Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51512 |
| ensemblid | ENSG00000075218.19 |
| hgncid | 13698 |
| symbol | GTSE1 |
| name | G2 and S-phase expressed 1 |
| refseq_nuc | NM_016426.7 |
| refseq_prot | NP_057510.5 |
| ensembl_nuc | ENST00000454366.2 |
| ensembl_prot | ENSP00000415430.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 46296870 |
| end | 46330810 |
| strand | + |
| ver | v1.2 |
| region | chr22:46296870-46330810 |
| region5000 | chr22:46291870-46335810 |
| regionname0 | GTSE1_chr22_46296870_46330810 |
| regionname5000 | GTSE1_chr22_46291870_46335810 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 739 | 120 | 30 | 31 | 40 | 1 | 17 | 26 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0002 | 0/0 | 739 | 28 | 21 | 3 | 0 | 2 | 2 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0003 | 0/0 | 739 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0004 | 0/0 | 739 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0005 | 1/0 | 739 | 5 | 1 | 2 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0006 | 0/0 | 739 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0007 | 0/0 | 739 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0008 | 0/0 | 739 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0009 | 0/0 | 739 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0010 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0011 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0012 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0013 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0014 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0015 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0016 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0017 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| a0018 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | MEGGG others(734): Show |
chr22 | 46291870 | 46335810 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2217 | 107 | 22 | 29 | 37 | 1 | 17 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0001c0009 | 0/0 | 2217 | 5 | 5 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0001c0011 | 0/0 | 2217 | 3 | 1 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0001c0012 | 0/0 | 2217 | 2 | 0 | 0 | 2 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0001c0017 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0001c0020 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0001c0025 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0002c0002 | 0/0 | 2217 | 16 | 16 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0002c0004 | 0/0 | 2217 | 8 | 1 | 3 | 0 | 2 | 2 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0002c0014 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0002c0026 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0002c0028 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0003c0003 | 0/0 | 2217 | 13 | 12 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0004c0005 | 0/0 | 2217 | 7 | 6 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0005c0008 | 1/0 | 2217 | 5 | 1 | 2 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0006c0006 | 0/0 | 2217 | 6 | 4 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0007c0007 | 0/0 | 2217 | 6 | 6 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0008c0010 | 0/0 | 2217 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0009c0013 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0010c0027 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0011c0016 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0012c0015 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0013c0023 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0014c0021 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0015c0018 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0016c0019 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0017c0022 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 | ||
| a0018c0024 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | ATGGA others(2212): Show |
chr22 | 46291870 | 46335810 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2983 | 105 | 22 | 28 | 36 | 1 | 17 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0001t0002 | 0/0 | 2983 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0001t0003 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0009t0001 | 0/0 | 2983 | 5 | 5 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0011t0001 | 0/0 | 2983 | 3 | 1 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0012t0001 | 0/0 | 2983 | 2 | 0 | 0 | 2 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0017t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0020t0001 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0001c0025t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0002c0002t0001 | 0/0 | 2983 | 16 | 16 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0002c0004t0001 | 0/0 | 2983 | 8 | 1 | 3 | 0 | 2 | 2 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0002c0014t0001 | 0/0 | 2983 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0002c0026t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0002c0028t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0003c0003t0001 | 0/0 | 2983 | 13 | 12 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0004c0005t0001 | 0/0 | 2983 | 7 | 6 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0005c0008t0001 | 1/0 | 2983 | 5 | 1 | 2 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0006c0006t0001 | 0/0 | 2983 | 6 | 4 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0007c0007t0001 | 0/0 | 2983 | 6 | 6 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0008c0010t0001 | 0/0 | 2983 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0009c0013t0001 | 0/0 | 2983 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0010c0027t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0011c0016t0001 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0012c0015t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0013c0023t0001 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0014c0021t0001 | 0/0 | 2983 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0015c0018t0001 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0016c0019t0001 | 0/0 | 2983 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0017c0022t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| a0018c0024t0001 | 0/0 | 2983 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | GTCTC others(2978): Show |
chr22 | 46291870 | 46335810 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 3 | 7 | 5 | 0 | 5 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0009t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0009t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0009t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0009t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0011t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0011t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0012t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0012t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0017t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0020t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0001c0025t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0014t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0014t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0026t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0002c0028t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0003c0003t0001g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0003c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0003c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0004c0005t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0004c0005t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0004c0005t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0004c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0004c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0005c0008t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0005c0008t0001g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0005c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0005c0008t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0006c0006t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0006c0006t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0006c0006t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0006c0006t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0006c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0007c0007t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0007c0007t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0007c0007t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0007c0007t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0007c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0008c0010t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0008c0010t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0009c0013t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0009c0013t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0010c0027t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0011c0016t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0012c0015t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0013c0023t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0014c0021t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0015c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0016c0019t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0017c0022t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| a0018c0024t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00639 | hp2 | a0001 | c0011 | t0001 | g0005 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00738 | hp2 | a0005 | c0008 | t0001 | g0122 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00741 | hp1 | a0005 | c0008 | t0001 | g0019 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01070 | hp1 | a0002 | c0004 | t0001 | g0042 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01106 | hp2 | a0002 | c0004 | t0001 | g0043 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01167 | hp1 | a0006 | c0006 | t0001 | g0142 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01169 | hp1 | a0006 | c0006 | t0001 | g0141 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01243 | hp1 | a0003 | c0003 | t0001 | g0114 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01358 | hp1 | a0002 | c0004 | t0001 | g0044 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01433 | hp1 | a0004 | c0005 | t0001 | g0118 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01433 | hp2 | a0001 | c0011 | t0001 | g0005 | AMR | CLM | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02145 | hp2 | a0006 | c0006 | t0001 | g0021 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CDX | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02257 | hp1 | a0001 | c0009 | t0001 | g0056 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02257 | hp2 | a0005 | c0008 | t0001 | g0019 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02258 | hp1 | a0010 | c0027 | t0001 | g0029 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02258 | hp2 | a0001 | c0011 | t0001 | g0030 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02572 | hp1 | a0001 | c0009 | t0001 | g0055 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02622 | hp2 | a0002 | c0028 | t0001 | g0037 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0115 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02647 | hp2 | a0008 | c0010 | t0001 | g0008 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02683 | hp1 | a0002 | c0004 | t0001 | g0041 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02723 | hp1 | a0004 | c0005 | t0001 | g0013 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02723 | hp2 | a0001 | c0009 | t0001 | g0054 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02738 | hp1 | a0011 | c0016 | t0001 | g0023 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02809 | hp1 | a0002 | c0014 | t0001 | g0126 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02809 | hp2 | a0007 | c0007 | t0001 | g0026 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02818 | hp1 | a0007 | c0007 | t0001 | g0028 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0139 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02895 | hp1 | a0007 | c0007 | t0001 | g0010 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02896 | hp1 | a0001 | c0017 | t0001 | g0099 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02922 | hp2 | a0009 | c0013 | t0001 | g0111 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02965 | hp1 | a0006 | c0006 | t0001 | g0021 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02965 | hp2 | a0012 | c0015 | t0001 | g0117 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03098 | hp1 | a0004 | c0005 | t0001 | g0013 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03098 | hp2 | a0008 | c0010 | t0001 | g0008 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03130 | hp1 | a0008 | c0010 | t0001 | g0038 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03130 | hp2 | a0007 | c0007 | t0001 | g0010 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03139 | hp1 | a0004 | c0005 | t0001 | g0020 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03139 | hp2 | a0009 | c0013 | t0001 | g0110 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03209 | hp1 | a0006 | c0006 | t0001 | g0143 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0002 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03453 | hp2 | a0008 | c0010 | t0001 | g0008 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03486 | hp1 | a0004 | c0005 | t0001 | g0119 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0138 | AFR | ESN | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03540 | hp1 | a0004 | c0005 | t0001 | g0137 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03540 | hp2 | a0002 | c0014 | t0001 | g0113 | AFR | GWD | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0140 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG04184 | hp2 | a0013 | c0023 | t0001 | g0070 | SAS | BEB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG04204 | hp2 | a0014 | c0021 | t0001 | g0005 | SAS | STU | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18522 | hp1 | a0001 | c0025 | t0001 | g0104 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18906 | hp1 | a0006 | c0006 | t0001 | g0144 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | YRI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18952 | hp2 | a0001 | c0020 | t0001 | g0131 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18968 | hp2 | a0001 | c0012 | t0001 | g0128 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA18998 | hp2 | a0015 | c0018 | t0001 | g0001 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19002 | hp1 | a0001 | c0012 | t0001 | g0129 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19012 | hp2 | a0016 | c0019 | t0001 | g0065 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19030 | hp1 | a0002 | c0026 | t0001 | g0034 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19030 | hp2 | a0017 | c0022 | t0001 | g0002 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19043 | hp1 | a0007 | c0007 | t0001 | g0024 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20752 | hp2 | a0002 | c0004 | t0001 | g0046 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20805 | hp1 | a0002 | c0004 | t0001 | g0048 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20805 | hp2 | a0005 | c0008 | t0001 | g0120 | EUR | TSI | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20905 | hp2 | a0002 | c0004 | t0001 | g0047 | SAS | GIH | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02486 | hp2 | a0007 | c0007 | t0001 | g0027 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02559 | hp1 | a0004 | c0005 | t0001 | g0020 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG02559 | hp2 | a0001 | c0009 | t0001 | g0012 | AFR | ACB | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0036 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| HG06807 | hp2 | a0002 | c0004 | t0001 | g0045 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA20300 | hp2 | a0001 | c0009 | t0001 | g0012 | AFR | USA | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| NA21309 | hp2 | a0018 | c0024 | t0001 | g0062 | AFR | LWK | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0059 | REF | REF | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| homoSapiens | grch38p0 | a0005 | c0008 | t0001 | g0071 | REF | REF | GTSE1_chr22_46291870_46335810 | GTSE1 | chr22 | 46291870 | 46335810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46308680 | T | G | 1 | a0011 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.499T>G | p.Tyr167Asp | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 582/2983 | 499/2220 | 167/739 | chr22 | 46308680 | |||
| chr22:46308713 | G | T | 1 | a0007 | 6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
missense_variant | MODERATE | c.532G>T | p.Val178Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 615/2983 | 532/2220 | 178/739 | chr22 | 46308713 | |||
| chr22:46308779 | A | G | 6 | a0002 a0006 a0007 others(3): Show |
46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
missense_variant | MODERATE | c.598A>G | p.Thr200Ala | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 681/2983 | 598/2220 | 200/739 | chr22 | 46308779 | |||
| chr22:46308837 | C | T | 2 | a0004 a0012 |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.656C>T | p.Ala219Val | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 739/2983 | 656/2220 | 219/739 | chr22 | 46308837 | |||
| chr22:46312255 | G | A | 2 | a0004 a0012 |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.877G>A | p.Ala293Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/12 | 960/2983 | 877/2220 | 293/739 | chr22 | 46312255 | |||
| chr22:46313984 | G | A | 4 | a0002 a0006 a0008 others(1): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
missense_variant | MODERATE | c.1022G>A | p.Ser341Asn | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/12 | 1105/2983 | 1022/2220 | 341/739 | chr22 | 46313984 | |||
| chr22:46316251 | C | T | 1 | a0013 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1271C>T | p.Pro424Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1354/2983 | 1271/2220 | 424/739 | chr22 | 46316251 | |||
| chr22:46316331 | C | T | 1 | a0010 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1351C>T | p.Arg451Trp | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1434/2983 | 1351/2220 | 451/739 | chr22 | 46316331 | |||
| chr22:46316332 | G | A | 1 | a0015 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.1352G>A | p.Arg451Gln | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1435/2983 | 1352/2220 | 451/739 | chr22 | 46316332 | |||
| chr22:46323203 | C | G | 5 | a0002 a0009 a0010 others(2): Show |
33 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(30): Show |
missense_variant | MODERATE | c.1446C>G | p.Asp482Glu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/12 | 1529/2983 | 1446/2220 | 482/739 | chr22 | 46323203 | |||
| chr22:46323244 | C | T | 1 | a0014 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1487C>T | p.Ser496Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/12 | 1570/2983 | 1487/2220 | 496/739 | chr22 | 46323244 | |||
| chr22:46326500 | G | A | 2 | a0006 a0007 |
12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
missense_variant | MODERATE | c.1570G>A | p.Ala524Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1653/2983 | 1570/2220 | 524/739 | chr22 | 46326500 | |||
| chr22:46326503 | T | C | 17 | a0001 a0002 a0003 others(14): Show |
194 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(191): Show |
missense_variant | MODERATE | c.1573T>C | p.Trp525Arg | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1656/2983 | 1573/2220 | 525/739 | chr22 | 46326503 | |||
| chr22:46326504 | G | A | 1 | a0001 | 2 | NA18968.hp2 NA19002.hp1 |
stop_gained | HIGH | c.1574G>A | p.Trp525* | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1657/2983 | 1574/2220 | 525/739 | chr22 | 46326504 | |||
| chr22:46328753 | G | C | 1 | a0016 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1790G>C | p.Arg597Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/12 | 1873/2983 | 1790/2220 | 597/739 | chr22 | 46328753 | |||
| chr22:46329391 | G | A | 3 | a0003 a0017 a0018 |
15 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(12): Show |
missense_variant | MODERATE | c.1960G>A | p.Ala654Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/12 | 2043/2983 | 1960/2220 | 654/739 | chr22 | 46329391 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46308166 | C | T | 1 | a0002c0028 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.96C>T | p.Ala32Ala | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 3/12 | 179/2983 | 96/2220 | 32/739 | chr22 | 46308166 | |||
| chr22:46308346 | C | T | 9 | a0002c0002 a0002c0004 a0002c0014 others(6): Show |
45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
synonymous_variant | LOW | c.165C>T | p.Phe55Phe | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 248/2983 | 165/2220 | 55/739 | chr22 | 46308346 | |||
| chr22:46308493 | A | G | 1 | a0001c0025 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.312A>G | p.Glu104Glu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 395/2983 | 312/2220 | 104/739 | chr22 | 46308493 | |||
| chr22:46308658 | G | A | 2 | a0004c0005 a0012c0015 |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.477G>A | p.Thr159Thr | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 560/2983 | 477/2220 | 159/739 | chr22 | 46308658 | |||
| chr22:46308683 | C | T | 1 | a0001c0009 | 5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
synonymous_variant | LOW | c.502C>T | p.Leu168Leu | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 585/2983 | 502/2220 | 168/739 | chr22 | 46308683 | |||
| chr22:46308790 | G | A | 1 | a0002c0026 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.609G>A | p.Pro203Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 692/2983 | 609/2220 | 203/739 | chr22 | 46308790 | |||
| chr22:46308793 | G | A | 1 | a0001c0017 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.612G>A | p.Gly204Gly | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 695/2983 | 612/2220 | 204/739 | chr22 | 46308793 | |||
| chr22:46308874 | C | T | 1 | a0011c0016 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.693C>T | p.Pro231Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/12 | 776/2983 | 693/2220 | 231/739 | chr22 | 46308874 | |||
| chr22:46316180 | C | T | 1 | a0002c0004 | 8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
synonymous_variant | LOW | c.1200C>T | p.Val400Val | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/12 | 1283/2983 | 1200/2220 | 400/739 | chr22 | 46316180 | |||
| chr22:46326529 | C | T | 4 | a0001c0009 a0003c0003 a0017c0022 others(1): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
synonymous_variant | LOW | c.1599C>T | p.Pro533Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1682/2983 | 1599/2220 | 533/739 | chr22 | 46326529 | |||
| chr22:46326634 | C | T | 3 | a0002c0004 a0002c0014 a0009c0013 |
12 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(9): Show |
synonymous_variant | LOW | c.1704C>T | p.Pro568Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/12 | 1787/2983 | 1704/2220 | 568/739 | chr22 | 46326634 | |||
| chr22:46328865 | G | C | 1 | a0001c0020 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.1902G>C | p.Pro634Pro | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/12 | 1985/2983 | 1902/2220 | 634/739 | chr22 | 46328865 | |||
| chr22:46329453 | T | C | 2 | a0001c0011 a0014c0021 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
synonymous_variant | LOW | c.2022T>C | p.Asp674Asp | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/12 | 2105/2983 | 2022/2220 | 674/739 | chr22 | 46329453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46330255 | C | T | 1 | a0001c0001t0003 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 12/12 | 125 | chr22 | 46330255 | ||||||
| chr22:46330324 | A | G | 1 | a0001c0001t0002 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*194A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 12/12 | 194 | chr22 | 46330324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46296988 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-22+57G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46296988 | |||||||
| chr22:46297008 | G | A | 24 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0004 others(21): Show |
31 | HG00639.hp2 HG01433.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.-22+77G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297008 | |||||||
| chr22:46297105 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-22+174C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297105 | |||||||
| chr22:46297137 | C | G | 1 | a0001c0001t0002g0145 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-22+206C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297137 | |||||||
| chr22:46297163 | A | T | 24 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0004 others(21): Show |
33 | HG00639.hp2 HG01433.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.-21-217A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297163 | |||||||
| chr22:46297181 | CG | C | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-196delG | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | 46297181 | ||||||
| chr22:46297195 | G | A | 1 | a0002c0004t0001g0041 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-21-185G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297195 | |||||||
| chr22:46297260 | C | T | 12 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0032 others(9): Show |
16 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-21-120C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 1/11 | chr22 | 46297260 | |||||||
| chr22:46297581 | T | G | 7 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0007c0007t0001g0010 others(4): Show |
9 | HG02486.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+102T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297581 | |||||||
| chr22:46297611 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG00408.hp2 HG00423.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.79+132T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297611 | |||||||
| chr22:46297669 | C | G | 6 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(3): Show |
9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+190C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297669 | |||||||
| chr22:46297764 | G | A | 1 | a0007c0007t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+285G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297764 | |||||||
| chr22:46297854 | A | C | 4 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0031 others(1): Show |
5 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+375A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297854 | |||||||
| chr22:46297936 | C | T | 1 | a0010c0027t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79+457C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46297936 | |||||||
| chr22:46297956 | T | TTTTATTT others(1): Show |
3 | a0003c0003t0001g0138 a0003c0003t0001g0139 a0003c0003t0001g0140 |
3 | HG02818.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.79+496_79+503dupTA others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46297956 | ||||||
| chr22:46298128 | C | A | 7 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0007c0007t0001g0010 others(4): Show |
9 | HG02486.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+649C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298128 | |||||||
| chr22:46298153 | G | A | 4 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0031 others(1): Show |
5 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+674G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298153 | |||||||
| chr22:46298226 | G | T | 8 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0007c0007t0001g0010 others(5): Show |
10 | HG02258.hp1 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+747G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298226 | |||||||
| chr22:46298411 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.79+932G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298411 | |||||||
| chr22:46298470 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.79+991G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298470 | |||||||
| chr22:46298519 | G | T | 1 | a0004c0005t0001g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.79+1040G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298519 | |||||||
| chr22:46298520 | C | A | 1 | a0004c0005t0001g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.79+1041C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298520 | |||||||
| chr22:46298600 | G | A | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1121G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298600 | |||||||
| chr22:46298892 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.79+1413C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298892 | |||||||
| chr22:46298970 | T | G | 1 | a0001c0001t0001g0057 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.79+1491T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46298970 | |||||||
| chr22:46299129 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.79+1650A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299129 | |||||||
| chr22:46299193 | T | C | 1 | a0010c0027t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79+1714T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299193 | |||||||
| chr22:46299271 | G | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(4): Show |
7 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+1792G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299271 | |||||||
| chr22:46299272 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.79+1793C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299272 | |||||||
| chr22:46299287 | C | T | 2 | a0001c0012t0001g0128 a0001c0012t0001g0129 |
2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.79+1808C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299287 | |||||||
| chr22:46299288 | G | A | 2 | a0003c0003t0001g0138 a0003c0003t0001g0139 |
2 | HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.79+1809G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299288 | |||||||
| chr22:46299353 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.79+1874C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299353 | |||||||
| chr22:46299357 | C | T | 1 | a0002c0014t0001g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+1878C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299357 | |||||||
| chr22:46299392 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.79+1913C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299392 | |||||||
| chr22:46299469 | T | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.79+1990T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299469 | |||||||
| chr22:46299556 | G | A | 3 | a0001c0011t0001g0030 a0002c0002t0001g0009 a0002c0002t0001g0025 |
4 | HG02258.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+2077G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299556 | |||||||
| chr22:46299652 | G | A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0032 others(8): Show |
15 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+2173G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299652 | |||||||
| chr22:46299706 | C | T | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+2227C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299706 | |||||||
| chr22:46299740 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.79+2261C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299740 | |||||||
| chr22:46299786 | T | A | 1 | a0010c0027t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79+2307T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299786 | |||||||
| chr22:46299792 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.79+2313T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299792 | |||||||
| chr22:46299862 | G | C | 2 | a0004c0005t0001g0013 a0004c0005t0001g0137 |
3 | HG02723.hp1 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.79+2383G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299862 | |||||||
| chr22:46299878 | C | T | 1 | a0004c0005t0001g0013 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.79+2399C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299878 | |||||||
| chr22:46299941 | C | T | 6 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(3): Show |
9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+2462C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299941 | |||||||
| chr22:46299942 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.79+2463G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46299942 | |||||||
| chr22:46299959 | A | AT | 31 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0123 others(28): Show |
36 | HG00609.hp2 HG00735.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.79+2505dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46299959 | ||||||
| chr22:46299959 | AT | A | 15 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0064 others(12): Show |
17 | HG01257.hp2 HG02155.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.79+2505delT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46299959 | ||||||
| chr22:46300021 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.79+2542T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300021 | |||||||
| chr22:46300427 | T | G | 1 | a0002c0014t0001g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.79+2948T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300427 | |||||||
| chr22:46300488 | C | G | 1 | a0006c0006t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79+3009C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300488 | |||||||
| chr22:46300548 | C | T | 1 | a0008c0010t0001g0008 | 3 | HG02647.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.79+3069C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300548 | |||||||
| chr22:46300565 | T | A | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79+3086T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300565 | |||||||
| chr22:46300635 | T | C | 1 | a0013c0023t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.79+3156T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300635 | |||||||
| chr22:46300733 | G | A | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+3254G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46300733 | |||||||
| chr22:46301005 | A | T | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+3526A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301005 | |||||||
| chr22:46301073 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.79+3594C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301073 | |||||||
| chr22:46301466 | A | C | 1 | a0004c0005t0001g0020 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.79+3987A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301466 | |||||||
| chr22:46301484 | A | AT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(138): Show |
191 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.79+4006dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46301484 | ||||||
| chr22:46301486 | A | T | 6 | a0001c0001t0001g0072 a0001c0011t0001g0030 a0002c0002t0001g0009 others(3): Show |
7 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4007A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301486 | |||||||
| chr22:46301487 | C | A | 6 | a0001c0001t0001g0072 a0001c0011t0001g0030 a0002c0002t0001g0009 others(3): Show |
7 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4008C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301487 | |||||||
| chr22:46301487 | CTT | C | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+4024_79+4025del others(2): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46301487 | ||||||
| chr22:46301488 | T | C | 6 | a0001c0001t0001g0072 a0001c0011t0001g0030 a0002c0002t0001g0009 others(3): Show |
7 | HG02258.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+4009T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301488 | |||||||
| chr22:46301557 | G | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0063 a0001c0001t0001g0073 others(3): Show |
7 | HG00741.hp2 HG01257.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4078G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301557 | |||||||
| chr22:46301576 | C | G | 5 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(2): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+4097C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301576 | |||||||
| chr22:46301644 | G | C | 10 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(7): Show |
12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+4165G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301644 | |||||||
| chr22:46301847 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.79+4368G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301847 | |||||||
| chr22:46301919 | G | A | 1 | a0007c0007t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79+4440G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301919 | |||||||
| chr22:46301927 | C | G | 14 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(11): Show |
19 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+4448C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46301927 | |||||||
| chr22:46302001 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79+4522A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302001 | |||||||
| chr22:46302006 | T | C | 9 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0004c0005t0001g0013 others(6): Show |
12 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+4527T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302006 | |||||||
| chr22:46302026 | A | G | 26 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(23): Show |
35 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.79+4547A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302026 | |||||||
| chr22:46302064 | G | T | 1 | a0003c0003t0001g0140 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79+4585G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302064 | |||||||
| chr22:46302121 | G | A | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4642G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302121 | |||||||
| chr22:46302341 | A | AC | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4862_79+4863ins others(1): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302341 | |||||||
| chr22:46302399 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+4920T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302399 | |||||||
| chr22:46302428 | G | A | 9 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0004c0005t0001g0013 others(6): Show |
12 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+4949G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302428 | |||||||
| chr22:46302493 | G | GCCT | 25 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0031 others(22): Show |
29 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+5017_79+5019dup others(3): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46302493 | ||||||
| chr22:46302522 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+5043T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302522 | |||||||
| chr22:46302562 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.79+5083A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302562 | |||||||
| chr22:46302664 | C | T | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+5185C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302664 | |||||||
| chr22:46302765 | T | G | 2 | a0002c0004t0001g0041 a0002c0004t0001g0042 |
2 | HG01070.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.79+5286T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302765 | |||||||
| chr22:46302783 | C | T | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.79+5304C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302783 | |||||||
| chr22:46302837 | T | C | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-5313T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302837 | |||||||
| chr22:46302895 | C | CT | 29 | a0001c0001t0001g0068 a0001c0001t0001g0134 a0001c0011t0001g0005 others(26): Show |
36 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.80-5237dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46302895 | ||||||
| chr22:46302911 | T | TC | 3 | a0007c0007t0001g0024 a0007c0007t0001g0026 a0007c0007t0001g0027 |
3 | HG02486.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.80-5239_80-5238ins others(1): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302911 | |||||||
| chr22:46302961 | G | A | 1 | a0016c0019t0001g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.80-5189G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302961 | |||||||
| chr22:46302962 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-5188T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46302962 | |||||||
| chr22:46303000 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-5150T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303000 | |||||||
| chr22:46303048 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-5102T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303048 | |||||||
| chr22:46303066 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.80-5084A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303066 | |||||||
| chr22:46303067 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.80-5083T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303067 | |||||||
| chr22:46303192 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.80-4958G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303192 | |||||||
| chr22:46303195 | C | T | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-4955C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303195 | |||||||
| chr22:46303240 | C | A | 2 | a0001c0011t0001g0005 a0014c0021t0001g0005 |
3 | HG00639.hp2 HG01433.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.80-4910C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303240 | |||||||
| chr22:46303291 | G | A | 1 | a0002c0004t0001g0042 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.80-4859G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303291 | |||||||
| chr22:46303322 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-4828C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303322 | |||||||
| chr22:46303364 | G | A | 1 | a0005c0008t0001g0120 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.80-4786G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303364 | |||||||
| chr22:46303422 | C | G | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-4728C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303422 | |||||||
| chr22:46303596 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-4554C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303596 | |||||||
| chr22:46303684 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | NA19063.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.80-4466T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303684 | |||||||
| chr22:46303886 | G | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-4264G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303886 | |||||||
| chr22:46303939 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.80-4211G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303939 | |||||||
| chr22:46303960 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.80-4190C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46303960 | |||||||
| chr22:46304038 | T | C | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-4112T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304038 | |||||||
| chr22:46304090 | C | T | 8 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(5): Show |
12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-4060C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304090 | |||||||
| chr22:46304180 | C | A | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-3970C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304180 | |||||||
| chr22:46304251 | T | A | 13 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0006c0006t0001g0021 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.80-3899T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304251 | |||||||
| chr22:46304312 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.80-3838G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304312 | |||||||
| chr22:46304504 | C | T | 1 | a0002c0002t0001g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-3646C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304504 | |||||||
| chr22:46304845 | T | G | 53 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(50): Show |
67 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.80-3305T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304845 | |||||||
| chr22:46304849 | C | T | 5 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(2): Show |
7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-3301C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46304849 | |||||||
| chr22:46305012 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.80-3138G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305012 | |||||||
| chr22:46305040 | A | G | 1 | a0002c0014t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.80-3110A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305040 | |||||||
| chr22:46305405 | C | G | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-2745C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305405 | |||||||
| chr22:46305505 | A | G | 2 | a0002c0002t0001g0009 a0002c0002t0001g0025 |
3 | HG02717.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.80-2645A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305505 | |||||||
| chr22:46305644 | C | T | 5 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-2506C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305644 | |||||||
| chr22:46305694 | G | A | 5 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(2): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2456G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305694 | |||||||
| chr22:46305780 | G | A | 9 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0004c0005t0001g0013 others(6): Show |
12 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.80-2370G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305780 | |||||||
| chr22:46305899 | T | G | 1 | a0002c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-2251T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46305899 | |||||||
| chr22:46306040 | C | T | 3 | a0001c0001t0001g0017 a0009c0013t0001g0110 a0009c0013t0001g0111 |
4 | HG02109.hp2 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-2110C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306040 | |||||||
| chr22:46306040 | CT | C | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-2106delT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46306040 | ||||||
| chr22:46306094 | A | G | 36 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(33): Show |
45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-2056A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306094 | |||||||
| chr22:46306323 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-1827A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306323 | |||||||
| chr22:46306442 | A | T | 14 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0031 others(11): Show |
20 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-1708A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306442 | |||||||
| chr22:46306460 | C | T | 1 | a0007c0007t0001g0010 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.80-1690C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306460 | |||||||
| chr22:46306552 | T | C | 37 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(34): Show |
46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.80-1598T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306552 | |||||||
| chr22:46306629 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.80-1521C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306629 | |||||||
| chr22:46306637 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG02132.hp1 HG02145.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.80-1513C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306637 | |||||||
| chr22:46306641 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.80-1509C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306641 | |||||||
| chr22:46306657 | T | G | 3 | a0001c0001t0001g0060 a0001c0011t0001g0005 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1493T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306657 | |||||||
| chr22:46306689 | C | T | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.80-1461C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46306689 | |||||||
| chr22:46307193 | C | T | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.80-957C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307193 | |||||||
| chr22:46307314 | A | C | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.80-836A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307314 | |||||||
| chr22:46307480 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.80-670C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307480 | |||||||
| chr22:46307511 | C | CT | 21 | a0002c0002t0001g0009 a0002c0004t0001g0041 a0002c0004t0001g0042 others(18): Show |
24 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-629dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307511 | ||||||
| chr22:46307511 | C | CTT | 14 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0025 others(11): Show |
20 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.80-630_80-629dupTT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307511 | ||||||
| chr22:46307606 | C | T | 1 | a0001c0025t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.80-544C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307606 | |||||||
| chr22:46307607 | G | A | 4 | a0001c0001t0001g0060 a0001c0011t0001g0005 a0001c0011t0001g0030 others(1): Show |
5 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-543G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307607 | |||||||
| chr22:46307608 | A | T | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-542A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307608 | |||||||
| chr22:46307699 | C | T | 5 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-451C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307699 | |||||||
| chr22:46307767 | T | C | 36 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(33): Show |
45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-383T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307767 | |||||||
| chr22:46307792 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.80-358C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307792 | |||||||
| chr22:46307813 | TA | T | 13 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(10): Show |
15 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.80-323delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307813 | ||||||
| chr22:46307813 | TAA | T | 28 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(25): Show |
37 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(34): Show |
intron_variant | MODIFIER | c.80-324_80-323delAA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | 46307813 | ||||||
| chr22:46307850 | G | A | 1 | a0002c0002t0001g0009 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.80-300G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307850 | |||||||
| chr22:46307879 | C | T | 36 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(33): Show |
45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.80-271C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307879 | |||||||
| chr22:46307963 | A | T | 37 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(34): Show |
46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.80-187A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46307963 | |||||||
| chr22:46308007 | A | C | 37 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(34): Show |
46 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.80-143A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46308007 | |||||||
| chr22:46308116 | G | A | 3 | a0003c0003t0001g0138 a0003c0003t0001g0139 a0003c0003t0001g0140 |
3 | HG02818.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.80-34G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46308116 | |||||||
| chr22:46308142 | C | T | 1 | a0002c0002t0001g0009 | 2 | HG02717.hp2 HG02886.hp2 |
splice_region_variant&intron_variant | LOW | c.80-8C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 2/11 | chr22 | 46308142 | |||||||
| chr22:46308977 | C | G | 1 | a0002c0014t0001g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.762+34C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46308977 | |||||||
| chr22:46309019 | C | G | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.762+76C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309019 | |||||||
| chr22:46309110 | G | T | 2 | a0001c0009t0001g0012 a0001c0009t0001g0056 |
3 | HG02257.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.762+167G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309110 | |||||||
| chr22:46309127 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.762+184G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309127 | |||||||
| chr22:46309237 | A | G | 1 | a0007c0007t0001g0010 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.762+294A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309237 | |||||||
| chr22:46309253 | C | G | 1 | a0002c0014t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.762+310C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309253 | |||||||
| chr22:46309254 | C | G | 1 | a0010c0027t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.762+311C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309254 | |||||||
| chr22:46309429 | C | G | 29 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(26): Show |
37 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.762+486C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309429 | |||||||
| chr22:46309506 | G | A | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.762+563G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309506 | |||||||
| chr22:46309510 | C | T | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.762+567C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309510 | |||||||
| chr22:46309523 | C | T | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.762+580C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309523 | |||||||
| chr22:46309543 | G | A | 6 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(3): Show |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.762+600G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309543 | |||||||
| chr22:46309590 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG00408.hp2 HG00423.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.762+647C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309590 | |||||||
| chr22:46309596 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.762+653G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309596 | |||||||
| chr22:46309687 | A | G | 30 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(27): Show |
38 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.762+744A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309687 | |||||||
| chr22:46309766 | G | A | 1 | a0002c0004t0001g0043 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.762+823G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309766 | |||||||
| chr22:46309774 | C | T | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.762+831C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309774 | |||||||
| chr22:46309848 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.762+905C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309848 | |||||||
| chr22:46309897 | A | G | 12 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0032 others(9): Show |
18 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.762+954A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309897 | |||||||
| chr22:46309932 | G | A | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.762+989G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309932 | |||||||
| chr22:46309934 | G | A | 1 | a0013c0023t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.762+991G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46309934 | |||||||
| chr22:46310092 | T | G | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1149T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310092 | |||||||
| chr22:46310341 | C | G | 1 | a0003c0003t0001g0115 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.762+1398C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310341 | |||||||
| chr22:46310352 | C | T | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.762+1409C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310352 | |||||||
| chr22:46310384 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.762+1441C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310384 | |||||||
| chr22:46310412 | CA | C | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.762+1476delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | 46310412 | ||||||
| chr22:46310700 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.763-1441G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310700 | |||||||
| chr22:46310799 | G | A | 1 | a0001c0012t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.763-1342G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46310799 | |||||||
| chr22:46311062 | GT | G | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-1068delT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | 46311062 | ||||||
| chr22:46311069 | T | G | 1 | a0004c0005t0001g0020 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.763-1072T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311069 | |||||||
| chr22:46311202 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.763-939C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311202 | |||||||
| chr22:46311213 | G | A | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.763-928G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311213 | |||||||
| chr22:46311222 | C | T | 6 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.763-919C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311222 | |||||||
| chr22:46311276 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.763-865T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311276 | |||||||
| chr22:46311290 | C | T | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-851C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311290 | |||||||
| chr22:46311329 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.763-812C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311329 | |||||||
| chr22:46311378 | G | A | 1 | a0002c0002t0001g0009 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.763-763G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311378 | |||||||
| chr22:46311482 | A | G | 1 | a0002c0002t0001g0009 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.763-659A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311482 | |||||||
| chr22:46311672 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0123 |
5 | HG00609.hp2 NA18964.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-469C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311672 | |||||||
| chr22:46311942 | C | G | 1 | a0002c0002t0001g0040 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.763-199C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46311942 | |||||||
| chr22:46312010 | G | A | 58 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(55): Show |
77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.763-131G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312010 | |||||||
| chr22:46312027 | G | T | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-114G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312027 | |||||||
| chr22:46312031 | G | A | 25 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(22): Show |
30 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.763-110G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312031 | |||||||
| chr22:46312057 | A | G | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.763-84A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 4/11 | chr22 | 46312057 | |||||||
| chr22:46312410 | T | C | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+105T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46312410 | |||||||
| chr22:46312638 | C | CA | 6 | a0001c0001t0001g0083 a0002c0002t0001g0025 a0002c0002t0001g0035 others(3): Show |
6 | HG00639.hp1 HG01358.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+351dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46312638 | ||||||
| chr22:46312638 | C | CAA | 5 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(2): Show |
8 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+350_927+351dup others(2): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46312638 | ||||||
| chr22:46312638 | CA | C | 16 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0101 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.927+351delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46312638 | ||||||
| chr22:46313166 | TA | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0100 a0002c0004t0001g0048 others(8): Show |
17 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-704delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | 46313166 | ||||||
| chr22:46313258 | G | A | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-632G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313258 | |||||||
| chr22:46313266 | C | A | 6 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(3): Show |
9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-624C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313266 | |||||||
| chr22:46313373 | C | T | 6 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-517C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313373 | |||||||
| chr22:46313404 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.928-486G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313404 | |||||||
| chr22:46313504 | C | G | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-386C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313504 | |||||||
| chr22:46313622 | C | T | 7 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(4): Show |
10 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.928-268C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313622 | |||||||
| chr22:46313752 | C | T | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-138C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 5/11 | chr22 | 46313752 | |||||||
| chr22:46314025 | G | A | 1 | a0003c0003t0001g0140 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1051+12G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314025 | |||||||
| chr22:46314127 | G | A | 24 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(21): Show |
29 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.1051+114G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314127 | |||||||
| chr22:46314144 | C | T | 2 | a0001c0012t0001g0128 a0001c0012t0001g0129 |
2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1051+131C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314144 | |||||||
| chr22:46314236 | C | T | 1 | a0008c0010t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1051+223C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314236 | |||||||
| chr22:46314237 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1051+224G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314237 | |||||||
| chr22:46314257 | G | A | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1051+244G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314257 | |||||||
| chr22:46314259 | A | G | 36 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(33): Show |
45 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1051+246A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314259 | |||||||
| chr22:46314535 | C | T | 1 | a0012c0015t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1051+522C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314535 | |||||||
| chr22:46314613 | C | T | 3 | a0006c0006t0001g0141 a0006c0006t0001g0142 a0006c0006t0001g0144 |
3 | HG01167.hp1 HG01169.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1051+600C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314613 | |||||||
| chr22:46314732 | C | T | 1 | a0001c0017t0001g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1051+719C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314732 | |||||||
| chr22:46314784 | G | A | 12 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0031 others(9): Show |
16 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+771G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314784 | |||||||
| chr22:46314796 | A | C | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1051+783A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314796 | |||||||
| chr22:46314801 | G | A | 6 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(3): Show |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1051+788G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314801 | |||||||
| chr22:46314806 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1051+793G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314806 | |||||||
| chr22:46314818 | A | G | 5 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0032 others(2): Show |
9 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1051+805A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314818 | |||||||
| chr22:46314825 | G | A | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1051+812G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314825 | |||||||
| chr22:46314850 | C | CA | 17 | a0001c0001t0001g0022 a0001c0009t0001g0054 a0002c0002t0001g0004 others(14): Show |
21 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1051+854dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46314850 | ||||||
| chr22:46314850 | C | CAA | 3 | a0006c0006t0001g0021 a0008c0010t0001g0008 a0010c0027t0001g0029 |
6 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+853_1051+854d others(4): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46314850 | ||||||
| chr22:46314850 | CA | C | 15 | a0001c0001t0001g0079 a0001c0001t0001g0098 a0001c0011t0001g0005 others(12): Show |
22 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051+854delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46314850 | ||||||
| chr22:46314940 | G | C | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1051+927G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46314940 | |||||||
| chr22:46315065 | G | GT | 35 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0073 others(32): Show |
43 | HG00408.hp1 HG00408.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1052-955dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46315065 | ||||||
| chr22:46315127 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1052-905T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315127 | |||||||
| chr22:46315168 | C | T | 11 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0004t0001g0041 others(8): Show |
12 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.1052-864C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315168 | |||||||
| chr22:46315279 | G | A | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052-753G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315279 | |||||||
| chr22:46315299 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1052-733C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315299 | |||||||
| chr22:46315426 | C | T | 31 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(28): Show |
39 | HG01070.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1052-606C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315426 | |||||||
| chr22:46315439 | T | C | 45 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0004 others(42): Show |
57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.1052-593T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315439 | |||||||
| chr22:46315472 | G | A | 14 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0004c0005t0001g0013 others(11): Show |
18 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1052-560G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315472 | |||||||
| chr22:46315492 | G | GC | 49 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(46): Show |
62 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.1052-539dupC | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46315492 | ||||||
| chr22:46315532 | C | T | 6 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1052-500C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315532 | |||||||
| chr22:46315550 | T | C | 6 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(3): Show |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1052-482T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315550 | |||||||
| chr22:46315826 | G | A | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052-206G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315826 | |||||||
| chr22:46315894 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1052-138T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | chr22 | 46315894 | |||||||
| chr22:46316023 | A | AC | 45 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0004 others(42): Show |
57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
splice_region_variant&intron_variant | LOW | c.1052-7dupC | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr22 | 46316023 | ||||||
| chr22:46316435 | T | C | 1 | a0002c0014t0001g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1432+23T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316435 | |||||||
| chr22:46316538 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1432+126G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316538 | |||||||
| chr22:46316562 | G | A | 4 | a0007c0007t0001g0024 a0007c0007t0001g0026 a0007c0007t0001g0027 others(1): Show |
4 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1432+150G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316562 | |||||||
| chr22:46316743 | T | G | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432+331T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316743 | |||||||
| chr22:46316947 | T | C | 1 | a0002c0002t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1432+535T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316947 | |||||||
| chr22:46316963 | T | A | 1 | a0002c0002t0001g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1432+551T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46316963 | |||||||
| chr22:46317122 | C | T | 45 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0004 others(42): Show |
57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.1432+710C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317122 | |||||||
| chr22:46317129 | T | A | 1 | a0001c0017t0001g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1432+717T>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317129 | |||||||
| chr22:46317175 | C | A | 1 | a0004c0005t0001g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1432+763C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317175 | |||||||
| chr22:46317218 | C | T | 1 | a0007c0007t0001g0010 | 2 | HG02895.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1432+806C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317218 | |||||||
| chr22:46317459 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1432+1047A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317459 | |||||||
| chr22:46317504 | C | T | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1432+1092C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317504 | |||||||
| chr22:46317646 | G | T | 1 | a0001c0025t0001g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1432+1234G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317646 | |||||||
| chr22:46317734 | C | T | 39 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0004 others(36): Show |
48 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.1432+1322C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317734 | |||||||
| chr22:46317754 | A | G | 6 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(3): Show |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432+1342A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317754 | |||||||
| chr22:46317881 | C | T | 8 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0007c0007t0001g0010 others(5): Show |
10 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1432+1469C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46317881 | |||||||
| chr22:46318020 | G | A | 45 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0002t0001g0004 others(42): Show |
57 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(54): Show |
intron_variant | MODIFIER | c.1432+1608G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318020 | |||||||
| chr22:46318431 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1432+2019C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318431 | |||||||
| chr22:46318432 | C | G | 5 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0032 others(2): Show |
9 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1432+2020C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318432 | |||||||
| chr22:46318516 | G | C | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1432+2104G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318516 | |||||||
| chr22:46318625 | C | A | 5 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(2): Show |
7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432+2213C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318625 | |||||||
| chr22:46318717 | G | A | 9 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(6): Show |
15 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1432+2305G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318717 | |||||||
| chr22:46318767 | C | T | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432+2355C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318767 | |||||||
| chr22:46318838 | A | G | 26 | a0002c0002t0001g0004 a0002c0002t0001g0009 a0002c0002t0001g0011 others(23): Show |
33 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.1432+2426A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318838 | |||||||
| chr22:46318851 | C | T | 26 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(23): Show |
37 | HG00639.hp2 HG01243.hp1 HG01433.hp1 others(34): Show |
intron_variant | MODIFIER | c.1432+2439C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318851 | |||||||
| chr22:46318855 | C | G | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1432+2443C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318855 | |||||||
| chr22:46318919 | G | T | 5 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(2): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2507G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318919 | |||||||
| chr22:46318920 | G | T | 5 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(2): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2508G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318920 | |||||||
| chr22:46318921 | C | CTTCT | 5 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(2): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2509_1432+251 others(8): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46318921 | |||||||
| chr22:46318923 | G | GGT | 5 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(2): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+2512_1432+251 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46318923 | ||||||
| chr22:46319002 | T | C | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1432+2590T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319002 | |||||||
| chr22:46319016 | G | T | 27 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(24): Show |
38 | HG00639.hp2 HG01243.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.1432+2604G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319016 | |||||||
| chr22:46319049 | C | T | 1 | a0010c0027t0001g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1432+2637C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319049 | |||||||
| chr22:46319172 | G | A | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432+2760G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319172 | |||||||
| chr22:46319201 | C | T | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432+2789C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319201 | |||||||
| chr22:46319207 | G | A | 1 | a0009c0013t0001g0110 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1432+2795G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319207 | |||||||
| chr22:46319256 | G | C | 1 | a0002c0014t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1432+2844G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319256 | |||||||
| chr22:46319310 | G | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG00408.hp2 HG00423.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1432+2898G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319310 | |||||||
| chr22:46319408 | C | T | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432+2996C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319408 | |||||||
| chr22:46319525 | G | A | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1432+3113G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319525 | |||||||
| chr22:46319539 | C | T | 2 | a0001c0012t0001g0128 a0001c0012t0001g0129 |
2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1432+3127C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319539 | |||||||
| chr22:46319581 | GAGGCCAC others(2): Show |
G | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432+3174_1432+318 others(13): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46319581 | ||||||
| chr22:46319628 | G | C | 9 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0114 others(6): Show |
15 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1432+3216G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319628 | |||||||
| chr22:46319803 | T | C | 1 | a0002c0004t0001g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1433-3387T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319803 | |||||||
| chr22:46319971 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1433-3219C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46319971 | |||||||
| chr22:46319982 | C | CA | 9 | a0001c0001t0001g0053 a0001c0001t0001g0112 a0001c0011t0001g0005 others(6): Show |
11 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1433-3194dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46319982 | ||||||
| chr22:46319982 | C | CAA | 12 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(9): Show |
19 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1433-3195_1433-319 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46319982 | ||||||
| chr22:46320057 | C | T | 3 | a0007c0007t0001g0024 a0007c0007t0001g0026 a0007c0007t0001g0027 |
3 | HG02486.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1433-3133C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320057 | |||||||
| chr22:46320139 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1433-3051A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320139 | |||||||
| chr22:46320308 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1433-2882G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320308 | |||||||
| chr22:46320372 | ATTCATCA others(34): Show |
A | 1 | a0001c0001t0001g0087 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1433-2817_1433-277 others(45): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320372 | |||||||
| chr22:46320425 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1433-2765C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320425 | |||||||
| chr22:46320430 | G | A | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1433-2760G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320430 | |||||||
| chr22:46320578 | C | T | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-2612C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320578 | |||||||
| chr22:46320706 | T | C | 58 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(55): Show |
77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1433-2484T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320706 | |||||||
| chr22:46320790 | G | A | 1 | a0002c0002t0001g0011 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1433-2400G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320790 | |||||||
| chr22:46320800 | G | C | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-2390G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320800 | |||||||
| chr22:46320963 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1433-2227G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46320963 | |||||||
| chr22:46321023 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0093 |
4 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1433-2167A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321023 | |||||||
| chr22:46321093 | G | T | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1433-2097G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321093 | |||||||
| chr22:46321306 | A | G | 1 | a0002c0004t0001g0047 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1433-1884A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321306 | |||||||
| chr22:46321419 | G | C | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-1771G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321419 | |||||||
| chr22:46321657 | C | T | 5 | a0007c0007t0001g0010 a0007c0007t0001g0024 a0007c0007t0001g0026 others(2): Show |
6 | HG02486.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-1533C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321657 | |||||||
| chr22:46321658 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1433-1532G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321658 | |||||||
| chr22:46321668 | T | G | 58 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(55): Show |
77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1433-1522T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321668 | |||||||
| chr22:46321774 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1433-1416A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321774 | |||||||
| chr22:46321848 | G | A | 1 | a0016c0019t0001g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1433-1342G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321848 | |||||||
| chr22:46321909 | A | G | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-1281A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321909 | |||||||
| chr22:46321928 | T | G | 52 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(49): Show |
69 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.1433-1262T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46321928 | |||||||
| chr22:46322052 | C | T | 1 | a0002c0026t0001g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1433-1138C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322052 | |||||||
| chr22:46322068 | TGTCTCAA others(1): Show |
T | 12 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(9): Show |
19 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1433-1121_1433-111 others(12): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322068 | |||||||
| chr22:46322073 | C | CA | 31 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0050 others(28): Show |
38 | HG00423.hp1 HG00735.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1433-1092dupA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | ||||||
| chr22:46322073 | C | CAA | 6 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0002c0028t0001g0037 others(3): Show |
6 | HG00408.hp2 HG02622.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1433-1093_1433-109 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | ||||||
| chr22:46322073 | CA | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0079 others(11): Show |
15 | HG00639.hp1 HG01070.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1433-1092delA | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | ||||||
| chr22:46322073 | CAA | C | 6 | a0002c0014t0001g0126 a0007c0007t0001g0010 a0007c0007t0001g0024 others(3): Show |
6 | HG02486.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1433-1093_1433-109 others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | ||||||
| chr22:46322073 | CAAA | C | 6 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0002c0014t0001g0113 others(3): Show |
7 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1433-1094_1433-109 others(7): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | 46322073 | ||||||
| chr22:46322076 | A | C | 1 | a0003c0003t0001g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1433-1114A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322076 | |||||||
| chr22:46322077 | A | C | 12 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(9): Show |
19 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1433-1113A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322077 | |||||||
| chr22:46322276 | G | T | 1 | a0002c0002t0001g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1433-914G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322276 | |||||||
| chr22:46322437 | C | T | 1 | a0002c0014t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1433-753C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322437 | |||||||
| chr22:46322477 | T | C | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1433-713T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322477 | |||||||
| chr22:46322520 | A | T | 58 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(55): Show |
77 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.1433-670A>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322520 | |||||||
| chr22:46322876 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1433-314C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322876 | |||||||
| chr22:46322933 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1433-257C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322933 | |||||||
| chr22:46322991 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1433-199C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46322991 | |||||||
| chr22:46323116 | C | T | 11 | a0001c0009t0001g0054 a0001c0009t0001g0055 a0001c0009t0001g0056 others(8): Show |
11 | HG02257.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1433-74C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46323116 | |||||||
| chr22:46323157 | T | C | 19 | a0001c0001t0001g0060 a0001c0009t0001g0054 a0001c0009t0001g0055 others(16): Show |
24 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1433-33T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 7/11 | chr22 | 46323157 | |||||||
| chr22:46323274 | T | C | 6 | a0002c0002t0001g0009 a0004c0005t0001g0013 a0004c0005t0001g0020 others(3): Show |
9 | HG01433.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1505+12T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323274 | |||||||
| chr22:46323280 | G | A | 5 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(2): Show |
7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1505+18G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323280 | |||||||
| chr22:46323288 | T | C | 1 | a0012c0015t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1505+26T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323288 | |||||||
| chr22:46323344 | T | G | 1 | a0011c0016t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1505+82T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323344 | |||||||
| chr22:46323396 | G | A | 4 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(1): Show |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1505+134G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323396 | |||||||
| chr22:46323460 | C | T | 19 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(16): Show |
29 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1505+198C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323460 | |||||||
| chr22:46323503 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1505+241C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323503 | |||||||
| chr22:46323627 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | NA19063.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1505+365T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323627 | |||||||
| chr22:46323648 | G | A | 16 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0025 others(13): Show |
26 | HG01243.hp1 HG01884.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1505+386G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323648 | |||||||
| chr22:46323700 | C | A | 4 | a0001c0001t0001g0060 a0001c0011t0001g0005 a0001c0011t0001g0030 others(1): Show |
5 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1505+438C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323700 | |||||||
| chr22:46323780 | C | T | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1505+518C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323780 | |||||||
| chr22:46323807 | C | T | 10 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(7): Show |
12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1505+545C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323807 | |||||||
| chr22:46323865 | A | AT | 6 | a0001c0001t0001g0060 a0001c0011t0001g0005 a0001c0011t0001g0030 others(3): Show |
8 | HG00639.hp2 HG01261.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1505+611dupT | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr22 | 46323865 | ||||||
| chr22:46323893 | C | T | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1505+631C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46323893 | |||||||
| chr22:46324051 | C | T | 1 | a0002c0014t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1505+789C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324051 | |||||||
| chr22:46324361 | TTTTTC | T | 3 | a0002c0002t0001g0009 a0002c0002t0001g0031 a0010c0027t0001g0029 |
4 | HG02258.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1505+1114_1505+111 others(9): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr22 | 46324361 | ||||||
| chr22:46324381 | T | C | 7 | a0002c0028t0001g0037 a0007c0007t0001g0010 a0007c0007t0001g0024 others(4): Show |
8 | HG02486.hp2 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1505+1119T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324381 | |||||||
| chr22:46324396 | C | T | 3 | a0002c0014t0001g0126 a0009c0013t0001g0110 a0009c0013t0001g0111 |
3 | HG02809.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1505+1134C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324396 | |||||||
| chr22:46324456 | C | T | 1 | a0001c0009t0001g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1505+1194C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324456 | |||||||
| chr22:46324513 | G | A | 5 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(2): Show |
7 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1505+1251G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324513 | |||||||
| chr22:46324524 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0146 |
2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1505+1262C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324524 | |||||||
| chr22:46324525 | G | A | 1 | a0002c0014t0001g0113 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1505+1263G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324525 | |||||||
| chr22:46324598 | G | A | 1 | a0002c0014t0001g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1505+1336G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324598 | |||||||
| chr22:46324625 | G | T | 2 | a0009c0013t0001g0110 a0009c0013t0001g0111 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1505+1363G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324625 | |||||||
| chr22:46324824 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1505+1562G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324824 | |||||||
| chr22:46324889 | A | C | 6 | a0004c0005t0001g0013 a0004c0005t0001g0020 a0004c0005t0001g0118 others(3): Show |
8 | HG01433.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-1547A>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324889 | |||||||
| chr22:46324957 | C | A | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-1479C>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46324957 | |||||||
| chr22:46325015 | C | T | 10 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(7): Show |
12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1506-1421C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325015 | |||||||
| chr22:46325024 | G | A | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-1412G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325024 | |||||||
| chr22:46325191 | C | T | 60 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(57): Show |
79 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.1506-1245C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325191 | |||||||
| chr22:46325326 | G | A | 61 | a0001c0001t0001g0127 a0001c0009t0001g0012 a0001c0009t0001g0054 others(58): Show |
80 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.1506-1110G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325326 | |||||||
| chr22:46325770 | G | A | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-666G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325770 | |||||||
| chr22:46325997 | G | A | 3 | a0007c0007t0001g0024 a0007c0007t0001g0026 a0007c0007t0001g0027 |
3 | HG02486.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1506-439G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46325997 | |||||||
| chr22:46326028 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1506-408C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326028 | |||||||
| chr22:46326031 | A | G | 1 | a0012c0015t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1506-405A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326031 | |||||||
| chr22:46326044 | C | T | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-392C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326044 | |||||||
| chr22:46326178 | T | C | 3 | a0002c0004t0001g0043 a0002c0004t0001g0045 a0002c0004t0001g0048 |
3 | HG01106.hp2 HG06807.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1506-258T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326178 | |||||||
| chr22:46326190 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1506-246T>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326190 | |||||||
| chr22:46326297 | G | A | 8 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 others(5): Show |
8 | HG01070.hp1 HG01106.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-139G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326297 | |||||||
| chr22:46326359 | A | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(80): Show |
109 | HG00408.hp2 HG00423.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.1506-77A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326359 | |||||||
| chr22:46326384 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1506-52C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 8/11 | chr22 | 46326384 | |||||||
| chr22:46326663 | C | T | 57 | a0001c0001t0001g0093 a0001c0009t0001g0012 a0001c0009t0001g0054 others(54): Show |
75 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(72): Show |
intron_variant | MODIFIER | c.1724+9C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46326663 | |||||||
| chr22:46326772 | AGTTT | A | 10 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(7): Show |
12 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1724+127_1724+130d others(6): Show |
GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr22 | 46326772 | ||||||
| chr22:46326861 | G | C | 58 | a0001c0001t0001g0060 a0001c0001t0001g0093 a0001c0009t0001g0012 others(55): Show |
76 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(73): Show |
intron_variant | MODIFIER | c.1724+207G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46326861 | |||||||
| chr22:46327020 | T | C | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1724+366T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327020 | |||||||
| chr22:46327096 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1724+442G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327096 | |||||||
| chr22:46327126 | C | T | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1724+472C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327126 | |||||||
| chr22:46327183 | C | T | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1724+529C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327183 | |||||||
| chr22:46327277 | C | G | 1 | a0018c0024t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1724+623C>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327277 | |||||||
| chr22:46327373 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1724+719G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327373 | |||||||
| chr22:46327476 | A | G | 62 | a0001c0001t0001g0060 a0001c0001t0001g0093 a0001c0009t0001g0012 others(59): Show |
81 | HG00639.hp2 HG01070.hp1 HG01106.hp2 others(78): Show |
intron_variant | MODIFIER | c.1724+822A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327476 | |||||||
| chr22:46327547 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1724+893C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327547 | |||||||
| chr22:46327800 | G | C | 1 | a0012c0015t0001g0117 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1725-888G>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46327800 | |||||||
| chr22:46328104 | G | A | 3 | a0001c0011t0001g0005 a0001c0011t0001g0030 a0014c0021t0001g0005 |
4 | HG00639.hp2 HG01433.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725-584G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328104 | |||||||
| chr22:46328168 | C | T | 1 | a0005c0008t0001g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1725-520C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328168 | |||||||
| chr22:46328263 | G | T | 13 | a0001c0001t0001g0093 a0002c0002t0001g0004 a0002c0002t0001g0011 others(10): Show |
19 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1725-425G>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328263 | |||||||
| chr22:46328363 | A | G | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1725-325A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328363 | |||||||
| chr22:46328661 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(141): Show |
194 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1725-27T>C | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 9/11 | chr22 | 46328661 | |||||||
| chr22:46328904 | C | T | 3 | a0003c0003t0001g0138 a0003c0003t0001g0139 a0003c0003t0001g0140 |
3 | HG02818.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1926+15C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46328904 | |||||||
| chr22:46328941 | G | A | 13 | a0001c0009t0001g0012 a0001c0009t0001g0054 a0001c0009t0001g0055 others(10): Show |
20 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1926+52G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46328941 | |||||||
| chr22:46328986 | C | T | 1 | a0007c0007t0001g0024 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1926+97C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46328986 | |||||||
| chr22:46329010 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1926+121G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329010 | |||||||
| chr22:46329120 | C | T | 1 | a0004c0005t0001g0020 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1926+231C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329120 | |||||||
| chr22:46329190 | G | A | 3 | a0002c0002t0001g0009 a0002c0002t0001g0025 a0002c0002t0001g0031 |
4 | HG02717.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1927-168G>A | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329190 | |||||||
| chr22:46329211 | A | G | 5 | a0006c0006t0001g0021 a0006c0006t0001g0141 a0006c0006t0001g0142 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927-147A>G | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 10/11 | chr22 | 46329211 | |||||||
| chr22:46329766 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01081.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2136+199C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/11 | chr22 | 46329766 | |||||||
| chr22:46329793 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2136+226C>T | GTSE1 | ENSG00000075218.19 | transcript | ENST00000454366.2 | protein_coding | 11/11 | chr22 | 46329793 |