0073 a0002c0002t0002g0075 others(2): Show |
5 | HG01256.hp2 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-481G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445442 | |||||||
| chr20:25445522 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0013g0047 |
2 | HG01255.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.523-401C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445522 | |||||||
| chr20:25445537 | C | T | 5 | a0002c0002t0002g0065 a0002c0002t0002g0080 a0002c0002t0002g0090 others(2): Show |
5 | HG00639.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-386C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445537 | |||||||
| chr20:25445538 | G | A | 5 | a0001c0001t0001g0336 a0001c0001t0009g0018 a0001c0001t0009g0019 others(2): Show |
5 | HG01346.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.523-385G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445538 | |||||||
| chr20:25445549 | G | A | 13 | a0001c0001t0002g0317 a0001c0001t0002g0318 a0001c0001t0002g0319 others(10): Show |
13 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.523-374G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445549 | |||||||
| chr20:25445598 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(156): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.523-325C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445598 | |||||||
| chr20:25445627 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.523-296G>A | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445627 | |||||||
| chr20:25445671 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.523-252C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445671 | |||||||
| chr20:25445771 | C | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0023 others(1): Show |
4 | HG01515.hp1 HG01975.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-152C>T | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445771 | |||||||
| chr20:25445816 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.523-107G>C | GINS1 | ENSG00000101003.12 | transcript | ENST00000262460.5 | protein_coding | 6/6 | chr20 | 25445816 |