Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3321 |
| ensemblid | ENSG00000143061.18 |
| hgncid | 5950 |
| symbol | IGSF3 |
| name | immunoglobulin superfamily member 3 |
| refseq_nuc | NM_001007237.3 |
| refseq_prot | NP_001007238.1 |
| ensembl_nuc | ENST00000369486.8 |
| ensembl_prot | ENSP00000358498.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 116574408 |
| end | 116667733 |
| strand | - |
| ver | v1.2 |
| region | chr1:116574408-116667733 |
| region5000 | chr1:116569408-116672733 |
| regionname0 | IGSF3_chr1_116574408_116667733 |
| regionname5000 | IGSF3_chr1_116569408_116672733 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1194 | 99 | 33 | 10 | 44 | 1 | 11 | 34 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0002 | 1/0 | 1194 | 88 | 35 | 17 | 22 | 5 | 8 | 13 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0003 | 0/1 | 1195 | 58 | 11 | 18 | 10 | 5 | 13 | 9 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1190): Show |
chr1 | 116569408 | 116672733 |
| a0004 | 0/0 | 1194 | 4 | 1 | 1 | 2 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0005 | 0/0 | 1194 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0006 | 0/0 | 1194 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0007 | 0/0 | 1194 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0008 | 0/0 | 1194 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0009 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0010 | 0/0 | 1195 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1190): Show |
chr1 | 116569408 | 116672733 |
| a0011 | 0/0 | 1195 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1190): Show |
chr1 | 116569408 | 116672733 |
| a0012 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0013 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0014 | 0/0 | 1194 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0015 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1189): Show |
chr1 | 116569408 | 116672733 |
| a0016 | 0/0 | 1195 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1190): Show |
chr1 | 116569408 | 116672733 |
| a0017 | 0/0 | 1195 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | MKCFF others(1190): Show |
chr1 | 116569408 | 116672733 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3582 | 72 | 19 | 10 | 34 | 1 | 8 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0001c0005 | 0/0 | 3582 | 8 | 6 | 0 | 0 | 0 | 2 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0001c0006 | 0/0 | 3582 | 7 | 0 | 0 | 7 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0001c0007 | 0/0 | 3582 | 5 | 5 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0001c0008 | 0/0 | 3582 | 4 | 0 | 0 | 3 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0001c0010 | 0/0 | 3582 | 2 | 2 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0001c0013 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0002c0002 | 1/0 | 3582 | 67 | 18 | 15 | 21 | 5 | 7 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0002c0004 | 0/0 | 3582 | 16 | 14 | 2 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0002c0014 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0002c0015 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0002c0022 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0002c0024 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0002c0031 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0003c0003 | 0/1 | 3585 | 56 | 11 | 18 | 9 | 5 | 12 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3580): Show |
chr1 | 116569408 | 116672733 | ||
| a0003c0017 | 0/0 | 3585 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3580): Show |
chr1 | 116569408 | 116672733 | ||
| a0003c0027 | 0/0 | 3585 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3580): Show |
chr1 | 116569408 | 116672733 | ||
| a0004c0009 | 0/0 | 3582 | 4 | 1 | 1 | 2 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0005c0011 | 0/0 | 3582 | 2 | 0 | 2 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0005c0026 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0006c0020 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0007c0021 | 0/0 | 3582 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0008c0032 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0009c0029 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0010c0028 | 0/0 | 3585 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3580): Show |
chr1 | 116569408 | 116672733 | ||
| a0011c0030 | 0/0 | 3585 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3580): Show |
chr1 | 116569408 | 116672733 | ||
| a0012c0012 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0013c0016 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0014c0019 | 0/0 | 3582 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0015c0025 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3577): Show |
chr1 | 116569408 | 116672733 | ||
| a0016c0023 | 0/0 | 3585 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3580): Show |
chr1 | 116569408 | 116672733 | ||
| a0017c0018 | 0/0 | 3585 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | ATGAA others(3580): Show |
chr1 | 116569408 | 116672733 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7235 | 48 | 2 | 10 | 27 | 1 | 8 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0001t0002 | 0/0 | 7217 | 7 | 0 | 0 | 7 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7212): Show |
chr1 | 116569408 | 116672733 |
| a0001c0001t0003 | 0/0 | 7235 | 2 | 2 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0001t0004 | 0/0 | 7235 | 7 | 7 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0001t0005 | 0/0 | 7235 | 5 | 5 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0001t0014 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0001t0016 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0001t0019 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0005t0001 | 0/0 | 7235 | 3 | 1 | 0 | 0 | 0 | 2 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0005t0003 | 0/0 | 7235 | 5 | 5 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0006t0001 | 0/0 | 7235 | 7 | 0 | 0 | 7 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0007t0003 | 0/0 | 7235 | 5 | 5 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0008t0001 | 0/0 | 7235 | 4 | 0 | 0 | 3 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0010t0001 | 0/0 | 7235 | 2 | 2 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0001c0013t0003 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0001 | 1/0 | 7235 | 46 | 8 | 15 | 13 | 5 | 4 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0002 | 0/0 | 7217 | 7 | 0 | 0 | 7 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7212): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0003 | 0/0 | 7235 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0004 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0006 | 0/0 | 7235 | 3 | 3 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0007 | 0/0 | 7235 | 2 | 1 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0010 | 0/0 | 7235 | 2 | 2 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0011 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0012 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0013 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0017 | 0/0 | 7235 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0002t0022 | 0/0 | 7217 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7212): Show |
chr1 | 116569408 | 116672733 |
| a0002c0004t0001 | 0/0 | 7235 | 15 | 13 | 2 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0004t0018 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0014t0003 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0015t0003 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0022t0001 | 0/0 | 7235 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0024t0001 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0002c0031t0002 | 0/0 | 7217 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7212): Show |
chr1 | 116569408 | 116672733 |
| a0003c0003t0001 | 0/1 | 7238 | 46 | 10 | 16 | 5 | 3 | 11 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0003c0003t0002 | 0/0 | 7220 | 3 | 0 | 0 | 3 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7215): Show |
chr1 | 116569408 | 116672733 |
| a0003c0003t0003 | 0/0 | 7238 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0003c0003t0008 | 0/0 | 7238 | 2 | 0 | 0 | 0 | 2 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0003c0003t0009 | 0/0 | 7238 | 2 | 0 | 2 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0003c0003t0015 | 0/0 | 7238 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0003c0003t0021 | 0/0 | 7220 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7215): Show |
chr1 | 116569408 | 116672733 |
| a0003c0017t0001 | 0/0 | 7238 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0003c0027t0001 | 0/0 | 7238 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0004c0009t0001 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0004c0009t0002 | 0/0 | 7217 | 2 | 0 | 1 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7212): Show |
chr1 | 116569408 | 116672733 |
| a0004c0009t0003 | 0/0 | 7235 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0005c0011t0001 | 0/0 | 7235 | 2 | 0 | 2 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0005c0026t0001 | 0/0 | 7235 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0006c0020t0001 | 0/0 | 7235 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0007c0021t0001 | 0/0 | 7235 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0008c0032t0001 | 0/0 | 7235 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0009c0029t0001 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0010c0028t0003 | 0/0 | 7238 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0011c0030t0001 | 0/0 | 7238 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| a0012c0012t0020 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0013c0016t0001 | 0/0 | 7235 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0014c0019t0001 | 0/0 | 7235 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7230): Show |
chr1 | 116569408 | 116672733 |
| a0015c0025t0002 | 0/0 | 7217 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7212): Show |
chr1 | 116569408 | 116672733 |
| a0016c0023t0002 | 0/0 | 7220 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7215): Show |
chr1 | 116569408 | 116672733 |
| a0017c0018t0001 | 0/0 | 7238 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | AGCGC others(7233): Show |
chr1 | 116569408 | 116672733 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0014g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0001t0019g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0005t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0006t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0006t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0007t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0007t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0007t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0007t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0008t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0008t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0008t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0008t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0010t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0010t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0001c0013t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0012 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0007g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0017g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0002t0022g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0004t0018g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0014t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0015t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0022t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0024t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0002c0031t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0008g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0015g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0003t0021g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0017t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0003c0027t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0004c0009t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0004c0009t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0004c0009t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0004c0009t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0005c0011t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0005c0026t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0006c0020t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0007c0021t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0008c0032t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0009c0029t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0010c0028t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0011c0030t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0012c0012t0020g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0013c0016t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0014c0019t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0015c0025t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0016c0023t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| a0017c0018t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0006 | c0020 | t0001 | g0079 | EUR | GBR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0206 | EUR | GBR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0091 | EUR | GBR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0128 | EUR | FIN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0092 | EUR | FIN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00609 | hp2 | a0002 | c0031 | t0002 | g0192 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00621 | hp2 | a0001 | c0008 | t0001 | g0156 | EAS | CHS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0078 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0172 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01070 | hp1 | a0005 | c0011 | t0001 | g0006 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01074 | hp1 | a0005 | c0011 | t0001 | g0006 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0125 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0088 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01099 | hp2 | a0002 | c0004 | t0001 | g0047 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01106 | hp2 | a0007 | c0021 | t0001 | g0064 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0059 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01192 | hp1 | a0003 | c0003 | t0009 | g0050 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0239 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0069 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0231 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0061 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01346 | hp1 | a0003 | c0003 | t0009 | g0101 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01433 | hp2 | a0002 | c0004 | t0001 | g0086 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0122 | EUR | IBS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01515 | hp2 | a0003 | c0003 | t0008 | g0007 | EUR | IBS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01517 | hp1 | a0008 | c0032 | t0001 | g0226 | EUR | IBS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01517 | hp2 | a0003 | c0003 | t0008 | g0007 | EUR | IBS | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01891 | hp1 | a0009 | c0029 | t0001 | g0157 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01891 | hp2 | a0001 | c0005 | t0003 | g0028 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01934 | hp1 | a0010 | c0028 | t0003 | g0033 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01943 | hp1 | a0004 | c0009 | t0002 | g0191 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0238 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0137 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG01993 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0083 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02074 | hp1 | a0004 | c0009 | t0003 | g0035 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02080 | hp2 | a0002 | c0002 | t0017 | g0117 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02257 | hp2 | a0011 | c0030 | t0001 | g0167 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0177 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0034 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02615 | hp1 | a0002 | c0002 | t0007 | g0170 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02615 | hp2 | a0001 | c0007 | t0003 | g0004 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0133 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02630 | hp1 | a0013 | c0016 | t0001 | g0051 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0151 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02647 | hp2 | a0002 | c0004 | t0001 | g0085 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0075 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02717 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02717 | hp2 | a0001 | c0005 | t0003 | g0018 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0098 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02809 | hp1 | a0001 | c0005 | t0003 | g0013 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0173 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02895 | hp1 | a0002 | c0002 | t0006 | g0015 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0109 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02896 | hp2 | a0001 | c0007 | t0003 | g0004 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02897 | hp2 | a0002 | c0002 | t0006 | g0016 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02922 | hp2 | a0002 | c0014 | t0003 | g0027 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02965 | hp1 | a0001 | c0005 | t0003 | g0026 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02970 | hp1 | a0002 | c0004 | t0001 | g0080 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02970 | hp2 | a0001 | c0007 | t0003 | g0032 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0119 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0221 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03017 | hp2 | a0003 | c0003 | t0021 | g0179 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0096 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03041 | hp2 | a0001 | c0013 | t0003 | g0019 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03098 | hp1 | a0002 | c0004 | t0001 | g0135 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0154 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0014 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03209 | hp1 | a0002 | c0004 | t0018 | g0071 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03209 | hp2 | a0002 | c0004 | t0001 | g0107 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03225 | hp2 | a0002 | c0002 | t0010 | g0175 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0076 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03453 | hp1 | a0001 | c0005 | t0003 | g0022 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03453 | hp2 | a0002 | c0002 | t0010 | g0176 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0204 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03490 | hp1 | a0014 | c0019 | t0001 | g0124 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0067 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0127 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0094 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0008 | AFR | ESN | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0203 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03579 | hp1 | a0002 | c0002 | t0013 | g0171 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03579 | hp2 | a0001 | c0010 | t0001 | g0246 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0062 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03654 | hp2 | a0001 | c0008 | t0001 | g0228 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0114 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03669 | hp2 | a0002 | c0022 | t0001 | g0074 | SAS | PJL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03688 | hp1 | a0001 | c0005 | t0001 | g0102 | SAS | STU | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0138 | SAS | STU | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03834 | hp1 | a0001 | c0005 | t0001 | g0099 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0063 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG04115 | hp1 | a0002 | c0002 | t0007 | g0089 | SAS | STU | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0123 | SAS | STU | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG04184 | hp2 | a0002 | c0002 | t0022 | g0187 | SAS | BEB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG04199 | hp1 | a0003 | c0027 | t0001 | g0097 | SAS | STU | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18522 | hp1 | a0002 | c0002 | t0012 | g0108 | AFR | YRI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18522 | hp2 | a0002 | c0004 | t0001 | g0048 | AFR | YRI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0181 | EAS | CHB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18747 | hp1 | a0015 | c0025 | t0002 | g0185 | EAS | CHB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | CHB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0244 | AFR | YRI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18941 | hp2 | a0001 | c0006 | t0001 | g0003 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18944 | hp1 | a0016 | c0023 | t0002 | g0182 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18946 | hp1 | a0001 | c0008 | t0001 | g0158 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0116 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18961 | hp2 | a0001 | c0006 | t0001 | g0143 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0242 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18969 | hp1 | a0003 | c0003 | t0002 | g0184 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18975 | hp2 | a0003 | c0003 | t0015 | g0234 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18977 | hp1 | a0001 | c0006 | t0001 | g0144 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18984 | hp2 | a0001 | c0006 | t0001 | g0150 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0003 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18994 | hp1 | a0003 | c0017 | t0001 | g0165 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19001 | hp1 | a0003 | c0003 | t0002 | g0200 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19002 | hp1 | a0001 | c0008 | t0001 | g0160 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0233 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19005 | hp1 | a0001 | c0006 | t0001 | g0003 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19009 | hp1 | a0004 | c0009 | t0002 | g0197 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19043 | hp1 | a0002 | c0015 | t0003 | g0020 | AFR | LWK | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19043 | hp2 | a0002 | c0004 | t0001 | g0134 | AFR | LWK | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19057 | hp2 | a0003 | c0003 | t0002 | g0201 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19076 | hp2 | a0001 | c0006 | t0001 | g0141 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19240 | hp1 | a0002 | c0004 | t0001 | g0073 | AFR | YRI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA19240 | hp2 | a0004 | c0009 | t0001 | g0072 | AFR | YRI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0057 | AFR | ASW | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20129 | hp2 | a0002 | c0024 | t0001 | g0087 | AFR | ASW | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0054 | EUR | TSI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0216 | EUR | TSI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20805 | hp1 | a0005 | c0026 | t0001 | g0044 | EUR | TSI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0210 | EUR | TSI | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20905 | hp1 | a0017 | c0018 | t0001 | g0056 | SAS | GIH | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0077 | SAS | GIH | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0111 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02109 | hp2 | a0001 | c0007 | t0003 | g0017 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02486 | hp1 | a0002 | c0002 | t0011 | g0040 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02486 | hp2 | a0012 | c0012 | t0020 | g0178 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | ACB | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03471 | hp1 | a0003 | c0003 | t0003 | g0030 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG03471 | hp2 | a0002 | c0004 | t0001 | g0082 | AFR | MSL | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG06807 | hp1 | a0001 | c0007 | t0003 | g0029 | AFR | USA | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | USA | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | LWK | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| NA21309 | hp2 | a0001 | c0010 | t0001 | g0245 | AFR | LWK | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0095 | REF | REF | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0012 | REF | REF | IGSF3_chr1_116569408_116672733 | IGSF3 | chr1 | 116569408 | 116672733 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116579508 | T | C | 5 | a0001 a0008 a0010 others(2): Show |
103 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
missense_variant | MODERATE | c.3218A>G | p.Gln1073Arg | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3964/7235 | 3218/3585 | 1073/1194 | chr1 | 116579508 | |||
| chr1:116579647 | GGTC | G | 4 | a0003 a0010 a0011 others(1): Show |
16 | HG00280.hp2 HG01099.hp1 HG01255.hp2 others(13): Show |
conservative_inframe_deletion | MODERATE | c.3076_3078delGAC | p.Asp1026del | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3824/7235 | 3076/3585 | 1026/1194 | chr1 | 116579647 | |||
| chr1:116579663 | G | C | 1 | a0007 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.3063C>G | p.Asp1021Glu | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3809/7235 | 3063/3585 | 1021/1194 | chr1 | 116579663 | |||
| chr1:116579663 | G | GTCC | 2 | a0003 a0017 |
45 | HG00140.hp2 HG00639.hp1 HG00738.hp2 others(42): Show |
disruptive_inframe_insertion | MODERATE | c.3062_3063insGGA | p.Asp1020_Asp1021ins others(3): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3808/7235 | 3062/3585 | 1021/1194 | chr1 | 116579663 | |||
| chr1:116579664 | T | A | 1 | a0014 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.3062A>T | p.Asp1021Val | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3808/7235 | 3062/3585 | 1021/1194 | chr1 | 116579664 | |||
| chr1:116579666 | G | C | 4 | a0003 a0006 a0007 others(1): Show |
47 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(44): Show |
missense_variant | MODERATE | c.3060C>G | p.Asp1020Glu | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3806/7235 | 3060/3585 | 1020/1194 | chr1 | 116579666 | |||
| chr1:116579666 | G | GTCCTCC | 4 | a0003 a0010 a0011 others(1): Show |
16 | HG00280.hp2 HG01099.hp1 HG01255.hp2 others(13): Show |
disruptive_inframe_insertion | MODERATE | c.3054_3059dupGGAGGA | p.Glu1018_Glu1019dup | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3805/7235 | 3059/3585 | 1020/1194 | chr1 | 116579666 | |||
| chr1:116584692 | C | T | 1 | a0017 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2801G>A | p.Arg934Gln | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/11 | 3547/7235 | 2801/3585 | 934/1194 | chr1 | 116584692 | |||
| chr1:116584795 | C | T | 1 | a0005 | 3 | HG01070.hp1 HG01074.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.2698G>A | p.Val900Met | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/11 | 3444/7235 | 2698/3585 | 900/1194 | chr1 | 116584795 | |||
| chr1:116585022 | C | T | 1 | a0004 | 4 | HG01943.hp1 HG02074.hp1 NA19009.hp1 others(1): Show |
missense_variant | MODERATE | c.2471G>A | p.Gly824Glu | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/11 | 3217/7235 | 2471/3585 | 824/1194 | chr1 | 116585022 | |||
| chr1:116600009 | T | C | 1 | a0016 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1961A>G | p.Tyr654Cys | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/11 | 2707/7235 | 1961/3585 | 654/1194 | chr1 | 116600009 | |||
| chr1:116600114 | A | G | 1 | a0013 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1856T>C | p.Ile619Thr | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/11 | 2602/7235 | 1856/3585 | 619/1194 | chr1 | 116600114 | |||
| chr1:116600234 | G | A | 1 | a0015 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1736C>T | p.Ser579Leu | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/11 | 2482/7235 | 1736/3585 | 579/1194 | chr1 | 116600234 | |||
| chr1:116603778 | C | G | 1 | a0012 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1470G>C | p.Gln490His | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/11 | 2216/7235 | 1470/3585 | 490/1194 | chr1 | 116603778 | |||
| chr1:116608064 | C | A | 1 | a0010 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1100G>T | p.Arg367Leu | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/11 | 1846/7235 | 1100/3585 | 367/1194 | chr1 | 116608064 | |||
| chr1:116608179 | C | A | 2 | a0009 a0011 |
2 | HG01891.hp1 HG02257.hp2 |
missense_variant | MODERATE | c.985G>T | p.Gly329Cys | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/11 | 1731/7235 | 985/3585 | 329/1194 | chr1 | 116608179 | |||
| chr1:116608274 | G | A | 1 | a0008 | 1 | HG01517.hp1 | missense_variant | MODERATE | c.890C>T | p.Pro297Leu | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/11 | 1636/7235 | 890/3585 | 297/1194 | chr1 | 116608274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116579522 | C | A | 2 | a0002c0004 a0013c0016 |
17 | HG01099.hp2 HG01433.hp2 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.3204G>T | p.Leu1068Leu | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/11 | 3950/7235 | 3204/3585 | 1068/1194 | chr1 | 116579522 | |||
| chr1:116588785 | G | A | 6 | a0001c0005 a0001c0007 a0001c0010 others(3): Show |
18 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(15): Show |
synonymous_variant | LOW | c.2349C>T | p.His783His | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/11 | 3095/7235 | 2349/3585 | 783/1194 | chr1 | 116588785 | |||
| chr1:116588803 | G | A | 1 | a0012c0012 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.2331C>T | p.Ser777Ser | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/11 | 3077/7235 | 2331/3585 | 777/1194 | chr1 | 116588803 | |||
| chr1:116588911 | G | A | 1 | a0002c0022 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.2223C>T | p.Tyr741Tyr | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/11 | 2969/7235 | 2223/3585 | 741/1194 | chr1 | 116588911 | |||
| chr1:116599984 | C | T | 1 | a0003c0017 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.1986G>A | p.Ala662Ala | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/11 | 2732/7235 | 1986/3585 | 662/1194 | chr1 | 116599984 | |||
| chr1:116600167 | G | A | 2 | a0002c0015 a0002c0024 |
2 | NA19043.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.1803C>T | p.Asp601Asp | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/11 | 2549/7235 | 1803/3585 | 601/1194 | chr1 | 116600167 | |||
| chr1:116600212 | C | T | 1 | a0001c0013 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1758G>A | p.Pro586Pro | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/11 | 2504/7235 | 1758/3585 | 586/1194 | chr1 | 116600212 | |||
| chr1:116603697 | C | T | 6 | a0001c0005 a0001c0008 a0001c0013 others(3): Show |
16 | HG00621.hp2 HG01891.hp2 HG02486.hp2 others(13): Show |
synonymous_variant | LOW | c.1551G>A | p.Val517Val | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/11 | 2297/7235 | 1551/3585 | 517/1194 | chr1 | 116603697 | |||
| chr1:116603754 | G | A | 1 | a0005c0026 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1494C>T | p.Ile498Ile | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/11 | 2240/7235 | 1494/3585 | 498/1194 | chr1 | 116603754 | |||
| chr1:116603844 | G | A | 1 | a0003c0027 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1404C>T | p.Thr468Thr | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/11 | 2150/7235 | 1404/3585 | 468/1194 | chr1 | 116603844 | |||
| chr1:116603940 | C | T | 1 | a0001c0010 | 2 | HG03579.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1308G>A | p.Thr436Thr | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/11 | 2054/7235 | 1308/3585 | 436/1194 | chr1 | 116603940 | |||
| chr1:116608234 | G | A | 1 | a0002c0031 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.930C>T | p.Pro310Pro | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/11 | 1676/7235 | 930/3585 | 310/1194 | chr1 | 116608234 | |||
| chr1:116608296 | G | T | 1 | a0001c0006 | 7 | NA18941.hp2 NA18961.hp2 NA18977.hp1 others(4): Show |
synonymous_variant | LOW | c.868C>A | p.Arg290Arg | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/11 | 1614/7235 | 868/3585 | 290/1194 | chr1 | 116608296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116575936 | A | G | 1 | a0003c0003t0008 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1376T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 1376 | chr1 | 116575936 | ||||||
| chr1:116575944 | C | T | 1 | a0003c0003t0021 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1368G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 1368 | chr1 | 116575944 | ||||||
| chr1:116576012 | C | G | 1 | a0003c0003t0015 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1300G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 1300 | chr1 | 116576012 | ||||||
| chr1:116576188 | C | T | 1 | a0002c0002t0017 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1124G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 1124 | chr1 | 116576188 | ||||||
| chr1:116576194 | C | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0019 others(1): Show |
14 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1118G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 1118 | chr1 | 116576194 | ||||||
| chr1:116576230 | G | A | 1 | a0001c0001t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1082C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 1082 | chr1 | 116576230 | ||||||
| chr1:116576452 | T | G | 1 | a0002c0002t0013 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*860A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 860 | chr1 | 116576452 | ||||||
| chr1:116576604 | C | T | 1 | a0001c0001t0014 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*708G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 708 | chr1 | 116576604 | ||||||
| chr1:116576761 | C | A | 1 | a0002c0002t0017 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*551G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 551 | chr1 | 116576761 | ||||||
| chr1:116576815 | T | C | 1 | a0002c0002t0022 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*497A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 497 | chr1 | 116576815 | ||||||
| chr1:116576989 | G | T | 3 | a0002c0002t0006 a0002c0002t0007 a0002c0002t0013 |
6 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*323C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 323 | chr1 | 116576989 | ||||||
| chr1:116577111 | C | T | 2 | a0002c0002t0011 a0002c0002t0012 |
2 | HG02486.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*201G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 201 | chr1 | 116577111 | ||||||
| chr1:116577112 | G | A | 1 | a0002c0004t0018 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 200 | chr1 | 116577112 | ||||||
| chr1:116577113 | C | A | 1 | a0003c0003t0009 | 2 | HG01192.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*199G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 199 | chr1 | 116577113 | ||||||
| chr1:116577115 | C | G | 1 | a0003c0003t0009 | 2 | HG01192.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*197G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 197 | chr1 | 116577115 | ||||||
| chr1:116577119 | T | A | 1 | a0003c0003t0009 | 2 | HG01192.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 11/11 | 193 | chr1 | 116577119 | ||||||
| chr1:116666337 | T | C | 1 | a0002c0002t0010 | 2 | HG03225.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-11A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/11 | 11 | chr1 | 116666337 | ||||||
| chr1:116666496 | G | A | 2 | a0001c0001t0019 a0012c0012t0020 |
2 | HG02280.hp2 HG02486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-170C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/11 | 170 | chr1 | 116666496 | ||||||
| chr1:116666799 | CTGCCTGG others(11): Show |
C | 9 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0022 others(6): Show |
24 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-491_-474delAACGGT others(12): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/11 | 474 | chr1 | 116666799 | ||||||
| chr1:116666802 | C | T | 2 | a0001c0001t0001 a0002c0002t0001 |
2 | HG02027.hp2 HG02074.hp2 |
5_prime_UTR_variant | MODIFIER | c.-476G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/11 | 476 | chr1 | 116666802 | ||||||
| chr1:116667652 | A | T | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0005t0003 others(11): Show |
31 | HG01891.hp2 HG01934.hp1 HG02074.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-665T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/11 | 1326 | chr1 | 116667652 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:116577633 | G | A | 2 | a0003c0003t0001g0076 a0003c0003t0001g0127 |
2 | HG03239.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.3335-71C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116577633 | |||||||
| chr1:116577698 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3335-136T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116577698 | |||||||
| chr1:116577746 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3335-184A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116577746 | |||||||
| chr1:116577941 | A | G | 5 | a0002c0002t0006g0014 a0002c0002t0006g0015 a0002c0002t0006g0016 others(2): Show |
5 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3335-379T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116577941 | |||||||
| chr1:116577981 | A | G | 14 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(11): Show |
14 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3335-419T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116577981 | |||||||
| chr1:116578089 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3335-527C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116578089 | |||||||
| chr1:116578266 | C | T | 1 | a0005c0011t0001g0006 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.3335-704G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116578266 | |||||||
| chr1:116578517 | C | G | 2 | a0003c0003t0009g0050 a0003c0003t0009g0101 |
2 | HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.3334+875G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116578517 | |||||||
| chr1:116578529 | G | T | 7 | a0002c0002t0001g0131 a0002c0002t0001g0152 a0002c0002t0001g0155 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3334+863C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116578529 | |||||||
| chr1:116578641 | A | C | 5 | a0002c0002t0006g0014 a0002c0002t0006g0015 a0002c0002t0006g0016 others(2): Show |
5 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3334+751T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116578641 | |||||||
| chr1:116578996 | G | A | 1 | a0004c0009t0002g0197 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3334+396C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116578996 | |||||||
| chr1:116579066 | A | G | 1 | a0002c0002t0001g0217 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3334+326T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116579066 | |||||||
| chr1:116579170 | T | C | 1 | a0001c0007t0003g0004 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3334+222A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116579170 | |||||||
| chr1:116579243 | G | A | 110 | a0001c0001t0001g0070 a0001c0001t0001g0136 a0001c0001t0001g0207 others(107): Show |
116 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(113): Show |
intron_variant | MODIFIER | c.3334+149C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116579243 | |||||||
| chr1:116579345 | A | G | 2 | a0003c0003t0001g0076 a0003c0003t0001g0127 |
2 | HG03239.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.3334+47T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 10/10 | chr1 | 116579345 | |||||||
| chr1:116580000 | T | C | 1 | a0001c0001t0019g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2849-123A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116580000 | |||||||
| chr1:116580022 | A | G | 1 | a0002c0002t0001g0155 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2849-145T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116580022 | |||||||
| chr1:116580079 | A | G | 16 | a0002c0004t0001g0048 a0002c0004t0001g0073 a0002c0004t0001g0080 others(13): Show |
16 | HG01433.hp2 HG02055.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.2849-202T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116580079 | |||||||
| chr1:116580265 | T | C | 64 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(61): Show |
68 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.2849-388A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116580265 | |||||||
| chr1:116580573 | G | T | 1 | a0002c0002t0001g0210 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2849-696C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116580573 | |||||||
| chr1:116580641 | A | ACCAGAAC others(9): Show |
1 | a0001c0001t0001g0205 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2849-765_2849-764i others(18): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116580641 | |||||||
| chr1:116580762 | C | G | 4 | a0002c0002t0006g0014 a0002c0002t0006g0015 a0002c0002t0006g0016 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2849-885G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116580762 | |||||||
| chr1:116581129 | C | T | 1 | a0009c0029t0001g0157 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2849-1252G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116581129 | |||||||
| chr1:116581320 | C | CT | 25 | a0001c0001t0001g0104 a0001c0001t0001g0146 a0001c0001t0005g0153 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.2849-1444dupA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116581320 | |||||||
| chr1:116581320 | CT | C | 21 | a0001c0001t0001g0136 a0001c0001t0001g0145 a0001c0001t0001g0148 others(18): Show |
22 | HG01943.hp1 HG01943.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2849-1444delA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116581320 | |||||||
| chr1:116581572 | G | A | 1 | a0001c0005t0001g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2849-1695C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116581572 | |||||||
| chr1:116581944 | G | A | 2 | a0001c0001t0002g0189 a0002c0002t0001g0128 |
2 | HG00280.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2849-2067C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116581944 | |||||||
| chr1:116581992 | A | G | 1 | a0003c0003t0008g0007 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2849-2115T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116581992 | |||||||
| chr1:116582140 | G | A | 7 | a0002c0002t0006g0014 a0002c0002t0006g0015 a0002c0002t0006g0016 others(4): Show |
7 | HG02486.hp1 HG02615.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2849-2263C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582140 | |||||||
| chr1:116582182 | A | C | 5 | a0001c0001t0003g0031 a0004c0009t0001g0072 a0004c0009t0002g0191 others(2): Show |
5 | HG01943.hp1 HG02074.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2849-2305T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582182 | |||||||
| chr1:116582343 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2848+2302G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582343 | |||||||
| chr1:116582400 | C | T | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2848+2245G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582400 | |||||||
| chr1:116582602 | A | G | 1 | a0010c0028t0003g0033 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2848+2043T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582602 | |||||||
| chr1:116582714 | A | G | 3 | a0002c0002t0006g0014 a0002c0002t0006g0015 a0002c0002t0006g0016 |
3 | HG02895.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2848+1931T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582714 | |||||||
| chr1:116582815 | T | G | 1 | a0002c0004t0001g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2848+1830A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582815 | |||||||
| chr1:116582831 | G | A | 4 | a0002c0002t0001g0206 a0002c0002t0001g0209 a0002c0002t0001g0221 others(1): Show |
4 | HG00140.hp1 HG00639.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2848+1814C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582831 | |||||||
| chr1:116582980 | G | A | 2 | a0001c0001t0019g0177 a0002c0002t0004g0021 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2848+1665C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116582980 | |||||||
| chr1:116583081 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2848+1564A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116583081 | |||||||
| chr1:116583299 | C | G | 7 | a0002c0002t0006g0014 a0002c0002t0006g0015 a0002c0002t0006g0016 others(4): Show |
7 | HG02486.hp1 HG02615.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2848+1346G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116583299 | |||||||
| chr1:116583308 | G | C | 1 | a0002c0002t0002g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2848+1337C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116583308 | |||||||
| chr1:116583419 | T | C | 2 | a0002c0015t0003g0020 a0002c0024t0001g0087 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2848+1226A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116583419 | |||||||
| chr1:116583505 | G | C | 1 | a0002c0002t0001g0168 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2848+1140C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116583505 | |||||||
| chr1:116583731 | T | A | 5 | a0001c0001t0003g0031 a0004c0009t0001g0072 a0004c0009t0002g0191 others(2): Show |
5 | HG01943.hp1 HG02074.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2848+914A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116583731 | |||||||
| chr1:116583764 | C | T | 1 | a0011c0030t0001g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2848+881G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116583764 | |||||||
| chr1:116584020 | C | G | 2 | a0002c0015t0003g0020 a0002c0024t0001g0087 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2848+625G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116584020 | |||||||
| chr1:116584046 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2848+599C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116584046 | |||||||
| chr1:116584057 | C | T | 17 | a0001c0001t0001g0070 a0002c0004t0001g0048 a0002c0004t0001g0073 others(14): Show |
17 | HG01433.hp2 HG02055.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.2848+588G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116584057 | |||||||
| chr1:116584190 | C | T | 2 | a0002c0002t0001g0110 a0002c0002t0001g0120 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2848+455G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116584190 | |||||||
| chr1:116584195 | CA | C | 126 | a0001c0001t0001g0070 a0001c0001t0001g0136 a0001c0001t0003g0023 others(123): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2848+449delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 9/10 | chr1 | 116584195 | |||||||
| chr1:116585056 | G | C | 1 | a0002c0002t0001g0112 | 1 | NA18956.hp1 | splice_region_variant&intron_variant | LOW | c.2441-4C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585056 | |||||||
| chr1:116585131 | T | C | 1 | a0002c0002t0001g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2441-79A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585131 | |||||||
| chr1:116585260 | A | G | 17 | a0001c0001t0001g0070 a0002c0004t0001g0048 a0002c0004t0001g0073 others(14): Show |
17 | HG01433.hp2 HG02055.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.2441-208T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585260 | |||||||
| chr1:116585361 | G | A | 1 | a0001c0005t0003g0026 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2441-309C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585361 | |||||||
| chr1:116585389 | C | G | 4 | a0002c0004t0001g0082 a0002c0004t0001g0083 a0002c0004t0001g0085 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441-337G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585389 | |||||||
| chr1:116585406 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2441-354G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585406 | |||||||
| chr1:116585439 | G | C | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2441-387C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585439 | |||||||
| chr1:116585496 | C | A | 1 | a0003c0003t0001g0116 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2441-444G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585496 | |||||||
| chr1:116585550 | C | A | 128 | a0001c0001t0001g0070 a0001c0001t0001g0136 a0001c0001t0003g0023 others(125): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2441-498G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585550 | |||||||
| chr1:116585648 | A | G | 1 | a0001c0001t0019g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2441-596T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585648 | |||||||
| chr1:116585702 | G | A | 127 | a0001c0001t0001g0070 a0001c0001t0001g0136 a0001c0001t0003g0023 others(124): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2441-650C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585702 | |||||||
| chr1:116585851 | T | C | 128 | a0001c0001t0001g0070 a0001c0001t0001g0136 a0001c0001t0003g0023 others(125): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2441-799A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116585851 | |||||||
| chr1:116586018 | G | A | 14 | a0001c0001t0016g0244 a0001c0005t0001g0099 a0001c0005t0001g0102 others(11): Show |
14 | HG01891.hp2 HG02109.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.2441-966C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116586018 | |||||||
| chr1:116586304 | T | C | 9 | a0001c0001t0005g0153 a0002c0002t0001g0131 a0002c0002t0001g0152 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2441-1252A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116586304 | |||||||
| chr1:116586389 | T | TTG | 15 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(12): Show |
15 | HG02027.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2441-1339_2441-133 others(6): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116586389 | |||||||
| chr1:116586512 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2441-1460C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116586512 | |||||||
| chr1:116586550 | G | C | 2 | a0002c0002t0001g0131 a0009c0029t0001g0157 |
2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2441-1498C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116586550 | |||||||
| chr1:116587089 | A | G | 18 | a0001c0001t0001g0070 a0002c0002t0006g0014 a0002c0002t0006g0015 others(15): Show |
18 | HG01433.hp2 HG02055.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.2440+1605T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587089 | |||||||
| chr1:116587160 | T | G | 1 | a0003c0003t0001g0116 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2440+1534A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587160 | |||||||
| chr1:116587187 | T | C | 1 | a0001c0001t0016g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2440+1507A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587187 | |||||||
| chr1:116587330 | T | G | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2440+1364A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587330 | |||||||
| chr1:116587448 | A | G | 3 | a0002c0004t0001g0134 a0002c0004t0001g0135 a0002c0004t0001g0203 |
3 | HG03098.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2440+1246T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587448 | |||||||
| chr1:116587500 | TA | T | 72 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(69): Show |
79 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.2440+1193delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587500 | |||||||
| chr1:116587540 | C | T | 3 | a0002c0002t0007g0170 a0002c0002t0013g0171 a0011c0030t0001g0167 |
3 | HG02257.hp2 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2440+1154G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587540 | |||||||
| chr1:116587668 | C | T | 11 | a0002c0002t0001g0120 a0002c0002t0011g0040 a0002c0002t0012g0108 others(8): Show |
13 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2440+1026G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587668 | |||||||
| chr1:116587673 | G | A | 42 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0107 others(39): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.2440+1021C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587673 | |||||||
| chr1:116587777 | A | C | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2440+917T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587777 | |||||||
| chr1:116587795 | G | C | 1 | a0003c0003t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2440+899C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116587795 | |||||||
| chr1:116588104 | C | T | 3 | a0002c0002t0007g0170 a0002c0002t0013g0171 a0011c0030t0001g0167 |
3 | HG02257.hp2 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2440+590G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116588104 | |||||||
| chr1:116588556 | G | C | 1 | a0003c0003t0001g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2440+138C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116588556 | |||||||
| chr1:116588560 | G | A | 1 | a0001c0007t0003g0004 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2440+134C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116588560 | |||||||
| chr1:116588634 | C | A | 1 | a0015c0025t0002g0185 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2440+60G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116588634 | |||||||
| chr1:116588670 | G | A | 1 | a0003c0003t0001g0173 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2440+24C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 8/10 | chr1 | 116588670 | |||||||
| chr1:116589182 | G | C | 1 | a0002c0002t0001g0090 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2030-78C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589182 | |||||||
| chr1:116589260 | A | ACCGCTAA others(8): Show |
1 | a0002c0024t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2030-171_2030-157d others(17): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589260 | |||||||
| chr1:116589282 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0003g0023 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2030-178G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589282 | |||||||
| chr1:116589442 | A | G | 2 | a0002c0002t0006g0015 a0002c0002t0006g0016 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2030-338T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589442 | |||||||
| chr1:116589471 | C | T | 41 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0107 others(38): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.2030-367G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589471 | |||||||
| chr1:116589556 | C | T | 69 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(66): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2030-452G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589556 | |||||||
| chr1:116589595 | G | A | 2 | a0002c0002t0011g0040 a0002c0002t0012g0108 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2030-491C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589595 | |||||||
| chr1:116589671 | C | T | 2 | a0002c0002t0006g0015 a0002c0002t0006g0016 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2030-567G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589671 | |||||||
| chr1:116589712 | T | C | 1 | a0011c0030t0001g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2030-608A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589712 | |||||||
| chr1:116589761 | G | A | 9 | a0002c0002t0001g0120 a0002c0004t0001g0047 a0003c0003t0001g0005 others(6): Show |
11 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2030-657C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589761 | |||||||
| chr1:116589965 | C | T | 11 | a0002c0002t0001g0120 a0002c0002t0011g0040 a0002c0002t0012g0108 others(8): Show |
13 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.2030-861G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116589965 | |||||||
| chr1:116590034 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2030-930C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590034 | |||||||
| chr1:116590063 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2030-959G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590063 | |||||||
| chr1:116590064 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0161 a0001c0001t0001g0162 others(7): Show |
11 | HG00423.hp2 HG01256.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.2030-960C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590064 | |||||||
| chr1:116590231 | C | T | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-1127G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590231 | |||||||
| chr1:116590306 | C | T | 2 | a0002c0002t0011g0040 a0002c0002t0012g0108 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2030-1202G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590306 | |||||||
| chr1:116590336 | A | G | 150 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(147): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.2030-1232T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590336 | |||||||
| chr1:116590371 | G | GA | 17 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0129 others(14): Show |
17 | HG00621.hp2 HG01099.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.2030-1268dupT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590371 | |||||||
| chr1:116590371 | GA | G | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-1268delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590371 | |||||||
| chr1:116590421 | A | C | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-1317T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590421 | |||||||
| chr1:116590422 | G | A | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-1318C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590422 | |||||||
| chr1:116590627 | A | G | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-1523T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590627 | |||||||
| chr1:116590762 | G | A | 1 | a0003c0003t0001g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2030-1658C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590762 | |||||||
| chr1:116590806 | C | T | 1 | a0002c0002t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2030-1702G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590806 | |||||||
| chr1:116590890 | C | T | 1 | a0014c0019t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2030-1786G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590890 | |||||||
| chr1:116590934 | A | G | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-1830T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116590934 | |||||||
| chr1:116591082 | C | T | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-1978G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116591082 | |||||||
| chr1:116591336 | T | C | 9 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(6): Show |
9 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2030-2232A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116591336 | |||||||
| chr1:116591515 | T | A | 150 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(147): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.2030-2411A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116591515 | |||||||
| chr1:116591665 | A | G | 1 | a0003c0003t0015g0234 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2030-2561T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116591665 | |||||||
| chr1:116591796 | A | G | 15 | a0001c0001t0001g0136 a0001c0001t0003g0023 a0001c0001t0004g0024 others(12): Show |
15 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2030-2692T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116591796 | |||||||
| chr1:116591850 | G | C | 8 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2030-2746C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116591850 | |||||||
| chr1:116591954 | A | G | 1 | a0003c0003t0001g0116 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2030-2850T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116591954 | |||||||
| chr1:116592225 | A | G | 1 | a0003c0003t0001g0046 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2030-3121T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592225 | |||||||
| chr1:116592497 | G | A | 41 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0107 others(38): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.2030-3393C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592497 | |||||||
| chr1:116592586 | G | A | 18 | a0001c0001t0001g0070 a0002c0002t0006g0014 a0002c0002t0006g0015 others(15): Show |
18 | HG01433.hp2 HG02055.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.2030-3482C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592586 | |||||||
| chr1:116592658 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2030-3554G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592658 | |||||||
| chr1:116592733 | G | C | 3 | a0002c0002t0010g0176 a0002c0002t0013g0171 a0011c0030t0001g0167 |
3 | HG02257.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2030-3629C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592733 | |||||||
| chr1:116592745 | C | T | 2 | a0002c0004t0001g0086 a0002c0004t0001g0094 |
2 | HG01433.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2030-3641G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592745 | |||||||
| chr1:116592841 | G | C | 8 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2030-3737C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592841 | |||||||
| chr1:116592905 | A | G | 3 | a0001c0007t0003g0017 a0001c0010t0001g0245 a0001c0010t0001g0246 |
3 | HG02109.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2030-3801T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592905 | |||||||
| chr1:116592946 | C | T | 1 | a0003c0003t0001g0137 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2030-3842G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116592946 | |||||||
| chr1:116593070 | A | G | 8 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2030-3966T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593070 | |||||||
| chr1:116593137 | A | G | 2 | a0002c0002t0011g0040 a0002c0002t0012g0108 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2030-4033T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593137 | |||||||
| chr1:116593256 | T | A | 2 | a0003c0003t0001g0075 a0003c0003t0001g0077 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2030-4152A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593256 | |||||||
| chr1:116593304 | G | A | 1 | a0003c0003t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2030-4200C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593304 | |||||||
| chr1:116593639 | TTTGGGCC others(30): Show |
T | 3 | a0003c0003t0002g0200 a0003c0017t0001g0165 a0016c0023t0002g0182 |
3 | NA18944.hp1 NA18994.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2030-4572_2030-453 others(41): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593639 | |||||||
| chr1:116593714 | C | A | 2 | a0001c0001t0001g0070 a0002c0004t0018g0071 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2030-4610G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593714 | |||||||
| chr1:116593831 | G | A | 2 | a0003c0003t0001g0002 a0003c0003t0001g0054 |
4 | HG01358.hp1 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.2030-4727C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593831 | |||||||
| chr1:116593891 | A | G | 1 | a0003c0003t0001g0061 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2030-4787T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593891 | |||||||
| chr1:116593950 | C | T | 69 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(66): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2030-4846G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593950 | |||||||
| chr1:116593954 | T | C | 3 | a0002c0002t0007g0170 a0002c0002t0013g0171 a0011c0030t0001g0167 |
3 | HG02257.hp2 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2030-4850A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116593954 | |||||||
| chr1:116594003 | C | T | 5 | a0003c0003t0001g0005 a0003c0003t0001g0008 a0003c0003t0001g0096 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2030-4899G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116594003 | |||||||
| chr1:116594283 | T | A | 18 | a0001c0001t0001g0070 a0002c0002t0006g0014 a0002c0002t0006g0015 others(15): Show |
18 | HG01433.hp2 HG02055.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.2030-5179A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116594283 | |||||||
| chr1:116594317 | A | G | 8 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0131 others(5): Show |
8 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2030-5213T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116594317 | |||||||
| chr1:116594477 | C | T | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2030-5373G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116594477 | |||||||
| chr1:116594748 | G | A | 69 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(66): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2029+5193C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116594748 | |||||||
| chr1:116594958 | G | A | 32 | a0002c0002t0001g0011 a0002c0002t0001g0043 a0002c0002t0001g0112 others(29): Show |
35 | HG00423.hp1 HG00621.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.2029+4983C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116594958 | |||||||
| chr1:116595073 | G | T | 1 | a0002c0024t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2029+4868C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116595073 | |||||||
| chr1:116595239 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2029+4702G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116595239 | |||||||
| chr1:116595376 | G | A | 1 | a0003c0003t0001g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2029+4565C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116595376 | |||||||
| chr1:116595661 | G | A | 1 | a0002c0002t0001g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2029+4280C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116595661 | |||||||
| chr1:116595759 | A | G | 7 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2029+4182T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116595759 | |||||||
| chr1:116595869 | G | T | 1 | a0001c0001t0001g0240 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2029+4072C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116595869 | |||||||
| chr1:116596327 | T | G | 1 | a0002c0004t0001g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2029+3614A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116596327 | |||||||
| chr1:116596434 | G | C | 71 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(68): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.2029+3507C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116596434 | |||||||
| chr1:116596912 | C | T | 13 | a0001c0001t0016g0244 a0001c0005t0001g0099 a0001c0005t0001g0102 others(10): Show |
13 | HG01891.hp2 HG02486.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.2029+3029G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116596912 | |||||||
| chr1:116597403 | G | A | 1 | a0009c0029t0001g0157 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2029+2538C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116597403 | |||||||
| chr1:116597489 | G | A | 13 | a0001c0005t0001g0099 a0001c0005t0001g0102 a0001c0005t0001g0109 others(10): Show |
13 | HG01192.hp1 HG01346.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2029+2452C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116597489 | |||||||
| chr1:116597685 | C | T | 1 | a0001c0001t0016g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2029+2256G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116597685 | |||||||
| chr1:116598236 | A | G | 11 | a0001c0005t0001g0099 a0001c0005t0001g0102 a0001c0005t0001g0109 others(8): Show |
11 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2029+1705T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116598236 | |||||||
| chr1:116598470 | C | T | 1 | a0001c0001t0016g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2029+1471G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116598470 | |||||||
| chr1:116598589 | C | T | 3 | a0002c0002t0007g0170 a0002c0002t0013g0171 a0011c0030t0001g0167 |
3 | HG02257.hp2 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2029+1352G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116598589 | |||||||
| chr1:116598739 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0003g0023 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2029+1202G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116598739 | |||||||
| chr1:116598818 | G | C | 1 | a0002c0024t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2029+1123C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116598818 | |||||||
| chr1:116598924 | C | T | 1 | a0008c0032t0001g0226 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2029+1017G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116598924 | |||||||
| chr1:116599037 | G | A | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2029+904C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599037 | |||||||
| chr1:116599124 | A | G | 8 | a0001c0001t0001g0207 a0002c0002t0001g0084 a0002c0002t0001g0212 others(5): Show |
8 | HG00609.hp2 NA18946.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.2029+817T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599124 | |||||||
| chr1:116599188 | C | T | 1 | a0005c0011t0001g0006 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2029+753G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599188 | |||||||
| chr1:116599327 | G | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0213 others(7): Show |
10 | HG01934.hp1 HG01943.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2029+614C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599327 | |||||||
| chr1:116599389 | T | TACACACA others(3): Show |
7 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2029+551_2029+552i others(12): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599389 | |||||||
| chr1:116599391 | T | C | 7 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2029+550A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599391 | |||||||
| chr1:116599391 | T | TAC | 62 | a0001c0001t0001g0009 a0001c0001t0001g0105 a0001c0001t0001g0139 others(59): Show |
72 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.2029+548_2029+549d others(4): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599391 | |||||||
| chr1:116599391 | T | TACAC | 12 | a0001c0001t0001g0103 a0001c0001t0001g0213 a0001c0001t0001g0240 others(9): Show |
12 | HG00423.hp1 HG01934.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.2029+546_2029+549d others(6): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599391 | |||||||
| chr1:116599391 | T | TACACAC | 23 | a0001c0001t0001g0104 a0001c0001t0004g0036 a0001c0001t0004g0037 others(20): Show |
23 | HG01433.hp2 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2029+544_2029+549d others(8): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599391 | |||||||
| chr1:116599391 | TAC | T | 12 | a0001c0005t0001g0099 a0001c0005t0001g0102 a0001c0005t0001g0109 others(9): Show |
12 | HG01169.hp2 HG01891.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2029+548_2029+549d others(4): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599391 | |||||||
| chr1:116599391 | TACACAC | T | 30 | a0001c0001t0003g0031 a0001c0001t0004g0024 a0001c0001t0004g0025 others(27): Show |
33 | HG01099.hp2 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.2029+544_2029+549d others(8): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599391 | |||||||
| chr1:116599467 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2029+474T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599467 | |||||||
| chr1:116599518 | G | C | 9 | a0002c0002t0001g0120 a0002c0004t0001g0047 a0003c0003t0001g0005 others(6): Show |
11 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2029+423C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599518 | |||||||
| chr1:116599593 | G | A | 8 | a0001c0001t0004g0025 a0001c0001t0005g0052 a0001c0001t0005g0053 others(5): Show |
8 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2029+348C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599593 | |||||||
| chr1:116599617 | G | A | 74 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0136 others(71): Show |
81 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.2029+324C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599617 | |||||||
| chr1:116599696 | A | C | 1 | a0001c0005t0001g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2029+245T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599696 | |||||||
| chr1:116599844 | G | A | 2 | a0001c0001t0001g0223 a0002c0002t0001g0227 |
2 | HG00558.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2029+97C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599844 | |||||||
| chr1:116599868 | C | T | 3 | a0002c0004t0001g0082 a0002c0004t0001g0083 a0002c0004t0001g0154 |
3 | HG02055.hp2 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2029+73G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599868 | |||||||
| chr1:116599909 | G | A | 187 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(184): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.2029+32C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599909 | |||||||
| chr1:116599910 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2029+31C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 7/10 | chr1 | 116599910 | |||||||
| chr1:116600445 | G | A | 30 | a0002c0002t0001g0011 a0002c0002t0001g0112 a0002c0002t0001g0115 others(27): Show |
33 | HG00423.hp1 HG00621.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1625-100C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600445 | |||||||
| chr1:116600446 | A | G | 30 | a0002c0002t0001g0011 a0002c0002t0001g0112 a0002c0002t0001g0115 others(27): Show |
33 | HG00423.hp1 HG00621.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1625-101T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600446 | |||||||
| chr1:116600561 | CT | C | 13 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1625-217delA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600561 | |||||||
| chr1:116600690 | T | C | 6 | a0001c0001t0003g0031 a0001c0007t0003g0017 a0001c0007t0003g0029 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1625-345A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600690 | |||||||
| chr1:116600775 | A | T | 3 | a0003c0003t0001g0061 a0003c0003t0001g0125 a0003c0003t0001g0172 |
3 | HG00738.hp2 HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1625-430T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600775 | |||||||
| chr1:116600794 | C | T | 3 | a0003c0003t0001g0061 a0003c0003t0001g0125 a0003c0003t0001g0172 |
3 | HG00738.hp2 HG01081.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1625-449G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600794 | |||||||
| chr1:116600936 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1625-591G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600936 | |||||||
| chr1:116600981 | T | C | 2 | a0002c0002t0007g0170 a0011c0030t0001g0167 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1625-636A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116600981 | |||||||
| chr1:116601462 | A | T | 10 | a0002c0002t0001g0120 a0002c0004t0001g0047 a0002c0024t0001g0087 others(7): Show |
12 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1625-1117T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601462 | |||||||
| chr1:116601575 | T | G | 1 | a0001c0005t0001g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1625-1230A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601575 | |||||||
| chr1:116601601 | A | C | 15 | a0001c0001t0001g0070 a0002c0002t0006g0014 a0002c0002t0006g0015 others(12): Show |
15 | HG01433.hp2 HG02630.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.1625-1256T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601601 | |||||||
| chr1:116601684 | A | G | 1 | a0001c0001t0004g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1625-1339T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601684 | |||||||
| chr1:116601694 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1625-1349G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601694 | |||||||
| chr1:116601725 | T | C | 7 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0017 others(4): Show |
8 | HG02109.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1625-1380A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601725 | |||||||
| chr1:116601735 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1625-1390T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601735 | |||||||
| chr1:116601752 | G | A | 7 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1625-1407C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601752 | |||||||
| chr1:116601768 | A | G | 25 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(22): Show |
25 | HG01433.hp2 HG01934.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.1625-1423T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601768 | |||||||
| chr1:116601860 | A | AC | 12 | a0001c0001t0001g0136 a0001c0001t0005g0153 a0002c0002t0001g0110 others(9): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1625-1516dupG | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116601860 | |||||||
| chr1:116602207 | C | A | 1 | a0003c0003t0001g0075 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1624+1417G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602207 | |||||||
| chr1:116602256 | G | A | 8 | a0002c0002t0001g0049 a0002c0002t0001g0090 a0002c0002t0001g0132 others(5): Show |
8 | HG01071.hp2 HG01106.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1624+1368C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602256 | |||||||
| chr1:116602282 | G | A | 1 | a0009c0029t0001g0157 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1624+1342C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602282 | |||||||
| chr1:116602362 | T | A | 4 | a0001c0005t0003g0013 a0001c0005t0003g0018 a0001c0013t0003g0019 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624+1262A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602362 | |||||||
| chr1:116602362 | T | TA | 109 | a0001c0001t0001g0103 a0001c0001t0001g0136 a0001c0001t0001g0213 others(106): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1624+1261dupT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602362 | |||||||
| chr1:116602452 | T | C | 1 | a0001c0007t0003g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1624+1172A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602452 | |||||||
| chr1:116602478 | G | A | 3 | a0004c0009t0002g0191 a0004c0009t0002g0197 a0004c0009t0003g0035 |
3 | HG01943.hp1 HG02074.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1624+1146C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602478 | |||||||
| chr1:116602657 | T | C | 10 | a0001c0001t0001g0136 a0001c0001t0005g0153 a0002c0002t0001g0110 others(7): Show |
10 | HG01891.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1624+967A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602657 | |||||||
| chr1:116602781 | T | G | 1 | a0003c0003t0001g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1624+843A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116602781 | |||||||
| chr1:116603348 | C | A | 1 | a0001c0001t0004g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1624+276G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116603348 | |||||||
| chr1:116603502 | T | C | 43 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0082 others(40): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1624+122A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 6/10 | chr1 | 116603502 | |||||||
| chr1:116604076 | G | A | 1 | a0003c0003t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1223-51C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604076 | |||||||
| chr1:116604219 | C | T | 43 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0082 others(40): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1223-194G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604219 | |||||||
| chr1:116604560 | G | A | 1 | a0003c0003t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1223-535C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604560 | |||||||
| chr1:116604635 | C | A | 1 | a0002c0002t0002g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1223-610G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604635 | |||||||
| chr1:116604679 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1223-654A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604679 | |||||||
| chr1:116604692 | C | T | 1 | a0014c0019t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1223-667G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604692 | |||||||
| chr1:116604734 | G | A | 31 | a0002c0002t0001g0011 a0002c0002t0001g0043 a0002c0002t0001g0112 others(28): Show |
34 | HG00423.hp1 HG00621.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1223-709C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604734 | |||||||
| chr1:116604892 | C | T | 1 | a0002c0024t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1223-867G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604892 | |||||||
| chr1:116604986 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1223-961G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116604986 | |||||||
| chr1:116605055 | T | C | 25 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(22): Show |
25 | HG01433.hp2 HG01934.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.1223-1030A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116605055 | |||||||
| chr1:116605153 | T | A | 1 | a0001c0001t0019g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1223-1128A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116605153 | |||||||
| chr1:116605275 | G | A | 4 | a0001c0005t0003g0013 a0001c0005t0003g0018 a0001c0013t0003g0019 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1223-1250C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116605275 | |||||||
| chr1:116605381 | T | C | 1 | a0009c0029t0001g0157 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1223-1356A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116605381 | |||||||
| chr1:116605416 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1223-1391T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116605416 | |||||||
| chr1:116605670 | G | A | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1223-1645C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116605670 | |||||||
| chr1:116605951 | A | C | 2 | a0002c0002t0007g0170 a0011c0030t0001g0167 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1223-1926T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116605951 | |||||||
| chr1:116606086 | G | A | 12 | a0002c0002t0001g0120 a0002c0002t0011g0040 a0002c0002t0012g0108 others(9): Show |
14 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1222+1856C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606086 | |||||||
| chr1:116606191 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1222+1751C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606191 | |||||||
| chr1:116606209 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0213 others(1): Show |
4 | NA18982.hp2 NA18994.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222+1733G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606209 | |||||||
| chr1:116606216 | C | T | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1222+1726G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606216 | |||||||
| chr1:116606252 | G | A | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1222+1690C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606252 | |||||||
| chr1:116606263 | T | C | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1222+1679A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606263 | |||||||
| chr1:116606517 | G | A | 1 | a0003c0003t0001g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1222+1425C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606517 | |||||||
| chr1:116606632 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1222+1310A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606632 | |||||||
| chr1:116606740 | G | A | 1 | a0013c0016t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1222+1202C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606740 | |||||||
| chr1:116606849 | A | C | 17 | a0001c0001t0001g0066 a0002c0004t0001g0080 a0002c0004t0001g0107 others(14): Show |
20 | HG00280.hp2 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1222+1093T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116606849 | |||||||
| chr1:116607065 | C | T | 17 | a0001c0001t0016g0244 a0001c0005t0001g0102 a0001c0005t0001g0109 others(14): Show |
17 | HG00621.hp2 HG01891.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1222+877G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116607065 | |||||||
| chr1:116607081 | A | G | 2 | a0002c0002t0007g0170 a0011c0030t0001g0167 |
2 | HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1222+861T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116607081 | |||||||
| chr1:116607321 | TG | T | 190 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(187): Show |
204 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1222+620delC | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116607321 | |||||||
| chr1:116607707 | C | T | 1 | a0002c0015t0003g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1222+235G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116607707 | |||||||
| chr1:116607865 | C | T | 3 | a0002c0002t0001g0110 a0002c0002t0011g0040 a0002c0002t0012g0108 |
3 | HG02486.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1222+77G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116607865 | |||||||
| chr1:116607872 | C | G | 11 | a0002c0002t0001g0120 a0002c0004t0001g0047 a0002c0024t0001g0087 others(8): Show |
13 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1222+70G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 5/10 | chr1 | 116607872 | |||||||
| chr1:116608443 | C | G | 1 | a0003c0003t0001g0059 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.833-112G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116608443 | |||||||
| chr1:116608608 | A | G | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.833-277T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116608608 | |||||||
| chr1:116608730 | T | G | 1 | a0001c0001t0004g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.833-399A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116608730 | |||||||
| chr1:116608865 | C | T | 13 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0208 others(10): Show |
13 | HG01934.hp1 HG01943.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-534G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116608865 | |||||||
| chr1:116609263 | C | T | 131 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(128): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.833-932G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116609263 | |||||||
| chr1:116609767 | G | A | 1 | a0001c0001t0002g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.833-1436C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116609767 | |||||||
| chr1:116609830 | T | G | 1 | a0001c0005t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.833-1499A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116609830 | |||||||
| chr1:116609912 | G | A | 1 | a0001c0001t0016g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.833-1581C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116609912 | |||||||
| chr1:116610091 | T | G | 1 | a0002c0002t0001g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.833-1760A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116610091 | |||||||
| chr1:116610107 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.833-1776G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116610107 | |||||||
| chr1:116610153 | C | G | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.833-1822G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116610153 | |||||||
| chr1:116610337 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.833-2006G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116610337 | |||||||
| chr1:116610944 | G | A | 41 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0082 others(38): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.833-2613C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116610944 | |||||||
| chr1:116610975 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.833-2644G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116610975 | |||||||
| chr1:116611710 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.832+2055C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116611710 | |||||||
| chr1:116611767 | A | G | 1 | a0001c0001t0005g0093 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+1998T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116611767 | |||||||
| chr1:116611772 | C | T | 2 | a0009c0029t0001g0157 a0011c0030t0001g0167 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.832+1993G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116611772 | |||||||
| chr1:116611838 | C | T | 126 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(123): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.832+1927G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116611838 | |||||||
| chr1:116611921 | G | A | 1 | a0003c0003t0001g0059 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.832+1844C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116611921 | |||||||
| chr1:116612167 | AAAT | A | 21 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(18): Show |
23 | HG01099.hp2 HG01433.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.832+1595_832+1597d others(5): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116612167 | |||||||
| chr1:116612288 | C | T | 21 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(18): Show |
23 | HG01099.hp2 HG01433.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.832+1477G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116612288 | |||||||
| chr1:116612349 | C | A | 1 | a0002c0004t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.832+1416G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116612349 | |||||||
| chr1:116612435 | T | C | 41 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0082 others(38): Show |
48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.832+1330A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116612435 | |||||||
| chr1:116612500 | C | T | 1 | a0003c0003t0001g0046 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.832+1265G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116612500 | |||||||
| chr1:116612850 | G | A | 1 | a0001c0001t0016g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.832+915C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116612850 | |||||||
| chr1:116612867 | C | T | 13 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.832+898G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116612867 | |||||||
| chr1:116613132 | T | C | 1 | a0003c0003t0001g0173 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.832+633A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116613132 | |||||||
| chr1:116613622 | C | T | 3 | a0002c0004t0001g0134 a0002c0004t0001g0135 a0002c0004t0001g0203 |
3 | HG03098.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+143G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 4/10 | chr1 | 116613622 | |||||||
| chr1:116614196 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.422-21C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614196 | |||||||
| chr1:116614273 | C | A | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.422-98G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614273 | |||||||
| chr1:116614301 | G | A | 13 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-126C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614301 | |||||||
| chr1:116614386 | C | T | 21 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(18): Show |
23 | HG01099.hp2 HG01433.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.422-211G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614386 | |||||||
| chr1:116614426 | G | A | 1 | a0002c0002t0001g0043 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.422-251C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614426 | |||||||
| chr1:116614590 | T | C | 13 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-415A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614590 | |||||||
| chr1:116614750 | A | G | 153 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(150): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.422-575T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614750 | |||||||
| chr1:116614820 | G | C | 13 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-645C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614820 | |||||||
| chr1:116614851 | T | C | 1 | a0014c0019t0001g0124 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.422-676A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614851 | |||||||
| chr1:116614949 | G | T | 2 | a0002c0002t0011g0040 a0002c0002t0012g0108 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.422-774C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116614949 | |||||||
| chr1:116615232 | C | T | 1 | a0001c0008t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.421+848G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615232 | |||||||
| chr1:116615286 | T | TAC | 29 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0136 others(26): Show |
30 | HG01934.hp1 HG01943.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.421+792_421+793dup others(2): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615286 | |||||||
| chr1:116615286 | T | TACAC | 3 | a0001c0001t0001g0070 a0002c0004t0001g0203 a0002c0004t0018g0071 |
3 | HG02723.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.421+790_421+793dup others(4): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615286 | |||||||
| chr1:116615518 | A | AATGGAAG others(103): Show |
1 | a0002c0002t0001g0132 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.421+452_421+561dup others(110): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615518 | |||||||
| chr1:116615603 | G | C | 3 | a0002c0002t0007g0170 a0009c0029t0001g0157 a0011c0030t0001g0167 |
3 | HG01891.hp1 HG02257.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.421+477C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615603 | |||||||
| chr1:116615605 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.421+475T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615605 | |||||||
| chr1:116615621 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0146 |
2 | NA18962.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.421+459A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615621 | |||||||
| chr1:116615754 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.421+326G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116615754 | |||||||
| chr1:116616022 | G | A | 25 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(22): Show |
25 | HG01934.hp1 HG01943.hp1 HG02074.hp1 others(22): Show |
intron_variant | MODIFIER | c.421+58C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116616022 | |||||||
| chr1:116616049 | C | T | 2 | a0001c0005t0003g0026 a0001c0005t0003g0028 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.421+31G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116616049 | |||||||
| chr1:116616059 | G | A | 1 | a0001c0006t0001g0144 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.421+21C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 3/10 | chr1 | 116616059 | |||||||
| chr1:116616846 | A | T | 1 | a0003c0003t0001g0060 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.44-389T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116616846 | |||||||
| chr1:116616907 | C | T | 1 | a0003c0003t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.44-450G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116616907 | |||||||
| chr1:116617023 | A | G | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-566T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116617023 | |||||||
| chr1:116617096 | A | G | 18 | a0001c0001t0016g0244 a0001c0005t0001g0099 a0001c0005t0001g0102 others(15): Show |
18 | HG00621.hp2 HG01891.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-639T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116617096 | |||||||
| chr1:116617194 | C | A | 21 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(18): Show |
23 | HG01099.hp2 HG01433.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.44-737G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116617194 | |||||||
| chr1:116617306 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.44-849C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116617306 | |||||||
| chr1:116617403 | C | T | 1 | a0002c0002t0001g0043 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.44-946G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116617403 | |||||||
| chr1:116617573 | G | C | 4 | a0002c0004t0001g0082 a0002c0004t0001g0083 a0002c0004t0001g0085 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-1116C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116617573 | |||||||
| chr1:116617964 | C | T | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-1507G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116617964 | |||||||
| chr1:116618283 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-1826T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116618283 | |||||||
| chr1:116618654 | G | A | 1 | a0002c0014t0003g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.44-2197C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116618654 | |||||||
| chr1:116618775 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-2318T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116618775 | |||||||
| chr1:116619054 | G | A | 1 | a0002c0024t0001g0087 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.44-2597C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619054 | |||||||
| chr1:116619191 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.44-2734G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619191 | |||||||
| chr1:116619220 | A | C | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.44-2763T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619220 | |||||||
| chr1:116619271 | T | C | 1 | a0001c0005t0003g0028 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.44-2814A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619271 | |||||||
| chr1:116619341 | C | T | 1 | a0002c0004t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.44-2884G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619341 | |||||||
| chr1:116619375 | G | A | 1 | a0002c0004t0001g0085 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.44-2918C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619375 | |||||||
| chr1:116619453 | T | C | 3 | a0003c0003t0001g0076 a0003c0003t0001g0078 a0003c0003t0001g0088 |
3 | HG00639.hp1 HG01099.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.44-2996A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619453 | |||||||
| chr1:116619516 | G | C | 1 | a0003c0003t0002g0200 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.44-3059C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619516 | |||||||
| chr1:116619588 | T | G | 2 | a0002c0002t0001g0121 a0002c0002t0001g0122 |
2 | HG01515.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.44-3131A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619588 | |||||||
| chr1:116619688 | A | C | 154 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(151): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.44-3231T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619688 | |||||||
| chr1:116619761 | G | A | 6 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-3304C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619761 | |||||||
| chr1:116619770 | CT | C | 18 | a0001c0005t0001g0099 a0001c0005t0001g0102 a0001c0005t0001g0109 others(15): Show |
18 | HG00621.hp2 HG01891.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-3314delA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116619770 | |||||||
| chr1:116620002 | T | A | 29 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(26): Show |
29 | HG01433.hp2 HG01891.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.44-3545A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620002 | |||||||
| chr1:116620004 | TA | T | 29 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(26): Show |
29 | HG01433.hp2 HG01891.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.44-3548delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620004 | |||||||
| chr1:116620040 | T | A | 1 | a0002c0002t0001g0227 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.44-3583A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620040 | |||||||
| chr1:116620357 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.44-3900A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620357 | |||||||
| chr1:116620442 | C | G | 2 | a0001c0001t0002g0188 a0001c0001t0002g0194 |
2 | NA18968.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.44-3985G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620442 | |||||||
| chr1:116620442 | C | T | 5 | a0001c0001t0003g0031 a0001c0001t0016g0244 a0001c0007t0003g0004 others(2): Show |
6 | HG02258.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-3985G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620442 | |||||||
| chr1:116620458 | G | C | 20 | a0001c0005t0001g0099 a0001c0005t0001g0102 a0001c0005t0001g0109 others(17): Show |
20 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.44-4001C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620458 | |||||||
| chr1:116620714 | A | G | 1 | a0001c0001t0016g0244 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.44-4257T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620714 | |||||||
| chr1:116620833 | G | A | 1 | a0003c0003t0001g0075 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.44-4376C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116620833 | |||||||
| chr1:116621410 | G | A | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-4953C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116621410 | |||||||
| chr1:116621648 | G | C | 44 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0001g0136 others(41): Show |
47 | HG00423.hp1 HG00621.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.44-5191C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116621648 | |||||||
| chr1:116621952 | T | G | 1 | a0002c0004t0001g0086 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-5495A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116621952 | |||||||
| chr1:116621969 | A | G | 118 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0042 others(115): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.44-5512T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116621969 | |||||||
| chr1:116621989 | T | C | 35 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(32): Show |
35 | HG01433.hp2 HG01891.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.44-5532A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116621989 | |||||||
| chr1:116622034 | C | T | 5 | a0001c0006t0001g0003 a0001c0006t0001g0141 a0001c0006t0001g0143 others(2): Show |
7 | NA18941.hp2 NA18961.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-5577G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622034 | |||||||
| chr1:116622172 | C | T | 1 | a0001c0007t0003g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44-5715G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622172 | |||||||
| chr1:116622174 | C | T | 1 | a0002c0002t0007g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.44-5717G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622174 | |||||||
| chr1:116622230 | T | C | 1 | a0002c0002t0001g0120 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.44-5773A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622230 | |||||||
| chr1:116622259 | C | T | 1 | a0001c0007t0003g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44-5802G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622259 | |||||||
| chr1:116622279 | C | T | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-5822G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622279 | |||||||
| chr1:116622466 | T | TA | 12 | a0001c0001t0003g0031 a0001c0001t0016g0244 a0001c0005t0003g0026 others(9): Show |
13 | HG01515.hp1 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-6010dupT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622466 | |||||||
| chr1:116622467 | A | T | 1 | a0001c0001t0002g0193 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.44-6010T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622467 | |||||||
| chr1:116622820 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-6363C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622820 | |||||||
| chr1:116622900 | G | A | 44 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0001g0136 others(41): Show |
47 | HG00423.hp1 HG00621.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.44-6443C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116622900 | |||||||
| chr1:116623033 | C | A | 1 | a0003c0003t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.44-6576G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623033 | |||||||
| chr1:116623165 | C | G | 1 | a0003c0003t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.44-6708G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623165 | |||||||
| chr1:116623324 | C | T | 2 | a0001c0006t0001g0143 a0001c0006t0001g0150 |
2 | NA18961.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.44-6867G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623324 | |||||||
| chr1:116623494 | T | C | 44 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0001g0136 others(41): Show |
47 | HG00423.hp1 HG00621.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.44-7037A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623494 | |||||||
| chr1:116623586 | T | C | 1 | a0003c0003t0001g0008 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.44-7129A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623586 | |||||||
| chr1:116623648 | T | C | 129 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(126): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.44-7191A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623648 | |||||||
| chr1:116623740 | T | G | 1 | a0003c0003t0001g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.44-7283A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623740 | |||||||
| chr1:116623861 | G | A | 5 | a0001c0001t0001g0070 a0002c0004t0001g0134 a0002c0004t0001g0135 others(2): Show |
5 | HG02723.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-7404C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623861 | |||||||
| chr1:116623913 | C | T | 1 | a0003c0003t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.44-7456G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623913 | |||||||
| chr1:116623981 | G | A | 6 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-7524C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116623981 | |||||||
| chr1:116624019 | G | A | 1 | a0002c0002t0001g0132 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.44-7562C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624019 | |||||||
| chr1:116624045 | T | TCTCGGCT others(11): Show |
27 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(24): Show |
27 | HG01433.hp2 HG01891.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.44-7589_44-7588ins others(18): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624045 | |||||||
| chr1:116624073 | A | C | 125 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(122): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.44-7616T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624073 | |||||||
| chr1:116624085 | TA | T | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-7629delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624085 | |||||||
| chr1:116624203 | CA | C | 9 | a0001c0001t0004g0025 a0001c0001t0004g0037 a0001c0001t0004g0038 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.44-7747delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624203 | |||||||
| chr1:116624246 | C | A | 1 | a0016c0023t0002g0182 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.44-7789G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624246 | |||||||
| chr1:116624296 | C | G | 52 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(49): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.44-7839G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624296 | |||||||
| chr1:116624520 | C | T | 1 | a0002c0004t0001g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.44-8063G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624520 | |||||||
| chr1:116624534 | T | C | 3 | a0001c0001t0003g0023 a0001c0001t0019g0177 a0002c0002t0004g0021 |
3 | HG02280.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-8077A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624534 | |||||||
| chr1:116624541 | T | A | 1 | a0002c0002t0001g0210 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.44-8084A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624541 | |||||||
| chr1:116624588 | C | G | 1 | a0001c0001t0002g0198 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-8131G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624588 | |||||||
| chr1:116624800 | C | T | 1 | a0001c0005t0003g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.44-8343G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624800 | |||||||
| chr1:116624827 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-8370G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624827 | |||||||
| chr1:116624911 | T | C | 1 | a0002c0002t0001g0211 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.44-8454A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624911 | |||||||
| chr1:116624918 | A | T | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-8461T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116624918 | |||||||
| chr1:116626104 | T | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
8 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-9647A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626104 | |||||||
| chr1:116626252 | T | TA | 15 | a0001c0001t0001g0070 a0001c0001t0001g0205 a0002c0002t0013g0171 others(12): Show |
15 | HG01433.hp2 HG01891.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.44-9796dupT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626252 | |||||||
| chr1:116626252 | TA | T | 13 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-9796delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626252 | |||||||
| chr1:116626263 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.44-9806A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626263 | |||||||
| chr1:116626272 | A | G | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.44-9815T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626272 | |||||||
| chr1:116626373 | CCTCA | C | 17 | a0001c0001t0001g0136 a0001c0001t0005g0153 a0002c0002t0001g0110 others(14): Show |
19 | HG01099.hp2 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-9920_44-9917del others(4): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626373 | |||||||
| chr1:116626449 | A | G | 3 | a0001c0007t0003g0017 a0001c0010t0001g0245 a0001c0010t0001g0246 |
3 | HG02109.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.44-9992T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626449 | |||||||
| chr1:116626466 | T | G | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-10009A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626466 | |||||||
| chr1:116626595 | T | C | 2 | a0003c0003t0001g0173 a0004c0009t0003g0035 |
2 | HG02074.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.44-10138A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626595 | |||||||
| chr1:116626659 | C | G | 40 | a0001c0007t0003g0017 a0001c0010t0001g0245 a0001c0010t0001g0246 others(37): Show |
47 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.44-10202G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626659 | |||||||
| chr1:116626725 | G | A | 1 | a0003c0003t0001g0075 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.44-10268C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626725 | |||||||
| chr1:116626817 | T | C | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-10360A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116626817 | |||||||
| chr1:116627147 | A | C | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.44-10690T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627147 | |||||||
| chr1:116627154 | G | T | 3 | a0001c0007t0003g0017 a0001c0010t0001g0245 a0001c0010t0001g0246 |
3 | HG02109.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.44-10697C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627154 | |||||||
| chr1:116627251 | A | G | 1 | a0010c0028t0003g0033 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.44-10794T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627251 | |||||||
| chr1:116627299 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.44-10842G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627299 | |||||||
| chr1:116627310 | C | T | 17 | a0001c0001t0001g0136 a0001c0001t0005g0153 a0002c0002t0001g0110 others(14): Show |
19 | HG01099.hp2 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.44-10853G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627310 | |||||||
| chr1:116627513 | G | A | 1 | a0002c0002t0002g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.44-11056C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627513 | |||||||
| chr1:116627531 | G | A | 3 | a0002c0002t0001g0209 a0002c0022t0001g0074 a0003c0003t0001g0111 |
3 | HG00639.hp2 HG02109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.44-11074C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627531 | |||||||
| chr1:116627613 | G | A | 1 | a0002c0002t0001g0212 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.44-11156C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116627613 | |||||||
| chr1:116628101 | T | C | 2 | a0002c0002t0007g0170 a0012c0012t0020g0178 |
2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.44-11644A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116628101 | |||||||
| chr1:116628115 | G | A | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-11658C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116628115 | |||||||
| chr1:116628184 | C | T | 1 | a0001c0005t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-11727G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116628184 | |||||||
| chr1:116628283 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-11826G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116628283 | |||||||
| chr1:116628399 | C | A | 3 | a0001c0001t0003g0023 a0001c0001t0019g0177 a0002c0002t0004g0021 |
3 | HG02280.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-11942G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116628399 | |||||||
| chr1:116628813 | A | G | 4 | a0002c0004t0001g0048 a0002c0004t0001g0073 a0002c0004t0001g0086 others(1): Show |
4 | HG01433.hp2 HG03516.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-12356T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116628813 | |||||||
| chr1:116629038 | G | A | 2 | a0001c0001t0002g0188 a0001c0001t0002g0194 |
2 | NA18968.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.44-12581C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629038 | |||||||
| chr1:116629080 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.44-12623C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629080 | |||||||
| chr1:116629082 | G | A | 1 | a0002c0015t0003g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.44-12625C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629082 | |||||||
| chr1:116629589 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-13132T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629589 | |||||||
| chr1:116629590 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-13133C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629590 | |||||||
| chr1:116629720 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-13263G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629720 | |||||||
| chr1:116629721 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-13264A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629721 | |||||||
| chr1:116629815 | A | C | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-13358T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629815 | |||||||
| chr1:116629973 | C | G | 7 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(4): Show |
7 | HG02451.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-13516G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116629973 | |||||||
| chr1:116630135 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-13678C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116630135 | |||||||
| chr1:116630690 | A | T | 1 | a0003c0003t0001g0046 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.44-14233T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116630690 | |||||||
| chr1:116630706 | G | A | 1 | a0003c0003t0001g0137 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.44-14249C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116630706 | |||||||
| chr1:116631012 | G | A | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-14555C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631012 | |||||||
| chr1:116631029 | A | G | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-14572T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631029 | |||||||
| chr1:116631042 | G | C | 11 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0036 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-14585C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631042 | |||||||
| chr1:116631103 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-14646C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631103 | |||||||
| chr1:116631224 | AG | A | 38 | a0002c0002t0001g0068 a0002c0004t0001g0080 a0002c0004t0001g0082 others(35): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.44-14768delC | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631224 | |||||||
| chr1:116631249 | C | T | 1 | a0002c0002t0011g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.44-14792G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631249 | |||||||
| chr1:116631317 | C | CA | 39 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0103 others(36): Show |
40 | HG01106.hp2 HG01433.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.44-14861dupT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631317 | |||||||
| chr1:116631317 | C | CAA | 5 | a0001c0001t0001g0104 a0001c0001t0001g0208 a0002c0002t0013g0171 others(2): Show |
5 | HG03516.hp1 HG03579.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-14862_44-14861d others(4): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631317 | |||||||
| chr1:116631317 | CA | C | 32 | a0001c0001t0001g0105 a0001c0001t0001g0149 a0001c0001t0001g0162 others(29): Show |
34 | HG01074.hp2 HG01081.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.44-14861delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631317 | |||||||
| chr1:116631317 | CAA | C | 5 | a0001c0001t0003g0023 a0001c0001t0004g0036 a0001c0001t0019g0177 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-14862_44-14861d others(4): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631317 | |||||||
| chr1:116631351 | C | T | 2 | a0002c0002t0007g0170 a0012c0012t0020g0178 |
2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.44-14894G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631351 | |||||||
| chr1:116631994 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-15537C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116631994 | |||||||
| chr1:116632245 | G | A | 6 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-15788C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116632245 | |||||||
| chr1:116632401 | T | A | 1 | a0002c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.44-15944A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116632401 | |||||||
| chr1:116632401 | T | C | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-15944A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116632401 | |||||||
| chr1:116632466 | A | C | 2 | a0002c0002t0013g0171 a0013c0016t0001g0051 |
2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.44-16009T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116632466 | |||||||
| chr1:116632483 | G | A | 151 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(148): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.44-16026C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116632483 | |||||||
| chr1:116632703 | G | A | 3 | a0001c0001t0003g0023 a0001c0001t0019g0177 a0002c0002t0004g0021 |
3 | HG02280.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-16246C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116632703 | |||||||
| chr1:116632706 | T | A | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-16249A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116632706 | |||||||
| chr1:116633059 | C | T | 1 | a0003c0003t0009g0050 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.44-16602G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116633059 | |||||||
| chr1:116634154 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-17697A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634154 | |||||||
| chr1:116634178 | T | C | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0042 others(243): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.44-17721A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634178 | |||||||
| chr1:116634189 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-17732G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634189 | |||||||
| chr1:116634214 | T | C | 2 | a0002c0004t0001g0107 a0004c0009t0001g0072 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-17757A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634214 | |||||||
| chr1:116634297 | A | T | 10 | a0001c0001t0004g0024 a0001c0001t0004g0036 a0001c0001t0004g0037 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.44-17840T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634297 | |||||||
| chr1:116634438 | G | GCCTGGCT others(17): Show |
1 | a0003c0003t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.44-18005_44-17982d others(26): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634438 | |||||||
| chr1:116634484 | C | A | 2 | a0002c0004t0001g0134 a0002c0004t0001g0135 |
2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.44-18027G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634484 | |||||||
| chr1:116634497 | C | CT | 3 | a0001c0007t0003g0017 a0001c0010t0001g0245 a0001c0010t0001g0246 |
3 | HG02109.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.44-18041dupA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634497 | |||||||
| chr1:116634500 | A | T | 3 | a0001c0007t0003g0017 a0001c0010t0001g0245 a0001c0010t0001g0246 |
3 | HG02109.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.44-18043T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634500 | |||||||
| chr1:116634696 | A | G | 10 | a0002c0002t0001g0120 a0002c0004t0001g0047 a0002c0024t0001g0087 others(7): Show |
12 | HG01099.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.44-18239T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634696 | |||||||
| chr1:116634854 | T | C | 196 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(193): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.44-18397A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634854 | |||||||
| chr1:116634881 | G | A | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-18424C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116634881 | |||||||
| chr1:116635024 | C | T | 6 | a0001c0001t0003g0023 a0001c0001t0019g0177 a0001c0007t0003g0017 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-18567G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635024 | |||||||
| chr1:116635247 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.44-18790T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635247 | |||||||
| chr1:116635250 | C | A | 1 | a0001c0001t0005g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.44-18793G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635250 | |||||||
| chr1:116635357 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.44-18900G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635357 | |||||||
| chr1:116635423 | C | T | 11 | a0001c0001t0002g0198 a0002c0022t0001g0074 a0003c0003t0001g0069 others(8): Show |
11 | HG00140.hp2 HG01099.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-18966G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635423 | |||||||
| chr1:116635447 | A | G | 5 | a0002c0002t0001g0128 a0002c0004t0001g0134 a0002c0004t0001g0135 others(2): Show |
5 | HG00280.hp1 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-18990T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635447 | |||||||
| chr1:116635456 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.44-18999G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635456 | |||||||
| chr1:116635483 | C | T | 20 | a0001c0001t0001g0070 a0001c0001t0003g0023 a0001c0001t0019g0177 others(17): Show |
20 | HG01433.hp2 HG01891.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.44-19026G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635483 | |||||||
| chr1:116635490 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.44-19033A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635490 | |||||||
| chr1:116635491 | G | A | 1 | a0002c0002t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.44-19034C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635491 | |||||||
| chr1:116635519 | G | C | 1 | a0002c0002t0001g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.44-19062C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635519 | |||||||
| chr1:116635680 | G | T | 193 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(190): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.44-19223C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635680 | |||||||
| chr1:116635765 | C | T | 4 | a0001c0001t0005g0052 a0001c0001t0005g0053 a0001c0001t0005g0093 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-19308G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635765 | |||||||
| chr1:116635925 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.44-19468A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116635925 | |||||||
| chr1:116636019 | C | T | 155 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(152): Show |
162 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.44-19562G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116636019 | |||||||
| chr1:116636020 | G | A | 1 | a0002c0002t0001g0212 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.44-19563C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116636020 | |||||||
| chr1:116636166 | G | A | 2 | a0001c0005t0001g0109 a0002c0002t0012g0108 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.44-19709C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116636166 | |||||||
| chr1:116636182 | C | T | 7 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-19725G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116636182 | |||||||
| chr1:116637036 | A | T | 13 | a0001c0005t0001g0109 a0001c0005t0003g0013 a0001c0005t0003g0018 others(10): Show |
13 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-20579T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116637036 | |||||||
| chr1:116637204 | T | C | 2 | a0009c0029t0001g0157 a0011c0030t0001g0167 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.44-20747A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116637204 | |||||||
| chr1:116637324 | T | C | 4 | a0002c0004t0001g0082 a0002c0004t0001g0083 a0002c0004t0001g0085 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-20867A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116637324 | |||||||
| chr1:116637807 | T | A | 16 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(13): Show |
18 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-21350A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116637807 | |||||||
| chr1:116638066 | T | C | 4 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(1): Show |
5 | HG02258.hp1 HG02615.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-21609A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638066 | |||||||
| chr1:116638088 | C | T | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-21631G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638088 | |||||||
| chr1:116638599 | C | T | 1 | a0002c0002t0001g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.44-22142G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638599 | |||||||
| chr1:116638694 | A | T | 1 | a0002c0002t0006g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.44-22237T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638694 | |||||||
| chr1:116638766 | T | A | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-22309A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638766 | |||||||
| chr1:116638768 | T | G | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-22311A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638768 | |||||||
| chr1:116638787 | T | C | 1 | a0001c0005t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-22330A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638787 | |||||||
| chr1:116638845 | T | C | 1 | a0001c0001t0005g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.44-22388A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638845 | |||||||
| chr1:116638890 | T | A | 16 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(13): Show |
18 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-22433A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638890 | |||||||
| chr1:116638900 | G | A | 16 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(13): Show |
18 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-22443C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638900 | |||||||
| chr1:116638905 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.44-22448C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638905 | |||||||
| chr1:116638942 | C | T | 3 | a0001c0007t0003g0017 a0001c0010t0001g0245 a0001c0010t0001g0246 |
3 | HG02109.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.44-22485G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116638942 | |||||||
| chr1:116639295 | T | A | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-22838A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639295 | |||||||
| chr1:116639398 | G | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | NA18944.hp2 NA19006.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-22941C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639398 | |||||||
| chr1:116639547 | C | A | 6 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-23090G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639547 | |||||||
| chr1:116639809 | G | A | 2 | a0002c0002t0001g0115 a0003c0003t0001g0116 |
2 | NA18747.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.44-23352C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639809 | |||||||
| chr1:116639833 | A | G | 1 | a0002c0002t0013g0171 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.44-23376T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639833 | |||||||
| chr1:116639918 | C | T | 14 | a0003c0003t0001g0002 a0003c0003t0001g0054 a0003c0003t0001g0069 others(11): Show |
17 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.44-23461G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639918 | |||||||
| chr1:116639939 | C | T | 13 | a0001c0005t0001g0109 a0001c0005t0003g0013 a0001c0005t0003g0018 others(10): Show |
13 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-23482G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639939 | |||||||
| chr1:116639959 | T | C | 16 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(13): Show |
18 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-23502A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116639959 | |||||||
| chr1:116640006 | C | T | 1 | a0003c0003t0001g0233 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.44-23549G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640006 | |||||||
| chr1:116640037 | C | CA | 8 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0002c0002t0001g0084 others(5): Show |
8 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-23581dupT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640037 | |||||||
| chr1:116640037 | C | CG | 13 | a0001c0005t0001g0109 a0001c0005t0003g0013 a0001c0005t0003g0018 others(10): Show |
13 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-23581_44-23580i others(3): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640037 | |||||||
| chr1:116640037 | CA | C | 26 | a0001c0001t0001g0103 a0001c0001t0001g0142 a0001c0001t0001g0208 others(23): Show |
26 | HG01071.hp2 HG01106.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.44-23581delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640037 | |||||||
| chr1:116640053 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-23596T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640053 | |||||||
| chr1:116640054 | A | AAAAG | 8 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0241 others(5): Show |
8 | HG00738.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-23601_44-23598d others(6): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640054 | |||||||
| chr1:116640054 | AAAAG | A | 16 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(13): Show |
18 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-23601_44-23598d others(6): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640054 | |||||||
| chr1:116640174 | C | A | 1 | a0001c0008t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-23717G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640174 | |||||||
| chr1:116640310 | G | T | 16 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(13): Show |
18 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-23853C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640310 | |||||||
| chr1:116640559 | T | A | 1 | a0002c0002t0001g0212 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.44-24102A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640559 | |||||||
| chr1:116640595 | C | T | 1 | a0010c0028t0003g0033 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.44-24138G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640595 | |||||||
| chr1:116640619 | G | A | 1 | a0001c0005t0001g0102 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-24162C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640619 | |||||||
| chr1:116640721 | C | T | 75 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(72): Show |
79 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.44-24264G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640721 | |||||||
| chr1:116640729 | T | C | 155 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(152): Show |
162 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.44-24272A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640729 | |||||||
| chr1:116640765 | G | A | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-24308C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640765 | |||||||
| chr1:116640826 | C | T | 2 | a0002c0002t0001g0112 a0002c0002t0017g0117 |
2 | HG02080.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.44-24369G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640826 | |||||||
| chr1:116640832 | C | T | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0136 others(24): Show |
28 | HG01071.hp2 HG01106.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.44-24375G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116640832 | |||||||
| chr1:116641080 | G | T | 1 | a0001c0001t0019g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.44-24623C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641080 | |||||||
| chr1:116641161 | T | C | 150 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(147): Show |
157 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.44-24704A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641161 | |||||||
| chr1:116641173 | C | T | 1 | a0002c0022t0001g0074 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.44-24716G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641173 | |||||||
| chr1:116641450 | T | C | 18 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(15): Show |
20 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.43+24834A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641450 | |||||||
| chr1:116641457 | C | T | 18 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(15): Show |
20 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.43+24827G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641457 | |||||||
| chr1:116641495 | C | CA | 30 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0136 others(27): Show |
31 | HG01071.hp2 HG01106.hp1 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.43+24788dupT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641495 | |||||||
| chr1:116641495 | C | CAA | 18 | a0001c0001t0001g0208 a0001c0001t0001g0230 a0001c0001t0005g0153 others(15): Show |
20 | HG01943.hp1 HG02109.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.43+24787_43+24788d others(4): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641495 | |||||||
| chr1:116641495 | CA | C | 73 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0070 others(70): Show |
77 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.43+24788delT | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641495 | |||||||
| chr1:116641495 | CAAAAA | C | 10 | a0001c0001t0004g0024 a0001c0001t0004g0036 a0001c0001t0004g0037 others(7): Show |
10 | HG02055.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+24784_43+24788d others(7): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641495 | |||||||
| chr1:116641495 | CAAAAAAA others(5): Show |
C | 2 | a0002c0002t0001g0115 a0003c0003t0001g0116 |
2 | NA18747.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.43+24777_43+24788d others(14): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641495 | |||||||
| chr1:116641547 | AGAAAAAG others(7): Show |
A | 68 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(65): Show |
72 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.43+24723_43+24736d others(16): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641547 | |||||||
| chr1:116641550 | A | AAAAG | 16 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0120 others(13): Show |
18 | HG01099.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.43+24730_43+24733d others(6): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641550 | |||||||
| chr1:116641561 | G | A | 82 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0136 others(79): Show |
85 | HG01071.hp2 HG01099.hp2 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.43+24723C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641561 | |||||||
| chr1:116641852 | CT | C | 15 | a0001c0001t0004g0025 a0001c0005t0001g0109 a0001c0005t0003g0013 others(12): Show |
15 | HG01891.hp2 HG02717.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.43+24431delA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116641852 | |||||||
| chr1:116642505 | A | G | 27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0136 others(24): Show |
28 | HG01071.hp2 HG01106.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.43+23779T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116642505 | |||||||
| chr1:116642549 | C | T | 1 | a0003c0003t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.43+23735G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116642549 | |||||||
| chr1:116642779 | C | T | 1 | a0002c0002t0004g0021 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.43+23505G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116642779 | |||||||
| chr1:116643030 | C | A | 1 | a0001c0007t0003g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.43+23254G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116643030 | |||||||
| chr1:116643310 | G | A | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+22974C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116643310 | |||||||
| chr1:116643387 | C | T | 26 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0208 others(23): Show |
27 | HG01071.hp2 HG01106.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.43+22897G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116643387 | |||||||
| chr1:116643537 | T | C | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+22747A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116643537 | |||||||
| chr1:116643591 | G | T | 2 | a0002c0002t0001g0216 a0002c0002t0001g0217 |
2 | HG01358.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.43+22693C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116643591 | |||||||
| chr1:116643722 | A | G | 3 | a0001c0001t0001g0136 a0002c0002t0001g0131 a0004c0009t0001g0072 |
3 | HG03486.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+22562T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116643722 | |||||||
| chr1:116643758 | C | T | 1 | a0001c0005t0001g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.43+22526G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116643758 | |||||||
| chr1:116644363 | G | A | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43+21921C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116644363 | |||||||
| chr1:116644445 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.43+21839G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116644445 | |||||||
| chr1:116644498 | T | C | 1 | a0003c0003t0001g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43+21786A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116644498 | |||||||
| chr1:116644691 | A | G | 2 | a0001c0001t0004g0036 a0001c0001t0004g0041 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.43+21593T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116644691 | |||||||
| chr1:116644703 | G | A | 1 | a0002c0002t0002g0195 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.43+21581C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116644703 | |||||||
| chr1:116644866 | G | A | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+21418C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116644866 | |||||||
| chr1:116644889 | C | A | 2 | a0001c0001t0001g0136 a0002c0002t0001g0131 |
2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.43+21395G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116644889 | |||||||
| chr1:116645074 | A | G | 21 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0208 others(18): Show |
21 | HG01071.hp2 HG01106.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.43+21210T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116645074 | |||||||
| chr1:116645157 | C | T | 1 | a0002c0002t0001g0043 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.43+21127G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116645157 | |||||||
| chr1:116645215 | A | T | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+21069T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116645215 | |||||||
| chr1:116645482 | T | A | 22 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0208 others(19): Show |
22 | HG00140.hp2 HG01071.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.43+20802A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116645482 | |||||||
| chr1:116645792 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+20492G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116645792 | |||||||
| chr1:116645895 | G | A | 1 | a0002c0002t0001g0113 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.43+20389C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116645895 | |||||||
| chr1:116645929 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.43+20355G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116645929 | |||||||
| chr1:116646170 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.43+20114G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646170 | |||||||
| chr1:116646342 | G | T | 1 | a0003c0003t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.43+19942C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646342 | |||||||
| chr1:116646343 | G | T | 1 | a0003c0003t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.43+19941C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646343 | |||||||
| chr1:116646355 | A | T | 1 | a0002c0002t0001g0212 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.43+19929T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646355 | |||||||
| chr1:116646507 | CACAA | C | 53 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0105 others(50): Show |
56 | HG00280.hp1 HG00558.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.43+19773_43+19776d others(6): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646507 | |||||||
| chr1:116646577 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43+19707T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646577 | |||||||
| chr1:116646642 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.43+19642T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646642 | |||||||
| chr1:116646735 | A | G | 1 | a0002c0002t0001g0210 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.43+19549T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646735 | |||||||
| chr1:116646858 | G | A | 5 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+19426C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646858 | |||||||
| chr1:116646861 | C | T | 3 | a0002c0002t0006g0014 a0002c0002t0006g0015 a0002c0002t0006g0016 |
3 | HG02895.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.43+19423G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646861 | |||||||
| chr1:116646924 | G | A | 1 | a0002c0002t0002g0196 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.43+19360C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646924 | |||||||
| chr1:116646950 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.43+19334C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116646950 | |||||||
| chr1:116647120 | A | T | 7 | a0001c0001t0005g0153 a0002c0002t0001g0110 a0002c0002t0001g0152 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+19164T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647120 | |||||||
| chr1:116647221 | C | T | 1 | a0001c0001t0019g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+19063G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647221 | |||||||
| chr1:116647232 | G | A | 1 | a0002c0002t0012g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43+19052C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647232 | |||||||
| chr1:116647403 | C | T | 1 | a0001c0001t0004g0024 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.43+18881G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647403 | |||||||
| chr1:116647416 | T | G | 9 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(6): Show |
10 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+18868A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647416 | |||||||
| chr1:116647479 | A | T | 11 | a0001c0001t0019g0177 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+18805T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647479 | |||||||
| chr1:116647570 | C | A | 1 | a0003c0003t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43+18714G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647570 | |||||||
| chr1:116647626 | C | T | 2 | a0002c0002t0001g0120 a0002c0004t0001g0119 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.43+18658G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647626 | |||||||
| chr1:116647682 | G | A | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+18602C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647682 | |||||||
| chr1:116647875 | G | A | 1 | a0003c0003t0001g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.43+18409C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116647875 | |||||||
| chr1:116648204 | A | G | 14 | a0001c0001t0001g0136 a0001c0001t0003g0023 a0001c0001t0019g0177 others(11): Show |
14 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.43+18080T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116648204 | |||||||
| chr1:116648267 | C | A | 66 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0105 others(63): Show |
70 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.43+18017G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116648267 | |||||||
| chr1:116648349 | T | G | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+17935A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116648349 | |||||||
| chr1:116648433 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | HG01074.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.43+17851C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116648433 | |||||||
| chr1:116648567 | G | C | 3 | a0001c0001t0005g0093 a0002c0002t0011g0040 a0003c0003t0001g0204 |
3 | HG02055.hp1 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.43+17717C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116648567 | |||||||
| chr1:116648649 | C | A | 1 | a0004c0009t0002g0197 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.43+17635G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116648649 | |||||||
| chr1:116649020 | A | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(90): Show |
97 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.43+17264T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649020 | |||||||
| chr1:116649339 | G | A | 1 | a0003c0003t0001g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.43+16945C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649339 | |||||||
| chr1:116649431 | A | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(77): Show |
84 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.43+16853T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649431 | |||||||
| chr1:116649475 | T | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+16809A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649475 | |||||||
| chr1:116649614 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.43+16670G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649614 | |||||||
| chr1:116649620 | A | G | 13 | a0001c0001t0003g0023 a0001c0001t0019g0177 a0001c0005t0003g0013 others(10): Show |
13 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+16664T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649620 | |||||||
| chr1:116649753 | C | T | 1 | a0002c0002t0011g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.43+16531G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649753 | |||||||
| chr1:116649754 | C | A | 1 | a0012c0012t0020g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43+16530G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649754 | |||||||
| chr1:116649796 | A | G | 13 | a0001c0001t0003g0023 a0001c0001t0019g0177 a0001c0005t0003g0013 others(10): Show |
13 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+16488T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649796 | |||||||
| chr1:116649801 | T | C | 2 | a0002c0002t0013g0171 a0002c0004t0001g0107 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.43+16483A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649801 | |||||||
| chr1:116649833 | G | A | 7 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(4): Show |
7 | HG02451.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+16451C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649833 | |||||||
| chr1:116649926 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.43+16358A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649926 | |||||||
| chr1:116649970 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.43+16314G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116649970 | |||||||
| chr1:116650100 | T | A | 9 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(6): Show |
10 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+16184A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650100 | |||||||
| chr1:116650130 | A | C | 72 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(69): Show |
75 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.43+16154T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650130 | |||||||
| chr1:116650253 | T | C | 1 | a0005c0026t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.43+16031A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650253 | |||||||
| chr1:116650263 | C | G | 1 | a0002c0002t0001g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.43+16021G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650263 | |||||||
| chr1:116650282 | C | T | 9 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(6): Show |
10 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+16002G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650282 | |||||||
| chr1:116650720 | A | C | 11 | a0001c0001t0019g0177 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+15564T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650720 | |||||||
| chr1:116650808 | C | T | 1 | a0002c0002t0012g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43+15476G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650808 | |||||||
| chr1:116650976 | G | A | 1 | a0001c0013t0003g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43+15308C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116650976 | |||||||
| chr1:116651086 | T | A | 5 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+15198A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116651086 | |||||||
| chr1:116651522 | T | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+14762A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116651522 | |||||||
| chr1:116651530 | A | T | 5 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+14754T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116651530 | |||||||
| chr1:116651569 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43+14715G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116651569 | |||||||
| chr1:116651614 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.43+14670A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116651614 | |||||||
| chr1:116651967 | C | T | 81 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0105 others(78): Show |
85 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.43+14317G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116651967 | |||||||
| chr1:116652068 | G | A | 2 | a0001c0001t0019g0177 a0002c0002t0004g0021 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.43+14216C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652068 | |||||||
| chr1:116652105 | C | G | 8 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(5): Show |
9 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+14179G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652105 | |||||||
| chr1:116652273 | T | C | 11 | a0001c0001t0019g0177 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+14011A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652273 | |||||||
| chr1:116652569 | C | G | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+13715G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652569 | |||||||
| chr1:116652672 | T | C | 1 | a0002c0002t0001g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.43+13612A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652672 | |||||||
| chr1:116652759 | C | A | 13 | a0001c0001t0001g0232 a0001c0001t0001g0240 a0002c0002t0001g0011 others(10): Show |
14 | HG00621.hp1 HG00738.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.43+13525G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652759 | |||||||
| chr1:116652874 | T | C | 2 | a0002c0002t0007g0170 a0002c0004t0001g0203 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.43+13410A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652874 | |||||||
| chr1:116652910 | C | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+13374G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652910 | |||||||
| chr1:116652985 | T | C | 36 | a0001c0001t0003g0023 a0001c0001t0003g0031 a0001c0001t0004g0024 others(33): Show |
37 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(34): Show |
intron_variant | MODIFIER | c.43+13299A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116652985 | |||||||
| chr1:116653039 | A | G | 9 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+13245T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116653039 | |||||||
| chr1:116653200 | G | A | 2 | a0001c0001t0001g0105 a0002c0002t0002g0199 |
2 | NA18612.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.43+13084C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116653200 | |||||||
| chr1:116653221 | A | G | 1 | a0003c0003t0002g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.43+13063T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116653221 | |||||||
| chr1:116653428 | C | G | 1 | a0001c0001t0002g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.43+12856G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116653428 | |||||||
| chr1:116653581 | C | T | 19 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0014g0057 others(16): Show |
23 | HG00738.hp2 HG01070.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.43+12703G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116653581 | |||||||
| chr1:116653700 | A | G | 9 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+12584T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116653700 | |||||||
| chr1:116653828 | G | C | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.43+12456C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116653828 | |||||||
| chr1:116654105 | T | A | 4 | a0002c0002t0001g0100 a0002c0002t0003g0034 a0004c0009t0003g0035 others(1): Show |
4 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+12179A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654105 | |||||||
| chr1:116654380 | C | G | 1 | a0001c0006t0001g0141 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.43+11904G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654380 | |||||||
| chr1:116654386 | T | A | 25 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(22): Show |
25 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.43+11898A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654386 | |||||||
| chr1:116654497 | C | A | 2 | a0001c0010t0001g0245 a0001c0010t0001g0246 |
2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.43+11787G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654497 | |||||||
| chr1:116654560 | C | T | 1 | a0001c0005t0003g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.43+11724G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654560 | |||||||
| chr1:116654576 | A | C | 1 | a0002c0002t0002g0202 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.43+11708T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654576 | |||||||
| chr1:116654593 | A | G | 2 | a0003c0003t0001g0002 a0003c0003t0001g0054 |
4 | HG01358.hp1 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+11691T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654593 | |||||||
| chr1:116654613 | T | C | 184 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(181): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.43+11671A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654613 | |||||||
| chr1:116654659 | C | T | 12 | a0001c0001t0003g0023 a0001c0001t0019g0177 a0001c0005t0003g0013 others(9): Show |
12 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+11625G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116654659 | |||||||
| chr1:116655053 | A | G | 24 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(21): Show |
24 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.43+11231T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116655053 | |||||||
| chr1:116655243 | C | G | 24 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(21): Show |
24 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.43+11041G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116655243 | |||||||
| chr1:116655389 | A | G | 185 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(182): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.43+10895T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116655389 | |||||||
| chr1:116655496 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+10788G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116655496 | |||||||
| chr1:116655512 | T | C | 1 | a0002c0002t0002g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+10772A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116655512 | |||||||
| chr1:116655688 | G | A | 1 | a0002c0004t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43+10596C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116655688 | |||||||
| chr1:116656073 | T | C | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.43+10211A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656073 | |||||||
| chr1:116656229 | C | G | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.43+10055G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656229 | |||||||
| chr1:116656249 | A | G | 16 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(13): Show |
16 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.43+10035T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656249 | |||||||
| chr1:116656292 | T | C | 1 | a0002c0031t0002g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.43+9992A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656292 | |||||||
| chr1:116656293 | C | CT | 5 | a0001c0001t0001g0222 a0001c0001t0004g0037 a0002c0002t0001g0113 others(2): Show |
5 | HG01169.hp2 HG02027.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+9990dupA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656293 | |||||||
| chr1:116656293 | CT | C | 146 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(143): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.43+9990delA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656293 | |||||||
| chr1:116656293 | CTTTTT | C | 15 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(12): Show |
15 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.43+9986_43+9990del others(5): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656293 | |||||||
| chr1:116656362 | G | A | 2 | a0002c0004t0001g0134 a0002c0004t0001g0135 |
2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.43+9922C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656362 | |||||||
| chr1:116656418 | C | T | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+9866G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656418 | |||||||
| chr1:116656436 | A | G | 106 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(103): Show |
110 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.43+9848T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656436 | |||||||
| chr1:116656785 | G | A | 1 | a0003c0003t0003g0030 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+9499C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656785 | |||||||
| chr1:116656942 | G | T | 9 | a0001c0001t0001g0139 a0001c0001t0003g0023 a0001c0001t0004g0024 others(6): Show |
9 | HG01981.hp2 HG02257.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+9342C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656942 | |||||||
| chr1:116656946 | T | G | 10 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(7): Show |
11 | HG01891.hp1 HG01934.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+9338A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656946 | |||||||
| chr1:116656959 | A | C | 1 | a0013c0016t0001g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.43+9325T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656959 | |||||||
| chr1:116656964 | A | T | 14 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(11): Show |
14 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.43+9320T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656964 | |||||||
| chr1:116656976 | G | A | 14 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(11): Show |
14 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.43+9308C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116656976 | |||||||
| chr1:116657010 | T | C | 24 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(21): Show |
24 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.43+9274A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657010 | |||||||
| chr1:116657036 | C | T | 13 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(10): Show |
13 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.43+9248G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657036 | |||||||
| chr1:116657047 | G | A | 24 | a0001c0001t0003g0023 a0001c0001t0004g0024 a0001c0001t0004g0025 others(21): Show |
24 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.43+9237C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657047 | |||||||
| chr1:116657253 | C | T | 2 | a0002c0002t0001g0152 a0002c0002t0001g0155 |
2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.43+9031G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657253 | |||||||
| chr1:116657262 | A | C | 185 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(182): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.43+9022T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657262 | |||||||
| chr1:116657463 | C | CAT | 104 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(101): Show |
108 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.43+8819_43+8820dup others(2): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657463 | |||||||
| chr1:116657540 | G | A | 12 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(9): Show |
12 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+8744C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657540 | |||||||
| chr1:116657588 | G | T | 12 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(9): Show |
12 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+8696C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657588 | |||||||
| chr1:116657858 | C | G | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+8426G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657858 | |||||||
| chr1:116657953 | T | A | 1 | a0002c0002t0007g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+8331A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116657953 | |||||||
| chr1:116658040 | A | G | 246 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0042 others(243): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.43+8244T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658040 | |||||||
| chr1:116658117 | T | C | 82 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0105 others(79): Show |
86 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.43+8167A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658117 | |||||||
| chr1:116658128 | G | A | 83 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0105 others(80): Show |
87 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.43+8156C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658128 | |||||||
| chr1:116658292 | G | A | 2 | a0002c0002t0013g0171 a0002c0004t0001g0107 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.43+7992C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658292 | |||||||
| chr1:116658633 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.43+7651A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658633 | |||||||
| chr1:116658817 | G | A | 1 | a0003c0003t0001g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.43+7467C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658817 | |||||||
| chr1:116658878 | A | T | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.43+7406T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658878 | |||||||
| chr1:116658924 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43+7360G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658924 | |||||||
| chr1:116658982 | G | T | 2 | a0002c0002t0010g0175 a0002c0002t0010g0176 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.43+7302C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116658982 | |||||||
| chr1:116659397 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.43+6887C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116659397 | |||||||
| chr1:116659540 | GT | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0161 a0001c0001t0001g0162 others(6): Show |
10 | HG00423.hp2 HG01256.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+6743delA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116659540 | |||||||
| chr1:116659810 | C | A | 2 | a0001c0001t0004g0036 a0001c0001t0004g0041 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.43+6474G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116659810 | |||||||
| chr1:116659973 | A | G | 185 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(182): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.43+6311T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116659973 | |||||||
| chr1:116659987 | C | T | 9 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(6): Show |
10 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+6297G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116659987 | |||||||
| chr1:116660027 | G | A | 2 | a0001c0001t0019g0177 a0012c0012t0020g0178 |
2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.43+6257C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660027 | |||||||
| chr1:116660358 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.43+5926C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660358 | |||||||
| chr1:116660479 | C | CT | 70 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(67): Show |
73 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.43+5804dupA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660479 | |||||||
| chr1:116660479 | CT | C | 35 | a0001c0001t0003g0023 a0001c0001t0003g0031 a0001c0001t0004g0037 others(32): Show |
36 | HG01934.hp1 HG01943.hp2 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.43+5804delA | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660479 | |||||||
| chr1:116660485 | T | C | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+5799A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660485 | |||||||
| chr1:116660606 | G | GAGCTGGG others(1586): Show |
1 | a0002c0002t0002g0181 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+5677_43+5678ins others(1593): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660606 | |||||||
| chr1:116660607 | T | A | 107 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(104): Show |
111 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.43+5677A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660607 | |||||||
| chr1:116660722 | G | A | 2 | a0001c0001t0001g0169 a0002c0002t0007g0170 |
2 | HG00423.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.43+5562C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660722 | |||||||
| chr1:116660738 | G | A | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.43+5546C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660738 | |||||||
| chr1:116660839 | A | C | 1 | a0002c0002t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.43+5445T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660839 | |||||||
| chr1:116660911 | C | T | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+5373G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660911 | |||||||
| chr1:116660923 | G | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0139 a0001c0001t0001g0140 others(11): Show |
17 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.43+5361C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660923 | |||||||
| chr1:116660927 | T | C | 2 | a0001c0005t0001g0099 a0003c0003t0001g0098 |
2 | HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.43+5357A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116660927 | |||||||
| chr1:116661007 | A | G | 1 | a0002c0002t0002g0180 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.43+5277T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661007 | |||||||
| chr1:116661219 | G | T | 1 | a0003c0003t0001g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.43+5065C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661219 | |||||||
| chr1:116661225 | G | A | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+5059C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661225 | |||||||
| chr1:116661294 | A | AAAAAAT | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+4989_43+4990ins others(6): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661294 | |||||||
| chr1:116661464 | T | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+4820A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661464 | |||||||
| chr1:116661548 | A | G | 1 | a0002c0002t0013g0171 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.43+4736T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661548 | |||||||
| chr1:116661631 | C | T | 7 | a0001c0005t0003g0013 a0001c0005t0003g0018 a0001c0007t0003g0017 others(4): Show |
7 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+4653G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661631 | |||||||
| chr1:116661669 | C | T | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+4615G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116661669 | |||||||
| chr1:116662010 | C | A | 9 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(6): Show |
10 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+4274G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662010 | |||||||
| chr1:116662060 | T | G | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+4224A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662060 | |||||||
| chr1:116662065 | G | A | 1 | a0004c0009t0003g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.43+4219C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662065 | |||||||
| chr1:116662133 | C | T | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.43+4151G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662133 | |||||||
| chr1:116662228 | G | C | 1 | a0002c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.43+4056C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662228 | |||||||
| chr1:116662231 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.43+4053G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662231 | |||||||
| chr1:116662259 | C | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+4025G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662259 | |||||||
| chr1:116662364 | C | T | 1 | a0002c0002t0001g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.43+3920G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662364 | |||||||
| chr1:116662374 | G | A | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+3910C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662374 | |||||||
| chr1:116662387 | C | A | 8 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+3897G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662387 | |||||||
| chr1:116662474 | T | C | 2 | a0001c0001t0019g0177 a0012c0012t0020g0178 |
2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.43+3810A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662474 | |||||||
| chr1:116662611 | A | C | 9 | a0001c0001t0003g0031 a0001c0007t0003g0004 a0001c0007t0003g0029 others(6): Show |
10 | HG01934.hp1 HG01952.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+3673T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662611 | |||||||
| chr1:116662971 | C | T | 1 | a0002c0004t0001g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.43+3313G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116662971 | |||||||
| chr1:116663162 | C | G | 75 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0070 others(72): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.43+3122G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663162 | |||||||
| chr1:116663192 | T | C | 8 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+3092A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663192 | |||||||
| chr1:116663432 | T | C | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+2852A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663432 | |||||||
| chr1:116663452 | A | G | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+2832T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663452 | |||||||
| chr1:116663491 | G | A | 8 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+2793C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663491 | |||||||
| chr1:116663495 | T | C | 1 | a0003c0003t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.43+2789A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663495 | |||||||
| chr1:116663714 | T | C | 74 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(71): Show |
77 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.43+2570A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663714 | |||||||
| chr1:116663767 | C | A | 1 | a0001c0001t0005g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.43+2517G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663767 | |||||||
| chr1:116663930 | T | A | 6 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+2354A>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663930 | |||||||
| chr1:116663959 | A | T | 74 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0045 others(71): Show |
77 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.43+2325T>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116663959 | |||||||
| chr1:116664013 | G | T | 2 | a0001c0005t0001g0109 a0002c0002t0012g0108 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.43+2271C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116664013 | |||||||
| chr1:116664280 | C | G | 1 | a0002c0004t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+2004G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116664280 | |||||||
| chr1:116664318 | G | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.43+1966C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116664318 | |||||||
| chr1:116664443 | C | T | 73 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0070 others(70): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.43+1841G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116664443 | |||||||
| chr1:116664624 | G | A | 1 | a0003c0003t0001g0172 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.43+1660C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116664624 | |||||||
| chr1:116665055 | C | G | 1 | a0002c0004t0001g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.43+1229G>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665055 | |||||||
| chr1:116665107 | T | C | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.43+1177A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665107 | |||||||
| chr1:116665227 | T | C | 1 | a0003c0003t0001g0173 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43+1057A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665227 | |||||||
| chr1:116665307 | G | A | 1 | a0001c0005t0003g0022 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.43+977C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665307 | |||||||
| chr1:116665326 | A | G | 1 | a0003c0003t0001g0046 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.43+958T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665326 | |||||||
| chr1:116665392 | G | A | 1 | a0002c0002t0002g0202 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.43+892C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665392 | |||||||
| chr1:116665470 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43+814G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665470 | |||||||
| chr1:116665607 | T | G | 1 | a0002c0004t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.43+677A>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665607 | |||||||
| chr1:116665664 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.43+620G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665664 | |||||||
| chr1:116665738 | G | A | 1 | a0002c0002t0001g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+546C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 2/10 | chr1 | 116665738 | |||||||
| chr1:116667043 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-630-87C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667043 | |||||||
| chr1:116667256 | C | A | 1 | a0001c0001t0004g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-630-300G>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667256 | |||||||
| chr1:116667294 | C | T | 1 | a0005c0026t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-631+324G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667294 | |||||||
| chr1:116667364 | G | C | 28 | a0001c0001t0003g0023 a0001c0001t0003g0031 a0001c0001t0004g0024 others(25): Show |
29 | HG01934.hp1 HG02074.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-631+254C>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667364 | |||||||
| chr1:116667369 | G | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0025 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-631+249C>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667369 | |||||||
| chr1:116667419 | T | C | 1 | a0003c0003t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-631+199A>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667419 | |||||||
| chr1:116667423 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-631+195C>T | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667423 | |||||||
| chr1:116667520 | G | GCTCCCCC | 3 | a0001c0001t0001g0042 a0002c0002t0001g0043 a0003c0003t0001g0005 |
4 | HG02027.hp2 HG02074.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-631+97_-631+98ins others(7): Show |
IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667520 | |||||||
| chr1:116667527 | A | C | 179 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0045 others(176): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-631+91T>G | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667527 | |||||||
| chr1:116667527 | A | G | 3 | a0001c0001t0001g0042 a0002c0002t0001g0043 a0003c0003t0001g0005 |
4 | HG02027.hp2 HG02074.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-631+91T>C | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667527 | |||||||
| chr1:116667605 | C | T | 11 | a0001c0001t0003g0023 a0001c0005t0003g0013 a0001c0005t0003g0018 others(8): Show |
11 | HG02109.hp2 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.-631+13G>A | IGSF3 | ENSG00000143061.18 | transcript | ENST00000369486.8 | protein_coding | 1/10 | chr1 | 116667605 |