Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54826 |
| ensemblid | ENSG00000145723.17 |
| hgncid | 25959 |
| symbol | GIN1 |
| name | gypsy retrotransposon integrase 1 |
| refseq_nuc | NM_017676.2 |
| refseq_prot | NP_060146.2 |
| ensembl_nuc | ENST00000399004.7 |
| ensembl_prot | ENSP00000381970.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 103086000 |
| end | 103120138 |
| strand | - |
| ver | v1.2 |
| region | chr5:103086000-103120138 |
| region5000 | chr5:103081000-103125138 |
| regionname0 | GIN1_chr5_103086000_103120138 |
| regionname5000 | GIN1_chr5_103081000_103125138 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 522 | 196 | 71 | 36 | 67 | 10 | 11 | 55 | GIN1_chr5_103081000_103125138 | GIN1 | MVRSG others(517): Show |
chr5 | 103081000 | 103125138 |
| a0002 | 0/1 | 522 | 118 | 16 | 18 | 70 | 4 | 9 | 59 | GIN1_chr5_103081000_103125138 | GIN1 | MVRSG others(517): Show |
chr5 | 103081000 | 103125138 |
| a0003 | 0/0 | 522 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | MVRSG others(517): Show |
chr5 | 103081000 | 103125138 |
| a0004 | 0/0 | 522 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | MVRSG others(517): Show |
chr5 | 103081000 | 103125138 |
| a0005 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | MVRSG others(517): Show |
chr5 | 103081000 | 103125138 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1566 | 196 | 71 | 36 | 67 | 10 | 11 | GIN1_chr5_103081000_103125138 | GIN1 | ATGGT others(1561): Show |
chr5 | 103081000 | 103125138 | ||
| a0002c0002 | 0/1 | 1566 | 113 | 14 | 17 | 70 | 4 | 7 | GIN1_chr5_103081000_103125138 | GIN1 | ATGGT others(1561): Show |
chr5 | 103081000 | 103125138 | ||
| a0002c0004 | 0/0 | 1566 | 3 | 0 | 1 | 0 | 0 | 2 | GIN1_chr5_103081000_103125138 | GIN1 | ATGGT others(1561): Show |
chr5 | 103081000 | 103125138 | ||
| a0002c0006 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | ATGGT others(1561): Show |
chr5 | 103081000 | 103125138 | ||
| a0003c0003 | 0/0 | 1566 | 4 | 4 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | ATGGT others(1561): Show |
chr5 | 103081000 | 103125138 | ||
| a0004c0005 | 0/0 | 1566 | 3 | 3 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | ATGGT others(1561): Show |
chr5 | 103081000 | 103125138 | ||
| a0005c0007 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | ATGGT others(1561): Show |
chr5 | 103081000 | 103125138 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3549 | 153 | 40 | 29 | 63 | 10 | 10 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0003 | 0/0 | 3549 | 11 | 11 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0004 | 0/0 | 3549 | 12 | 11 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0005 | 0/0 | 3541 | 2 | 0 | 2 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3536): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0006 | 0/0 | 3549 | 5 | 5 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0008 | 0/0 | 3542 | 4 | 4 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3537): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0011 | 0/0 | 3549 | 3 | 0 | 3 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0012 | 0/0 | 3549 | 3 | 0 | 0 | 3 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0014 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0015 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0001c0001t0016 | 0/0 | 3549 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0002c0002t0002 | 0/1 | 3549 | 102 | 10 | 15 | 67 | 3 | 6 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0002c0002t0007 | 0/0 | 3549 | 4 | 1 | 1 | 0 | 1 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0002c0002t0009 | 0/0 | 3549 | 3 | 3 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0002c0002t0010 | 0/0 | 3549 | 3 | 0 | 0 | 3 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0002c0002t0017 | 0/0 | 3549 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0002c0004t0002 | 0/0 | 3549 | 3 | 0 | 1 | 0 | 0 | 2 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0002c0006t0013 | 0/0 | 3549 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0003c0003t0003 | 0/0 | 3549 | 4 | 4 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| a0004c0005t0005 | 0/0 | 3541 | 3 | 3 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3536): Show |
chr5 | 103081000 | 103125138 |
| a0005c0007t0002 | 0/0 | 3549 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | AGTTC others(3544): Show |
chr5 | 103081000 | 103125138 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 26 | 0 | 3 | 22 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0003 | 0/0 | 16 | 3 | 6 | 6 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0004g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0006g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0008g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0011g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0012g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0012g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0014g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0015g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0001c0001t0016g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0002 | 0/0 | 19 | 0 | 2 | 14 | 2 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0007g0021 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0007g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0010g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0010g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0002t0017g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0004t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0002c0006t0013g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0003c0003t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0003c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0003c0003t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0004c0005t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0004c0005t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| a0005c0007t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0007 | g0021 | EUR | GBR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00408 | hp2 | a0001 | c0001 | t0012 | g0111 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00597 | hp2 | a0005 | c0007 | t0002 | g0147 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00642 | hp1 | a0002 | c0002 | t0017 | g0188 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0182 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0143 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01081 | hp1 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01099 | hp1 | a0002 | c0004 | t0002 | g0039 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0170 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0177 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0105 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0176 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0103 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01433 | hp2 | a0002 | c0002 | t0007 | g0021 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0159 | AMR | CLM | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | CDX | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0167 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02572 | hp2 | a0003 | c0003 | t0003 | g0062 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0042 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02630 | hp1 | a0004 | c0005 | t0005 | g0134 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0146 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02886 | hp2 | a0003 | c0003 | t0003 | g0025 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02895 | hp1 | a0004 | c0005 | t0005 | g0035 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0153 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0032 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02897 | hp2 | a0004 | c0005 | t0005 | g0035 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02970 | hp2 | a0002 | c0002 | t0009 | g0148 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03098 | hp2 | a0002 | c0006 | t0013 | g0037 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03139 | hp2 | a0003 | c0003 | t0003 | g0025 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0144 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03453 | hp1 | a0002 | c0002 | t0009 | g0149 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0161 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03490 | hp1 | a0002 | c0002 | t0007 | g0162 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03490 | hp2 | a0002 | c0004 | t0002 | g0156 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03492 | hp2 | a0002 | c0004 | t0002 | g0039 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0158 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0157 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03834 | hp1 | a0001 | c0001 | t0016 | g0081 | SAS | BEB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0163 | SAS | BEB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18906 | hp1 | a0002 | c0002 | t0009 | g0145 | AFR | YRI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18943 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18957 | hp1 | a0002 | c0002 | t0010 | g0160 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18963 | hp1 | a0001 | c0001 | t0014 | g0059 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19003 | hp2 | a0002 | c0002 | t0010 | g0142 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | LWK | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | LWK | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19064 | hp1 | a0002 | c0002 | t0010 | g0045 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19074 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | YRI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | YRI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0150 | AFR | ASW | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0155 | EUR | TSI | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02109 | hp1 | a0002 | c0002 | t0007 | g0021 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG03471 | hp2 | a0003 | c0003 | t0003 | g0061 | AFR | MSL | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG06807 | hp1 | a0002 | c0006 | t0013 | g0037 | AFR | USA | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | LWK | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0151 | REF | REF | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0097 | REF | REF | GIN1_chr5_103081000_103125138 | GIN1 | chr5 | 103081000 | 103125138 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:103087924 | T | C | 1 | a0004 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.1543A>G | p.Asn515Asp | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1625/3549 | 1543/1569 | 515/522 | chr5 | 103087924 | |||
| chr5:103097378 | T | C | 1 | a0005 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.944A>G | p.Lys315Arg | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 6/8 | 1026/3549 | 944/1569 | 315/522 | chr5 | 103097378 | |||
| chr5:103097394 | T | C | 1 | a0003 | 4 | HG02572.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.928A>G | p.Thr310Ala | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 6/8 | 1010/3549 | 928/1569 | 310/522 | chr5 | 103097394 | |||
| chr5:103097645 | T | C | 1 | a0004 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.776A>G | p.Asn259Ser | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 5/8 | 858/3549 | 776/1569 | 259/522 | chr5 | 103097645 | |||
| chr5:103097705 | G | A | 2 | a0002 a0005 |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
missense_variant | MODERATE | c.716C>T | p.Thr239Met | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 5/8 | 798/3549 | 716/1569 | 239/522 | chr5 | 103097705 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:103096800 | T | C | 1 | a0002c0006 | 2 | HG03098.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.1035A>G | p.Leu345Leu | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/8 | 1117/3549 | 1035/1569 | 345/522 | chr5 | 103096800 | |||
| chr5:103104679 | C | T | 1 | a0002c0004 | 3 | HG01099.hp1 HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.501G>A | p.Leu167Leu | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/8 | 583/3549 | 501/1569 | 167/522 | chr5 | 103104679 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:103086041 | GCAAAAGT | G | 1 | a0001c0001t0008 | 4 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1850_*1856delACTT others(3): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1850 | chr5 | 103086041 | ||||||
| chr5:103086074 | G | C | 1 | a0001c0001t0008 | 4 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1824C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1824 | chr5 | 103086074 | ||||||
| chr5:103086109 | C | T | 1 | a0001c0001t0014 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1789G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1789 | chr5 | 103086109 | ||||||
| chr5:103086254 | ATACTGTA others(1): Show |
A | 2 | a0001c0001t0005 a0004c0005t0005 |
5 | HG01099.hp2 HG01167.hp2 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1636_*1643delATAC others(4): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1636 | chr5 | 103086254 | ||||||
| chr5:103086316 | C | T | 1 | a0002c0002t0010 | 3 | NA18957.hp1 NA19003.hp2 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1582G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1582 | chr5 | 103086316 | ||||||
| chr5:103086481 | C | G | 1 | a0001c0001t0011 | 3 | HG01081.hp1 HG01106.hp2 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1417G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1417 | chr5 | 103086481 | ||||||
| chr5:103086613 | C | T | 1 | a0002c0006t0013 | 2 | HG03098.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1285G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1285 | chr5 | 103086613 | ||||||
| chr5:103086739 | C | T | 8 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0009 others(5): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1159G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1159 | chr5 | 103086739 | ||||||
| chr5:103086804 | G | A | 1 | a0001c0001t0006 | 5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1094 | chr5 | 103086804 | ||||||
| chr5:103086881 | T | C | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(10): Show |
154 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 1017 | chr5 | 103086881 | ||||||
| chr5:103087039 | C | T | 1 | a0002c0002t0009 | 3 | HG02970.hp2 HG03453.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*859G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 859 | chr5 | 103087039 | ||||||
| chr5:103087129 | C | A | 1 | a0001c0001t0012 | 3 | HG00408.hp2 NA18943.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*769G>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 769 | chr5 | 103087129 | ||||||
| chr5:103087167 | G | C | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 731 | chr5 | 103087167 | ||||||
| chr5:103087264 | C | T | 1 | a0002c0002t0007 | 4 | HG00099.hp1 HG01433.hp2 HG02109.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*634G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 634 | chr5 | 103087264 | ||||||
| chr5:103087275 | C | T | 1 | a0001c0001t0004 | 12 | HG00741.hp1 HG02145.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*623G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 623 | chr5 | 103087275 | ||||||
| chr5:103087664 | T | A | 8 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0009 others(5): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*234A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 234 | chr5 | 103087664 | ||||||
| chr5:103087827 | G | A | 1 | a0001c0001t0016 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 71 | chr5 | 103087827 | ||||||
| chr5:103087872 | A | G | 8 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0009 others(5): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*26T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 26 | chr5 | 103087872 | ||||||
| chr5:103087875 | A | C | 8 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0009 others(5): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*23T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 8/8 | 23 | chr5 | 103087875 | ||||||
| chr5:103120099 | T | G | 1 | a0002c0002t0017 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/8 | 11392 | chr5 | 103120099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:103088267 | A | C | 1 | a0002c0002t0002g0168 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1295-95T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088267 | |||||||
| chr5:103088332 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1295-160T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088332 | |||||||
| chr5:103088454 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1295-282G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088454 | |||||||
| chr5:103088462 | G | A | 6 | a0001c0001t0001g0083 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
10 | HG01884.hp2 HG01928.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1295-290C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088462 | |||||||
| chr5:103088509 | A | G | 63 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(60): Show |
110 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.1295-337T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088509 | |||||||
| chr5:103088716 | C | T | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-544G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088716 | |||||||
| chr5:103088725 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-553A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088725 | |||||||
| chr5:103088910 | C | G | 1 | a0002c0002t0002g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1295-738G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103088910 | |||||||
| chr5:103089083 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1295-911A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089083 | |||||||
| chr5:103089119 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1295-947A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089119 | |||||||
| chr5:103089271 | T | G | 3 | a0001c0001t0006g0015 a0001c0001t0006g0065 a0001c0001t0006g0074 |
5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-1099A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089271 | |||||||
| chr5:103089296 | G | A | 3 | a0001c0001t0006g0015 a0001c0001t0006g0065 a0001c0001t0006g0074 |
5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-1124C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089296 | |||||||
| chr5:103089315 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0016g0081 |
3 | HG02257.hp1 HG02293.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1295-1143T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089315 | |||||||
| chr5:103089436 | TTTCA | T | 20 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0023 others(17): Show |
36 | HG00741.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1295-1268_1295-126 others(8): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089436 | |||||||
| chr5:103089461 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-1289A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089461 | |||||||
| chr5:103089465 | C | T | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-1293G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089465 | |||||||
| chr5:103089491 | C | G | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1295-1319G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089491 | |||||||
| chr5:103089513 | A | G | 1 | a0002c0002t0010g0142 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1295-1341T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089513 | |||||||
| chr5:103089611 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0070 a0001c0001t0001g0091 |
4 | HG01516.hp1 HG01517.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1295-1439A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089611 | |||||||
| chr5:103089828 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1295-1656C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089828 | |||||||
| chr5:103089962 | C | T | 2 | a0001c0001t0004g0008 a0001c0001t0004g0053 |
5 | HG02145.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1295-1790G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089962 | |||||||
| chr5:103089982 | A | T | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1295-1810T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103089982 | |||||||
| chr5:103090023 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-1851A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090023 | |||||||
| chr5:103090047 | G | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-1875C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090047 | |||||||
| chr5:103090106 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1295-1934G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090106 | |||||||
| chr5:103090219 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1295-2047C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090219 | |||||||
| chr5:103090432 | T | C | 9 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(6): Show |
16 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1295-2260A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090432 | |||||||
| chr5:103090495 | A | C | 3 | a0001c0001t0003g0014 a0001c0001t0008g0031 a0001c0001t0008g0032 |
7 | HG01884.hp2 HG02486.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1295-2323T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090495 | |||||||
| chr5:103090498 | A | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-2326T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090498 | |||||||
| chr5:103090598 | T | A | 1 | a0001c0001t0006g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1295-2426A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090598 | |||||||
| chr5:103090650 | T | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
8 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1295-2478A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090650 | |||||||
| chr5:103090712 | A | G | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1295-2540T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090712 | |||||||
| chr5:103090799 | C | T | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-2627G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090799 | |||||||
| chr5:103090809 | T | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-2637A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090809 | |||||||
| chr5:103090900 | A | AAC | 8 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0001g0114 others(5): Show |
11 | HG00738.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1295-2730_1295-272 others(6): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090900 | |||||||
| chr5:103090900 | A | AACAC | 5 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0003g0014 others(2): Show |
9 | HG01884.hp2 HG02280.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1295-2732_1295-272 others(8): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090900 | |||||||
| chr5:103090900 | AAC | A | 66 | a0001c0001t0005g0046 a0001c0001t0005g0105 a0002c0002t0002g0002 others(63): Show |
112 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1295-2730_1295-272 others(6): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103090900 | |||||||
| chr5:103091301 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-3129A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091301 | |||||||
| chr5:103091366 | AC | A | 2 | a0004c0005t0005g0035 a0004c0005t0005g0134 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1295-3195delG | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091366 | |||||||
| chr5:103091411 | T | C | 2 | a0002c0002t0002g0040 a0002c0002t0002g0153 |
3 | HG02055.hp1 HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1295-3239A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091411 | |||||||
| chr5:103091477 | A | G | 1 | a0001c0001t0001g0005 | 6 | HG00673.hp1 HG01978.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-3305T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091477 | |||||||
| chr5:103091609 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-3437A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091609 | |||||||
| chr5:103091675 | G | T | 3 | a0001c0001t0006g0015 a0001c0001t0006g0065 a0001c0001t0006g0074 |
5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-3503C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091675 | |||||||
| chr5:103091722 | G | A | 9 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(6): Show |
16 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1295-3550C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091722 | |||||||
| chr5:103091898 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1295-3726C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091898 | |||||||
| chr5:103091924 | C | T | 8 | a0001c0001t0003g0013 a0001c0001t0003g0050 a0001c0001t0004g0007 others(5): Show |
16 | HG00741.hp1 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1295-3752G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091924 | |||||||
| chr5:103091953 | A | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-3781T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103091953 | |||||||
| chr5:103092139 | G | C | 117 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0034 others(114): Show |
188 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(185): Show |
intron_variant | MODIFIER | c.1295-3967C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092139 | |||||||
| chr5:103092414 | G | T | 78 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(75): Show |
134 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.1294+4127C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092414 | |||||||
| chr5:103092535 | G | A | 29 | a0002c0002t0002g0002 a0002c0002t0002g0011 a0002c0002t0002g0012 others(26): Show |
61 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1294+4006C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092535 | |||||||
| chr5:103092608 | A | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1294+3933T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092608 | |||||||
| chr5:103092668 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG01243.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294+3873G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092668 | |||||||
| chr5:103092733 | T | C | 78 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(75): Show |
134 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.1294+3808A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092733 | |||||||
| chr5:103092789 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0096 |
2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1294+3752G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092789 | |||||||
| chr5:103092818 | T | C | 67 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(64): Show |
115 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.1294+3723A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092818 | |||||||
| chr5:103092945 | C | CA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(82): Show |
160 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1294+3595dupT | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092945 | |||||||
| chr5:103092945 | C | CAA | 13 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0057 others(10): Show |
16 | HG01109.hp2 HG01243.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.1294+3594_1294+359 others(6): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092945 | |||||||
| chr5:103092945 | CAAA | C | 70 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(67): Show |
126 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.1294+3593_1294+359 others(7): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092945 | |||||||
| chr5:103092945 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1294+3582_1294+359 others(18): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092945 | |||||||
| chr5:103092950 | A | G | 9 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(6): Show |
16 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1294+3591T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092950 | |||||||
| chr5:103092984 | GA | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1294+3556delT | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103092984 | |||||||
| chr5:103093005 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1294+3536T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093005 | |||||||
| chr5:103093104 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1294+3437G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093104 | |||||||
| chr5:103093172 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1294+3369T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093172 | |||||||
| chr5:103093464 | C | T | 3 | a0001c0001t0006g0015 a0001c0001t0006g0065 a0001c0001t0006g0074 |
5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1294+3077G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093464 | |||||||
| chr5:103093484 | T | A | 63 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(60): Show |
110 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.1294+3057A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093484 | |||||||
| chr5:103093711 | T | G | 9 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(6): Show |
16 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1294+2830A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093711 | |||||||
| chr5:103093722 | C | G | 9 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(6): Show |
16 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1294+2819G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093722 | |||||||
| chr5:103093963 | A | G | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294+2578T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103093963 | |||||||
| chr5:103094116 | A | G | 1 | a0004c0005t0005g0134 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1294+2425T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103094116 | |||||||
| chr5:103094179 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1294+2362C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103094179 | |||||||
| chr5:103094387 | A | G | 1 | a0001c0001t0012g0028 | 2 | NA18943.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1294+2154T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103094387 | |||||||
| chr5:103094413 | C | A | 63 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(60): Show |
110 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.1294+2128G>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103094413 | |||||||
| chr5:103094804 | T | C | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1294+1737A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103094804 | |||||||
| chr5:103094865 | G | A | 8 | a0001c0001t0003g0013 a0001c0001t0003g0050 a0001c0001t0004g0007 others(5): Show |
16 | HG00741.hp1 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1294+1676C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103094865 | |||||||
| chr5:103095045 | A | T | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1294+1496T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095045 | |||||||
| chr5:103095168 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1294+1373C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095168 | |||||||
| chr5:103095214 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
317 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.1294+1327A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095214 | |||||||
| chr5:103095368 | A | C | 1 | a0002c0002t0002g0036 | 2 | HG00738.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1294+1173T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095368 | |||||||
| chr5:103095570 | T | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0071 others(14): Show |
36 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1294+971A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095570 | |||||||
| chr5:103095642 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1294+899G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095642 | |||||||
| chr5:103095786 | T | C | 3 | a0002c0002t0002g0163 a0002c0004t0002g0039 a0002c0004t0002g0156 |
4 | HG01099.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294+755A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095786 | |||||||
| chr5:103095894 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1294+647T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095894 | |||||||
| chr5:103095906 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA19006.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1294+635T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095906 | |||||||
| chr5:103095946 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1294+595A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103095946 | |||||||
| chr5:103096074 | T | C | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294+467A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103096074 | |||||||
| chr5:103096117 | A | G | 79 | a0001c0001t0003g0014 a0001c0001t0003g0052 a0001c0001t0006g0015 others(76): Show |
135 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.1294+424T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103096117 | |||||||
| chr5:103096151 | A | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1294+390T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103096151 | |||||||
| chr5:103096259 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1294+282C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103096259 | |||||||
| chr5:103096320 | G | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1294+221C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103096320 | |||||||
| chr5:103096360 | C | A | 6 | a0001c0001t0003g0014 a0001c0001t0008g0031 a0001c0001t0008g0032 others(3): Show |
11 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1294+181G>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 7/7 | chr5 | 103096360 | |||||||
| chr5:103097039 | C | T | 4 | a0002c0002t0002g0176 a0002c0002t0002g0177 a0002c0002t0002g0182 others(1): Show |
4 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-213G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 6/7 | chr5 | 103097039 | |||||||
| chr5:103097068 | GACT | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1008+243_1009-243d others(5): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 6/7 | chr5 | 103097068 | |||||||
| chr5:103097171 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1008+143G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 6/7 | chr5 | 103097171 | |||||||
| chr5:103097906 | G | A | 3 | a0002c0002t0002g0012 a0002c0002t0002g0143 a0002c0002t0002g0170 |
6 | HG01071.hp2 HG01106.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-125C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103097906 | |||||||
| chr5:103098132 | T | C | 78 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(75): Show |
134 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.640-351A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103098132 | |||||||
| chr5:103098335 | T | TACA | 78 | a0001c0001t0003g0014 a0001c0001t0006g0015 a0001c0001t0006g0065 others(75): Show |
134 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.640-557_640-555dup others(3): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103098335 | |||||||
| chr5:103098561 | C | T | 67 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(64): Show |
115 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.640-780G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103098561 | |||||||
| chr5:103098645 | G | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.640-864C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103098645 | |||||||
| chr5:103098736 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0096 |
2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.640-955C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103098736 | |||||||
| chr5:103098836 | G | A | 1 | a0001c0001t0008g0031 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.640-1055C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103098836 | |||||||
| chr5:103098941 | T | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0006 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.640-1160A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103098941 | |||||||
| chr5:103099522 | G | T | 1 | a0001c0001t0004g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.640-1741C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103099522 | |||||||
| chr5:103099556 | G | T | 66 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0003g0014 others(63): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.640-1775C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103099556 | |||||||
| chr5:103099885 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.640-2104G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103099885 | |||||||
| chr5:103099966 | C | T | 3 | a0001c0001t0006g0015 a0001c0001t0006g0065 a0001c0001t0006g0074 |
5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.640-2185G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103099966 | |||||||
| chr5:103099976 | T | C | 3 | a0003c0003t0003g0025 a0003c0003t0003g0061 a0003c0003t0003g0062 |
4 | HG02572.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-2195A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103099976 | |||||||
| chr5:103100023 | T | G | 1 | a0001c0001t0001g0029 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.640-2242A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100023 | |||||||
| chr5:103100039 | G | A | 5 | a0001c0001t0003g0052 a0002c0002t0009g0145 a0002c0002t0009g0148 others(2): Show |
6 | HG02970.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.640-2258C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100039 | |||||||
| chr5:103100112 | A | AT | 11 | a0001c0001t0003g0013 a0001c0001t0003g0023 a0001c0001t0003g0050 others(8): Show |
20 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.640-2332dupA | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100112 | |||||||
| chr5:103100316 | T | C | 1 | a0002c0006t0013g0037 | 2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.640-2535A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100316 | |||||||
| chr5:103100384 | C | CTAT | 3 | a0001c0001t0006g0015 a0001c0001t0006g0065 a0001c0001t0006g0074 |
5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.640-2606_640-2604d others(5): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100384 | |||||||
| chr5:103100401 | A | ATTG | 2 | a0002c0002t0002g0036 a0002c0002t0002g0146 |
3 | HG00738.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.640-2621_640-2620i others(5): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100401 | |||||||
| chr5:103100404 | A | T | 2 | a0001c0001t0003g0014 a0002c0002t0002g0073 |
4 | HG01884.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-2623T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100404 | |||||||
| chr5:103100404 | ATTT | A | 2 | a0001c0001t0004g0008 a0001c0001t0004g0053 |
5 | HG02145.hp1 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-2626_640-2624d others(5): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100404 | |||||||
| chr5:103100407 | T | A | 78 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0023 others(75): Show |
133 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.640-2626A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100407 | |||||||
| chr5:103100420 | G | T | 1 | a0001c0001t0003g0014 | 3 | HG01884.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.640-2639C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100420 | |||||||
| chr5:103100447 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.640-2666T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100447 | |||||||
| chr5:103100515 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.640-2734G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100515 | |||||||
| chr5:103100560 | T | C | 1 | a0002c0002t0002g0165 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.640-2779A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100560 | |||||||
| chr5:103100564 | A | T | 1 | a0002c0002t0002g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.640-2783T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100564 | |||||||
| chr5:103100565 | A | T | 68 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(65): Show |
117 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.640-2784T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100565 | |||||||
| chr5:103100566 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0033 |
6 | HG01243.hp1 HG02486.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-2785A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100566 | |||||||
| chr5:103100588 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0003c0003t0003g0062 |
3 | HG01109.hp2 HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.640-2807C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100588 | |||||||
| chr5:103100933 | A | G | 1 | a0002c0006t0013g0037 | 2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.640-3152T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103100933 | |||||||
| chr5:103101164 | A | G | 88 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(85): Show |
152 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.639+3377T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101164 | |||||||
| chr5:103101300 | G | A | 1 | a0002c0002t0002g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.639+3241C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101300 | |||||||
| chr5:103101312 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.639+3229G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101312 | |||||||
| chr5:103101505 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.639+3036C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101505 | |||||||
| chr5:103101531 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.639+3010A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101531 | |||||||
| chr5:103101539 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG01168.hp1 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.639+3002G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101539 | |||||||
| chr5:103101719 | A | T | 1 | a0002c0002t0002g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.639+2822T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101719 | |||||||
| chr5:103101856 | A | G | 3 | a0001c0001t0006g0015 a0001c0001t0006g0065 a0001c0001t0006g0074 |
5 | HG02280.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+2685T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101856 | |||||||
| chr5:103101913 | T | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.639+2628A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103101913 | |||||||
| chr5:103102003 | T | C | 2 | a0002c0002t0002g0168 a0002c0002t0002g0169 |
2 | NA19000.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.639+2538A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102003 | |||||||
| chr5:103102007 | T | C | 86 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(83): Show |
149 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.639+2534A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102007 | |||||||
| chr5:103102109 | A | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
6 | NA18963.hp1 NA19006.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+2432T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102109 | |||||||
| chr5:103102190 | C | T | 2 | a0002c0002t0002g0036 a0002c0002t0002g0146 |
3 | HG00738.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.639+2351G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102190 | |||||||
| chr5:103102587 | A | G | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.639+1954T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102587 | |||||||
| chr5:103102800 | A | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
5 | NA18961.hp2 NA18964.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+1741T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102800 | |||||||
| chr5:103102874 | C | T | 1 | a0002c0002t0002g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.639+1667G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102874 | |||||||
| chr5:103102943 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.639+1598G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103102943 | |||||||
| chr5:103103029 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.639+1512T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103029 | |||||||
| chr5:103103155 | C | G | 1 | a0001c0001t0004g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.639+1386G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103155 | |||||||
| chr5:103103227 | A | C | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.639+1314T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103227 | |||||||
| chr5:103103565 | T | A | 11 | a0001c0001t0003g0013 a0001c0001t0003g0023 a0001c0001t0003g0050 others(8): Show |
20 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.639+976A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103565 | |||||||
| chr5:103103614 | T | C | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.639+927A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103614 | |||||||
| chr5:103103882 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0187 |
2 | HG01109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.639+659G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103882 | |||||||
| chr5:103103883 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.639+658C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103883 | |||||||
| chr5:103103985 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.639+556C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103103985 | |||||||
| chr5:103104121 | A | T | 86 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(83): Show |
149 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.639+420T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103104121 | |||||||
| chr5:103104228 | T | A | 2 | a0002c0002t0002g0036 a0002c0002t0002g0146 |
3 | HG00738.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.639+313A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103104228 | |||||||
| chr5:103104399 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.639+142C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 4/7 | chr5 | 103104399 | |||||||
| chr5:103105020 | A | G | 1 | a0002c0002t0002g0174 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.334-174T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103105020 | |||||||
| chr5:103105168 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.334-322G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103105168 | |||||||
| chr5:103105276 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.334-430G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103105276 | |||||||
| chr5:103105497 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.334-651T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103105497 | |||||||
| chr5:103105660 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0121 |
2 | NA18950.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.334-814C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103105660 | |||||||
| chr5:103105778 | A | G | 80 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0023 others(77): Show |
138 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.334-932T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103105778 | |||||||
| chr5:103106034 | C | T | 1 | a0001c0001t0016g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.333+682G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103106034 | |||||||
| chr5:103106044 | T | C | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.333+672A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103106044 | |||||||
| chr5:103106347 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.333+369T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103106347 | |||||||
| chr5:103106363 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.333+353G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 3/7 | chr5 | 103106363 | |||||||
| chr5:103106985 | T | C | 1 | a0002c0002t0002g0011 | 4 | NA18965.hp2 NA18988.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.140-76A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103106985 | |||||||
| chr5:103107168 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.140-259G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107168 | |||||||
| chr5:103107186 | C | T | 11 | a0001c0001t0003g0013 a0001c0001t0003g0023 a0001c0001t0003g0050 others(8): Show |
20 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.140-277G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107186 | |||||||
| chr5:103107209 | C | A | 80 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0023 others(77): Show |
138 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.140-300G>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107209 | |||||||
| chr5:103107323 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.140-414C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107323 | |||||||
| chr5:103107339 | AT | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.140-431delA | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107339 | |||||||
| chr5:103107341 | T | C | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.140-432A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107341 | |||||||
| chr5:103107365 | GCTT | G | 3 | a0003c0003t0003g0025 a0003c0003t0003g0061 a0003c0003t0003g0062 |
4 | HG02572.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-459_140-457del others(3): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107365 | |||||||
| chr5:103107425 | C | A | 2 | a0004c0005t0005g0035 a0004c0005t0005g0134 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.140-516G>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107425 | |||||||
| chr5:103107596 | T | G | 3 | a0003c0003t0003g0025 a0003c0003t0003g0061 a0003c0003t0003g0062 |
4 | HG02572.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-687A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107596 | |||||||
| chr5:103107609 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.140-700T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107609 | |||||||
| chr5:103107749 | T | G | 1 | a0001c0001t0008g0032 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.139+820A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103107749 | |||||||
| chr5:103108085 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.139+484C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108085 | |||||||
| chr5:103108106 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.139+463G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108106 | |||||||
| chr5:103108131 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.139+438C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108131 | |||||||
| chr5:103108157 | A | C | 8 | a0001c0001t0003g0013 a0001c0001t0003g0050 a0001c0001t0004g0007 others(5): Show |
16 | HG00741.hp1 HG01891.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.139+412T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108157 | |||||||
| chr5:103108160 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.139+409T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108160 | |||||||
| chr5:103108170 | C | T | 2 | a0001c0001t0008g0031 a0001c0001t0008g0032 |
4 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.139+399G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108170 | |||||||
| chr5:103108216 | A | G | 1 | a0002c0002t0002g0155 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.139+353T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108216 | |||||||
| chr5:103108234 | A | T | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.139+335T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108234 | |||||||
| chr5:103108260 | A | T | 89 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(86): Show |
154 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.139+309T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108260 | |||||||
| chr5:103108349 | A | G | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.139+220T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108349 | |||||||
| chr5:103108385 | C | T | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.139+184G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108385 | |||||||
| chr5:103108412 | T | C | 3 | a0003c0003t0003g0025 a0003c0003t0003g0061 a0003c0003t0003g0062 |
4 | HG02572.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+157A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 2/7 | chr5 | 103108412 | |||||||
| chr5:103108891 | T | C | 63 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(60): Show |
110 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7-177A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103108891 | |||||||
| chr5:103108914 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0130 others(1): Show |
7 | HG02965.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-200G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103108914 | |||||||
| chr5:103109019 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-7-305A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103109019 | |||||||
| chr5:103109480 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-7-766T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103109480 | |||||||
| chr5:103109738 | AT | A | 3 | a0003c0003t0003g0025 a0003c0003t0003g0061 a0003c0003t0003g0062 |
4 | HG02572.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-1025delA | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103109738 | |||||||
| chr5:103109766 | C | T | 86 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(83): Show |
149 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.-7-1052G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103109766 | |||||||
| chr5:103110123 | T | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-1409A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103110123 | |||||||
| chr5:103110200 | CA | C | 70 | a0001c0001t0001g0172 a0001c0001t0003g0050 a0002c0002t0002g0002 others(67): Show |
119 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.-7-1487delT | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103110200 | |||||||
| chr5:103110202 | A | C | 5 | a0001c0001t0001g0026 a0001c0001t0003g0014 a0001c0001t0008g0031 others(2): Show |
10 | HG01884.hp2 HG02486.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-1488T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103110202 | |||||||
| chr5:103110310 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-1596G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103110310 | |||||||
| chr5:103110340 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0051 |
3 | HG02055.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-7-1626A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103110340 | |||||||
| chr5:103110496 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7-1782T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103110496 | |||||||
| chr5:103110758 | C | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-2044G>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103110758 | |||||||
| chr5:103111033 | C | T | 9 | a0002c0002t0002g0004 a0002c0002t0002g0006 a0002c0002t0002g0136 others(6): Show |
20 | HG00609.hp2 HG02056.hp1 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-7-2319G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111033 | |||||||
| chr5:103111175 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-2461G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111175 | |||||||
| chr5:103111182 | T | TA | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-2469dupT | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111182 | |||||||
| chr5:103111253 | A | G | 86 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(83): Show |
149 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.-7-2539T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111253 | |||||||
| chr5:103111345 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-7-2631A>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111345 | |||||||
| chr5:103111423 | C | T | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-2709G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111423 | |||||||
| chr5:103111508 | A | C | 1 | a0001c0001t0003g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-7-2794T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111508 | |||||||
| chr5:103111523 | T | C | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-2809A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111523 | |||||||
| chr5:103111600 | T | C | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-2886A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111600 | |||||||
| chr5:103111601 | G | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-2887C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111601 | |||||||
| chr5:103111942 | A | C | 63 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(60): Show |
110 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7-3228T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103111942 | |||||||
| chr5:103112025 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-7-3311G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103112025 | |||||||
| chr5:103112166 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-7-3452C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103112166 | |||||||
| chr5:103112199 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-7-3485A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103112199 | |||||||
| chr5:103112313 | T | TCAA | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-3602_-7-3600dup others(3): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103112313 | |||||||
| chr5:103112351 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-7-3637A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103112351 | |||||||
| chr5:103112699 | T | A | 2 | a0002c0002t0002g0139 a0002c0002t0002g0140 |
2 | NA18946.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-7-3985A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103112699 | |||||||
| chr5:103112995 | A | C | 1 | a0002c0002t0002g0153 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-7-4281T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103112995 | |||||||
| chr5:103113338 | C | G | 1 | a0002c0002t0002g0173 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-7-4624G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103113338 | |||||||
| chr5:103113489 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0051 |
3 | HG02055.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-7-4775A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103113489 | |||||||
| chr5:103113521 | C | CT | 68 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(65): Show |
117 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.-7-4808dupA | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103113521 | |||||||
| chr5:103113521 | CT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0128 a0001c0001t0003g0014 others(4): Show |
10 | HG00323.hp1 HG00323.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-4808delA | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103113521 | |||||||
| chr5:103113748 | C | T | 3 | a0002c0002t0002g0011 a0002c0002t0002g0020 a0002c0002t0002g0152 |
8 | HG02135.hp1 NA18953.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-5034G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103113748 | |||||||
| chr5:103113850 | C | G | 1 | a0001c0001t0001g0033 | 2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-7-5136G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103113850 | |||||||
| chr5:103114083 | CT | C | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-7-5370delA | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103114083 | |||||||
| chr5:103114713 | G | A | 85 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0023 others(82): Show |
146 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8+5351C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103114713 | |||||||
| chr5:103114725 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-8+5339G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103114725 | |||||||
| chr5:103114740 | A | G | 3 | a0001c0001t0001g0172 a0002c0002t0002g0043 a0002c0002t0002g0180 |
4 | NA18956.hp2 NA18961.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+5324T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103114740 | |||||||
| chr5:103114808 | C | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+5256G>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103114808 | |||||||
| chr5:103114872 | C | G | 86 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(83): Show |
149 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.-8+5192G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103114872 | |||||||
| chr5:103115112 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8+4952T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115112 | |||||||
| chr5:103115116 | G | T | 80 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0023 others(77): Show |
138 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.-8+4948C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115116 | |||||||
| chr5:103115188 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-8+4876G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115188 | |||||||
| chr5:103115276 | A | G | 1 | a0002c0006t0013g0037 | 2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-8+4788T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115276 | |||||||
| chr5:103115431 | T | C | 1 | a0002c0002t0009g0149 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-8+4633A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115431 | |||||||
| chr5:103115465 | G | C | 1 | a0001c0001t0003g0014 | 3 | HG01884.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-8+4599C>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115465 | |||||||
| chr5:103115572 | C | T | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+4492G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115572 | |||||||
| chr5:103115605 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-8+4459C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115605 | |||||||
| chr5:103115691 | T | C | 1 | a0002c0002t0002g0178 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-8+4373A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115691 | |||||||
| chr5:103115868 | A | C | 1 | a0001c0001t0006g0065 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8+4196T>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103115868 | |||||||
| chr5:103116090 | C | G | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+3974G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103116090 | |||||||
| chr5:103116298 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-8+3766G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103116298 | |||||||
| chr5:103116554 | C | T | 80 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0023 others(77): Show |
138 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.-8+3510G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103116554 | |||||||
| chr5:103116572 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-8+3492G>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103116572 | |||||||
| chr5:103116851 | A | T | 1 | a0002c0002t0002g0152 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-8+3213T>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103116851 | |||||||
| chr5:103116852 | C | T | 86 | a0001c0001t0001g0172 a0001c0001t0003g0013 a0001c0001t0003g0014 others(83): Show |
149 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.-8+3212G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103116852 | |||||||
| chr5:103116962 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-8+3102A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103116962 | |||||||
| chr5:103117064 | A | G | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+3000T>C | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117064 | |||||||
| chr5:103117226 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8+2838A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117226 | |||||||
| chr5:103117304 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0051 |
3 | HG02055.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-8+2760A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117304 | |||||||
| chr5:103117398 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0130 others(1): Show |
7 | HG02965.hp1 HG03130.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+2666A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117398 | |||||||
| chr5:103117581 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8+2483A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TAC | 3 | a0001c0001t0005g0046 a0001c0001t0008g0031 a0001c0001t0008g0032 |
5 | HG01099.hp2 HG02486.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+2481_-8+2482dup others(2): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATACACA others(21): Show |
1 | a0002c0002t0002g0179 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(28): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATACACA others(25): Show |
1 | a0002c0002t0002g0185 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(32): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATACACA others(27): Show |
1 | a0002c0002t0002g0186 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(34): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(9): Show |
1 | a0002c0002t0002g0141 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(16): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(13): Show |
6 | a0002c0002t0002g0036 a0002c0002t0002g0143 a0002c0002t0002g0144 others(3): Show |
7 | HG00738.hp1 HG01071.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(20): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(15): Show |
3 | a0002c0002t0009g0148 a0002c0002t0009g0149 a0005c0007t0002g0147 |
3 | HG00597.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(22): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(17): Show |
3 | a0002c0002t0002g0038 a0002c0002t0002g0150 a0002c0006t0013g0037 |
5 | HG01081.hp2 HG03098.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(24): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(19): Show |
27 | a0002c0002t0002g0002 a0002c0002t0002g0011 a0002c0002t0002g0012 others(24): Show |
57 | HG00099.hp1 HG00423.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(26): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(21): Show |
4 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0170 others(1): Show |
6 | HG00609.hp1 HG01106.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(28): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(23): Show |
12 | a0001c0001t0001g0172 a0002c0002t0002g0004 a0002c0002t0002g0006 others(9): Show |
26 | HG00609.hp2 HG00642.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(30): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(25): Show |
8 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0139 others(5): Show |
8 | HG00733.hp1 HG02155.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(32): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATACA others(27): Show |
1 | a0002c0002t0002g0184 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(34): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117581 | T | TATATATA others(23): Show |
1 | a0002c0002t0002g0136 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-8+2482_-8+2483ins others(30): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117581 | |||||||
| chr5:103117853 | G | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+2211C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103117853 | |||||||
| chr5:103118176 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0033 |
6 | HG01243.hp1 HG02486.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+1888A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118176 | |||||||
| chr5:103118252 | G | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
7 | HG02074.hp2 NA18963.hp1 NA19006.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+1812C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118252 | |||||||
| chr5:103118297 | T | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0132 |
4 | HG03195.hp1 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+1767A>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118297 | |||||||
| chr5:103118314 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-8+1750G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118314 | |||||||
| chr5:103118352 | AATT | A | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+1709_-8+1711del others(3): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118352 | |||||||
| chr5:103118600 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0133 |
3 | NA18964.hp1 NA18968.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-8+1464A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118600 | |||||||
| chr5:103118705 | C | T | 4 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0139 others(1): Show |
4 | NA18946.hp1 NA18983.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+1359G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118705 | |||||||
| chr5:103118735 | C | T | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+1329G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118735 | |||||||
| chr5:103118745 | AGTT | A | 2 | a0004c0005t0005g0035 a0004c0005t0005g0134 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-8+1316_-8+1318del others(3): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118745 | |||||||
| chr5:103118749 | G | GT | 11 | a0001c0001t0003g0013 a0001c0001t0003g0023 a0001c0001t0003g0050 others(8): Show |
20 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8+1314dupA | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118749 | |||||||
| chr5:103118766 | G | T | 69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+1298C>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118766 | |||||||
| chr5:103118773 | C | CATACACT others(38): Show |
69 | a0001c0001t0001g0172 a0002c0002t0002g0002 a0002c0002t0002g0004 others(66): Show |
118 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+1290_-8+1291ins others(45): Show |
GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103118773 | |||||||
| chr5:103119039 | G | A | 1 | a0001c0001t0001g0044 | 2 | NA18980.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-8+1025C>T | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103119039 | |||||||
| chr5:103119443 | C | T | 11 | a0001c0001t0003g0013 a0001c0001t0003g0023 a0001c0001t0003g0050 others(8): Show |
20 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8+621G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103119443 | |||||||
| chr5:103119667 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8+397A>G | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103119667 | |||||||
| chr5:103119684 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-8+380G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103119684 | |||||||
| chr5:103119777 | C | T | 1 | a0002c0002t0010g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+287G>A | GIN1 | ENSG00000145723.17 | transcript | ENST00000399004.7 | protein_coding | 1/7 | chr5 | 103119777 |