Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27244 |
| ensemblid | ENSG00000080546.14 |
| hgncid | 21595 |
| symbol | SESN1 |
| name | sestrin 1 |
| refseq_nuc | NM_014454.3 |
| refseq_prot | NP_055269.1 |
| ensembl_nuc | ENST00000436639.7 |
| ensembl_prot | ENSP00000393762.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 108984309 |
| end | 109094846 |
| strand | - |
| ver | v1.2 |
| region | chr6:108984309-109094846 |
| region5000 | chr6:108979309-109099846 |
| regionname0 | SESN1_chr6_108984309_109094846 |
| regionname5000 | SESN1_chr6_108979309_109099846 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 551 | 155 | 62 | 26 | 40 | 5 | 20 | 29 | SESN1_chr6_108979309_109099846 | SESN1 | MAEGE others(546): Show |
chr6 | 108979309 | 109099846 |
| a0002 | 0/0 | 551 | 26 | 1 | 6 | 8 | 3 | 8 | 7 | SESN1_chr6_108979309_109099846 | SESN1 | MAEGE others(546): Show |
chr6 | 108979309 | 109099846 |
| a0003 | 0/0 | 550 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | MAEGE others(545): Show |
chr6 | 108979309 | 109099846 |
| a0004 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | MAEGE others(546): Show |
chr6 | 108979309 | 109099846 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1653 | 143 | 54 | 24 | 38 | 5 | 20 | SESN1_chr6_108979309_109099846 | SESN1 | ATGGC others(1648): Show |
chr6 | 108979309 | 109099846 | ||
| a0001c0003 | 0/0 | 1653 | 6 | 6 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | ATGGC others(1648): Show |
chr6 | 108979309 | 109099846 | ||
| a0001c0004 | 0/0 | 1653 | 4 | 2 | 2 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | ATGGC others(1648): Show |
chr6 | 108979309 | 109099846 | ||
| a0001c0005 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | ATGGC others(1648): Show |
chr6 | 108979309 | 109099846 | ||
| a0002c0002 | 0/0 | 1653 | 26 | 1 | 6 | 8 | 3 | 8 | SESN1_chr6_108979309_109099846 | SESN1 | ATGGC others(1648): Show |
chr6 | 108979309 | 109099846 | ||
| a0003c0006 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | ATGGC others(1645): Show |
chr6 | 108979309 | 109099846 | ||
| a0004c0007 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | ATGGC others(1648): Show |
chr6 | 108979309 | 109099846 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5664 | 108 | 35 | 20 | 30 | 5 | 16 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0003 | 0/0 | 5668 | 18 | 8 | 2 | 6 | 0 | 2 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5663): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0006 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0007 | 0/0 | 5664 | 3 | 0 | 2 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0008 | 0/0 | 5664 | 3 | 3 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0009 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0010 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0011 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0012 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0013 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0014 | 0/0 | 5664 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0015 | 0/0 | 5664 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0001t0016 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0003t0002 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5655): Show |
chr6 | 108979309 | 109099846 |
| a0001c0003t0004 | 0/0 | 5664 | 5 | 5 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0001c0004t0005 | 0/0 | 5668 | 4 | 2 | 2 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5663): Show |
chr6 | 108979309 | 109099846 |
| a0001c0005t0001 | 0/0 | 5664 | 2 | 0 | 0 | 2 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| a0002c0002t0002 | 0/0 | 5660 | 26 | 1 | 6 | 8 | 3 | 8 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5655): Show |
chr6 | 108979309 | 109099846 |
| a0003c0006t0001 | 0/0 | 5661 | 2 | 2 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5656): Show |
chr6 | 108979309 | 109099846 |
| a0004c0007t0001 | 0/0 | 5664 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | GCTCC others(5659): Show |
chr6 | 108979309 | 109099846 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0014g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0015g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0001t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0003t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0003t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0003t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0003t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0003t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0003t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0004t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0004t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0004t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0004t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0001c0005t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0003c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0003c0006t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| a0004c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0031 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0032 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0047 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01168 | hp2 | a0001 | c0004 | t0005 | g0023 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01169 | hp2 | a0001 | c0004 | t0005 | g0022 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0065 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02055 | hp1 | a0003 | c0006 | t0001 | g0059 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0183 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02451 | hp1 | a0001 | c0004 | t0005 | g0020 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0005 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02630 | hp2 | a0004 | c0007 | t0001 | g0017 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0066 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0015 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02886 | hp1 | a0001 | c0004 | t0005 | g0021 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0182 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03130 | hp2 | a0003 | c0006 | t0001 | g0057 | AFR | ESN | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0004 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0003 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03669 | hp2 | a0001 | c0001 | t0014 | g0158 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0041 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | STU | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | YRI | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18906 | hp2 | a0001 | c0003 | t0004 | g0002 | AFR | YRI | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18998 | hp1 | a0001 | c0005 | t0001 | g0009 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19012 | hp1 | a0001 | c0001 | t0015 | g0141 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19080 | hp2 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA19089 | hp2 | a0001 | c0001 | t0011 | g0146 | EAS | JPT | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ASW | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ASW | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | GIH | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | USA | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0083 | REF | REF | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0089 | REF | REF | SESN1_chr6_108979309_109099846 | SESN1 | chr6 | 108979309 | 109099846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108992887 | ACTT | A | 1 | a0003 | 2 | HG02055.hp1 HG03130.hp2 |
disruptive_inframe_deletion | MODERATE | c.1130_1132delAAG | p.Glu377del | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/10 | 1905/5664 | 1130/1656 | 377/551 | chr6 | 108992887 | |||
| chr6:108998551 | C | T | 1 | a0004 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.934G>A | p.Val312Met | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/10 | 1707/5664 | 934/1656 | 312/551 | chr6 | 108998551 | |||
| chr6:109002316 | G | T | 1 | a0002 | 26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
missense_variant | MODERATE | c.307C>A | p.Leu103Ile | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/10 | 1080/5664 | 307/1656 | 103/551 | chr6 | 109002316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108998567 | T | C | 1 | a0001c0004 | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
synonymous_variant | LOW | c.918A>G | p.Thr306Thr | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/10 | 1691/5664 | 918/1656 | 306/551 | chr6 | 108998567 | |||
| chr6:109001351 | C | T | 2 | a0001c0003 a0002c0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
synonymous_variant | LOW | c.483G>A | p.Gln161Gln | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/10 | 1256/5664 | 483/1656 | 161/551 | chr6 | 109001351 | |||
| chr6:109093977 | A | G | 1 | a0001c0005 | 2 | NA18998.hp1 NA19080.hp2 |
synonymous_variant | LOW | c.97T>C | p.Leu33Leu | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 870/5664 | 97/1656 | 33/551 | chr6 | 109093977 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108984362 | C | T | 1 | a0001c0001t0012 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 3182 | chr6 | 108984362 | ||||||
| chr6:108984540 | T | C | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3004A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 3004 | chr6 | 108984540 | ||||||
| chr6:108984848 | T | C | 1 | a0001c0004t0005 | 4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2696A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2696 | chr6 | 108984848 | ||||||
| chr6:108984907 | A | G | 1 | a0001c0001t0007 | 3 | HG01106.hp2 HG01361.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2637T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2637 | chr6 | 108984907 | ||||||
| chr6:108984962 | G | A | 1 | a0001c0001t0013 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2582C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2582 | chr6 | 108984962 | ||||||
| chr6:108985143 | T | C | 1 | a0001c0001t0014 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2401 | chr6 | 108985143 | ||||||
| chr6:108985198 | T | G | 1 | a0001c0001t0015 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2346A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2346 | chr6 | 108985198 | ||||||
| chr6:108985277 | C | T | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2267G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2267 | chr6 | 108985277 | ||||||
| chr6:108985286 | C | A | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2258G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2258 | chr6 | 108985286 | ||||||
| chr6:108985290 | T | G | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2254A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2254 | chr6 | 108985290 | ||||||
| chr6:108985291 | CA | C | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2252delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2252 | chr6 | 108985291 | ||||||
| chr6:108985478 | T | C | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2066A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 2066 | chr6 | 108985478 | ||||||
| chr6:108985760 | C | A | 2 | a0001c0003t0002 a0002c0002t0002 |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1784G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1784 | chr6 | 108985760 | ||||||
| chr6:108985773 | A | T | 1 | a0001c0001t0011 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1771T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1771 | chr6 | 108985773 | ||||||
| chr6:108986078 | TATC | T | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1463_*1465delGAT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1463 | chr6 | 108986078 | ||||||
| chr6:108986370 | G | GTAGA | 3 | a0001c0001t0003 a0001c0003t0004 a0001c0004t0005 |
27 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1170_*1173dupTCTA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1173 | chr6 | 108986370 | ||||||
| chr6:108986507 | G | A | 3 | a0001c0003t0002 a0001c0003t0004 a0002c0002t0002 |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1037C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 1037 | chr6 | 108986507 | ||||||
| chr6:108986684 | C | T | 1 | a0001c0001t0010 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 860 | chr6 | 108986684 | ||||||
| chr6:108986703 | C | T | 1 | a0001c0001t0006 | 3 | HG01891.hp1 HG02647.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*841G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 841 | chr6 | 108986703 | ||||||
| chr6:108987518 | G | C | 1 | a0001c0001t0008 | 3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*26C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 10/10 | 26 | chr6 | 108987518 | ||||||
| chr6:109094079 | T | C | 1 | a0001c0001t0016 | 1 | HG02280.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | chr6 | 109094079 | |||||||
| chr6:109094312 | T | G | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-239A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 239 | chr6 | 109094312 | ||||||
| chr6:109094453 | C | T | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-380G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 380 | chr6 | 109094453 | ||||||
| chr6:109094567 | C | T | 1 | a0001c0001t0009 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-494G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 494 | chr6 | 109094567 | ||||||
| chr6:109094662 | C | A | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-589G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 589 | chr6 | 109094662 | ||||||
| chr6:109094809 | C | T | 1 | a0001c0003t0004 | 5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-736G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/10 | 736 | chr6 | 109094809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108987647 | A | G | 1 | a0002c0002t0002g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1570-17T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987647 | |||||||
| chr6:108987749 | C | A | 33 | a0001c0001t0010g0010 a0001c0003t0002g0182 a0001c0003t0004g0002 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1570-119G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987749 | |||||||
| chr6:108987806 | C | CTTTT | 23 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1570-180_1570-177d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | |||||||
| chr6:108987806 | C | CTTTTT | 13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0058 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1570-181_1570-177d others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | |||||||
| chr6:108987806 | C | CTTTTTT | 48 | a0001c0001t0001g0019 a0001c0001t0001g0125 a0001c0001t0001g0126 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1570-182_1570-177d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | |||||||
| chr6:108987806 | C | CTTTTTTT | 12 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0003g0167 others(9): Show |
12 | HG01168.hp2 HG01169.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1570-183_1570-177d others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987806 | |||||||
| chr6:108987905 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1570-275G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987905 | |||||||
| chr6:108987947 | T | C | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1570-317A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108987947 | |||||||
| chr6:108988050 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0134 |
2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1570-420A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108988050 | |||||||
| chr6:108988084 | A | G | 62 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(59): Show |
62 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1570-454T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108988084 | |||||||
| chr6:108988239 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1569+304A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 9/9 | chr6 | 108988239 | |||||||
| chr6:108988799 | G | C | 2 | a0001c0004t0005g0020 a0001c0004t0005g0021 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1425-112C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108988799 | |||||||
| chr6:108988822 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0013g0015 |
2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1425-135T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108988822 | |||||||
| chr6:108989065 | C | T | 28 | a0001c0001t0010g0010 a0001c0003t0002g0182 a0002c0002t0002g0013 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1425-378G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989065 | |||||||
| chr6:108989070 | T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1425-383A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989070 | |||||||
| chr6:108989222 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1425-535T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989222 | |||||||
| chr6:108989391 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1425-704G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989391 | |||||||
| chr6:108989393 | C | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(148): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.1425-706G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989393 | |||||||
| chr6:108989424 | G | GAT | 27 | a0001c0003t0002g0182 a0002c0002t0002g0013 a0002c0002t0002g0014 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1425-739_1425-738d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989424 | |||||||
| chr6:108989425 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1425-738T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989425 | |||||||
| chr6:108989427 | ATATATCT others(17): Show |
A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1425-764_1425-741d others(26): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989427 | |||||||
| chr6:108989428 | T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1425-741A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989428 | |||||||
| chr6:108989446 | C | T | 60 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1425-759G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989446 | |||||||
| chr6:108989454 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1425-767A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989454 | |||||||
| chr6:108989454 | TATCTAGA others(31): Show |
T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 |
3 | HG01168.hp1 HG02486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1425-805_1425-768d others(40): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989454 | |||||||
| chr6:108989505 | CTA | C | 55 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1425-820_1425-819d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989505 | |||||||
| chr6:108989516 | T | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1425-829A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989516 | |||||||
| chr6:108989529 | ATAGAGAT others(31): Show |
A | 55 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1425-880_1425-843d others(40): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989529 | |||||||
| chr6:108989546 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1425-859A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989546 | |||||||
| chr6:108989567 | C | A | 1 | a0003c0006t0001g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1425-880G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108989567 | |||||||
| chr6:108990158 | G | A | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1424+487C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990158 | |||||||
| chr6:108990224 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1424+421C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990224 | |||||||
| chr6:108990357 | T | G | 55 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1424+288A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990357 | |||||||
| chr6:108990483 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1424+162C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990483 | |||||||
| chr6:108990529 | T | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA19012.hp2 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1424+116A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990529 | |||||||
| chr6:108990561 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1424+84C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 8/9 | chr6 | 108990561 | |||||||
| chr6:108991021 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1234-186A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991021 | |||||||
| chr6:108991036 | C | T | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-201G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991036 | |||||||
| chr6:108991066 | C | CA | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-232dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991066 | |||||||
| chr6:108991073 | A | AAAC | 25 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(22): Show |
25 | HG01109.hp1 HG01891.hp2 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.1234-241_1234-239d others(5): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991073 | |||||||
| chr6:108991073 | A | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(65): Show |
69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1234-238T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991073 | |||||||
| chr6:108991074 | AAC | A | 21 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0026 others(18): Show |
21 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1234-241_1234-240d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991074 | |||||||
| chr6:108991075 | AC | A | 4 | a0002c0002t0002g0027 a0002c0002t0002g0029 a0002c0002t0002g0043 others(1): Show |
4 | HG00438.hp1 HG01175.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-241delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991075 | |||||||
| chr6:108991076 | C | A | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-241G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991076 | |||||||
| chr6:108991079 | C | A | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-244G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991079 | |||||||
| chr6:108991082 | C | A | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-247G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991082 | |||||||
| chr6:108991082 | C | CAAA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-250_1234-248d others(5): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991082 | |||||||
| chr6:108991085 | A | C | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1234-250T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991085 | |||||||
| chr6:108991228 | A | AGT | 11 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
11 | HG00280.hp1 HG01168.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1234-395_1234-394d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | |||||||
| chr6:108991228 | AGT | A | 9 | a0001c0001t0001g0179 a0001c0001t0003g0135 a0001c0001t0003g0159 others(6): Show |
9 | HG01891.hp2 HG02258.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-395_1234-394d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | |||||||
| chr6:108991228 | AGTGT | A | 47 | a0001c0001t0001g0126 a0001c0001t0003g0131 a0001c0001t0003g0161 others(44): Show |
47 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1234-397_1234-394d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | |||||||
| chr6:108991228 | AGTGTGT | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(7): Show |
10 | HG01168.hp2 HG01169.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1234-399_1234-394d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991228 | |||||||
| chr6:108991295 | A | G | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-460T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991295 | |||||||
| chr6:108991486 | C | T | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1234-651G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991486 | |||||||
| chr6:108991830 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1233+957G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108991830 | |||||||
| chr6:108992068 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1233+719T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992068 | |||||||
| chr6:108992100 | C | T | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1233+687G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992100 | |||||||
| chr6:108992291 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0113 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1233+496A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992291 | |||||||
| chr6:108992308 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0113 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1233+479C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992308 | |||||||
| chr6:108992397 | G | A | 3 | a0001c0001t0006g0070 a0001c0001t0006g0091 a0001c0001t0006g0092 |
3 | HG01891.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1233+390C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992397 | |||||||
| chr6:108992426 | T | C | 33 | a0001c0001t0010g0010 a0001c0003t0002g0182 a0001c0003t0004g0002 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.1233+361A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992426 | |||||||
| chr6:108992525 | C | T | 65 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1233+262G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 7/9 | chr6 | 108992525 | |||||||
| chr6:108993147 | T | C | 65 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1121-248A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993147 | |||||||
| chr6:108993190 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121-291C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993190 | |||||||
| chr6:108993272 | AGATT | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02280.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1121-377_1121-374d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993272 | |||||||
| chr6:108993753 | G | GT | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120+708dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993753 | |||||||
| chr6:108993788 | C | A | 2 | a0001c0004t0005g0022 a0001c0004t0005g0023 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1120+674G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993788 | |||||||
| chr6:108993828 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120+634G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993828 | |||||||
| chr6:108993906 | C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1120+556G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993906 | |||||||
| chr6:108993912 | T | C | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.1120+550A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108993912 | |||||||
| chr6:108994018 | T | C | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+444A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994018 | |||||||
| chr6:108994078 | T | G | 16 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(13): Show |
16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.1120+384A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994078 | |||||||
| chr6:108994096 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1120+366G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994096 | |||||||
| chr6:108994140 | T | TA | 8 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0093 others(5): Show |
8 | HG02055.hp1 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1120+321dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994140 | |||||||
| chr6:108994140 | TA | T | 15 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0073 others(12): Show |
15 | HG00323.hp2 HG01168.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1120+321delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994140 | |||||||
| chr6:108994163 | A | AG | 3 | a0002c0002t0002g0029 a0002c0002t0002g0041 a0002c0002t0002g0044 |
3 | HG01123.hp2 HG02738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1120+298dupC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994163 | |||||||
| chr6:108994163 | A | G | 29 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(26): Show |
29 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1120+299T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 6/9 | chr6 | 108994163 | |||||||
| chr6:108994698 | C | CT | 57 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.973-90dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994698 | |||||||
| chr6:108994753 | A | T | 17 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(14): Show |
17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.973-144T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994753 | |||||||
| chr6:108994796 | A | G | 101 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(98): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.973-187T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994796 | |||||||
| chr6:108994879 | T | G | 9 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0001c0001t0001g0143 others(6): Show |
9 | HG02293.hp1 HG02523.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.973-270A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994879 | |||||||
| chr6:108994970 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.973-361G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108994970 | |||||||
| chr6:108995199 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0113 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.973-590C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995199 | |||||||
| chr6:108995200 | T | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0113 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.973-591A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995200 | |||||||
| chr6:108995449 | C | G | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-840G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995449 | |||||||
| chr6:108995471 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.973-862T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995471 | |||||||
| chr6:108995551 | C | G | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-942G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995551 | |||||||
| chr6:108995674 | G | T | 2 | a0001c0001t0003g0167 a0001c0001t0003g0171 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.973-1065C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995674 | |||||||
| chr6:108995752 | C | T | 2 | a0001c0005t0001g0008 a0001c0005t0001g0009 |
2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.973-1143G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995752 | |||||||
| chr6:108995838 | AT | A | 27 | a0001c0003t0002g0182 a0002c0002t0002g0013 a0002c0002t0002g0014 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.973-1230delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108995838 | |||||||
| chr6:108996024 | T | C | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.973-1415A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996024 | |||||||
| chr6:108996064 | G | T | 1 | a0002c0002t0002g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.973-1455C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996064 | |||||||
| chr6:108996127 | C | T | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-1518G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996127 | |||||||
| chr6:108996185 | A | G | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-1576T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996185 | |||||||
| chr6:108996191 | C | G | 34 | a0001c0001t0010g0010 a0001c0001t0013g0015 a0001c0003t0002g0182 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.973-1582G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996191 | |||||||
| chr6:108996432 | C | T | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.973-1823G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108996432 | |||||||
| chr6:108997076 | G | T | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1437C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997076 | |||||||
| chr6:108997077 | A | T | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1436T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997077 | |||||||
| chr6:108997117 | A | G | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.972+1396T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997117 | |||||||
| chr6:108997132 | CAA | C | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1379_972+1380d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997132 | |||||||
| chr6:108997313 | G | C | 66 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.972+1200C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997313 | |||||||
| chr6:108997501 | T | G | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.972+1012A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997501 | |||||||
| chr6:108997557 | G | A | 1 | a0001c0001t0003g0181 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.972+956C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997557 | |||||||
| chr6:108997640 | A | G | 34 | a0001c0001t0010g0010 a0001c0001t0013g0015 a0001c0003t0002g0182 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.972+873T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997640 | |||||||
| chr6:108997884 | T | C | 1 | a0001c0001t0006g0092 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.972+629A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997884 | |||||||
| chr6:108997995 | A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.972+518T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108997995 | |||||||
| chr6:108998104 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+409G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 5/9 | chr6 | 108998104 | |||||||
| chr6:108998776 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.730-21C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108998776 | |||||||
| chr6:108999238 | T | C | 34 | a0001c0001t0010g0010 a0001c0001t0013g0015 a0001c0003t0002g0182 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.730-483A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999238 | |||||||
| chr6:108999543 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.730-788A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999543 | |||||||
| chr6:108999692 | T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.729+799A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999692 | |||||||
| chr6:108999855 | C | T | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.729+636G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 108999855 | |||||||
| chr6:109000128 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0105 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+363A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000128 | |||||||
| chr6:109000146 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.729+345C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000146 | |||||||
| chr6:109000294 | G | A | 27 | a0001c0003t0002g0182 a0002c0002t0002g0013 a0002c0002t0002g0014 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.729+197C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000294 | |||||||
| chr6:109000378 | CA | C | 17 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(14): Show |
17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.729+112delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000378 | |||||||
| chr6:109000399 | T | G | 4 | a0002c0002t0002g0027 a0002c0002t0002g0032 a0002c0002t0002g0033 others(1): Show |
4 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+92A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 4/9 | chr6 | 109000399 | |||||||
| chr6:109000795 | C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.547-122G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000795 | |||||||
| chr6:109000842 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.547-169C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000842 | |||||||
| chr6:109000846 | G | A | 1 | a0001c0004t0005g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547-173C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000846 | |||||||
| chr6:109000980 | A | C | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.547-307T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109000980 | |||||||
| chr6:109001163 | G | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.546+125C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109001163 | |||||||
| chr6:109001274 | G | C | 27 | a0001c0003t0002g0182 a0002c0002t0002g0013 a0002c0002t0002g0014 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.546+14C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 3/9 | chr6 | 109001274 | |||||||
| chr6:109001498 | T | TGA | 33 | a0001c0001t0010g0010 a0001c0003t0002g0182 a0001c0003t0004g0002 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.346-12_346-11dupTC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109001498 | |||||||
| chr6:109001751 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.346-263T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109001751 | |||||||
| chr6:109001929 | TC | T | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+348delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109001929 | |||||||
| chr6:109002016 | ATGT | A | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.345+259_345+261del others(3): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 2/9 | chr6 | 109002016 | |||||||
| chr6:109002378 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.280-35C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109002378 | |||||||
| chr6:109002720 | G | A | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280-377C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109002720 | |||||||
| chr6:109003150 | T | C | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-807A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003150 | |||||||
| chr6:109003250 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-907G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003250 | |||||||
| chr6:109003372 | T | TGGGGTG | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1035_280-1030d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003372 | |||||||
| chr6:109003499 | G | T | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-1156C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003499 | |||||||
| chr6:109003715 | TA | T | 2 | a0001c0001t0008g0051 a0001c0001t0008g0052 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-1373delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003715 | |||||||
| chr6:109003782 | G | GCCATTTA others(4): Show |
1 | a0002c0002t0002g0037 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.280-1450_280-1440d others(13): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109003782 | |||||||
| chr6:109004011 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-1668C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004011 | |||||||
| chr6:109004014 | T | C | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.280-1671A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004014 | |||||||
| chr6:109004421 | C | A | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-2078G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004421 | |||||||
| chr6:109004422 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.280-2079C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004422 | |||||||
| chr6:109004438 | C | CT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0179 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-2096dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004438 | |||||||
| chr6:109004584 | C | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-2241G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004584 | |||||||
| chr6:109004608 | TTTTAGTA others(2): Show |
T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-2274_280-2266d others(11): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004608 | |||||||
| chr6:109004618 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-2275C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004618 | |||||||
| chr6:109004622 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-2279C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004622 | |||||||
| chr6:109004682 | G | A | 17 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(14): Show |
17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-2339C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004682 | |||||||
| chr6:109004719 | G | A | 8 | a0002c0002t0002g0035 a0002c0002t0002g0037 a0002c0002t0002g0038 others(5): Show |
8 | HG00438.hp1 NA18951.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-2376C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004719 | |||||||
| chr6:109004759 | C | CACAG | 39 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(36): Show |
39 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.280-2420_280-2417d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004759 | |||||||
| chr6:109004931 | T | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0115 a0001c0001t0001g0128 others(1): Show |
4 | HG00323.hp2 HG02523.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-2588A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004931 | |||||||
| chr6:109004980 | A | T | 40 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.280-2637T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109004980 | |||||||
| chr6:109005418 | T | G | 32 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-3075A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005418 | |||||||
| chr6:109005537 | A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-3194T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005537 | |||||||
| chr6:109005596 | T | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-3253A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005596 | |||||||
| chr6:109005632 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280-3289C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005632 | |||||||
| chr6:109005685 | G | A | 1 | a0002c0002t0002g0041 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.280-3342C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005685 | |||||||
| chr6:109005707 | C | T | 2 | a0001c0001t0008g0051 a0001c0001t0008g0052 |
2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-3364G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005707 | |||||||
| chr6:109005727 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.280-3384A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109005727 | |||||||
| chr6:109006084 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280-3741G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006084 | |||||||
| chr6:109006205 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-3862T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006205 | |||||||
| chr6:109006280 | A | C | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.280-3937T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006280 | |||||||
| chr6:109006336 | A | C | 1 | a0001c0003t0004g0003 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280-3993T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006336 | |||||||
| chr6:109006379 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.280-4036T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006379 | |||||||
| chr6:109006387 | T | G | 1 | a0002c0002t0002g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.280-4044A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006387 | |||||||
| chr6:109006449 | A | T | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.280-4106T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006449 | |||||||
| chr6:109006469 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.280-4126G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109006469 | |||||||
| chr6:109007040 | T | C | 2 | a0002c0002t0002g0028 a0002c0002t0002g0029 |
2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.280-4697A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007040 | |||||||
| chr6:109007225 | CTA | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.280-4884_280-4883d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007225 | |||||||
| chr6:109007229 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-4886C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007229 | |||||||
| chr6:109007309 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0094 others(5): Show |
8 | HG02083.hp2 HG02129.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-4966A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007309 | |||||||
| chr6:109007556 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.280-5213G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007556 | |||||||
| chr6:109007570 | G | A | 1 | a0001c0001t0003g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.280-5227C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007570 | |||||||
| chr6:109007718 | ACTAAC | A | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5380_280-5376d others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007718 | |||||||
| chr6:109007723 | C | T | 2 | a0001c0001t0003g0167 a0001c0001t0003g0171 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.280-5380G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007723 | |||||||
| chr6:109007724 | A | T | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5381T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007724 | |||||||
| chr6:109007773 | A | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-5430T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007773 | |||||||
| chr6:109007785 | CT | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(17): Show |
20 | HG01257.hp2 HG02004.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.280-5443delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007785 | |||||||
| chr6:109007785 | CTT | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-5444_280-5443d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007785 | |||||||
| chr6:109007785 | CTTTTTT | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-5448_280-5443d others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007785 | |||||||
| chr6:109007857 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.280-5514C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109007857 | |||||||
| chr6:109008130 | C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-5787G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008130 | |||||||
| chr6:109008187 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.280-5844C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008187 | |||||||
| chr6:109008270 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-5927C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008270 | |||||||
| chr6:109008334 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.280-5991A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008334 | |||||||
| chr6:109008438 | A | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-6095T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008438 | |||||||
| chr6:109008450 | AT | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-6108delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008450 | |||||||
| chr6:109008454 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280-6111A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008454 | |||||||
| chr6:109008792 | C | T | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.280-6449G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008792 | |||||||
| chr6:109008803 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-6460C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008803 | |||||||
| chr6:109008916 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.280-6573C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008916 | |||||||
| chr6:109008977 | C | A | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.280-6634G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109008977 | |||||||
| chr6:109009164 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-6821T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009164 | |||||||
| chr6:109009214 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-6871G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009214 | |||||||
| chr6:109009515 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-7172G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009515 | |||||||
| chr6:109009532 | A | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-7189T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009532 | |||||||
| chr6:109009656 | C | T | 61 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.280-7313G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009656 | |||||||
| chr6:109009725 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.280-7382T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109009725 | |||||||
| chr6:109010306 | C | A | 18 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(15): Show |
18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-7963G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010306 | |||||||
| chr6:109010355 | TTC | T | 2 | a0001c0001t0001g0130 a0001c0001t0003g0131 |
2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.280-8014_280-8013d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010355 | |||||||
| chr6:109010574 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-8231T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010574 | |||||||
| chr6:109010672 | T | C | 9 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0001c0001t0001g0143 others(6): Show |
9 | HG02293.hp1 HG02818.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-8329A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109010672 | |||||||
| chr6:109011008 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-8665T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011008 | |||||||
| chr6:109011136 | C | G | 2 | a0001c0001t0006g0070 a0001c0001t0006g0091 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.280-8793G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011136 | |||||||
| chr6:109011467 | T | C | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.280-9124A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011467 | |||||||
| chr6:109011494 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280-9151T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011494 | |||||||
| chr6:109011632 | CT | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-9290delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011632 | |||||||
| chr6:109011660 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.280-9317G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011660 | |||||||
| chr6:109011792 | C | A | 2 | a0001c0004t0005g0020 a0001c0004t0005g0021 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.280-9449G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011792 | |||||||
| chr6:109011843 | G | A | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.280-9500C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011843 | |||||||
| chr6:109011892 | G | C | 1 | a0002c0002t0002g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.280-9549C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011892 | |||||||
| chr6:109011904 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-9561G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011904 | |||||||
| chr6:109011927 | C | T | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-9584G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109011927 | |||||||
| chr6:109012244 | C | CT | 7 | a0001c0001t0001g0063 a0001c0003t0004g0002 a0001c0003t0004g0003 others(4): Show |
7 | HG00639.hp2 HG02572.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-9902dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012244 | |||||||
| chr6:109012623 | A | T | 17 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(14): Show |
17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-10280T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012623 | |||||||
| chr6:109012881 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-10538C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012881 | |||||||
| chr6:109012933 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-10590C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012933 | |||||||
| chr6:109012959 | C | CA | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-10617dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109012959 | |||||||
| chr6:109013097 | AG | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-10755delC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013097 | |||||||
| chr6:109013100 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-10757C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013100 | |||||||
| chr6:109013255 | C | G | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-10912G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013255 | |||||||
| chr6:109013434 | T | G | 12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.280-11091A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013434 | |||||||
| chr6:109013520 | A | C | 1 | a0002c0002t0002g0032 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.280-11177T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013520 | |||||||
| chr6:109013768 | C | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-11425G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013768 | |||||||
| chr6:109013906 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0105 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-11563A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109013906 | |||||||
| chr6:109014157 | G | A | 3 | a0002c0002t0002g0032 a0002c0002t0002g0033 a0002c0002t0002g0044 |
3 | HG00280.hp2 HG01123.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.280-11814C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014157 | |||||||
| chr6:109014239 | A | G | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-11896T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014239 | |||||||
| chr6:109014257 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-11914C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014257 | |||||||
| chr6:109014431 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.280-12088C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014431 | |||||||
| chr6:109014743 | T | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0058 others(12): Show |
15 | HG01257.hp2 HG02004.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-12400A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014743 | |||||||
| chr6:109014766 | C | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-12423G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014766 | |||||||
| chr6:109014848 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-12505C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109014848 | |||||||
| chr6:109015414 | A | G | 26 | a0001c0001t0001g0049 a0002c0002t0002g0013 a0002c0002t0002g0014 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-13071T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109015414 | |||||||
| chr6:109015777 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.280-13434G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109015777 | |||||||
| chr6:109016368 | T | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-14025A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016368 | |||||||
| chr6:109016520 | G | A | 29 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-14177C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016520 | |||||||
| chr6:109016574 | G | A | 2 | a0001c0004t0005g0022 a0001c0004t0005g0023 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.280-14231C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016574 | |||||||
| chr6:109016907 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14564A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016907 | |||||||
| chr6:109016944 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14601G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016944 | |||||||
| chr6:109016958 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14615A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016958 | |||||||
| chr6:109016984 | C | T | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.280-14641G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109016984 | |||||||
| chr6:109017198 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280-14855A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109017198 | |||||||
| chr6:109017230 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-14887G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109017230 | |||||||
| chr6:109017580 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0003g0131 |
2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.280-15237G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109017580 | |||||||
| chr6:109018280 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.280-15937T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018280 | |||||||
| chr6:109018311 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.280-15968A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018311 | |||||||
| chr6:109018314 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.280-15971G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018314 | |||||||
| chr6:109018569 | AG | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-16227delC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018569 | |||||||
| chr6:109018732 | CA | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0177 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.280-16390delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018732 | |||||||
| chr6:109018925 | C | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-16582G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109018925 | |||||||
| chr6:109019078 | TTAAA | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-16739_280-1673 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019078 | |||||||
| chr6:109019088 | C | T | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-16745G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019088 | |||||||
| chr6:109019343 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.280-17000T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019343 | |||||||
| chr6:109019355 | G | A | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-17012C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019355 | |||||||
| chr6:109019495 | A | T | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-17152T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019495 | |||||||
| chr6:109019611 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280-17268T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019611 | |||||||
| chr6:109019670 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-17327T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019670 | |||||||
| chr6:109019965 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-17622G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109019965 | |||||||
| chr6:109020095 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-17752T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020095 | |||||||
| chr6:109020175 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.280-17832C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020175 | |||||||
| chr6:109020192 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.280-17849A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020192 | |||||||
| chr6:109020589 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-18246T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020589 | |||||||
| chr6:109020631 | C | T | 65 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.280-18288G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020631 | |||||||
| chr6:109020638 | GAGA | G | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-18298_280-1829 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020638 | |||||||
| chr6:109020796 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.280-18453G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020796 | |||||||
| chr6:109020966 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-18623A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109020966 | |||||||
| chr6:109021330 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.280-18987A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021330 | |||||||
| chr6:109021440 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.280-19097C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021440 | |||||||
| chr6:109021456 | T | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0123 |
2 | HG01168.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.280-19113A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021456 | |||||||
| chr6:109021490 | T | G | 26 | a0001c0001t0001g0049 a0002c0002t0002g0013 a0002c0002t0002g0014 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-19147A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021490 | |||||||
| chr6:109021554 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.280-19211G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021554 | |||||||
| chr6:109021596 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-19253G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109021596 | |||||||
| chr6:109022049 | A | ATT | 26 | a0001c0001t0001g0049 a0002c0002t0002g0013 a0002c0002t0002g0014 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-19708_280-1970 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022049 | |||||||
| chr6:109022137 | A | T | 65 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.280-19794T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022137 | |||||||
| chr6:109022353 | C | T | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.280-20010G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022353 | |||||||
| chr6:109022411 | C | CT | 19 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0054 others(16): Show |
19 | HG01109.hp2 HG01361.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.280-20069dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | |||||||
| chr6:109022411 | CT | C | 24 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0067 others(21): Show |
24 | HG00323.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.280-20069delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | |||||||
| chr6:109022411 | CTT | C | 37 | a0001c0001t0001g0019 a0001c0001t0001g0060 a0001c0001t0001g0063 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.280-20070_280-2006 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | |||||||
| chr6:109022411 | CTTTTTT | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-20074_280-2006 others(10): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | |||||||
| chr6:109022411 | CTTTTTTT others(1): Show |
C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-20076_280-2006 others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | |||||||
| chr6:109022411 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-20078_280-2006 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022411 | |||||||
| chr6:109022445 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-20102A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022445 | |||||||
| chr6:109022537 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.280-20194G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022537 | |||||||
| chr6:109022549 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-20206G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022549 | |||||||
| chr6:109022599 | A | G | 1 | a0002c0002t0002g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.280-20256T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022599 | |||||||
| chr6:109022642 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-20299G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109022642 | |||||||
| chr6:109023402 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-21059G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023402 | |||||||
| chr6:109023436 | A | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-21093T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023436 | |||||||
| chr6:109023458 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280-21115A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023458 | |||||||
| chr6:109023772 | T | G | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-21429A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023772 | |||||||
| chr6:109023838 | AAAT | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-21498_280-2149 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023838 | |||||||
| chr6:109023863 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-21520G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109023863 | |||||||
| chr6:109024288 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-21945C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024288 | |||||||
| chr6:109024727 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-22384A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024727 | |||||||
| chr6:109024889 | T | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.280-22546A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024889 | |||||||
| chr6:109024981 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-22638T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109024981 | |||||||
| chr6:109025303 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.280-22960G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025303 | |||||||
| chr6:109025415 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-23072T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025415 | |||||||
| chr6:109025747 | A | G | 9 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0001c0001t0001g0143 others(6): Show |
9 | HG02293.hp1 HG02523.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.280-23404T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025747 | |||||||
| chr6:109025854 | A | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-23511T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025854 | |||||||
| chr6:109025951 | C | CT | 31 | a0001c0001t0001g0049 a0001c0001t0003g0166 a0001c0001t0010g0010 others(28): Show |
31 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.280-23609dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025951 | |||||||
| chr6:109025951 | C | CTT | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-23610_280-2360 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109025951 | |||||||
| chr6:109026059 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-23716G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026059 | |||||||
| chr6:109026119 | A | G | 3 | a0001c0001t0008g0050 a0001c0001t0008g0051 a0001c0001t0008g0052 |
3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-23776T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026119 | |||||||
| chr6:109026528 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-24185G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026528 | |||||||
| chr6:109026609 | A | T | 2 | a0001c0003t0004g0005 a0001c0003t0004g0006 |
2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.280-24266T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026609 | |||||||
| chr6:109026672 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280-24329A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026672 | |||||||
| chr6:109026690 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-24347G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026690 | |||||||
| chr6:109026724 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.280-24381G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026724 | |||||||
| chr6:109026756 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.280-24413C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026756 | |||||||
| chr6:109026777 | G | A | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-24434C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026777 | |||||||
| chr6:109026798 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.280-24455G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026798 | |||||||
| chr6:109026943 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(168): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.280-24600T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109026943 | |||||||
| chr6:109027084 | C | T | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280-24741G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027084 | |||||||
| chr6:109027434 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0179 a0001c0001t0008g0050 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-25091C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027434 | |||||||
| chr6:109027476 | C | CA | 10 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0124 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-25134dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | |||||||
| chr6:109027476 | C | CAAA | 6 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(3): Show |
6 | HG00280.hp2 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-25136_280-2513 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | |||||||
| chr6:109027476 | C | CAAAA | 21 | a0001c0001t0001g0147 a0001c0003t0002g0182 a0001c0003t0004g0005 others(18): Show |
21 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.280-25137_280-2513 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | |||||||
| chr6:109027476 | C | CAAAAA | 6 | a0001c0001t0001g0049 a0002c0002t0002g0014 a0002c0002t0002g0026 others(3): Show |
6 | HG00438.hp1 HG00639.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-25138_280-2513 others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | |||||||
| chr6:109027476 | CA | C | 11 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG00099.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.280-25134delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109027476 | |||||||
| chr6:109028152 | TC | T | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-25810delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028152 | |||||||
| chr6:109028223 | G | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0148 |
2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.280-25880C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028223 | |||||||
| chr6:109028593 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.280-26250C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028593 | |||||||
| chr6:109028690 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-26347C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028690 | |||||||
| chr6:109028925 | C | A | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-26582G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028925 | |||||||
| chr6:109028979 | T | C | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-26636A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109028979 | |||||||
| chr6:109029018 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-26675T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029018 | |||||||
| chr6:109029087 | C | T | 26 | a0001c0001t0001g0049 a0002c0002t0002g0013 a0002c0002t0002g0014 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-26744G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029087 | |||||||
| chr6:109029148 | G | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-26805C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029148 | |||||||
| chr6:109029178 | T | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0086 |
2 | HG00738.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.280-26835A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029178 | |||||||
| chr6:109029286 | G | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-26943C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029286 | |||||||
| chr6:109029316 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.280-26973G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029316 | |||||||
| chr6:109029347 | T | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-27004A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029347 | |||||||
| chr6:109029413 | A | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-27070T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029413 | |||||||
| chr6:109029590 | G | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-27247C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029590 | |||||||
| chr6:109029638 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.280-27295G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029638 | |||||||
| chr6:109029656 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.280-27313G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029656 | |||||||
| chr6:109029922 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-27579T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109029922 | |||||||
| chr6:109030556 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.280-28213A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109030556 | |||||||
| chr6:109031342 | G | A | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-28999C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031342 | |||||||
| chr6:109031401 | C | A | 1 | a0002c0002t0002g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.280-29058G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031401 | |||||||
| chr6:109031415 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG00280.hp1 HG02258.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.280-29072G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031415 | |||||||
| chr6:109031498 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-29155G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031498 | |||||||
| chr6:109031552 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-29209C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031552 | |||||||
| chr6:109031596 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.280-29253G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031596 | |||||||
| chr6:109031702 | T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-29359A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109031702 | |||||||
| chr6:109032013 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-29670G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032013 | |||||||
| chr6:109032204 | G | A | 26 | a0001c0001t0001g0049 a0002c0002t0002g0013 a0002c0002t0002g0014 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-29861C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032204 | |||||||
| chr6:109032210 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-29867A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032210 | |||||||
| chr6:109032212 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-29869G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032212 | |||||||
| chr6:109032226 | A | C | 65 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.280-29883T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032226 | |||||||
| chr6:109032244 | C | T | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-29901G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032244 | |||||||
| chr6:109032316 | C | A | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-29973G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032316 | |||||||
| chr6:109032351 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-30008C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032351 | |||||||
| chr6:109032378 | G | C | 1 | a0002c0002t0002g0041 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.280-30035C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032378 | |||||||
| chr6:109032617 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-30274G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032617 | |||||||
| chr6:109032619 | T | TG | 34 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(31): Show |
34 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.280-30277dupC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032619 | |||||||
| chr6:109032659 | T | C | 5 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(2): Show |
5 | HG01891.hp2 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-30316A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109032659 | |||||||
| chr6:109033657 | G | T | 28 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(25): Show |
28 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-31314C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109033657 | |||||||
| chr6:109033706 | T | C | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-31363A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109033706 | |||||||
| chr6:109033823 | A | C | 1 | a0001c0001t0003g0165 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.280-31480T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109033823 | |||||||
| chr6:109034158 | T | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-31815A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034158 | |||||||
| chr6:109034469 | T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-32126A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034469 | |||||||
| chr6:109034514 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-32171A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034514 | |||||||
| chr6:109034587 | G | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-32244C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034587 | |||||||
| chr6:109034683 | A | G | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-32340T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034683 | |||||||
| chr6:109034808 | C | G | 28 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(25): Show |
28 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-32465G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034808 | |||||||
| chr6:109034901 | A | T | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-32558T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109034901 | |||||||
| chr6:109035386 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-33043G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035386 | |||||||
| chr6:109035548 | G | GA | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-33206dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035548 | |||||||
| chr6:109035794 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-33451C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035794 | |||||||
| chr6:109035887 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-33544G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109035887 | |||||||
| chr6:109036121 | G | T | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-33778C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036121 | |||||||
| chr6:109036498 | T | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-34155A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036498 | |||||||
| chr6:109036626 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-34283T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036626 | |||||||
| chr6:109036936 | TA | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 others(1): Show |
4 | HG01168.hp1 HG02486.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-34594delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109036936 | |||||||
| chr6:109037043 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.280-34700A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037043 | |||||||
| chr6:109037142 | C | G | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-34799G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037142 | |||||||
| chr6:109037587 | T | G | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.280-35244A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037587 | |||||||
| chr6:109037911 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-35568A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037911 | |||||||
| chr6:109037914 | GCTGA | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-35575_280-3557 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109037914 | |||||||
| chr6:109038484 | GC | G | 66 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.280-36142delG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038484 | |||||||
| chr6:109038760 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-36417C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038760 | |||||||
| chr6:109038911 | A | AAGG | 29 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.280-36571_280-3656 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038911 | |||||||
| chr6:109038911 | A | AAGGAGG | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-36574_280-3656 others(10): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038911 | |||||||
| chr6:109038985 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-36642T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109038985 | |||||||
| chr6:109039041 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-36698T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039041 | |||||||
| chr6:109039045 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-36702T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039045 | |||||||
| chr6:109039046 | G | A | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-36703C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039046 | |||||||
| chr6:109039046 | G | GGGA | 103 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.280-36706_280-3670 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039046 | |||||||
| chr6:109039154 | G | GAGGAGAA others(9): Show |
32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-36812_280-3681 others(20): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039154 | |||||||
| chr6:109039407 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.280-37064A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039407 | |||||||
| chr6:109039502 | C | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-37159G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039502 | |||||||
| chr6:109039545 | T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-37202A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039545 | |||||||
| chr6:109039641 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-37298A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039641 | |||||||
| chr6:109039742 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.280-37399G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109039742 | |||||||
| chr6:109040224 | A | G | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-37881T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040224 | |||||||
| chr6:109040292 | C | T | 3 | a0001c0001t0008g0050 a0001c0001t0008g0051 a0001c0001t0008g0052 |
3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-37949G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040292 | |||||||
| chr6:109040329 | CTG | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-37988_280-3798 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040329 | |||||||
| chr6:109040519 | G | C | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-38176C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040519 | |||||||
| chr6:109040572 | C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-38229G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040572 | |||||||
| chr6:109040657 | C | CT | 6 | a0001c0001t0010g0010 a0001c0004t0005g0020 a0001c0004t0005g0021 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-38315dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040657 | |||||||
| chr6:109040657 | C | CTT | 31 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(28): Show |
31 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.280-38316_280-3831 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040657 | |||||||
| chr6:109040714 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-38371C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040714 | |||||||
| chr6:109040935 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-38592T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040935 | |||||||
| chr6:109040962 | T | A | 2 | a0001c0001t0006g0070 a0001c0001t0006g0091 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.280-38619A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040962 | |||||||
| chr6:109040999 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-38656C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109040999 | |||||||
| chr6:109041042 | C | T | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-38699G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041042 | |||||||
| chr6:109041047 | T | A | 1 | a0001c0001t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.280-38704A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041047 | |||||||
| chr6:109041133 | T | C | 1 | a0002c0002t0002g0035 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.280-38790A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041133 | |||||||
| chr6:109041138 | T | TA | 5 | a0001c0001t0001g0126 a0001c0004t0005g0020 a0001c0004t0005g0021 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-38796dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041138 | |||||||
| chr6:109041138 | TA | T | 33 | a0001c0001t0001g0049 a0001c0001t0003g0176 a0001c0001t0003g0178 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-38796delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041138 | |||||||
| chr6:109041149 | A | C | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-38806T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041149 | |||||||
| chr6:109041324 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280-38981A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041324 | |||||||
| chr6:109041524 | AT | A | 27 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.280-39182delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041524 | |||||||
| chr6:109041546 | T | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-39203A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041546 | |||||||
| chr6:109041921 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.280-39578A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109041921 | |||||||
| chr6:109042014 | C | T | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-39671G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042014 | |||||||
| chr6:109042171 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-39828T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042171 | |||||||
| chr6:109042177 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-39834A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042177 | |||||||
| chr6:109042312 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | NA19012.hp2 NA19063.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-39969A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042312 | |||||||
| chr6:109042442 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.280-40099T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042442 | |||||||
| chr6:109042530 | C | CA | 36 | a0001c0001t0001g0049 a0001c0001t0001g0073 a0001c0001t0001g0088 others(33): Show |
36 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.280-40188_280-4018 others(5): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042530 | |||||||
| chr6:109042531 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.280-40188C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042531 | |||||||
| chr6:109042768 | A | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0100 |
3 | HG00140.hp2 HG01123.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.280-40425T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042768 | |||||||
| chr6:109042868 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-40525T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109042868 | |||||||
| chr6:109043463 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-41120T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109043463 | |||||||
| chr6:109043495 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-41152A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109043495 | |||||||
| chr6:109043622 | G | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-41279C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109043622 | |||||||
| chr6:109044054 | C | T | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-41711G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044054 | |||||||
| chr6:109044064 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-41721G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044064 | |||||||
| chr6:109044122 | C | T | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-41779G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044122 | |||||||
| chr6:109044191 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.280-41848C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044191 | |||||||
| chr6:109044213 | G | A | 1 | a0002c0002t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.280-41870C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044213 | |||||||
| chr6:109044311 | C | CA | 32 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0034 others(29): Show |
33 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-41969dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | C | CAA | 15 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0024 others(12): Show |
15 | HG01891.hp1 HG02004.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.280-41970_280-4196 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | C | CAAA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0071 others(4): Show |
7 | HG02027.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-41971_280-4196 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | CA | C | 13 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0077 others(10): Show |
13 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.280-41969delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | CAAAAAAA | C | 7 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(4): Show |
7 | HG02027.hp2 HG02572.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-41975_280-4196 others(11): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | CAAAAAAA others(1): Show |
C | 17 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0125 others(14): Show |
17 | HG01109.hp1 HG01169.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.280-41976_280-4196 others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0003g0135 a0001c0001t0010g0010 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.280-41978_280-4196 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | CAAAAAAA others(6): Show |
C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-41981_280-4196 others(17): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | CAAAAAAA others(11): Show |
C | 27 | a0001c0001t0001g0049 a0001c0001t0001g0087 a0001c0003t0002g0182 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-41986_280-4196 others(22): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044311 | CAAAAAAA others(12): Show |
C | 1 | a0002c0002t0002g0037 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.280-41987_280-4196 others(23): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044311 | |||||||
| chr6:109044430 | C | T | 1 | a0001c0001t0011g0146 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.280-42087G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044430 | |||||||
| chr6:109044556 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.280-42213T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044556 | |||||||
| chr6:109044572 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280-42229T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044572 | |||||||
| chr6:109044708 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-42365G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044708 | |||||||
| chr6:109044868 | A | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.280-42525T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044868 | |||||||
| chr6:109044884 | G | A | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-42541C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044884 | |||||||
| chr6:109044891 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-42548G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044891 | |||||||
| chr6:109044980 | G | A | 1 | a0001c0003t0004g0004 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.280-42637C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109044980 | |||||||
| chr6:109045103 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.280-42760C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045103 | |||||||
| chr6:109045212 | A | G | 2 | a0001c0005t0001g0008 a0001c0005t0001g0009 |
2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.280-42869T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045212 | |||||||
| chr6:109045291 | CT | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-42949delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045291 | |||||||
| chr6:109045319 | C | T | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-42976G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045319 | |||||||
| chr6:109045423 | C | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-43080G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045423 | |||||||
| chr6:109045454 | GCATATAA others(3): Show |
G | 33 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(30): Show |
33 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.280-43121_280-4311 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045454 | |||||||
| chr6:109045480 | C | G | 14 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(11): Show |
14 | HG01106.hp2 HG01361.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.280-43137G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045480 | |||||||
| chr6:109045536 | A | G | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-43193T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045536 | |||||||
| chr6:109045537 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-43194C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045537 | |||||||
| chr6:109045628 | A | G | 18 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(15): Show |
18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-43285T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045628 | |||||||
| chr6:109045750 | T | C | 15 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(12): Show |
15 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-43407A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045750 | |||||||
| chr6:109045854 | TAC | T | 3 | a0001c0001t0008g0050 a0001c0001t0008g0051 a0001c0001t0008g0052 |
3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.280-43513_280-4351 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045854 | |||||||
| chr6:109045860 | G | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-43517C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045860 | |||||||
| chr6:109045966 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-43623G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109045966 | |||||||
| chr6:109046027 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.280-43684A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046027 | |||||||
| chr6:109046052 | T | C | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-43709A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046052 | |||||||
| chr6:109046084 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0113 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.280-43741T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046084 | |||||||
| chr6:109046100 | G | GCCCTCT | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-43763_280-4375 others(10): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046100 | |||||||
| chr6:109046141 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-43798C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046141 | |||||||
| chr6:109046157 | T | G | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.280-43814A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046157 | |||||||
| chr6:109046229 | G | A | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-43886C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046229 | |||||||
| chr6:109046229 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0109 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.280-43886C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046229 | |||||||
| chr6:109046294 | G | A | 16 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(13): Show |
16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-43951C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046294 | |||||||
| chr6:109046343 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.280-44000G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046343 | |||||||
| chr6:109046352 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-44009G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046352 | |||||||
| chr6:109046416 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44073T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046416 | |||||||
| chr6:109046451 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280-44108G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046451 | |||||||
| chr6:109046499 | C | T | 1 | a0001c0001t0003g0170 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.280-44156G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046499 | |||||||
| chr6:109046503 | A | AC | 5 | a0001c0001t0001g0144 a0001c0001t0003g0170 a0001c0004t0005g0022 others(2): Show |
5 | HG01169.hp2 HG02055.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44161dupG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046503 | |||||||
| chr6:109046540 | A | G | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44197T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046540 | |||||||
| chr6:109046602 | G | A | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-44259C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046602 | |||||||
| chr6:109046615 | C | T | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44272G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046615 | |||||||
| chr6:109046628 | A | G | 1 | a0002c0002t0002g0036 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.280-44285T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046628 | |||||||
| chr6:109046682 | G | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44339C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046682 | |||||||
| chr6:109046692 | G | A | 1 | a0001c0001t0008g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.280-44349C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046692 | |||||||
| chr6:109046720 | C | T | 7 | a0001c0001t0003g0161 a0001c0001t0003g0164 a0001c0001t0003g0165 others(4): Show |
7 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.280-44377G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046720 | |||||||
| chr6:109046757 | T | C | 34 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0010g0010 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.280-44414A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046757 | |||||||
| chr6:109046772 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG02109.hp1 HG02293.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-44429C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046772 | |||||||
| chr6:109046779 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.280-44436G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046779 | |||||||
| chr6:109046800 | C | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-44457G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046800 | |||||||
| chr6:109046856 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-44513G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046856 | |||||||
| chr6:109046859 | A | C | 4 | a0001c0001t0001g0101 a0001c0001t0001g0115 a0001c0001t0001g0128 others(1): Show |
4 | HG00323.hp2 HG02523.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-44516T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046859 | |||||||
| chr6:109046882 | T | C | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44539A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046882 | |||||||
| chr6:109046897 | G | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0114 others(2): Show |
5 | HG02083.hp2 NA18747.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-44554C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046897 | |||||||
| chr6:109046925 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44582C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046925 | |||||||
| chr6:109046928 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44585T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046928 | |||||||
| chr6:109046955 | G | A | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44612C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046955 | |||||||
| chr6:109046961 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44618T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046961 | |||||||
| chr6:109046965 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-44622C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046965 | |||||||
| chr6:109046986 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44643C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109046986 | |||||||
| chr6:109047006 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG00140.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.280-44663G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047006 | |||||||
| chr6:109047009 | T | C | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44666A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047009 | |||||||
| chr6:109047027 | A | ATCCGGGA others(92): Show |
1 | a0002c0002t0002g0029 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.280-44685_280-4468 others(103): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | |||||||
| chr6:109047027 | A | ATCCGGGA others(91): Show |
5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44685_280-4468 others(102): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | |||||||
| chr6:109047027 | A | ATCCGGGA others(91): Show |
25 | a0001c0001t0001g0049 a0002c0002t0002g0013 a0002c0002t0002g0014 others(22): Show |
25 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.280-44685_280-4468 others(102): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | |||||||
| chr6:109047027 | A | ATCCGGGA others(91): Show |
1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-44685_280-4468 others(102): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047027 | |||||||
| chr6:109047041 | T | TGGGGGGG others(671): Show |
1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(671): Show |
1 | a0001c0001t0003g0164 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(673): Show |
1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(684): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
1 | a0001c0001t0003g0161 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(671): Show |
1 | a0001c0001t0001g0061 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
11 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0067 others(8): Show |
11 | HG01106.hp2 HG01361.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(671): Show |
2 | a0001c0001t0001g0060 a0001c0001t0001g0094 |
2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
2 | a0001c0001t0003g0160 a0001c0001t0003g0162 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(493): Show |
4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(504): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(493): Show |
1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(504): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(495): Show |
1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(506): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
1 | a0001c0001t0003g0171 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
15 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(12): Show |
15 | HG02027.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(1071): Show |
2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG01109.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(1082): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(671): Show |
1 | a0001c0001t0001g0128 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
4 | a0001c0001t0001g0122 a0001c0001t0006g0070 a0001c0001t0006g0091 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0113 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
1 | a0001c0001t0001g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(670): Show |
85 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.280-44699_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(671): Show |
1 | a0001c0001t0001g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047041 | T | TGGGGGGT others(671): Show |
1 | a0001c0005t0001g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.280-44699_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047041 | |||||||
| chr6:109047042 | G | GGGGGGTC others(671): Show |
2 | a0001c0004t0005g0020 a0001c0004t0005g0021 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.280-44700_280-4469 others(682): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047042 | |||||||
| chr6:109047042 | G | GGGGGGTC others(670): Show |
3 | a0001c0001t0013g0015 a0001c0004t0005g0022 a0001c0004t0005g0023 |
3 | HG01168.hp2 HG01169.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.280-44700_280-4469 others(681): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047042 | |||||||
| chr6:109047055 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44712A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047055 | |||||||
| chr6:109047058 | A | G | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44715T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047058 | |||||||
| chr6:109047075 | A | G | 28 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-44732T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047075 | |||||||
| chr6:109047078 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44735A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047078 | |||||||
| chr6:109047135 | T | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44792A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047135 | |||||||
| chr6:109047139 | C | T | 33 | a0001c0001t0001g0049 a0001c0001t0001g0100 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-44796G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047139 | |||||||
| chr6:109047148 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44805C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047148 | |||||||
| chr6:109047152 | G | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44809C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047152 | |||||||
| chr6:109047157 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44814C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047157 | |||||||
| chr6:109047166 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-44823C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047166 | |||||||
| chr6:109047178 | G | GC | 28 | a0001c0001t0001g0049 a0001c0001t0003g0176 a0001c0003t0002g0182 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.280-44836dupG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047178 | |||||||
| chr6:109047184 | C | CCACCCGG others(347): Show |
5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44842_280-4484 others(358): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047184 | |||||||
| chr6:109047185 | G | A | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44842C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047185 | |||||||
| chr6:109047189 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44846C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047189 | |||||||
| chr6:109047201 | C | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44858G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047201 | |||||||
| chr6:109047231 | T | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44888A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047231 | |||||||
| chr6:109047237 | C | T | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44894G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047237 | |||||||
| chr6:109047247 | C | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-44904G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047247 | |||||||
| chr6:109047251 | G | A | 26 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.280-44908C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047251 | |||||||
| chr6:109047254 | T | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44911A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047254 | |||||||
| chr6:109047311 | T | A | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-44968A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047311 | |||||||
| chr6:109047312 | G | GCCTGGCC others(269): Show |
1 | a0002c0002t0002g0029 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.280-44970_280-4496 others(280): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047312 | |||||||
| chr6:109047312 | G | GCCTGGCC others(268): Show |
25 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(22): Show |
25 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.280-44970_280-4496 others(279): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047312 | |||||||
| chr6:109047312 | G | GCCTGGCC others(268): Show |
1 | a0002c0002t0002g0031 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.280-44970_280-4496 others(279): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047312 | |||||||
| chr6:109047316 | G | A | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.280-44973C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047316 | |||||||
| chr6:109047323 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-44980G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047323 | |||||||
| chr6:109047358 | C | T | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45015G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047358 | |||||||
| chr6:109047360 | T | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45017A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047360 | |||||||
| chr6:109047364 | C | T | 16 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(13): Show |
16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-45021G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047364 | |||||||
| chr6:109047373 | G | C | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-45030C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047373 | |||||||
| chr6:109047381 | C | T | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45038G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047381 | |||||||
| chr6:109047405 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-45062G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047405 | |||||||
| chr6:109047456 | A | G | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-45113T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047456 | |||||||
| chr6:109047499 | C | T | 28 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(25): Show |
28 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.280-45156G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047499 | |||||||
| chr6:109047505 | G | A | 1 | a0003c0006t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280-45162C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047505 | |||||||
| chr6:109047532 | C | T | 1 | a0001c0001t0003g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.280-45189G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047532 | |||||||
| chr6:109047650 | A | G | 2 | a0001c0004t0005g0022 a0001c0004t0005g0023 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.280-45307T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047650 | |||||||
| chr6:109047655 | G | C | 34 | a0001c0001t0001g0049 a0001c0001t0001g0118 a0001c0001t0010g0010 others(31): Show |
34 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.280-45312C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047655 | |||||||
| chr6:109047696 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280-45353C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047696 | |||||||
| chr6:109047745 | C | T | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-45402G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047745 | |||||||
| chr6:109047856 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-45513A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047856 | |||||||
| chr6:109047903 | G | C | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45560C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047903 | |||||||
| chr6:109047904 | G | A | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280-45561C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047904 | |||||||
| chr6:109047910 | A | AGTCATCA others(7): Show |
2 | a0001c0004t0005g0020 a0001c0004t0005g0021 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.280-45581_280-4556 others(18): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047910 | |||||||
| chr6:109047921 | C | A | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45578G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047921 | |||||||
| chr6:109047938 | C | A | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45595G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047938 | |||||||
| chr6:109047939 | C | T | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45596G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047939 | |||||||
| chr6:109047952 | C | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-45609G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047952 | |||||||
| chr6:109047966 | A | G | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.280-45623T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109047966 | |||||||
| chr6:109048043 | A | G | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.280-45700T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048043 | |||||||
| chr6:109048104 | TA | T | 45 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.279+45690delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048104 | |||||||
| chr6:109048104 | TAA | T | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0001t0013g0015 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.279+45689_279+4569 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048104 | |||||||
| chr6:109048106 | A | T | 16 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(13): Show |
16 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.279+45689T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048106 | |||||||
| chr6:109048200 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+45595A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048200 | |||||||
| chr6:109048367 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+45428T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048367 | |||||||
| chr6:109048542 | T | C | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+45253A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048542 | |||||||
| chr6:109048624 | G | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+45171C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048624 | |||||||
| chr6:109048637 | C | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+45158G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048637 | |||||||
| chr6:109048646 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+45149C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048646 | |||||||
| chr6:109048800 | T | C | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.279+44995A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048800 | |||||||
| chr6:109048803 | A | G | 53 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.279+44992T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048803 | |||||||
| chr6:109048824 | T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+44971A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109048824 | |||||||
| chr6:109049008 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.279+44787G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049008 | |||||||
| chr6:109049238 | T | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+44557A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049238 | |||||||
| chr6:109049287 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.279+44508G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049287 | |||||||
| chr6:109049486 | T | C | 22 | a0001c0001t0001g0053 a0001c0001t0001g0097 a0001c0001t0003g0135 others(19): Show |
22 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+44309A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049486 | |||||||
| chr6:109049620 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.279+44175G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049620 | |||||||
| chr6:109049650 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.279+44145T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049650 | |||||||
| chr6:109049694 | G | A | 2 | a0001c0001t0003g0167 a0001c0001t0003g0171 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.279+44101C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049694 | |||||||
| chr6:109049926 | T | C | 39 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(36): Show |
39 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.279+43869A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109049926 | |||||||
| chr6:109050371 | G | A | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.279+43424C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050371 | |||||||
| chr6:109050388 | T | TA | 38 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(35): Show |
38 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.279+43406dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050388 | |||||||
| chr6:109050388 | T | TAA | 14 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(11): Show |
14 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+43405_279+4340 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050388 | |||||||
| chr6:109050388 | TA | T | 6 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0117 others(3): Show |
6 | HG01168.hp1 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+43406delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050388 | |||||||
| chr6:109050460 | T | G | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.279+43335A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050460 | |||||||
| chr6:109050506 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+43289C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050506 | |||||||
| chr6:109050703 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.279+43092T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050703 | |||||||
| chr6:109050765 | ATCATAAG others(13): Show |
A | 1 | a0001c0001t0003g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.279+43010_279+4302 others(24): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050765 | |||||||
| chr6:109050863 | C | A | 1 | a0001c0001t0003g0166 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.279+42932G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050863 | |||||||
| chr6:109050917 | G | A | 32 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0001c0003t0004g0002 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.279+42878C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109050917 | |||||||
| chr6:109051150 | C | CA | 8 | a0001c0001t0008g0050 a0001c0001t0008g0051 a0001c0001t0008g0052 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+42644dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051150 | |||||||
| chr6:109051163 | C | CA | 26 | a0001c0001t0001g0049 a0001c0001t0012g0163 a0001c0003t0002g0182 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.279+42631dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051163 | |||||||
| chr6:109051172 | A | C | 3 | a0001c0001t0008g0050 a0001c0001t0008g0051 a0001c0001t0008g0052 |
3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.279+42623T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051172 | |||||||
| chr6:109051322 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.279+42473T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051322 | |||||||
| chr6:109051325 | GAGTC | G | 27 | a0001c0001t0001g0049 a0001c0003t0002g0182 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+42466_279+4246 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051325 | |||||||
| chr6:109051348 | T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+42447A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051348 | |||||||
| chr6:109051557 | C | T | 5 | a0001c0001t0001g0049 a0002c0002t0002g0027 a0002c0002t0002g0032 others(2): Show |
5 | HG00280.hp2 HG01123.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+42238G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051557 | |||||||
| chr6:109051559 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+42236G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109051559 | |||||||
| chr6:109052306 | T | TA | 5 | a0001c0001t0001g0019 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+41488dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109052306 | |||||||
| chr6:109052542 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.279+41253A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109052542 | |||||||
| chr6:109052798 | A | G | 1 | a0001c0001t0012g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.279+40997T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109052798 | |||||||
| chr6:109053022 | T | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18979.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.279+40773A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053022 | |||||||
| chr6:109053045 | G | GATGT | 3 | a0001c0001t0001g0179 a0001c0001t0008g0051 a0001c0001t0008g0052 |
3 | HG03453.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.279+40746_279+4074 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053045 | |||||||
| chr6:109053046 | A | ATG | 5 | a0001c0001t0001g0100 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+40747_279+4074 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053046 | |||||||
| chr6:109053046 | A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+40749T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053046 | |||||||
| chr6:109053262 | T | C | 33 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.279+40533A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053262 | |||||||
| chr6:109053353 | G | A | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+40442C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053353 | |||||||
| chr6:109053502 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0008g0051 a0001c0001t0008g0052 |
3 | HG03453.hp2 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.279+40293C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053502 | |||||||
| chr6:109053778 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.279+40017C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109053778 | |||||||
| chr6:109054078 | A | AT | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+39716dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054078 | |||||||
| chr6:109054084 | T | G | 18 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(15): Show |
18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+39711A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054084 | |||||||
| chr6:109054154 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+39641C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054154 | |||||||
| chr6:109054157 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+39638A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054157 | |||||||
| chr6:109054252 | G | A | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+39543C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054252 | |||||||
| chr6:109054370 | A | G | 1 | a0001c0001t0003g0180 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.279+39425T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054370 | |||||||
| chr6:109054387 | T | C | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+39408A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054387 | |||||||
| chr6:109054392 | T | A | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+39403A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054392 | |||||||
| chr6:109054736 | T | C | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.279+39059A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054736 | |||||||
| chr6:109054769 | A | AC | 66 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.279+39025dupG | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054769 | |||||||
| chr6:109054915 | T | C | 33 | a0001c0001t0001g0049 a0001c0001t0010g0010 a0001c0003t0002g0182 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.279+38880A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109054915 | |||||||
| chr6:109055117 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.279+38678A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055117 | |||||||
| chr6:109055218 | G | A | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.279+38577C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055218 | |||||||
| chr6:109055234 | G | C | 1 | a0002c0002t0002g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.279+38561C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055234 | |||||||
| chr6:109055269 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+38526G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055269 | |||||||
| chr6:109055421 | G | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0074 others(7): Show |
10 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+38374C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055421 | |||||||
| chr6:109055444 | C | G | 26 | a0001c0001t0001g0049 a0002c0002t0002g0013 a0002c0002t0002g0014 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.279+38351G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055444 | |||||||
| chr6:109055503 | A | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+38292T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055503 | |||||||
| chr6:109055505 | A | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0009g0007 |
3 | HG02109.hp2 HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.279+38290T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055505 | |||||||
| chr6:109055519 | C | T | 23 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(20): Show |
23 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.279+38276G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055519 | |||||||
| chr6:109055520 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+38275C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055520 | |||||||
| chr6:109055661 | C | CA | 31 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0018 others(28): Show |
31 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.279+38133dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055661 | |||||||
| chr6:109055661 | CA | C | 6 | a0001c0001t0003g0135 a0001c0001t0006g0070 a0001c0001t0006g0091 others(3): Show |
6 | HG02647.hp2 HG02735.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+38133delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055661 | |||||||
| chr6:109055830 | C | A | 66 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0053 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.279+37965G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055830 | |||||||
| chr6:109055838 | G | A | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+37957C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109055838 | |||||||
| chr6:109056185 | T | C | 1 | a0001c0001t0006g0091 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.279+37610A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056185 | |||||||
| chr6:109056262 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+37533G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056262 | |||||||
| chr6:109056408 | AAAC | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+37384_279+3738 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056408 | |||||||
| chr6:109056566 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+37229G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056566 | |||||||
| chr6:109056667 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+37128G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056667 | |||||||
| chr6:109056671 | T | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+37124A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056671 | |||||||
| chr6:109056848 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0123 |
3 | HG01168.hp1 HG02486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.279+36947C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109056848 | |||||||
| chr6:109057049 | C | A | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+36746G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057049 | |||||||
| chr6:109057169 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.279+36626C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057169 | |||||||
| chr6:109057285 | A | T | 1 | a0001c0004t0005g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.279+36510T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057285 | |||||||
| chr6:109057315 | G | C | 6 | a0001c0003t0002g0182 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03130.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+36480C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057315 | |||||||
| chr6:109057406 | G | A | 26 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.279+36389C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057406 | |||||||
| chr6:109057639 | T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+36156A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057639 | |||||||
| chr6:109057766 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.279+36029G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057766 | |||||||
| chr6:109057867 | G | A | 2 | a0001c0001t0006g0070 a0001c0001t0006g0091 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.279+35928C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109057867 | |||||||
| chr6:109058037 | C | CT | 15 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(12): Show |
15 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+35757dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058037 | |||||||
| chr6:109058147 | C | T | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+35648G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058147 | |||||||
| chr6:109058154 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279+35641C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058154 | |||||||
| chr6:109058579 | CTAGATGC others(3): Show |
C | 5 | a0001c0001t0013g0015 a0001c0004t0005g0020 a0001c0004t0005g0021 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+35206_279+3521 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058579 | |||||||
| chr6:109058623 | A | G | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+35172T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058623 | |||||||
| chr6:109058667 | ACCT | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+35125_279+3512 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058667 | |||||||
| chr6:109058705 | G | C | 14 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(11): Show |
14 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.279+35090C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058705 | |||||||
| chr6:109058752 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0148 |
2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.279+35043T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058752 | |||||||
| chr6:109058810 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.279+34985G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109058810 | |||||||
| chr6:109059096 | T | TAC | 6 | a0001c0001t0001g0145 a0001c0001t0001g0177 a0001c0001t0008g0051 others(3): Show |
6 | HG03453.hp2 HG03654.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+34697_279+3469 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059096 | |||||||
| chr6:109059096 | T | TACACACA others(11): Show |
4 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(1): Show |
4 | HG03225.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+34681_279+3469 others(22): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059096 | |||||||
| chr6:109059118 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0008g0050 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+34677A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059118 | |||||||
| chr6:109059431 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.279+34364C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059431 | |||||||
| chr6:109059710 | A | T | 7 | a0001c0001t0001g0126 a0001c0001t0008g0050 a0001c0003t0004g0002 others(4): Show |
7 | HG01891.hp2 HG02572.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+34085T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059710 | |||||||
| chr6:109059937 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+33858T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109059937 | |||||||
| chr6:109060210 | G | T | 2 | a0001c0005t0001g0008 a0001c0005t0001g0009 |
2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.279+33585C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109060210 | |||||||
| chr6:109060449 | G | T | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+33346C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109060449 | |||||||
| chr6:109060897 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+32898G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109060897 | |||||||
| chr6:109061170 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+32625A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109061170 | |||||||
| chr6:109061423 | A | G | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+32372T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109061423 | |||||||
| chr6:109061492 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.279+32303G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109061492 | |||||||
| chr6:109062071 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+31724A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062071 | |||||||
| chr6:109062197 | C | T | 24 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.279+31598G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062197 | |||||||
| chr6:109062364 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.279+31431G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062364 | |||||||
| chr6:109062373 | C | T | 20 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0001c0001t0001g0137 others(17): Show |
20 | HG00438.hp2 HG01099.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.279+31422G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062373 | |||||||
| chr6:109062424 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0076 a0001c0003t0004g0002 others(4): Show |
7 | HG02109.hp1 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+31371A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062424 | |||||||
| chr6:109062456 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0049 others(43): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.279+31339A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062456 | |||||||
| chr6:109062556 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+31239C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062556 | |||||||
| chr6:109062620 | C | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+31175G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062620 | |||||||
| chr6:109062924 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.279+30871T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109062924 | |||||||
| chr6:109063073 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279+30722A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063073 | |||||||
| chr6:109063109 | C | T | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+30686G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063109 | |||||||
| chr6:109063275 | G | GA | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+30519dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063275 | |||||||
| chr6:109063362 | C | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+30433G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063362 | |||||||
| chr6:109063433 | A | C | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.279+30362T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063433 | |||||||
| chr6:109063511 | T | C | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+30284A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063511 | |||||||
| chr6:109063615 | G | T | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+30180C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063615 | |||||||
| chr6:109063731 | T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+30064A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063731 | |||||||
| chr6:109063758 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.279+30037C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063758 | |||||||
| chr6:109063892 | T | TA | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29902dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109063892 | |||||||
| chr6:109064076 | T | C | 19 | a0001c0001t0001g0126 a0001c0001t0003g0135 a0001c0001t0003g0159 others(16): Show |
19 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.279+29719A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064076 | |||||||
| chr6:109064443 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+29352A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064443 | |||||||
| chr6:109064448 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29347T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064448 | |||||||
| chr6:109064576 | A | G | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+29219T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064576 | |||||||
| chr6:109064584 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0001g0086 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.279+29210_279+2921 others(20): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064584 | |||||||
| chr6:109064584 | A | AGAGGAGA others(28): Show |
1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+29210_279+2921 others(39): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064584 | |||||||
| chr6:109064584 | A | AGAGGGGA others(8): Show |
1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+29210_279+2921 others(19): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064584 | |||||||
| chr6:109064589 | A | AGAGGG | 52 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0053 others(49): Show |
52 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+29201_279+2920 others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | A | AGAGGGGA others(3): Show |
22 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(19): Show |
22 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+29196_279+2920 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | A | AGAGGGGA others(8): Show |
12 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+29191_279+2920 others(19): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | A | AGAGGGGA others(13): Show |
1 | a0001c0001t0001g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.279+29186_279+2920 others(24): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | A | AGAGGGGA others(18): Show |
1 | a0001c0001t0001g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.279+29181_279+2920 others(29): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | A | AGAGGGGA others(23): Show |
3 | a0002c0002t0002g0027 a0002c0002t0002g0032 a0002c0002t0002g0033 |
3 | HG00280.hp2 HG01175.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.279+29176_279+2920 others(34): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0179 a0001c0001t0006g0091 others(1): Show |
4 | HG00738.hp2 HG02647.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+29206T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | AGAGGG | A | 4 | a0001c0001t0001g0148 a0001c0001t0003g0135 a0001c0001t0003g0176 others(1): Show |
4 | HG01175.hp2 HG02258.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+29201_279+2920 others(9): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064589 | AGAGGGGA others(3): Show |
A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0150 |
2 | HG02523.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.279+29196_279+2920 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064589 | |||||||
| chr6:109064590 | G | GAGGGGAG others(3): Show |
15 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 others(12): Show |
15 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.279+29204_279+2920 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064590 | |||||||
| chr6:109064605 | G | A | 1 | a0001c0001t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.279+29190C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064605 | |||||||
| chr6:109064622 | G | GGGGAGGG others(17): Show |
1 | a0002c0002t0002g0044 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.279+29172_279+2917 others(28): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064622 | |||||||
| chr6:109064623 | GGGAGGGG others(8): Show |
G | 1 | a0002c0002t0002g0047 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.279+29157_279+2917 others(19): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064623 | |||||||
| chr6:109064629 | G | A | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+29166C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064629 | |||||||
| chr6:109064633 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29162C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064633 | |||||||
| chr6:109064638 | A | G | 32 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.279+29157T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064638 | |||||||
| chr6:109064782 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+29013G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064782 | |||||||
| chr6:109064903 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+28892C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064903 | |||||||
| chr6:109064954 | G | A | 27 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.279+28841C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109064954 | |||||||
| chr6:109065009 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.279+28786G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065009 | |||||||
| chr6:109065106 | G | A | 26 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.279+28689C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065106 | |||||||
| chr6:109065256 | TA | T | 30 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(27): Show |
30 | HG01109.hp1 HG01168.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.279+28538delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065256 | |||||||
| chr6:109065628 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+28167T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065628 | |||||||
| chr6:109065798 | A | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+27997T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065798 | |||||||
| chr6:109065809 | A | G | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+27986T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065809 | |||||||
| chr6:109065818 | A | T | 7 | a0002c0002t0002g0028 a0002c0002t0002g0029 a0002c0002t0002g0030 others(4): Show |
7 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+27977T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065818 | |||||||
| chr6:109065989 | A | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+27806T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109065989 | |||||||
| chr6:109066312 | CT | C | 16 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0001g0117 others(13): Show |
16 | HG01168.hp1 HG01168.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.279+27482delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066312 | |||||||
| chr6:109066414 | G | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+27381C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066414 | |||||||
| chr6:109066508 | C | T | 1 | a0001c0001t0003g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+27287G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066508 | |||||||
| chr6:109066883 | G | GTAAGTCA others(3): Show |
67 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(64): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+26911_279+2691 others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109066883 | |||||||
| chr6:109067034 | G | C | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+26761C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067034 | |||||||
| chr6:109067155 | C | T | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+26640G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067155 | |||||||
| chr6:109067212 | C | T | 52 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+26583G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067212 | |||||||
| chr6:109067396 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02280.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.279+26399A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067396 | |||||||
| chr6:109067410 | G | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+26385C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067410 | |||||||
| chr6:109067740 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+26055A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067740 | |||||||
| chr6:109067919 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.279+25876T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109067919 | |||||||
| chr6:109068006 | T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+25789A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068006 | |||||||
| chr6:109068048 | A | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25747T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068048 | |||||||
| chr6:109068062 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25733G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068062 | |||||||
| chr6:109068196 | T | C | 1 | a0001c0001t0003g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.279+25599A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068196 | |||||||
| chr6:109068305 | A | C | 67 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(64): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+25490T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068305 | |||||||
| chr6:109068333 | G | A | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+25462C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068333 | |||||||
| chr6:109068418 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25377T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068418 | |||||||
| chr6:109068477 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25318C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068477 | |||||||
| chr6:109068486 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.279+25309T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068486 | |||||||
| chr6:109068611 | T | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25184A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068611 | |||||||
| chr6:109068721 | C | CT | 18 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0079 others(15): Show |
18 | HG00280.hp1 HG01099.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.279+25073dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068721 | |||||||
| chr6:109068772 | G | A | 5 | a0001c0001t0013g0015 a0001c0004t0005g0020 a0001c0004t0005g0021 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+25023C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068772 | |||||||
| chr6:109068807 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.279+24988C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068807 | |||||||
| chr6:109068870 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+24925T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068870 | |||||||
| chr6:109068880 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+24915G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109068880 | |||||||
| chr6:109069021 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279+24774G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069021 | |||||||
| chr6:109069116 | T | C | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+24679A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069116 | |||||||
| chr6:109069173 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.279+24622C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069173 | |||||||
| chr6:109069206 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+24589C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069206 | |||||||
| chr6:109069304 | T | C | 2 | a0001c0004t0005g0022 a0001c0004t0005g0023 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.279+24491A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069304 | |||||||
| chr6:109069331 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.279+24464T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069331 | |||||||
| chr6:109069485 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.279+24310C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069485 | |||||||
| chr6:109069567 | G | C | 23 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.279+24228C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069567 | |||||||
| chr6:109069700 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.279+24095G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069700 | |||||||
| chr6:109069707 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.279+24088T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069707 | |||||||
| chr6:109069743 | A | AG | 30 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0093 others(27): Show |
30 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.279+24051dupC | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069743 | |||||||
| chr6:109069745 | G | C | 1 | a0001c0001t0014g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.279+24050C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069745 | |||||||
| chr6:109069871 | A | C | 1 | a0002c0002t0002g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.279+23924T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109069871 | |||||||
| chr6:109070095 | T | C | 1 | a0003c0006t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.279+23700A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070095 | |||||||
| chr6:109070111 | A | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+23684T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070111 | |||||||
| chr6:109070291 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.279+23504T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070291 | |||||||
| chr6:109070321 | T | G | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+23474A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070321 | |||||||
| chr6:109070538 | C | T | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+23257G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070538 | |||||||
| chr6:109070882 | T | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22913A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109070882 | |||||||
| chr6:109071238 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22557G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071238 | |||||||
| chr6:109071239 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.279+22556C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071239 | |||||||
| chr6:109071265 | A | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22530T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071265 | |||||||
| chr6:109071353 | C | CTTTTTTT others(1): Show |
5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+22434_279+2244 others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071353 | |||||||
| chr6:109071397 | T | C | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+22398A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071397 | |||||||
| chr6:109071434 | T | G | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+22361A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071434 | |||||||
| chr6:109071518 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.279+22277C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071518 | |||||||
| chr6:109071788 | C | T | 18 | a0001c0001t0003g0135 a0001c0001t0003g0159 a0001c0001t0003g0160 others(15): Show |
18 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+22007G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071788 | |||||||
| chr6:109071955 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.279+21840A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109071955 | |||||||
| chr6:109072077 | ATC | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+21716_279+2171 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072077 | |||||||
| chr6:109072195 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+21600A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072195 | |||||||
| chr6:109072351 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+21444A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072351 | |||||||
| chr6:109072452 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+21343G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072452 | |||||||
| chr6:109072672 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+21123A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072672 | |||||||
| chr6:109072899 | AT | A | 6 | a0001c0001t0001g0087 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG02683.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+20895delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072899 | |||||||
| chr6:109072964 | G | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+20831C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109072964 | |||||||
| chr6:109073011 | TTTTG | T | 28 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0001c0003t0002g0182 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+20780_279+2078 others(8): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073011 | |||||||
| chr6:109073065 | A | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02280.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.279+20730T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073065 | |||||||
| chr6:109073093 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+20702C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073093 | |||||||
| chr6:109073130 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.279+20665T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073130 | |||||||
| chr6:109073244 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+20551G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073244 | |||||||
| chr6:109073275 | C | T | 4 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0005 others(1): Show |
4 | HG02572.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+20520G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073275 | |||||||
| chr6:109073322 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.279+20473G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073322 | |||||||
| chr6:109073729 | A | G | 3 | a0001c0001t0006g0070 a0001c0001t0006g0091 a0001c0001t0006g0092 |
3 | HG01891.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.279+20066T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073729 | |||||||
| chr6:109073819 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.279+19976A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073819 | |||||||
| chr6:109073868 | C | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+19927G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109073868 | |||||||
| chr6:109074306 | A | ACC | 67 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(64): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+19487_279+1948 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074306 | |||||||
| chr6:109074559 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+19236A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074559 | |||||||
| chr6:109074607 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+19188T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074607 | |||||||
| chr6:109074699 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.279+19096A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074699 | |||||||
| chr6:109074744 | C | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.279+19051G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074744 | |||||||
| chr6:109074858 | T | C | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+18937A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074858 | |||||||
| chr6:109074981 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+18814T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109074981 | |||||||
| chr6:109075000 | A | T | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+18795T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075000 | |||||||
| chr6:109075125 | C | A | 1 | a0001c0001t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.279+18670G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075125 | |||||||
| chr6:109075140 | G | A | 24 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(21): Show |
24 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+18655C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075140 | |||||||
| chr6:109075723 | C | T | 57 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.279+18072G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075723 | |||||||
| chr6:109075806 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.279+17989A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075806 | |||||||
| chr6:109075868 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+17927C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109075868 | |||||||
| chr6:109076046 | C | T | 1 | a0001c0001t0016g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.279+17749G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076046 | |||||||
| chr6:109076222 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02630.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+17573A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076222 | |||||||
| chr6:109076224 | T | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+17571A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076224 | |||||||
| chr6:109076418 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02630.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.279+17377C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076418 | |||||||
| chr6:109076662 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+17133G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076662 | |||||||
| chr6:109076747 | A | G | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+17048T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109076747 | |||||||
| chr6:109077054 | C | T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+16741G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077054 | |||||||
| chr6:109077059 | C | T | 1 | a0001c0003t0004g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279+16736G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077059 | |||||||
| chr6:109077215 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+16580T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077215 | |||||||
| chr6:109077276 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0074 others(6): Show |
9 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+16519C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077276 | |||||||
| chr6:109077291 | C | A | 2 | a0001c0004t0005g0022 a0001c0004t0005g0023 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.279+16504G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077291 | |||||||
| chr6:109077302 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.279+16493A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077302 | |||||||
| chr6:109077533 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+16262G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077533 | |||||||
| chr6:109077552 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+16243A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077552 | |||||||
| chr6:109077651 | A | G | 1 | a0001c0001t0016g0183 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.279+16144T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109077651 | |||||||
| chr6:109078001 | T | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+15794A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078001 | |||||||
| chr6:109078170 | C | T | 67 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(64): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+15625G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078170 | |||||||
| chr6:109078194 | A | C | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+15601T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078194 | |||||||
| chr6:109078416 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.279+15379G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078416 | |||||||
| chr6:109078436 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+15359G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078436 | |||||||
| chr6:109078860 | C | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+14935G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078860 | |||||||
| chr6:109078868 | T | G | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+14927A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078868 | |||||||
| chr6:109078951 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+14844C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109078951 | |||||||
| chr6:109079062 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+14733C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079062 | |||||||
| chr6:109079076 | T | C | 57 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(54): Show |
57 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.279+14719A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079076 | |||||||
| chr6:109079194 | G | GA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.279+14600dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079194 | |||||||
| chr6:109079194 | G | GAA | 25 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(22): Show |
25 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.279+14599_279+1460 others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079194 | |||||||
| chr6:109079355 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+14440T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079355 | |||||||
| chr6:109079832 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.279+13963G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079832 | |||||||
| chr6:109079842 | G | T | 26 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.279+13953C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109079842 | |||||||
| chr6:109080170 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+13625G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080170 | |||||||
| chr6:109080593 | T | C | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+13202A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080593 | |||||||
| chr6:109080652 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.279+13143T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080652 | |||||||
| chr6:109080659 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+13136A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080659 | |||||||
| chr6:109080914 | C | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12881G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080914 | |||||||
| chr6:109080998 | T | G | 2 | a0002c0002t0002g0047 a0002c0002t0002g0048 |
2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.279+12797A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109080998 | |||||||
| chr6:109081041 | C | CA | 28 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0001c0001t0003g0135 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.279+12753dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081041 | |||||||
| chr6:109081075 | C | G | 67 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(64): Show |
67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.279+12720G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081075 | |||||||
| chr6:109081207 | A | G | 1 | a0001c0003t0004g0004 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.279+12588T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081207 | |||||||
| chr6:109081231 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12564A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081231 | |||||||
| chr6:109081343 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.279+12452C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081343 | |||||||
| chr6:109081368 | G | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12427C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081368 | |||||||
| chr6:109081437 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+12358G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081437 | |||||||
| chr6:109081715 | T | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+12080A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081715 | |||||||
| chr6:109081842 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.279+11953A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109081842 | |||||||
| chr6:109082122 | T | C | 52 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+11673A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082122 | |||||||
| chr6:109082216 | A | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+11579T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082216 | |||||||
| chr6:109082777 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.279+11018A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082777 | |||||||
| chr6:109082963 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+10832C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109082963 | |||||||
| chr6:109083018 | GTAT | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+10774_279+1077 others(7): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083018 | |||||||
| chr6:109083463 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+10332T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083463 | |||||||
| chr6:109083629 | G | T | 1 | a0001c0001t0009g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.279+10166C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083629 | |||||||
| chr6:109083952 | C | T | 3 | a0001c0001t0008g0050 a0001c0001t0008g0051 a0001c0001t0008g0052 |
3 | HG01891.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.279+9843G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109083952 | |||||||
| chr6:109084058 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.279+9737G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084058 | |||||||
| chr6:109084070 | T | G | 73 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.279+9725A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084070 | |||||||
| chr6:109084122 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9673G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084122 | |||||||
| chr6:109084199 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9596C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084199 | |||||||
| chr6:109084407 | A | G | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+9388T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084407 | |||||||
| chr6:109084423 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9372C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084423 | |||||||
| chr6:109084425 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.279+9370C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084425 | |||||||
| chr6:109084480 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+9315C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084480 | |||||||
| chr6:109084856 | A | G | 13 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(10): Show |
13 | HG01106.hp2 HG01361.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.279+8939T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084856 | |||||||
| chr6:109084998 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0058 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+8797G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109084998 | |||||||
| chr6:109085020 | G | A | 52 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(49): Show |
52 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+8775C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085020 | |||||||
| chr6:109085041 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.279+8754A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085041 | |||||||
| chr6:109085050 | G | GT | 51 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(48): Show |
51 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.279+8744dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085050 | |||||||
| chr6:109085096 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.279+8699A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085096 | |||||||
| chr6:109085128 | GA | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+8666delT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085128 | |||||||
| chr6:109085251 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.279+8544C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085251 | |||||||
| chr6:109085310 | T | G | 63 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.279+8485A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085310 | |||||||
| chr6:109085347 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02280.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.279+8448C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085347 | |||||||
| chr6:109085432 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+8363A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085432 | |||||||
| chr6:109085445 | G | A | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+8350C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085445 | |||||||
| chr6:109085500 | C | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+8295G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085500 | |||||||
| chr6:109085515 | T | TCA | 8 | a0001c0001t0001g0123 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
8 | HG00280.hp1 HG01106.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+8278_279+8279d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | |||||||
| chr6:109085515 | T | TCACACAC others(3): Show |
2 | a0001c0003t0004g0003 a0001c0003t0004g0006 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.279+8270_279+8279d others(12): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | |||||||
| chr6:109085515 | T | TCACACAC others(5): Show |
3 | a0001c0003t0004g0002 a0001c0003t0004g0004 a0001c0003t0004g0005 |
3 | HG02572.hp1 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.279+8268_279+8279d others(14): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | |||||||
| chr6:109085515 | TCA | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0018 others(66): Show |
69 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.279+8278_279+8279d others(4): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | |||||||
| chr6:109085515 | TCACA | T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+8276_279+8279d others(6): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085515 | |||||||
| chr6:109085626 | G | A | 2 | a0001c0004t0005g0022 a0001c0004t0005g0023 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.279+8169C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085626 | |||||||
| chr6:109085638 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.279+8157T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085638 | |||||||
| chr6:109085693 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.279+8102C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109085693 | |||||||
| chr6:109086276 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.279+7519G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086276 | |||||||
| chr6:109086304 | A | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+7491T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086304 | |||||||
| chr6:109086492 | C | A | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+7303G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086492 | |||||||
| chr6:109086655 | T | G | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+7140A>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086655 | |||||||
| chr6:109086755 | AATAACTA others(2): Show |
A | 53 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(50): Show |
53 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.279+7031_279+7039d others(11): Show |
SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086755 | |||||||
| chr6:109086773 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+7022T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086773 | |||||||
| chr6:109086900 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.279+6895C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086900 | |||||||
| chr6:109086968 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6827G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109086968 | |||||||
| chr6:109087225 | C | G | 27 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+6570G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087225 | |||||||
| chr6:109087288 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6507A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087288 | |||||||
| chr6:109087315 | G | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6480C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087315 | |||||||
| chr6:109087346 | G | GA | 68 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0049 others(65): Show |
68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.279+6448dupT | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087346 | |||||||
| chr6:109087399 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.279+6396T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087399 | |||||||
| chr6:109087470 | A | G | 4 | a0001c0001t0001g0179 a0001c0001t0008g0050 a0001c0001t0008g0051 others(1): Show |
4 | HG01891.hp2 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+6325T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087470 | |||||||
| chr6:109087567 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6228A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087567 | |||||||
| chr6:109087632 | T | A | 5 | a0001c0001t0013g0015 a0001c0004t0005g0020 a0001c0004t0005g0021 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+6163A>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087632 | |||||||
| chr6:109087817 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.279+5978G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087817 | |||||||
| chr6:109087982 | T | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+5813A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109087982 | |||||||
| chr6:109088071 | A | G | 27 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0002c0002t0002g0013 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.279+5724T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088071 | |||||||
| chr6:109088146 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG01257.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.279+5649G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088146 | |||||||
| chr6:109088510 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.279+5285A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088510 | |||||||
| chr6:109088600 | A | AT | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+5194dupA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109088600 | |||||||
| chr6:109089059 | AT | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0130 a0001c0001t0001g0132 others(4): Show |
7 | HG02083.hp1 HG02109.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+4735delA | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089059 | |||||||
| chr6:109089122 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+4673C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089122 | |||||||
| chr6:109089256 | G | A | 19 | a0001c0001t0001g0134 a0001c0001t0003g0135 a0001c0001t0003g0159 others(16): Show |
19 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.279+4539C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089256 | |||||||
| chr6:109089293 | C | T | 4 | a0001c0004t0005g0020 a0001c0004t0005g0021 a0001c0004t0005g0022 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+4502G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089293 | |||||||
| chr6:109089366 | T | C | 26 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(23): Show |
26 | HG00280.hp1 HG00438.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.279+4429A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089366 | |||||||
| chr6:109089502 | A | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+4293T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089502 | |||||||
| chr6:109089586 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+4209C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089586 | |||||||
| chr6:109089901 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+3894G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109089901 | |||||||
| chr6:109090082 | C | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+3713G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090082 | |||||||
| chr6:109090110 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.279+3685G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090110 | |||||||
| chr6:109090507 | A | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+3288T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090507 | |||||||
| chr6:109090547 | A | C | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+3248T>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090547 | |||||||
| chr6:109090649 | C | T | 1 | a0001c0001t0001g0018 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.279+3146G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090649 | |||||||
| chr6:109090685 | G | A | 17 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(14): Show |
17 | HG01109.hp1 HG02004.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.279+3110C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090685 | |||||||
| chr6:109090806 | C | T | 1 | a0004c0007t0001g0017 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.279+2989G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090806 | |||||||
| chr6:109090937 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2858A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109090937 | |||||||
| chr6:109091053 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA19060.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+2742C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091053 | |||||||
| chr6:109091172 | C | G | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2623G>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091172 | |||||||
| chr6:109091251 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01081.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.279+2544C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091251 | |||||||
| chr6:109091285 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.279+2510T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091285 | |||||||
| chr6:109091356 | G | A | 1 | a0001c0001t0003g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.279+2439C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091356 | |||||||
| chr6:109091390 | C | T | 1 | a0001c0001t0013g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.279+2405G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091390 | |||||||
| chr6:109091398 | T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+2397A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091398 | |||||||
| chr6:109091443 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.279+2352C>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091443 | |||||||
| chr6:109091507 | T | C | 1 | a0001c0001t0003g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.279+2288A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091507 | |||||||
| chr6:109091539 | G | T | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2256C>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091539 | |||||||
| chr6:109091573 | C | T | 1 | a0001c0003t0004g0002 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279+2222G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091573 | |||||||
| chr6:109091730 | T | C | 1 | a0001c0001t0010g0010 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.279+2065A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091730 | |||||||
| chr6:109091863 | A | T | 2 | a0002c0002t0002g0013 a0002c0002t0002g0014 |
2 | HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.279+1932T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091863 | |||||||
| chr6:109091895 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.279+1900T>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109091895 | |||||||
| chr6:109092362 | C | T | 2 | a0001c0005t0001g0008 a0001c0005t0001g0009 |
2 | NA18998.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.279+1433G>A | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109092362 | |||||||
| chr6:109092572 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.279+1223G>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109092572 | |||||||
| chr6:109092707 | G | A | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG01109.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.279+1088C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109092707 | |||||||
| chr6:109093159 | T | C | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+636A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093159 | |||||||
| chr6:109093265 | T | C | 1 | a0001c0003t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.279+530A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093265 | |||||||
| chr6:109093279 | A | G | 6 | a0001c0001t0010g0010 a0001c0003t0004g0002 a0001c0003t0004g0003 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+516T>C | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093279 | |||||||
| chr6:109093470 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+325C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093470 | |||||||
| chr6:109093493 | T | C | 1 | a0001c0003t0004g0006 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.279+302A>G | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093493 | |||||||
| chr6:109093504 | G | A | 5 | a0001c0003t0004g0002 a0001c0003t0004g0003 a0001c0003t0004g0004 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+291C>T | SESN1 | ENSG00000080546.14 | transcript | ENST00000436639.7 | protein_coding | 1/9 | chr6 | 109093504 |