Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 375337 |
| ensemblid | ENSG00000173769.4 |
| hgncid | 24746 |
| symbol | TOPAZ1 |
| name | testis and ovary specific TOPAZ 1 |
| refseq_nuc | NM_001145030.2 |
| refseq_prot | NP_001138502.1 |
| ensembl_nuc | ENST00000309765.4 |
| ensembl_prot | ENSP00000310303.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 44241886 |
| end | 44332098 |
| strand | + |
| ver | v1.2 |
| region | chr3:44241886-44332098 |
| region5000 | chr3:44236886-44337098 |
| regionname0 | TOPAZ1_chr3_44241886_44332098 |
| regionname5000 | TOPAZ1_chr3_44236886_44337098 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1692 | 97 | 22 | 26 | 27 | 6 | 15 | 16 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0002 | 0/0 | 1692 | 79 | 44 | 18 | 4 | 7 | 6 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0003 | 1/0 | 1692 | 55 | 11 | 8 | 30 | 1 | 4 | 20 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0004 | 0/0 | 1692 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0005 | 0/0 | 1692 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0006 | 0/0 | 1692 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0007 | 0/0 | 1692 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0008 | 0/0 | 1692 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0009 | 0/0 | 1692 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0010 | 0/0 | 1692 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0011 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0012 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0013 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0014 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0015 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0016 | 0/0 | 1692 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0017 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0018 | 0/0 | 1692 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| a0019 | 0/0 | 1692 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | MRRPP others(1687): Show |
chr3 | 44236886 | 44337098 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5076 | 94 | 20 | 26 | 27 | 6 | 14 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0001c0015 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0001c0016 | 0/0 | 5076 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0001c0017 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0002c0002 | 0/0 | 5076 | 62 | 34 | 15 | 4 | 3 | 6 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0002c0005 | 0/0 | 5076 | 7 | 0 | 3 | 0 | 4 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0002c0006 | 0/0 | 5076 | 7 | 7 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0002c0024 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0002c0025 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0002c0026 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0003c0003 | 1/0 | 5076 | 45 | 11 | 8 | 20 | 1 | 4 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0003c0004 | 0/0 | 5076 | 10 | 0 | 0 | 10 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0004c0007 | 0/0 | 5076 | 5 | 5 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0005c0008 | 0/0 | 5076 | 4 | 4 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0006c0010 | 0/0 | 5076 | 2 | 0 | 1 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0007c0011 | 0/0 | 5076 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0008c0012 | 0/0 | 5076 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0009c0009 | 0/0 | 5076 | 2 | 0 | 0 | 0 | 0 | 2 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0010c0023 | 0/0 | 5076 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0011c0018 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0012c0028 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0013c0021 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0014c0022 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0015c0019 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0016c0020 | 0/0 | 5076 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0017c0014 | 0/0 | 5076 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0018c0013 | 0/0 | 5076 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 | ||
| a0019c0027 | 0/0 | 5076 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ATGCG others(5071): Show |
chr3 | 44236886 | 44337098 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5334 | 94 | 20 | 26 | 27 | 6 | 14 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0001c0015t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0001c0016t0001 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0001c0017t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0002c0002t0001 | 0/0 | 5334 | 62 | 34 | 15 | 4 | 3 | 6 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0002c0005t0001 | 0/0 | 5334 | 7 | 0 | 3 | 0 | 4 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0002c0006t0001 | 0/0 | 5334 | 7 | 7 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0002c0024t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0002c0025t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0002c0026t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0003c0003t0002 | 1/0 | 5334 | 45 | 11 | 8 | 20 | 1 | 4 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0003c0004t0002 | 0/0 | 5334 | 10 | 0 | 0 | 10 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0004c0007t0001 | 0/0 | 5334 | 5 | 5 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0005c0008t0002 | 0/0 | 5334 | 4 | 4 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0006c0010t0001 | 0/0 | 5334 | 2 | 0 | 1 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0007c0011t0001 | 0/0 | 5334 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0008c0012t0001 | 0/0 | 5334 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0009c0009t0001 | 0/0 | 5334 | 2 | 0 | 0 | 0 | 0 | 2 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0010c0023t0001 | 0/0 | 5334 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0011c0018t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0012c0028t0002 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0013c0021t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0014c0022t0001 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0015c0019t0002 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0016c0020t0002 | 0/0 | 5334 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0017c0014t0001 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0018c0013t0001 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| a0019c0027t0001 | 0/0 | 5334 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | ACTTC others(5329): Show |
chr3 | 44236886 | 44337098 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0015t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0016t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0001c0017t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0006t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0024t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0025t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0002c0026t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0193 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0003c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0004c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0005c0008t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0006c0010t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0006c0010t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0007c0011t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0008c0012t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0008c0012t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0009c0009t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0009c0009t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0010c0023t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0011c0018t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0012c0028t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0013c0021t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0014c0022t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0015c0019t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0016c0020t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0017c0014t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0018c0013t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| a0019c0027t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0005 | t0001 | g0125 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0129 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00408 | hp1 | a0003 | c0004 | t0002 | g0197 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0208 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00558 | hp2 | a0003 | c0004 | t0002 | g0239 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00597 | hp2 | a0003 | c0004 | t0002 | g0188 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0213 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0240 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00642 | hp2 | a0006 | c0010 | t0001 | g0053 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00673 | hp1 | a0003 | c0004 | t0002 | g0196 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00733 | hp1 | a0002 | c0005 | t0001 | g0127 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00738 | hp2 | a0003 | c0003 | t0002 | g0217 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01106 | hp2 | a0003 | c0003 | t0002 | g0214 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01109 | hp1 | a0002 | c0005 | t0001 | g0128 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01167 | hp2 | a0007 | c0011 | t0001 | g0005 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01169 | hp2 | a0007 | c0011 | t0001 | g0005 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01175 | hp1 | a0003 | c0003 | t0002 | g0220 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PUR | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01346 | hp1 | a0010 | c0023 | t0001 | g0152 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01358 | hp1 | a0003 | c0003 | t0002 | g0211 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0147 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0138 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01516 | hp1 | a0002 | c0005 | t0001 | g0126 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01517 | hp2 | a0002 | c0005 | t0001 | g0006 | EUR | IBS | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01928 | hp2 | a0003 | c0003 | t0002 | g0215 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0207 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0210 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02004 | hp2 | a0002 | c0005 | t0001 | g0006 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0203 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02132 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0194 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02257 | hp1 | a0003 | c0003 | t0002 | g0007 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02257 | hp2 | a0004 | c0007 | t0001 | g0172 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02258 | hp1 | a0005 | c0008 | t0002 | g0183 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02258 | hp2 | a0002 | c0006 | t0001 | g0244 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02280 | hp1 | a0003 | c0003 | t0002 | g0226 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | PEL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02451 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0162 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02622 | hp2 | a0005 | c0008 | t0002 | g0185 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02630 | hp1 | a0013 | c0021 | t0001 | g0181 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02647 | hp1 | a0003 | c0003 | t0002 | g0190 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02647 | hp2 | a0003 | c0003 | t0002 | g0199 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02683 | hp1 | a0003 | c0003 | t0002 | g0218 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0212 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02717 | hp1 | a0001 | c0017 | t0001 | g0095 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02717 | hp2 | a0005 | c0008 | t0002 | g0184 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02723 | hp1 | a0003 | c0003 | t0002 | g0191 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02723 | hp2 | a0004 | c0007 | t0001 | g0170 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02809 | hp2 | a0002 | c0006 | t0001 | g0247 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02818 | hp1 | a0003 | c0003 | t0002 | g0189 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02818 | hp2 | a0008 | c0012 | t0001 | g0023 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02886 | hp2 | a0002 | c0006 | t0001 | g0009 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02895 | hp2 | a0002 | c0006 | t0001 | g0248 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02897 | hp1 | a0002 | c0006 | t0001 | g0246 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02965 | hp2 | a0014 | c0022 | t0001 | g0169 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02976 | hp1 | a0002 | c0024 | t0001 | g0113 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03041 | hp1 | a0015 | c0019 | t0002 | g0236 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03098 | hp1 | a0016 | c0020 | t0002 | g0235 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03130 | hp1 | a0002 | c0026 | t0001 | g0230 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0237 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03139 | hp2 | a0004 | c0007 | t0001 | g0171 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03195 | hp1 | a0001 | c0015 | t0001 | g0104 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03209 | hp2 | a0003 | c0003 | t0002 | g0200 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03453 | hp1 | a0003 | c0003 | t0002 | g0201 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03486 | hp1 | a0004 | c0007 | t0001 | g0232 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03490 | hp2 | a0017 | c0014 | t0001 | g0020 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | ESN | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03540 | hp1 | a0008 | c0012 | t0001 | g0022 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03540 | hp2 | a0004 | c0007 | t0001 | g0173 | AFR | GWD | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03579 | hp2 | a0002 | c0025 | t0001 | g0243 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03654 | hp2 | a0018 | c0013 | t0001 | g0011 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03927 | hp1 | a0001 | c0016 | t0001 | g0088 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04115 | hp1 | a0009 | c0009 | t0001 | g0085 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0216 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04184 | hp2 | a0009 | c0009 | t0001 | g0084 | SAS | BEB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04199 | hp2 | a0003 | c0003 | t0002 | g0242 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG04228 | hp2 | a0006 | c0010 | t0001 | g0050 | SAS | STU | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18747 | hp2 | a0003 | c0003 | t0002 | g0202 | EAS | CHB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18943 | hp1 | a0003 | c0003 | t0002 | g0206 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18945 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18947 | hp2 | a0003 | c0003 | t0002 | g0228 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18953 | hp1 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18953 | hp2 | a0003 | c0003 | t0002 | g0192 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18957 | hp1 | a0019 | c0027 | t0001 | g0066 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0219 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18961 | hp2 | a0003 | c0003 | t0002 | g0204 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18966 | hp2 | a0003 | c0004 | t0002 | g0001 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18967 | hp2 | a0003 | c0003 | t0002 | g0241 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18970 | hp1 | a0003 | c0004 | t0002 | g0223 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18974 | hp1 | a0003 | c0003 | t0002 | g0221 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0209 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18986 | hp1 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0227 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18999 | hp1 | a0003 | c0003 | t0002 | g0222 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA18999 | hp2 | a0003 | c0004 | t0002 | g0229 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19002 | hp2 | a0003 | c0003 | t0002 | g0205 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0233 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19056 | hp1 | a0003 | c0003 | t0002 | g0238 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0187 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA19065 | hp2 | a0003 | c0003 | t0002 | g0195 | EAS | JPT | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ASW | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20752 | hp2 | a0003 | c0003 | t0002 | g0007 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0182 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20805 | hp2 | a0002 | c0005 | t0001 | g0231 | EUR | TSI | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | GIH | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02109 | hp1 | a0011 | c0018 | t0001 | g0083 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02109 | hp2 | a0002 | c0006 | t0001 | g0245 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0165 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02486 | hp2 | a0012 | c0028 | t0002 | g0198 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | USA | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0145 | AFR | USA | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA21309 | hp1 | a0003 | c0003 | t0002 | g0225 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| NA21309 | hp2 | a0005 | c0008 | t0002 | g0186 | AFR | LWK | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0041 | REF | REF | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0002 | g0193 | REF | REF | TOPAZ1_chr3_44236886_44337098 | TOPAZ1 | chr3 | 44236886 | 44337098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242174 | G | A | 1 | a0018 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.121G>A | p.Gly41Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 289/5334 | 121/5079 | 41/1692 | chr3 | 44242174 | |||
| chr3:44242180 | T | C | 17 | a0001 a0002 a0004 others(14): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
missense_variant | MODERATE | c.127T>C | p.Cys43Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 295/5334 | 127/5079 | 43/1692 | chr3 | 44242180 | |||
| chr3:44242316 | C | A | 16 | a0001 a0002 a0004 others(13): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
missense_variant | MODERATE | c.263C>A | p.Pro88Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 431/5334 | 263/5079 | 88/1692 | chr3 | 44242316 | |||
| chr3:44243092 | G | A | 8 | a0001 a0006 a0007 others(5): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
missense_variant | MODERATE | c.586G>A | p.Val196Ile | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 754/5334 | 586/5079 | 196/1692 | chr3 | 44243092 | |||
| chr3:44243633 | G | C | 1 | a0017 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1127G>C | p.Ser376Thr | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1295/5334 | 1127/5079 | 376/1692 | chr3 | 44243633 | |||
| chr3:44243654 | A | G | 1 | a0008 | 2 | HG02818.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1148A>G | p.Lys383Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1316/5334 | 1148/5079 | 383/1692 | chr3 | 44243654 | |||
| chr3:44243756 | A | G | 1 | a0007 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1250A>G | p.Gln417Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1418/5334 | 1250/5079 | 417/1692 | chr3 | 44243756 | |||
| chr3:44243954 | A | G | 1 | a0005 | 4 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
missense_variant | MODERATE | c.1448A>G | p.Gln483Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1616/5334 | 1448/5079 | 483/1692 | chr3 | 44243954 | |||
| chr3:44244200 | T | C | 1 | a0015 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1694T>C | p.Leu565Ser | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1862/5334 | 1694/5079 | 565/1692 | chr3 | 44244200 | |||
| chr3:44244383 | C | T | 1 | a0006 | 2 | HG00642.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.1877C>T | p.Thr626Met | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2045/5334 | 1877/5079 | 626/1692 | chr3 | 44244383 | |||
| chr3:44244523 | C | G | 1 | a0011 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.2017C>G | p.Pro673Ala | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2185/5334 | 2017/5079 | 673/1692 | chr3 | 44244523 | |||
| chr3:44244599 | A | G | 1 | a0009 | 2 | HG04115.hp1 HG04184.hp2 |
missense_variant | MODERATE | c.2093A>G | p.Lys698Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2261/5334 | 2093/5079 | 698/1692 | chr3 | 44244599 | |||
| chr3:44244638 | C | T | 1 | a0010 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2132C>T | p.Ala711Val | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2300/5334 | 2132/5079 | 711/1692 | chr3 | 44244638 | |||
| chr3:44244749 | G | A | 1 | a0016 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2243G>A | p.Arg748Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2411/5334 | 2243/5079 | 748/1692 | chr3 | 44244749 | |||
| chr3:44244892 | A | G | 3 | a0005 a0015 a0016 |
6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
missense_variant | MODERATE | c.2386A>G | p.Lys796Glu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2554/5334 | 2386/5079 | 796/1692 | chr3 | 44244892 | |||
| chr3:44254982 | T | C | 1 | a0013 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.2780T>C | p.Leu927Pro | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/20 | 2948/5334 | 2780/5079 | 927/1692 | chr3 | 44254982 | |||
| chr3:44269299 | G | A | 1 | a0007 | 2 | HG01167.hp2 HG01169.hp2 |
missense_variant&splice_region_variant | MODERATE | c.3244G>A | p.Gly1082Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/20 | 3412/5334 | 3244/5079 | 1082/1692 | chr3 | 44269299 | |||
| chr3:44290811 | A | G | 1 | a0014 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.3722A>G | p.Asn1241Ser | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/20 | 3890/5334 | 3722/5079 | 1241/1692 | chr3 | 44290811 | |||
| chr3:44304029 | G | A | 1 | a0008 | 2 | HG02818.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.3812G>A | p.Arg1271Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/20 | 3980/5334 | 3812/5079 | 1271/1692 | chr3 | 44304029 | |||
| chr3:44306341 | A | G | 1 | a0004 | 5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.4055A>G | p.Gln1352Arg | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/20 | 4223/5334 | 4055/5079 | 1352/1692 | chr3 | 44306341 | |||
| chr3:44323169 | A | T | 1 | a0012 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.4549A>T | p.Met1517Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/20 | 4717/5334 | 4549/5079 | 1517/1692 | chr3 | 44323169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242351 | C | T | 3 | a0002c0024 a0002c0025 a0002c0026 |
3 | HG02976.hp1 HG03130.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.298C>T | p.Leu100Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 466/5334 | 298/5079 | 100/1692 | chr3 | 44242351 | |||
| chr3:44243118 | G | A | 1 | a0002c0005 | 7 | HG00099.hp1 HG00733.hp1 HG01109.hp1 others(4): Show |
synonymous_variant | LOW | c.612G>A | p.Lys204Lys | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 780/5334 | 612/5079 | 204/1692 | chr3 | 44243118 | |||
| chr3:44243793 | G | A | 1 | a0002c0024 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1287G>A | p.Glu429Glu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1455/5334 | 1287/5079 | 429/1692 | chr3 | 44243793 | |||
| chr3:44243955 | G | A | 1 | a0001c0015 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1449G>A | p.Gln483Gln | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 1617/5334 | 1449/5079 | 483/1692 | chr3 | 44243955 | |||
| chr3:44244417 | G | A | 1 | a0012c0028 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1911G>A | p.Thr637Thr | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2079/5334 | 1911/5079 | 637/1692 | chr3 | 44244417 | |||
| chr3:44244441 | C | A | 1 | a0003c0004 | 10 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(7): Show |
synonymous_variant | LOW | c.1935C>A | p.Ser645Ser | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/20 | 2103/5334 | 1935/5079 | 645/1692 | chr3 | 44244441 | |||
| chr3:44267027 | C | T | 2 | a0002c0024 a0002c0026 |
2 | HG02976.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.3051C>T | p.Val1017Val | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/20 | 3219/5334 | 3051/5079 | 1017/1692 | chr3 | 44267027 | |||
| chr3:44270769 | C | T | 1 | a0015c0019 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.3331C>T | p.Leu1111Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/20 | 3499/5334 | 3331/5079 | 1111/1692 | chr3 | 44270769 | |||
| chr3:44290782 | C | T | 1 | a0001c0017 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.3693C>T | p.Ala1231Ala | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/20 | 3861/5334 | 3693/5079 | 1231/1692 | chr3 | 44290782 | |||
| chr3:44321172 | A | C | 1 | a0001c0016 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.4452A>C | p.Pro1484Pro | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/20 | 4620/5334 | 4452/5079 | 1484/1692 | chr3 | 44321172 | |||
| chr3:44328279 | T | C | 1 | a0002c0006 | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
synonymous_variant | LOW | c.4705T>C | p.Leu1569Leu | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/20 | 4873/5334 | 4705/5079 | 1569/1692 | chr3 | 44328279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242033 | A | G | 22 | a0001c0001t0001 a0001c0015t0001 a0001c0016t0001 others(19): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
5_prime_UTR_variant | MODIFIER | c.-21A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/20 | 21 | chr3 | 44242033 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44242422 | T | C | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.346+23T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/19 | chr3 | 44242422 | |||||||
| chr3:44242456 | C | T | 5 | a0002c0006t0001g0244 a0002c0006t0001g0245 a0002c0006t0001g0246 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.346+57C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/19 | chr3 | 44242456 | |||||||
| chr3:44242822 | C | A | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.347-31C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 1/19 | chr3 | 44242822 | |||||||
| chr3:44245286 | G | A | 1 | a0018c0013t0001g0011 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2765+15G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245286 | |||||||
| chr3:44245307 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2765+36G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245307 | |||||||
| chr3:44245530 | C | CT | 9 | a0002c0025t0001g0243 a0003c0003t0002g0237 a0003c0003t0002g0238 others(6): Show |
9 | HG00558.hp2 HG00642.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2765+285dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | ||||||
| chr3:44245530 | CT | C | 21 | a0002c0002t0001g0163 a0002c0002t0001g0164 a0002c0002t0001g0165 others(18): Show |
21 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.2765+285delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | ||||||
| chr3:44245530 | CTT | C | 55 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(52): Show |
58 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2765+284_2765+285d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | ||||||
| chr3:44245530 | CTTTTT | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(9): Show |
13 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2765+281_2765+285d others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | ||||||
| chr3:44245530 | CTTTTTT | C | 86 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(83): Show |
87 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2765+280_2765+285d others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | ||||||
| chr3:44245530 | CTTTTTTT | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(5): Show |
9 | HG01074.hp1 HG01099.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.2765+279_2765+285d others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44245530 | ||||||
| chr3:44245630 | A | G | 1 | a0002c0002t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2765+359A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245630 | |||||||
| chr3:44245632 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2765+361G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245632 | |||||||
| chr3:44245737 | C | T | 2 | a0002c0002t0001g0002 a0002c0002t0001g0161 |
4 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2765+466C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245737 | |||||||
| chr3:44245786 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18975.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2765+515G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245786 | |||||||
| chr3:44245818 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2765+547C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245818 | |||||||
| chr3:44245897 | A | G | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+626A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245897 | |||||||
| chr3:44245974 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2765+703A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44245974 | |||||||
| chr3:44246037 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+766C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246037 | |||||||
| chr3:44246039 | C | A | 6 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2765+768C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246039 | |||||||
| chr3:44246047 | A | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+776A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246047 | |||||||
| chr3:44246165 | G | T | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2765+894G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246165 | |||||||
| chr3:44246227 | C | T | 3 | a0002c0002t0001g0158 a0002c0002t0001g0159 a0002c0002t0001g0160 |
3 | HG00423.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2765+956C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246227 | |||||||
| chr3:44246268 | A | AT | 75 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2765+999dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44246268 | ||||||
| chr3:44246319 | G | A | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2765+1048G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246319 | |||||||
| chr3:44246353 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2765+1082T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246353 | |||||||
| chr3:44246578 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+1307C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246578 | |||||||
| chr3:44246655 | A | G | 2 | a0002c0024t0001g0113 a0002c0026t0001g0230 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2765+1384A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246655 | |||||||
| chr3:44246664 | G | A | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+1393G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246664 | |||||||
| chr3:44246773 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2765+1502C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44246773 | |||||||
| chr3:44247111 | A | C | 75 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.2765+1840A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247111 | |||||||
| chr3:44247398 | T | G | 2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2765+2127T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247398 | |||||||
| chr3:44247523 | T | C | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2765+2252T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247523 | |||||||
| chr3:44247719 | G | A | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2765+2448G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247719 | |||||||
| chr3:44247881 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2765+2610T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247881 | |||||||
| chr3:44247941 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2765+2670G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247941 | |||||||
| chr3:44247974 | C | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2765+2703C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44247974 | |||||||
| chr3:44248099 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2765+2828A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248099 | |||||||
| chr3:44248289 | A | G | 1 | a0003c0004t0002g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2765+3018A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248289 | |||||||
| chr3:44248324 | A | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2765+3053A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248324 | |||||||
| chr3:44248337 | G | A | 6 | a0002c0002t0001g0139 a0002c0002t0001g0140 a0002c0002t0001g0141 others(3): Show |
6 | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2765+3066G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248337 | |||||||
| chr3:44248906 | A | G | 7 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0132 others(4): Show |
7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+3635A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248906 | |||||||
| chr3:44248907 | G | A | 2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2765+3636G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248907 | |||||||
| chr3:44248914 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 |
3 | HG01123.hp1 HG01358.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.2765+3643T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44248914 | |||||||
| chr3:44249093 | T | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2765+3822T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249093 | |||||||
| chr3:44249268 | T | C | 1 | a0002c0002t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2765+3997T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249268 | |||||||
| chr3:44249419 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2765+4148C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249419 | |||||||
| chr3:44249700 | A | C | 3 | a0005c0008t0002g0184 a0005c0008t0002g0185 a0005c0008t0002g0186 |
3 | HG02622.hp2 HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2765+4429A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249700 | |||||||
| chr3:44249974 | A | G | 7 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0132 others(4): Show |
7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2765+4703A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249974 | |||||||
| chr3:44249994 | C | T | 5 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG01074.hp2 HG01243.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2765+4723C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44249994 | |||||||
| chr3:44250008 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2765+4737T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250008 | |||||||
| chr3:44250243 | C | CA | 65 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0025 others(62): Show |
65 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.2766-4707dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | ||||||
| chr3:44250243 | C | CAA | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(39): Show |
45 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.2766-4708_2766-470 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | ||||||
| chr3:44250243 | C | CAAA | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2766-4709_2766-470 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | ||||||
| chr3:44250243 | CA | C | 33 | a0003c0003t0002g0007 a0003c0003t0002g0162 a0003c0003t0002g0187 others(30): Show |
34 | HG00408.hp2 HG00609.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.2766-4707delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44250243 | ||||||
| chr3:44250354 | A | G | 1 | a0002c0002t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2766-4614A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250354 | |||||||
| chr3:44250358 | C | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2766-4610C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250358 | |||||||
| chr3:44250359 | G | A | 6 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2766-4609G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250359 | |||||||
| chr3:44250568 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2766-4400T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250568 | |||||||
| chr3:44250907 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(94): Show |
99 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.2766-4061A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44250907 | |||||||
| chr3:44251109 | T | A | 1 | a0003c0003t0002g0202 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2766-3859T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251109 | |||||||
| chr3:44251114 | TTC | T | 7 | a0002c0002t0001g0139 a0002c0002t0001g0140 a0002c0002t0001g0141 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2766-3848_2766-384 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44251114 | ||||||
| chr3:44251146 | G | T | 1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2766-3822G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251146 | |||||||
| chr3:44251189 | T | C | 2 | a0003c0003t0002g0190 a0003c0003t0002g0191 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2766-3779T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251189 | |||||||
| chr3:44251223 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2766-3745C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251223 | |||||||
| chr3:44251310 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2766-3658C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251310 | |||||||
| chr3:44251456 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2766-3512G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251456 | |||||||
| chr3:44251463 | A | G | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2766-3505A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251463 | |||||||
| chr3:44251512 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2766-3456C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251512 | |||||||
| chr3:44251580 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2766-3388G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251580 | |||||||
| chr3:44251761 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2766-3207A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251761 | |||||||
| chr3:44251762 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2766-3206C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251762 | |||||||
| chr3:44251783 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-3185T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251783 | |||||||
| chr3:44251834 | T | C | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2766-3134T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251834 | |||||||
| chr3:44251845 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2766-3123C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251845 | |||||||
| chr3:44251846 | G | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2766-3122G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44251846 | |||||||
| chr3:44252021 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(43): Show |
47 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.2766-2947A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252021 | |||||||
| chr3:44252055 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2766-2913A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252055 | |||||||
| chr3:44252188 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2766-2780G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252188 | |||||||
| chr3:44252267 | C | T | 2 | a0002c0002t0001g0002 a0002c0002t0001g0161 |
4 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2766-2701C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252267 | |||||||
| chr3:44252306 | A | G | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2766-2662A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252306 | |||||||
| chr3:44252308 | G | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2766-2660G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252308 | |||||||
| chr3:44252347 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-2621C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252347 | |||||||
| chr3:44252453 | G | T | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2766-2515G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252453 | |||||||
| chr3:44252562 | G | C | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2766-2406G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252562 | |||||||
| chr3:44252589 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2766-2379G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252589 | |||||||
| chr3:44252826 | AG | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-2141delG | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44252826 | |||||||
| chr3:44253056 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2766-1912C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253056 | |||||||
| chr3:44253094 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2766-1874T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253094 | |||||||
| chr3:44253152 | T | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-1816T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253152 | |||||||
| chr3:44253183 | C | T | 35 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(32): Show |
38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.2766-1785C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253183 | |||||||
| chr3:44253190 | T | TAATATGC others(6): Show |
1 | a0002c0002t0001g0143 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2766-1775_2766-176 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44253190 | ||||||
| chr3:44253356 | G | A | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2766-1612G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253356 | |||||||
| chr3:44253395 | A | G | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2766-1573A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253395 | |||||||
| chr3:44253468 | G | C | 1 | a0002c0002t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2766-1500G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253468 | |||||||
| chr3:44253544 | T | C | 1 | a0002c0002t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2766-1424T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253544 | |||||||
| chr3:44253626 | A | G | 1 | a0003c0003t0002g0228 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2766-1342A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253626 | |||||||
| chr3:44253682 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-1286G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253682 | |||||||
| chr3:44253692 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2766-1276T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253692 | |||||||
| chr3:44253724 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0089 |
2 | HG02129.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2766-1244A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253724 | |||||||
| chr3:44253968 | T | A | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2766-1000T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44253968 | |||||||
| chr3:44254015 | T | A | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2766-953T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254015 | |||||||
| chr3:44254221 | A | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2766-747A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254221 | |||||||
| chr3:44254378 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-590G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254378 | |||||||
| chr3:44254380 | C | A | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2766-588C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254380 | |||||||
| chr3:44254386 | G | A | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2766-582G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254386 | |||||||
| chr3:44254456 | C | T | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2766-512C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254456 | |||||||
| chr3:44254467 | A | C | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2766-501A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254467 | |||||||
| chr3:44254623 | G | A | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2766-345G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254623 | |||||||
| chr3:44254627 | CAA | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.2766-321_2766-320d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr3 | 44254627 | ||||||
| chr3:44254648 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2766-320A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254648 | |||||||
| chr3:44254879 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG01891.hp1 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2766-89G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254879 | |||||||
| chr3:44254911 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2766-57T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 2/19 | chr3 | 44254911 | |||||||
| chr3:44255226 | A | G | 6 | a0003c0003t0002g0189 a0003c0003t0002g0190 a0003c0003t0002g0191 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2827+197A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255226 | |||||||
| chr3:44255238 | A | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2827+209A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255238 | |||||||
| chr3:44255304 | AAAATG | A | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2827+280_2827+284d others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255304 | ||||||
| chr3:44255374 | TA | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2827+346delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255374 | |||||||
| chr3:44255543 | T | A | 2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2827+514T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255543 | |||||||
| chr3:44255583 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2827+554C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255583 | |||||||
| chr3:44255623 | G | A | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2828-528G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255623 | |||||||
| chr3:44255651 | C | CA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(4): Show |
7 | HG01515.hp2 HG01517.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2828-488dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255651 | ||||||
| chr3:44255651 | C | CAA | 17 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0033 others(14): Show |
17 | HG00639.hp2 HG00673.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.2828-489_2828-488d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255651 | ||||||
| chr3:44255662 | A | T | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2828-489A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255662 | |||||||
| chr3:44255663 | AT | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0062 others(5): Show |
10 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2828-487delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255663 | |||||||
| chr3:44255664 | T | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(145): Show |
149 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.2828-487T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255664 | |||||||
| chr3:44255666 | T | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(91): Show |
96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2828-485T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255666 | |||||||
| chr3:44255668 | T | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(86): Show |
90 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2828-483T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255668 | |||||||
| chr3:44255670 | T | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(67): Show |
71 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.2828-481T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255670 | |||||||
| chr3:44255670 | T | C | 3 | a0003c0003t0002g0189 a0003c0003t0002g0200 a0003c0003t0002g0237 |
3 | HG02818.hp1 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2828-481T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255670 | |||||||
| chr3:44255670 | T | TAC | 7 | a0003c0003t0002g0192 a0003c0003t0002g0203 a0003c0003t0002g0204 others(4): Show |
7 | HG00642.hp1 HG01952.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2828-431_2828-430d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255670 | T | TACACACA others(3): Show |
1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2828-439_2828-430d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255670 | TAC | T | 7 | a0003c0003t0002g0199 a0003c0003t0002g0218 a0003c0003t0002g0219 others(4): Show |
7 | HG01175.hp1 HG02647.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.2828-431_2828-430d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255670 | TACAC | T | 9 | a0003c0003t0002g0007 a0003c0003t0002g0195 a0003c0003t0002g0224 others(6): Show |
10 | HG00673.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2828-433_2828-430d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255670 | TACACAC | T | 4 | a0003c0004t0002g0001 a0003c0004t0002g0188 a0003c0004t0002g0197 others(1): Show |
7 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.2828-435_2828-430d others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255670 | TACACACA others(3): Show |
T | 1 | a0002c0002t0001g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2828-439_2828-430d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255670 | TACACACA others(7): Show |
T | 1 | a0012c0028t0002g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2828-443_2828-430d others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255670 | TACACACA others(9): Show |
T | 1 | a0003c0003t0002g0227 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2828-445_2828-430d others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255670 | ||||||
| chr3:44255672 | C | A | 2 | a0001c0001t0001g0004 a0001c0016t0001g0088 |
3 | HG01074.hp1 HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2828-479C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255672 | |||||||
| chr3:44255672 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(174): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2828-479C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255672 | |||||||
| chr3:44255674 | C | A | 1 | a0001c0016t0001g0088 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2828-477C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255674 | |||||||
| chr3:44255674 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
105 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2828-477C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255674 | |||||||
| chr3:44255676 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2828-475C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255676 | |||||||
| chr3:44255678 | C | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0018 others(66): Show |
70 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.2828-473C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255678 | |||||||
| chr3:44255680 | C | T | 4 | a0001c0016t0001g0088 a0009c0009t0001g0084 a0009c0009t0001g0085 others(1): Show |
4 | HG03654.hp2 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2828-471C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255680 | |||||||
| chr3:44255682 | C | T | 2 | a0001c0016t0001g0088 a0002c0002t0001g0156 |
2 | HG03471.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2828-469C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255682 | |||||||
| chr3:44255696 | CACACACA others(19): Show |
C | 1 | a0002c0006t0001g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2828-453_2828-428d others(28): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255696 | ||||||
| chr3:44255708 | CACACACA others(7): Show |
C | 8 | a0002c0002t0001g0140 a0002c0002t0001g0142 a0002c0002t0001g0166 others(5): Show |
8 | HG01884.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2828-441_2828-428d others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255708 | ||||||
| chr3:44255708 | CACACACA others(9): Show |
C | 1 | a0002c0002t0001g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2828-441_2828-426d others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255708 | ||||||
| chr3:44255710 | CACACACA others(5): Show |
C | 2 | a0002c0002t0001g0002 a0002c0002t0001g0143 |
3 | HG02895.hp1 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2828-439_2828-428d others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255710 | ||||||
| chr3:44255712 | CACACACA others(3): Show |
C | 38 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(35): Show |
39 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.2828-437_2828-428d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255712 | ||||||
| chr3:44255714 | CACACACA others(1): Show |
C | 27 | a0002c0002t0001g0122 a0002c0002t0001g0131 a0002c0002t0001g0134 others(24): Show |
27 | HG00639.hp1 HG00741.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.2828-435_2828-428d others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255714 | ||||||
| chr3:44255716 | CACACAT | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG01123.hp1 HG01358.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.2828-433_2828-428d others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255716 | ||||||
| chr3:44255718 | CACAT | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0075 others(9): Show |
12 | HG00609.hp1 HG02559.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2828-431_2828-428d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255718 | ||||||
| chr3:44255720 | CAT | C | 19 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0069 others(16): Show |
20 | HG00642.hp2 HG00741.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2828-422_2828-421d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 44255720 | ||||||
| chr3:44255722 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(77): Show |
82 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.2828-429T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255722 | |||||||
| chr3:44255724 | T | C | 2 | a0001c0001t0001g0044 a0018c0013t0001g0011 |
2 | HG03654.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2828-427T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255724 | |||||||
| chr3:44255881 | T | C | 1 | a0002c0002t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2828-270T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 3/19 | chr3 | 44255881 | |||||||
| chr3:44256350 | A | C | 1 | a0002c0002t0001g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2955+72A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256350 | |||||||
| chr3:44256456 | A | G | 31 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(28): Show |
31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.2955+178A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256456 | |||||||
| chr3:44256539 | A | C | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+261A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256539 | |||||||
| chr3:44256598 | G | C | 1 | a0002c0002t0001g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2955+320G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256598 | |||||||
| chr3:44256658 | T | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2955+380T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256658 | |||||||
| chr3:44256885 | G | T | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2955+607G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256885 | |||||||
| chr3:44256937 | T | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0039 others(13): Show |
16 | HG00738.hp1 HG01074.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2955+659T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256937 | |||||||
| chr3:44256983 | G | A | 2 | a0002c0002t0001g0121 a0002c0002t0001g0122 |
2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2955+705G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44256983 | |||||||
| chr3:44257086 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA18961.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.2955+808T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257086 | |||||||
| chr3:44257174 | A | T | 2 | a0002c0026t0001g0230 a0007c0011t0001g0005 |
3 | HG01167.hp2 HG01169.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2955+896A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257174 | |||||||
| chr3:44257351 | GGGTGTGT others(6): Show |
G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0006c0010t0001g0053 |
3 | HG00642.hp2 HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2955+1075_2955+108 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257351 | ||||||
| chr3:44257351 | GGGTGTGT others(10): Show |
G | 1 | a0002c0002t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2955+1075_2955+109 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257351 | ||||||
| chr3:44257352 | G | GGGGTGTG others(3): Show |
1 | a0003c0004t0002g0001 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2955+1075_2955+107 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGGGTGTG others(5): Show |
2 | a0002c0002t0001g0114 a0003c0003t0002g0220 |
2 | HG01175.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2955+1075_2955+107 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGT | 7 | a0002c0002t0001g0132 a0003c0003t0002g0007 a0003c0003t0002g0187 others(4): Show |
7 | HG00642.hp1 HG01346.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+1129_2955+113 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGT | 10 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0165 others(7): Show |
10 | HG00609.hp2 HG01192.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2955+1127_2955+113 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGTGT | 12 | a0002c0002t0001g0133 a0002c0002t0001g0135 a0002c0002t0001g0136 others(9): Show |
12 | HG00639.hp1 HG00741.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.2955+1125_2955+113 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGTGTG others(1): Show |
10 | a0002c0002t0001g0117 a0002c0002t0001g0134 a0002c0002t0001g0164 others(7): Show |
11 | HG02109.hp2 HG02132.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2955+1123_2955+113 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGTGTG others(3): Show |
5 | a0002c0002t0001g0124 a0003c0003t0002g0208 a0003c0003t0002g0210 others(2): Show |
5 | HG00408.hp2 HG00738.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1121_2955+113 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGTGTG others(5): Show |
1 | a0003c0003t0002g0202 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2955+1119_2955+113 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGTGTG others(9): Show |
1 | a0003c0004t0002g0188 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2955+1115_2955+113 others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGTGTG others(11): Show |
1 | a0003c0004t0002g0239 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2955+1113_2955+113 others(22): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GGTGTGTG others(13): Show |
2 | a0002c0006t0001g0248 a0003c0004t0002g0001 |
2 | HG02895.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2955+1111_2955+113 others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | G | GTGTGTGT others(12): Show |
1 | a0002c0006t0001g0246 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2955+1074_2955+107 others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257352 | |||||||
| chr3:44257352 | G | T | 1 | a0002c0006t0001g0009 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2955+1074G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257352 | |||||||
| chr3:44257352 | GGT | G | 4 | a0003c0003t0002g0007 a0003c0003t0002g0190 a0003c0003t0002g0201 others(1): Show |
4 | HG02647.hp1 HG03453.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1129_2955+113 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGT | G | 4 | a0003c0003t0002g0191 a0003c0003t0002g0212 a0003c0003t0002g0237 others(1): Show |
4 | HG02698.hp2 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1127_2955+113 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGTGT | G | 5 | a0002c0002t0001g0168 a0003c0003t0002g0189 a0003c0003t0002g0226 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1125_2955+113 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGTGTG others(3): Show |
G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0093 a0004c0007t0001g0170 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+1121_2955+113 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGTGTG others(5): Show |
G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(39): Show |
44 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.2955+1119_2955+113 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGTGTG others(7): Show |
G | 53 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.2955+1117_2955+113 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGTGTG others(9): Show |
G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
10 | HG01099.hp1 HG01123.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.2955+1115_2955+113 others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGTGTG others(11): Show |
G | 14 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0123 others(11): Show |
15 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.2955+1113_2955+113 others(22): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257352 | GGTGTGTG others(15): Show |
G | 1 | a0003c0003t0002g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2955+1109_2955+113 others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257352 | ||||||
| chr3:44257353 | GTGTGTGT others(4): Show |
G | 1 | a0001c0016t0001g0088 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2955+1076_2955+108 others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257353 | |||||||
| chr3:44257353 | GTGTGTGT others(6): Show |
G | 2 | a0009c0009t0001g0084 a0018c0013t0001g0011 |
2 | HG03654.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2955+1076_2955+108 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257353 | |||||||
| chr3:44257354 | T | G | 1 | a0002c0002t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2955+1076T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257354 | |||||||
| chr3:44257358 | T | G | 1 | a0016c0020t0002g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2955+1080T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257358 | |||||||
| chr3:44257360 | T | G | 2 | a0005c0008t0002g0183 a0016c0020t0002g0235 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2955+1082T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257360 | |||||||
| chr3:44257364 | T | G | 2 | a0008c0012t0001g0023 a0015c0019t0002g0236 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2955+1086T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257364 | |||||||
| chr3:44257365 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0026 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2955+1088_2955+110 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257365 | |||||||
| chr3:44257368 | T | G | 9 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0070 others(6): Show |
9 | HG00140.hp1 HG01167.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+1090T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257368 | |||||||
| chr3:44257370 | T | G | 1 | a0002c0002t0001g0002 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2955+1092T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257370 | |||||||
| chr3:44257381 | G | GTGTGTGT others(5): Show |
1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2955+1114_2955+111 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257381 | ||||||
| chr3:44257396 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2955+1118T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257396 | |||||||
| chr3:44257397 | GTGTGTGT others(12): Show |
G | 2 | a0002c0002t0001g0145 a0002c0002t0001g0174 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2955+1121_2955+113 others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257397 | ||||||
| chr3:44257399 | GTGTGTGT others(10): Show |
G | 1 | a0002c0002t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2955+1123_2955+113 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257399 | ||||||
| chr3:44257401 | GTGTGTGT others(8): Show |
G | 6 | a0002c0002t0001g0177 a0002c0002t0001g0178 a0002c0002t0001g0179 others(3): Show |
6 | HG01192.hp2 HG01884.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2955+1125_2955+113 others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257401 | ||||||
| chr3:44257405 | GTGTCTAT others(4): Show |
G | 2 | a0002c0002t0001g0175 a0002c0002t0001g0233 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2955+1129_2955+113 others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257405 | ||||||
| chr3:44257407 | GTCTAT | G | 4 | a0002c0002t0001g0138 a0002c0002t0001g0144 a0002c0002t0001g0151 others(1): Show |
4 | HG01123.hp2 HG01515.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1131_2955+113 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257407 | ||||||
| chr3:44257407 | GTCTATTT | G | 3 | a0002c0002t0001g0141 a0002c0002t0001g0142 a0002c0002t0001g0154 |
3 | HG02886.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2955+1131_2955+113 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257407 | ||||||
| chr3:44257409 | C | G | 8 | a0002c0002t0001g0140 a0002c0002t0001g0149 a0002c0002t0001g0150 others(5): Show |
8 | HG01261.hp1 HG01346.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2955+1131C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257409 | |||||||
| chr3:44257409 | CTATTTTA others(2): Show |
C | 4 | a0002c0002t0001g0139 a0002c0002t0001g0146 a0002c0002t0001g0147 others(1): Show |
4 | HG01361.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1144_2955+115 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257409 | ||||||
| chr3:44257411 | A | G | 7 | a0002c0002t0001g0140 a0002c0002t0001g0149 a0002c0002t0001g0150 others(4): Show |
7 | HG01261.hp1 HG01346.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2955+1133A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257411 | |||||||
| chr3:44257412 | T | G | 2 | a0002c0002t0001g0143 a0002c0002t0001g0176 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2955+1134T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257412 | |||||||
| chr3:44257412 | T | TG | 4 | a0002c0002t0001g0140 a0002c0002t0001g0150 a0002c0002t0001g0153 others(1): Show |
4 | HG01346.hp1 HG02630.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1134_2955+113 others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257412 | |||||||
| chr3:44257414 | T | G | 13 | a0002c0002t0001g0138 a0002c0002t0001g0140 a0002c0002t0001g0143 others(10): Show |
13 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2955+1136T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257414 | |||||||
| chr3:44257416 | A | G | 16 | a0002c0002t0001g0138 a0002c0002t0001g0140 a0002c0002t0001g0141 others(13): Show |
16 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.2955+1138A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257416 | |||||||
| chr3:44257418 | A | C | 27 | a0002c0002t0001g0138 a0002c0002t0001g0140 a0002c0002t0001g0141 others(24): Show |
27 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.2955+1140A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257418 | |||||||
| chr3:44257467 | ATAGT | A | 3 | a0002c0002t0001g0121 a0002c0002t0001g0122 a0002c0002t0001g0135 |
3 | HG00639.hp1 HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | |||||||
| chr3:44257467 | ATAGTGT | A | 22 | a0002c0002t0001g0002 a0002c0002t0001g0118 a0002c0002t0001g0119 others(19): Show |
25 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | |||||||
| chr3:44257467 | ATAGTGTG others(1): Show |
A | 14 | a0002c0002t0001g0114 a0002c0002t0001g0115 a0002c0002t0001g0116 others(11): Show |
14 | HG00741.hp1 HG01192.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | |||||||
| chr3:44257467 | ATAGTGTG others(3): Show |
A | 27 | a0002c0002t0001g0138 a0002c0002t0001g0140 a0002c0002t0001g0141 others(24): Show |
27 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.2955+1190_2955+119 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | |||||||
| chr3:44257467 | ATAGTGTG others(5): Show |
A | 3 | a0002c0002t0001g0139 a0002c0006t0001g0009 a0002c0006t0001g0010 |
3 | HG02451.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2955+1190_2955+120 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | |||||||
| chr3:44257467 | ATAGTGTG others(7): Show |
A | 2 | a0002c0002t0001g0148 a0002c0002t0001g0157 |
2 | HG02559.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2955+1190_2955+120 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | |||||||
| chr3:44257467 | ATAGTGTG others(19): Show |
A | 1 | a0001c0001t0001g0025 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2955+1190_2955+121 others(30): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257467 | |||||||
| chr3:44257468 | T | G | 4 | a0004c0007t0001g0171 a0004c0007t0001g0172 a0004c0007t0001g0173 others(1): Show |
4 | HG02257.hp2 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1190T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257468 | |||||||
| chr3:44257469 | A | T | 4 | a0004c0007t0001g0171 a0004c0007t0001g0172 a0004c0007t0001g0173 others(1): Show |
4 | HG02257.hp2 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1191A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257469 | |||||||
| chr3:44257469 | AGT | A | 15 | a0003c0003t0002g0162 a0003c0003t0002g0187 a0003c0003t0002g0195 others(12): Show |
15 | HG00408.hp1 HG01358.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.2955+1231_2955+123 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257469 | AGTGT | A | 7 | a0003c0003t0002g0194 a0003c0003t0002g0200 a0003c0003t0002g0201 others(4): Show |
7 | HG00609.hp2 HG00738.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2955+1229_2955+123 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257469 | AGTGTGT | A | 7 | a0003c0003t0002g0189 a0003c0003t0002g0190 a0003c0003t0002g0191 others(4): Show |
7 | HG02132.hp1 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+1227_2955+123 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257469 | AGTGTGTG others(1): Show |
A | 3 | a0002c0024t0001g0113 a0005c0008t0002g0186 a0016c0020t0002g0235 |
3 | HG02976.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2955+1225_2955+123 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257469 | AGTGTGTG others(3): Show |
A | 5 | a0002c0006t0001g0246 a0002c0006t0001g0247 a0002c0006t0001g0248 others(2): Show |
5 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1223_2955+123 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257469 | AGTGTGTG others(5): Show |
A | 4 | a0002c0006t0001g0244 a0002c0006t0001g0245 a0002c0026t0001g0230 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+1221_2955+123 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257469 | AGTGTGTG others(7): Show |
A | 2 | a0005c0008t0002g0184 a0005c0008t0002g0185 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2955+1219_2955+123 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257469 | AGTGTGTG others(17): Show |
A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
105 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.2955+1209_2955+123 others(28): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44257469 | ||||||
| chr3:44257514 | G | A | 2 | a0003c0003t0002g0195 a0003c0003t0002g0238 |
2 | NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2955+1236G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257514 | |||||||
| chr3:44257713 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2955+1435C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257713 | |||||||
| chr3:44257813 | G | T | 1 | a0002c0006t0001g0009 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2955+1535G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257813 | |||||||
| chr3:44257847 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2955+1569T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44257847 | |||||||
| chr3:44258054 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2955+1776A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258054 | |||||||
| chr3:44258114 | T | C | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.2955+1836T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258114 | |||||||
| chr3:44258152 | A | G | 1 | a0003c0003t0002g0222 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2955+1874A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258152 | |||||||
| chr3:44258274 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2955+1996G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258274 | |||||||
| chr3:44258396 | G | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2955+2118G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258396 | |||||||
| chr3:44258464 | C | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2955+2186C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258464 | |||||||
| chr3:44258476 | A | G | 4 | a0002c0002t0001g0117 a0002c0002t0001g0124 a0002c0002t0001g0164 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+2198A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258476 | |||||||
| chr3:44258600 | A | G | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+2322A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258600 | |||||||
| chr3:44258744 | G | A | 1 | a0002c0002t0001g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2955+2466G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258744 | |||||||
| chr3:44258862 | C | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2955+2584C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44258862 | |||||||
| chr3:44259133 | C | A | 6 | a0003c0004t0002g0001 a0003c0004t0002g0188 a0003c0004t0002g0196 others(3): Show |
9 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+2855C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259133 | |||||||
| chr3:44259250 | G | GTTCTGCC others(2261): Show |
1 | a0011c0018t0001g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2955+2987_2955+298 others(2272): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr3 | 44259250 | ||||||
| chr3:44259312 | G | A | 2 | a0002c0002t0001g0149 a0002c0002t0001g0156 |
2 | HG02300.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2955+3034G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259312 | |||||||
| chr3:44259344 | C | T | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2955+3066C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259344 | |||||||
| chr3:44259416 | C | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2956-3003C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259416 | |||||||
| chr3:44259590 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG00639.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2956-2829T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259590 | |||||||
| chr3:44259765 | C | A | 1 | a0002c0002t0001g0123 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2956-2654C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259765 | |||||||
| chr3:44259899 | C | G | 1 | a0003c0003t0002g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2956-2520C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44259899 | |||||||
| chr3:44260116 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0037 others(2): Show |
5 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.2956-2303C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260116 | |||||||
| chr3:44260165 | G | A | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2956-2254G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260165 | |||||||
| chr3:44260233 | G | A | 31 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(28): Show |
31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.2956-2186G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260233 | |||||||
| chr3:44260257 | A | G | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2956-2162A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260257 | |||||||
| chr3:44260433 | T | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2956-1986T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260433 | |||||||
| chr3:44260603 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2956-1816G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260603 | |||||||
| chr3:44260708 | G | A | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2956-1711G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260708 | |||||||
| chr3:44260980 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2956-1439T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44260980 | |||||||
| chr3:44261053 | A | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(92): Show |
96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2956-1366A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261053 | |||||||
| chr3:44261185 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2956-1234C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261185 | |||||||
| chr3:44261196 | A | G | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2956-1223A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261196 | |||||||
| chr3:44261550 | T | A | 4 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2956-869T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261550 | |||||||
| chr3:44261551 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2956-868T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261551 | |||||||
| chr3:44261632 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2956-787A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261632 | |||||||
| chr3:44261641 | C | G | 1 | a0002c0002t0001g0160 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2956-778C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261641 | |||||||
| chr3:44261693 | A | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0025 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.2956-726A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261693 | |||||||
| chr3:44261795 | T | C | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.2956-624T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261795 | |||||||
| chr3:44261816 | C | T | 1 | a0002c0002t0001g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2956-603C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44261816 | |||||||
| chr3:44262177 | G | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2956-242G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 4/19 | chr3 | 44262177 | |||||||
| chr3:44262760 | A | G | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3020+277A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44262760 | |||||||
| chr3:44263763 | C | A | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3020+1280C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44263763 | |||||||
| chr3:44263991 | G | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3020+1508G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44263991 | |||||||
| chr3:44264103 | C | T | 1 | a0002c0002t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3020+1620C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264103 | |||||||
| chr3:44264135 | A | G | 4 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3020+1652A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264135 | |||||||
| chr3:44264191 | A | G | 4 | a0003c0003t0002g0187 a0003c0003t0002g0224 a0003c0003t0002g0225 others(1): Show |
4 | HG02280.hp1 NA18986.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.3020+1708A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264191 | |||||||
| chr3:44264339 | ATTTT | A | 75 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3020+1860_3020+186 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 44264339 | ||||||
| chr3:44264359 | G | A | 1 | a0003c0003t0002g0227 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3020+1876G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264359 | |||||||
| chr3:44264367 | G | T | 1 | a0003c0003t0002g0221 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3020+1884G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264367 | |||||||
| chr3:44264581 | A | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3020+2098A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264581 | |||||||
| chr3:44264620 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
12 | HG00558.hp1 HG00673.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.3020+2137A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264620 | |||||||
| chr3:44264627 | A | G | 7 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0132 others(4): Show |
7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.3020+2144A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264627 | |||||||
| chr3:44264707 | T | G | 1 | a0003c0003t0002g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3020+2224T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264707 | |||||||
| chr3:44264739 | T | C | 1 | a0003c0003t0002g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3020+2256T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264739 | |||||||
| chr3:44264815 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3021-2182A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264815 | |||||||
| chr3:44264956 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3021-2041C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44264956 | |||||||
| chr3:44265109 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.3021-1888C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265109 | |||||||
| chr3:44265136 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3021-1861A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265136 | |||||||
| chr3:44265249 | G | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3021-1748G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265249 | |||||||
| chr3:44265328 | A | C | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3021-1669A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265328 | |||||||
| chr3:44265426 | G | A | 1 | a0003c0004t0002g0197 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3021-1571G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265426 | |||||||
| chr3:44265824 | A | G | 2 | a0003c0003t0002g0207 a0003c0003t0002g0217 |
2 | HG00738.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.3021-1173A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265824 | |||||||
| chr3:44265871 | C | T | 1 | a0016c0020t0002g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3021-1126C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44265871 | |||||||
| chr3:44266043 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3021-954G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266043 | |||||||
| chr3:44266065 | G | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3021-932G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266065 | |||||||
| chr3:44266396 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3021-601A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266396 | |||||||
| chr3:44266755 | T | G | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3021-242T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266755 | |||||||
| chr3:44266903 | T | A | 7 | a0003c0003t0002g0192 a0003c0003t0002g0204 a0003c0003t0002g0205 others(4): Show |
7 | HG00408.hp2 HG01358.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3021-94T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 5/19 | chr3 | 44266903 | |||||||
| chr3:44267289 | C | CT | 9 | a0002c0002t0001g0136 a0002c0002t0001g0137 a0002c0005t0001g0128 others(6): Show |
9 | HG00741.hp1 HG01109.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.3160+175dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44267289 | ||||||
| chr3:44267289 | CT | C | 56 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0043 others(53): Show |
56 | HG00642.hp2 HG00741.hp2 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.3160+175delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44267289 | ||||||
| chr3:44267289 | CTT | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
95 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3160+174_3160+175d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44267289 | ||||||
| chr3:44267371 | G | C | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+235G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267371 | |||||||
| chr3:44267455 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+319C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267455 | |||||||
| chr3:44267516 | T | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+380T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267516 | |||||||
| chr3:44267553 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3160+417C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267553 | |||||||
| chr3:44267584 | C | T | 75 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3160+448C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267584 | |||||||
| chr3:44267685 | T | C | 6 | a0002c0005t0001g0006 a0002c0005t0001g0125 a0002c0005t0001g0126 others(3): Show |
7 | HG00099.hp1 HG00733.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3160+549T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267685 | |||||||
| chr3:44267776 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3160+640A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267776 | |||||||
| chr3:44267786 | A | G | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3160+650A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267786 | |||||||
| chr3:44267801 | A | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+665A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44267801 | |||||||
| chr3:44268128 | G | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3160+992G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268128 | |||||||
| chr3:44268165 | A | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3160+1029A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268165 | |||||||
| chr3:44268365 | TC | T | 30 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(27): Show |
33 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.3161-850delC | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268365 | |||||||
| chr3:44268366 | C | CT | 11 | a0002c0002t0001g0141 a0002c0002t0001g0143 a0002c0002t0001g0147 others(8): Show |
11 | HG00673.hp1 HG01361.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.3161-824dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | ||||||
| chr3:44268366 | C | CTTTTTTT others(4): Show |
1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3161-834_3161-824d others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | ||||||
| chr3:44268366 | C | T | 4 | a0002c0002t0001g0116 a0002c0002t0001g0123 a0002c0002t0001g0137 others(1): Show |
4 | HG01109.hp1 HG02148.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.3161-850C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268366 | |||||||
| chr3:44268366 | CT | C | 11 | a0001c0001t0001g0049 a0001c0001t0001g0073 a0001c0001t0001g0093 others(8): Show |
11 | HG01175.hp2 HG01928.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.3161-824delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | ||||||
| chr3:44268366 | CTT | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(91): Show |
96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.3161-825_3161-824d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr3 | 44268366 | ||||||
| chr3:44268413 | G | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3161-803G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268413 | |||||||
| chr3:44268434 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3161-782T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268434 | |||||||
| chr3:44268636 | G | A | 1 | a0002c0002t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3161-580G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268636 | |||||||
| chr3:44268640 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3161-576C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268640 | |||||||
| chr3:44268892 | G | C | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3161-324G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44268892 | |||||||
| chr3:44269100 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3161-116T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 6/19 | chr3 | 44269100 | |||||||
| chr3:44269395 | C | T | 1 | a0014c0022t0001g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3246+94C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269395 | |||||||
| chr3:44269458 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3246+157A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269458 | |||||||
| chr3:44269471 | C | CT | 6 | a0003c0003t0002g0194 a0003c0003t0002g0205 a0003c0003t0002g0210 others(3): Show |
6 | HG01358.hp1 HG01975.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.3246+201dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(3): Show |
18 | a0002c0002t0001g0120 a0002c0002t0001g0122 a0002c0002t0001g0129 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.3246+192_3246+201d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(4): Show |
16 | a0002c0002t0001g0002 a0002c0002t0001g0117 a0002c0002t0001g0118 others(13): Show |
19 | HG00423.hp2 HG00741.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.3246+191_3246+201d others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(5): Show |
6 | a0002c0002t0001g0116 a0002c0002t0001g0124 a0002c0002t0001g0157 others(3): Show |
6 | HG00733.hp1 HG01109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3246+190_3246+201d others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(6): Show |
1 | a0004c0007t0001g0170 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3246+189_3246+201d others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(7): Show |
5 | a0002c0002t0001g0114 a0003c0003t0002g0191 a0004c0007t0001g0171 others(2): Show |
5 | HG02257.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3246+188_3246+201d others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(8): Show |
6 | a0002c0002t0001g0133 a0002c0002t0001g0144 a0002c0002t0001g0154 others(3): Show |
6 | HG01952.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3246+187_3246+201d others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(9): Show |
9 | a0002c0002t0001g0115 a0002c0002t0001g0132 a0002c0002t0001g0134 others(6): Show |
9 | HG01346.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3246+186_3246+201d others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(10): Show |
6 | a0002c0002t0001g0153 a0002c0002t0001g0180 a0002c0002t0001g0182 others(3): Show |
6 | HG01192.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3246+185_3246+201d others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(11): Show |
3 | a0002c0002t0001g0174 a0002c0006t0001g0246 a0002c0006t0001g0247 |
3 | HG01243.hp2 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3246+184_3246+201d others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(12): Show |
3 | a0002c0002t0001g0149 a0002c0002t0001g0151 a0005c0008t0002g0186 |
3 | HG01123.hp2 HG02300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3246+183_3246+201d others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(14): Show |
1 | a0002c0002t0001g0156 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3246+181_3246+201d others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(15): Show |
1 | a0016c0020t0002g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3246+180_3246+201d others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(16): Show |
1 | a0010c0023t0001g0152 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3246+179_3246+201d others(25): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(17): Show |
1 | a0002c0002t0001g0155 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3246+178_3246+201d others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(22): Show |
2 | a0002c0002t0001g0147 a0003c0003t0002g0200 |
2 | HG01361.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3246+173_3246+201d others(31): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | C | CTTTTTTT others(68): Show |
1 | a0002c0002t0001g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3246+201_3246+202i others(77): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | CTTT | C | 9 | a0001c0001t0001g0033 a0001c0001t0001g0038 a0001c0001t0001g0057 others(6): Show |
9 | HG00597.hp1 HG01106.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.3246+199_3246+201d others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | CTTTT | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(87): Show |
93 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.3246+198_3246+201d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269471 | CTTTTTTT others(3): Show |
C | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3246+192_3246+201d others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 44269471 | ||||||
| chr3:44269477 | T | G | 1 | a0003c0003t0002g0227 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3246+176T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269477 | |||||||
| chr3:44269508 | G | A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3246+207G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269508 | |||||||
| chr3:44269509 | G | T | 1 | a0002c0002t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3246+208G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269509 | |||||||
| chr3:44269581 | A | T | 1 | a0002c0006t0001g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3246+280A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269581 | |||||||
| chr3:44269582 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3246+281T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269582 | |||||||
| chr3:44269596 | A | G | 1 | a0001c0016t0001g0088 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3246+295A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269596 | |||||||
| chr3:44269789 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3246+488G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269789 | |||||||
| chr3:44269900 | G | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3246+599G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269900 | |||||||
| chr3:44269903 | C | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3246+602C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44269903 | |||||||
| chr3:44270061 | C | G | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3247-624C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270061 | |||||||
| chr3:44270084 | A | G | 1 | a0002c0002t0001g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3247-601A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270084 | |||||||
| chr3:44270087 | C | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.3247-598C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270087 | |||||||
| chr3:44270166 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3247-519C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270166 | |||||||
| chr3:44270176 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3247-509G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270176 | |||||||
| chr3:44270245 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0006c0010t0001g0050 others(1): Show |
4 | HG00642.hp2 HG03654.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3247-440A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270245 | |||||||
| chr3:44270457 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3247-228C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270457 | |||||||
| chr3:44270472 | T | A | 1 | a0002c0002t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3247-213T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270472 | |||||||
| chr3:44270483 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3247-202C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 7/19 | chr3 | 44270483 | |||||||
| chr3:44270829 | TTAAAG | T | 6 | a0002c0006t0001g0009 a0002c0006t0001g0244 a0002c0006t0001g0245 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3372+22_3372+26del others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44270829 | ||||||
| chr3:44270947 | C | A | 1 | a0002c0002t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3372+137C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44270947 | |||||||
| chr3:44270955 | T | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3372+145T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44270955 | |||||||
| chr3:44271163 | A | G | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3372+353A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271163 | |||||||
| chr3:44271355 | G | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+545G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271355 | |||||||
| chr3:44271600 | ATT | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3372+793_3372+794d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44271600 | ||||||
| chr3:44271824 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3372+1014T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271824 | |||||||
| chr3:44271841 | A | G | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3372+1031A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271841 | |||||||
| chr3:44271974 | T | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+1164T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271974 | |||||||
| chr3:44271978 | A | G | 1 | a0002c0002t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3372+1168A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44271978 | |||||||
| chr3:44272281 | C | A | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3372+1471C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44272281 | |||||||
| chr3:44272550 | T | A | 1 | a0005c0008t0002g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3372+1740T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44272550 | |||||||
| chr3:44272930 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3372+2120A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44272930 | |||||||
| chr3:44273286 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(94): Show |
99 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.3372+2476C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273286 | |||||||
| chr3:44273405 | T | G | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3372+2595T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273405 | |||||||
| chr3:44273579 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3372+2769A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273579 | |||||||
| chr3:44273627 | C | G | 1 | a0001c0001t0001g0025 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3372+2817C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273627 | |||||||
| chr3:44273923 | T | C | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3372+3113T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273923 | |||||||
| chr3:44273952 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3372+3142A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44273952 | |||||||
| chr3:44274008 | G | A | 2 | a0002c0006t0001g0244 a0013c0021t0001g0181 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3372+3198G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274008 | |||||||
| chr3:44274139 | G | A | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3372+3329G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274139 | |||||||
| chr3:44274145 | G | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3372+3335G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274145 | |||||||
| chr3:44274282 | G | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+3472G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274282 | |||||||
| chr3:44274406 | AAAAAG | A | 32 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(29): Show |
32 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.3372+3621_3372+362 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274406 | ||||||
| chr3:44274406 | AAAAAGAA others(3): Show |
A | 40 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(37): Show |
43 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.3372+3616_3372+362 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274406 | ||||||
| chr3:44274409 | A | G | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3372+3599A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274409 | |||||||
| chr3:44274561 | A | AT | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
105 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3372+3766dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274561 | ||||||
| chr3:44274641 | G | A | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3372+3831G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274641 | |||||||
| chr3:44274715 | C | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3372+3905C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274715 | |||||||
| chr3:44274715 | C | T | 6 | a0002c0006t0001g0009 a0002c0006t0001g0244 a0002c0006t0001g0245 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3372+3905C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274715 | |||||||
| chr3:44274839 | G | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+4029G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44274839 | |||||||
| chr3:44274840 | CACCCGGC others(1195): Show |
C | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3372+4032_3372+523 others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44274840 | ||||||
| chr3:44275155 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3372+4345C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44275155 | |||||||
| chr3:44275311 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3372+4501T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44275311 | |||||||
| chr3:44275364 | T | C | 1 | a0002c0002t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3372+4554T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44275364 | |||||||
| chr3:44276420 | T | C | 9 | a0003c0003t0002g0162 a0003c0004t0002g0001 a0003c0004t0002g0188 others(6): Show |
12 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.3373-5548T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276420 | |||||||
| chr3:44276624 | C | CT | 34 | a0002c0002t0001g0129 a0002c0002t0001g0138 a0002c0002t0001g0139 others(31): Show |
34 | HG00099.hp2 HG00673.hp1 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.3373-5315dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | ||||||
| chr3:44276624 | C | CTT | 16 | a0002c0002t0001g0140 a0002c0002t0001g0142 a0002c0002t0001g0143 others(13): Show |
16 | HG01123.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.3373-5316_3373-531 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | ||||||
| chr3:44276624 | C | CTTTTT | 5 | a0002c0002t0001g0114 a0002c0002t0001g0130 a0002c0002t0001g0132 others(2): Show |
5 | HG01192.hp1 HG01346.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-5319_3373-531 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | ||||||
| chr3:44276624 | C | CTTTTTT | 8 | a0002c0002t0001g0002 a0002c0002t0001g0115 a0002c0002t0001g0117 others(5): Show |
10 | HG00099.hp1 HG00639.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.3373-5320_3373-531 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | ||||||
| chr3:44276624 | C | CTTTTTTT | 12 | a0002c0002t0001g0116 a0002c0002t0001g0120 a0002c0002t0001g0124 others(9): Show |
12 | HG00741.hp1 HG01099.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3373-5321_3373-531 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | ||||||
| chr3:44276624 | C | CTTTTTTT others(3): Show |
4 | a0002c0002t0001g0119 a0002c0002t0001g0121 a0002c0002t0001g0122 others(1): Show |
4 | HG01258.hp2 HG02148.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.3373-5324_3373-531 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 44276624 | ||||||
| chr3:44276641 | TTTTTTTT others(6): Show |
T | 3 | a0002c0024t0001g0113 a0008c0012t0001g0022 a0008c0012t0001g0023 |
3 | HG02818.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-5326_3373-531 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276641 | |||||||
| chr3:44276646 | TTTTTTTT others(1): Show |
T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
45 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3373-5321_3373-531 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276646 | |||||||
| chr3:44276647 | TTTTTTTC | T | 42 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0026 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.3373-5320_3373-531 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276647 | |||||||
| chr3:44276648 | TTTTTTC | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(8): Show |
12 | HG01258.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.3373-5319_3373-531 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276648 | |||||||
| chr3:44276654 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3373-5314C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276654 | |||||||
| chr3:44276831 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-5137G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276831 | |||||||
| chr3:44276851 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-5117C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276851 | |||||||
| chr3:44276860 | G | A | 7 | a0003c0004t0002g0001 a0003c0004t0002g0188 a0003c0004t0002g0196 others(4): Show |
10 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.3373-5108G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276860 | |||||||
| chr3:44276896 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3373-5072C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276896 | |||||||
| chr3:44276948 | G | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG00738.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3373-5020G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44276948 | |||||||
| chr3:44277068 | G | A | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3373-4900G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277068 | |||||||
| chr3:44277377 | A | G | 1 | a0002c0005t0001g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3373-4591A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277377 | |||||||
| chr3:44277660 | A | G | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-4308A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277660 | |||||||
| chr3:44277701 | G | T | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-4267G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277701 | |||||||
| chr3:44277750 | C | T | 1 | a0003c0003t0002g0194 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3373-4218C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277750 | |||||||
| chr3:44277790 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3373-4178G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277790 | |||||||
| chr3:44277983 | A | G | 3 | a0003c0003t0002g0195 a0003c0003t0002g0222 a0003c0003t0002g0238 |
3 | NA18999.hp1 NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3373-3985A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44277983 | |||||||
| chr3:44278002 | T | C | 1 | a0002c0002t0001g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3373-3966T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278002 | |||||||
| chr3:44278202 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3373-3766G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278202 | |||||||
| chr3:44278627 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0039 others(2): Show |
5 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-3341A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278627 | |||||||
| chr3:44278673 | A | G | 2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3373-3295A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278673 | |||||||
| chr3:44278878 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-3090G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278878 | |||||||
| chr3:44278967 | T | A | 3 | a0002c0002t0001g0117 a0002c0002t0001g0124 a0002c0002t0001g0165 |
3 | HG02486.hp1 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3373-3001T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278967 | |||||||
| chr3:44278981 | T | G | 1 | a0002c0006t0001g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3373-2987T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44278981 | |||||||
| chr3:44279088 | T | C | 2 | a0002c0024t0001g0113 a0002c0026t0001g0230 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3373-2880T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279088 | |||||||
| chr3:44279130 | C | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3373-2838C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279130 | |||||||
| chr3:44279301 | G | A | 1 | a0003c0003t0002g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3373-2667G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279301 | |||||||
| chr3:44279351 | T | G | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3373-2617T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279351 | |||||||
| chr3:44279444 | A | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-2524A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279444 | |||||||
| chr3:44279497 | G | A | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3373-2471G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279497 | |||||||
| chr3:44279574 | A | G | 1 | a0002c0002t0001g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3373-2394A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279574 | |||||||
| chr3:44279581 | T | C | 3 | a0002c0002t0001g0158 a0002c0002t0001g0159 a0002c0002t0001g0160 |
3 | HG00423.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3373-2387T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279581 | |||||||
| chr3:44279692 | A | G | 1 | a0001c0001t0001g0004 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.3373-2276A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279692 | |||||||
| chr3:44279751 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3373-2217T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279751 | |||||||
| chr3:44279811 | A | G | 1 | a0002c0006t0001g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3373-2157A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279811 | |||||||
| chr3:44279843 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3373-2125T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279843 | |||||||
| chr3:44279890 | C | A | 1 | a0002c0006t0001g0009 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3373-2078C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279890 | |||||||
| chr3:44279895 | T | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-2073T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279895 | |||||||
| chr3:44279994 | G | A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3373-1974G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44279994 | |||||||
| chr3:44280001 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3373-1967T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280001 | |||||||
| chr3:44280423 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3373-1545C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280423 | |||||||
| chr3:44280504 | T | A | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3373-1464T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280504 | |||||||
| chr3:44280570 | A | C | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3373-1398A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280570 | |||||||
| chr3:44280846 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3373-1122T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280846 | |||||||
| chr3:44280950 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3373-1018A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44280950 | |||||||
| chr3:44281055 | C | G | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3373-913C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281055 | |||||||
| chr3:44281135 | T | C | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3373-833T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281135 | |||||||
| chr3:44281236 | A | G | 6 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3373-732A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281236 | |||||||
| chr3:44281329 | C | T | 2 | a0009c0009t0001g0085 a0018c0013t0001g0011 |
2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.3373-639C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281329 | |||||||
| chr3:44281648 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373-320G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281648 | |||||||
| chr3:44281887 | C | G | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG00738.hp1 HG02145.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3373-81C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 8/19 | chr3 | 44281887 | |||||||
| chr3:44282070 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3436+39G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282070 | |||||||
| chr3:44282189 | G | C | 6 | a0003c0003t0002g0189 a0003c0003t0002g0190 a0003c0003t0002g0191 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3436+158G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282189 | |||||||
| chr3:44282208 | A | G | 1 | a0002c0002t0001g0143 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3436+177A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282208 | |||||||
| chr3:44282269 | A | G | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3436+238A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282269 | |||||||
| chr3:44282335 | G | A | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3436+304G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282335 | |||||||
| chr3:44282436 | G | T | 1 | a0003c0003t0002g0226 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3436+405G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282436 | |||||||
| chr3:44282622 | C | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3436+591C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282622 | |||||||
| chr3:44282650 | G | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3436+619G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282650 | |||||||
| chr3:44282714 | A | C | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3436+683A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44282714 | |||||||
| chr3:44283073 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3436+1042G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283073 | |||||||
| chr3:44283177 | A | AAGCACCT others(13): Show |
2 | a0002c0024t0001g0113 a0002c0026t0001g0230 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3436+1158_3436+117 others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44283177 | ||||||
| chr3:44283566 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3436+1535G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283566 | |||||||
| chr3:44283767 | G | A | 3 | a0003c0003t0002g0212 a0003c0003t0002g0218 a0003c0003t0002g0220 |
3 | HG01175.hp1 HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3436+1736G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283767 | |||||||
| chr3:44283772 | C | G | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3436+1741C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283772 | |||||||
| chr3:44283919 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3436+1888C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283919 | |||||||
| chr3:44283977 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3436+1946G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283977 | |||||||
| chr3:44283979 | G | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3436+1948G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44283979 | |||||||
| chr3:44284090 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3436+2059T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284090 | |||||||
| chr3:44284116 | T | TA | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3436+2089dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44284116 | ||||||
| chr3:44284125 | C | T | 3 | a0002c0002t0001g0131 a0002c0002t0001g0135 a0002c0002t0001g0136 |
3 | HG00639.hp1 HG00741.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.3436+2094C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284125 | |||||||
| chr3:44284138 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3436+2107A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284138 | |||||||
| chr3:44284157 | G | A | 1 | a0003c0003t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3436+2126G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284157 | |||||||
| chr3:44284249 | G | A | 35 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(32): Show |
38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3436+2218G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284249 | |||||||
| chr3:44284252 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3436+2221T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284252 | |||||||
| chr3:44284399 | C | T | 31 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(28): Show |
31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.3436+2368C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284399 | |||||||
| chr3:44284403 | G | A | 9 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3436+2372G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284403 | |||||||
| chr3:44284500 | T | G | 9 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3436+2469T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284500 | |||||||
| chr3:44284722 | A | C | 7 | a0003c0004t0002g0001 a0003c0004t0002g0188 a0003c0004t0002g0196 others(4): Show |
10 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.3437-2667A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284722 | |||||||
| chr3:44284832 | A | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3437-2557A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44284832 | |||||||
| chr3:44285082 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3437-2307T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285082 | |||||||
| chr3:44285145 | G | A | 5 | a0002c0006t0001g0244 a0002c0006t0001g0245 a0002c0006t0001g0246 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-2244G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285145 | |||||||
| chr3:44285157 | C | A | 1 | a0003c0003t0002g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3437-2232C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285157 | |||||||
| chr3:44285396 | G | A | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-1993G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285396 | |||||||
| chr3:44285415 | G | A | 75 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(72): Show |
78 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3437-1974G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285415 | |||||||
| chr3:44285509 | T | C | 4 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3437-1880T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285509 | |||||||
| chr3:44285544 | C | T | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3437-1845C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285544 | |||||||
| chr3:44285566 | CATT | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3437-1819_3437-181 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44285566 | ||||||
| chr3:44285656 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3437-1733G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285656 | |||||||
| chr3:44285813 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3437-1576C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285813 | |||||||
| chr3:44285814 | G | A | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3437-1575G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285814 | |||||||
| chr3:44285868 | G | A | 2 | a0003c0003t0002g0215 a0003c0003t0002g0241 |
2 | HG01928.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.3437-1521G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285868 | |||||||
| chr3:44285937 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3437-1452A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44285937 | |||||||
| chr3:44286034 | C | T | 1 | a0016c0020t0002g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3437-1355C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286034 | |||||||
| chr3:44286054 | CA | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(195): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.3437-1325delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr3 | 44286054 | ||||||
| chr3:44286163 | T | C | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3437-1226T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286163 | |||||||
| chr3:44286202 | G | A | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-1187G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286202 | |||||||
| chr3:44286237 | C | T | 1 | a0011c0018t0001g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3437-1152C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286237 | |||||||
| chr3:44286247 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3437-1142A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286247 | |||||||
| chr3:44286372 | C | T | 8 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0177 others(5): Show |
8 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3437-1017C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286372 | |||||||
| chr3:44286388 | G | A | 5 | a0002c0002t0001g0121 a0002c0002t0001g0122 a0002c0002t0001g0158 others(2): Show |
5 | HG00423.hp2 HG02040.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.3437-1001G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286388 | |||||||
| chr3:44286617 | A | G | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3437-772A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286617 | |||||||
| chr3:44286635 | C | G | 7 | a0002c0002t0001g0139 a0002c0002t0001g0140 a0002c0002t0001g0141 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3437-754C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286635 | |||||||
| chr3:44286712 | G | A | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3437-677G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286712 | |||||||
| chr3:44286741 | C | G | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-648C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286741 | |||||||
| chr3:44286743 | A | G | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3437-646A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286743 | |||||||
| chr3:44286997 | A | G | 5 | a0002c0006t0001g0244 a0002c0006t0001g0245 a0002c0006t0001g0246 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3437-392A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44286997 | |||||||
| chr3:44287056 | C | T | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3437-333C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 9/19 | chr3 | 44287056 | |||||||
| chr3:44287902 | TG | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3681+70delG | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 44287902 | ||||||
| chr3:44287940 | G | A | 1 | a0002c0002t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3681+101G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44287940 | |||||||
| chr3:44288235 | C | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0098 |
3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3681+396C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288235 | |||||||
| chr3:44288331 | T | C | 1 | a0003c0003t0002g0227 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3681+492T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288331 | |||||||
| chr3:44288469 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3681+630G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288469 | |||||||
| chr3:44288543 | G | A | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3681+704G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288543 | |||||||
| chr3:44288987 | C | T | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3681+1148C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44288987 | |||||||
| chr3:44289123 | G | A | 1 | a0003c0003t0002g0208 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3681+1284G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289123 | |||||||
| chr3:44289272 | C | T | 2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3681+1433C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289272 | |||||||
| chr3:44289482 | A | AT | 35 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(32): Show |
38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3682-1280dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 44289482 | ||||||
| chr3:44289961 | C | T | 1 | a0002c0002t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3682-810C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289961 | |||||||
| chr3:44289975 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3682-796T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44289975 | |||||||
| chr3:44290025 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3682-746A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290025 | |||||||
| chr3:44290100 | A | G | 4 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3682-671A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290100 | |||||||
| chr3:44290110 | ACTGCCAG others(8): Show |
A | 31 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(28): Show |
31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.3682-658_3682-644d others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 44290110 | ||||||
| chr3:44290326 | T | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3682-445T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290326 | |||||||
| chr3:44290332 | C | T | 1 | a0002c0002t0001g0167 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3682-439C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290332 | |||||||
| chr3:44290431 | A | T | 7 | a0002c0002t0001g0139 a0002c0002t0001g0140 a0002c0002t0001g0141 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-340A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290431 | |||||||
| chr3:44290639 | T | A | 35 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(32): Show |
38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3682-132T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290639 | |||||||
| chr3:44290684 | T | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.3682-87T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290684 | |||||||
| chr3:44290749 | C | T | 1 | a0002c0002t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3682-22C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 11/19 | chr3 | 44290749 | |||||||
| chr3:44291018 | C | A | 2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3797+132C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291018 | |||||||
| chr3:44291043 | T | C | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3797+157T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291043 | |||||||
| chr3:44291070 | C | T | 9 | a0002c0002t0001g0114 a0002c0002t0001g0115 a0002c0002t0001g0130 others(6): Show |
9 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.3797+184C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291070 | |||||||
| chr3:44291203 | G | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.3797+317G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291203 | |||||||
| chr3:44291205 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3797+319G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291205 | |||||||
| chr3:44291308 | T | TA | 34 | a0001c0001t0001g0072 a0001c0001t0001g0099 a0002c0002t0001g0131 others(31): Show |
34 | HG00609.hp1 HG01123.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.3797+435dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44291308 | ||||||
| chr3:44291347 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3797+461A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291347 | |||||||
| chr3:44291354 | G | T | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3797+468G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291354 | |||||||
| chr3:44291378 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3797+492G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291378 | |||||||
| chr3:44291433 | T | C | 1 | a0003c0003t0002g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3797+547T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291433 | |||||||
| chr3:44291504 | G | A | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3797+618G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291504 | |||||||
| chr3:44291587 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3797+701C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291587 | |||||||
| chr3:44291661 | T | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3797+775T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291661 | |||||||
| chr3:44291808 | T | C | 2 | a0003c0003t0002g0187 a0003c0003t0002g0224 |
2 | NA18986.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.3797+922T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291808 | |||||||
| chr3:44291832 | G | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
45 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.3797+946G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291832 | |||||||
| chr3:44291857 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3797+971C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291857 | |||||||
| chr3:44291885 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3797+999T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291885 | |||||||
| chr3:44291898 | G | A | 8 | a0002c0002t0001g0138 a0002c0002t0001g0147 a0002c0002t0001g0149 others(5): Show |
8 | HG01123.hp2 HG01261.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.3797+1012G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291898 | |||||||
| chr3:44291905 | A | G | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3797+1019A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44291905 | |||||||
| chr3:44292102 | G | A | 1 | a0003c0003t0002g0227 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3797+1216G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292102 | |||||||
| chr3:44292145 | T | C | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3797+1259T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292145 | |||||||
| chr3:44292274 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0111 |
2 | HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.3797+1388G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292274 | |||||||
| chr3:44292551 | TC | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3797+1666delC | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292551 | |||||||
| chr3:44292607 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3797+1721T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292607 | |||||||
| chr3:44292619 | A | G | 1 | a0003c0003t0002g0226 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3797+1733A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292619 | |||||||
| chr3:44292707 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3797+1821G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292707 | |||||||
| chr3:44292807 | C | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3797+1921C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292807 | |||||||
| chr3:44292852 | G | A | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3797+1966G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44292852 | |||||||
| chr3:44293002 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3797+2116A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293002 | |||||||
| chr3:44293026 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3797+2140C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293026 | |||||||
| chr3:44293378 | G | C | 5 | a0002c0006t0001g0244 a0002c0006t0001g0245 a0002c0006t0001g0246 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3797+2492G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293378 | |||||||
| chr3:44293483 | A | G | 1 | a0002c0002t0001g0144 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3797+2597A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293483 | |||||||
| chr3:44293572 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3797+2686A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293572 | |||||||
| chr3:44293616 | T | C | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3797+2730T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293616 | |||||||
| chr3:44293968 | C | T | 2 | a0002c0024t0001g0113 a0002c0026t0001g0230 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3797+3082C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44293968 | |||||||
| chr3:44294004 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3797+3118G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294004 | |||||||
| chr3:44294009 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3797+3123G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294009 | |||||||
| chr3:44294233 | C | G | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3797+3347C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294233 | |||||||
| chr3:44294239 | C | CA | 84 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(81): Show |
87 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.3797+3364dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44294239 | ||||||
| chr3:44294272 | G | A | 6 | a0003c0003t0002g0189 a0003c0003t0002g0190 a0003c0003t0002g0191 others(3): Show |
6 | HG02647.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3797+3386G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294272 | |||||||
| chr3:44294485 | T | C | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3797+3599T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294485 | |||||||
| chr3:44294523 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3797+3637C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294523 | |||||||
| chr3:44294725 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3797+3839C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294725 | |||||||
| chr3:44294869 | G | A | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3797+3983G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44294869 | |||||||
| chr3:44295126 | G | A | 1 | a0002c0002t0001g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3797+4240G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295126 | |||||||
| chr3:44295145 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3797+4259T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295145 | |||||||
| chr3:44295206 | A | G | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3797+4320A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295206 | |||||||
| chr3:44295233 | A | G | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3797+4347A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295233 | |||||||
| chr3:44295420 | G | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3797+4534G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295420 | |||||||
| chr3:44295551 | C | A | 1 | a0002c0002t0001g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3797+4665C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295551 | |||||||
| chr3:44295681 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(94): Show |
99 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.3797+4795A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295681 | |||||||
| chr3:44295858 | C | T | 23 | a0002c0002t0001g0138 a0002c0002t0001g0144 a0002c0002t0001g0145 others(20): Show |
23 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.3797+4972C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44295858 | |||||||
| chr3:44296311 | A | G | 1 | a0003c0003t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3797+5425A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296311 | |||||||
| chr3:44296393 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3797+5507A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296393 | |||||||
| chr3:44296421 | T | TA | 8 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3797+5545dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296421 | ||||||
| chr3:44296421 | T | TAA | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.3797+5544_3797+554 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296421 | ||||||
| chr3:44296505 | A | C | 1 | a0002c0002t0001g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3797+5619A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296505 | |||||||
| chr3:44296555 | T | C | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3797+5669T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296555 | |||||||
| chr3:44296750 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3797+5864G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296750 | |||||||
| chr3:44296852 | AAAAAAAA others(6): Show |
A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3797+5977_3797+598 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296852 | ||||||
| chr3:44296860 | A | AAAAG | 87 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0072 others(84): Show |
90 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3797+5977_3797+597 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296860 | ||||||
| chr3:44296860 | A | AAAG | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(92): Show |
98 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.3797+5976_3797+597 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44296860 | ||||||
| chr3:44296865 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(180): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.3797+5979G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296865 | |||||||
| chr3:44296871 | A | G | 81 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(78): Show |
84 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.3797+5985A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296871 | |||||||
| chr3:44296907 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3797+6021C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296907 | |||||||
| chr3:44296989 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3797+6103T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44296989 | |||||||
| chr3:44297065 | A | T | 1 | a0003c0003t0002g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3797+6179A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297065 | |||||||
| chr3:44297152 | C | CAA | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3797+6266_3797+626 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297152 | |||||||
| chr3:44297169 | C | CAA | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.3797+6294_3797+629 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44297169 | ||||||
| chr3:44297180 | A | C | 9 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(6): Show |
9 | HG02257.hp2 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3797+6294A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297180 | |||||||
| chr3:44297377 | TAAG | T | 35 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(32): Show |
38 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3797+6497_3797+649 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44297377 | ||||||
| chr3:44297542 | A | G | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-6473A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297542 | |||||||
| chr3:44297578 | A | G | 2 | a0003c0003t0002g0190 a0003c0003t0002g0191 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3798-6437A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297578 | |||||||
| chr3:44297689 | A | G | 1 | a0003c0003t0002g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3798-6326A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297689 | |||||||
| chr3:44297709 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3798-6306A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297709 | |||||||
| chr3:44297750 | T | A | 2 | a0002c0024t0001g0113 a0002c0026t0001g0230 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3798-6265T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297750 | |||||||
| chr3:44297750 | T | TA | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3798-6255dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44297750 | ||||||
| chr3:44297912 | C | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3798-6103C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44297912 | |||||||
| chr3:44298051 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3798-5964A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298051 | |||||||
| chr3:44298071 | A | G | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3798-5944A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298071 | |||||||
| chr3:44298292 | C | T | 3 | a0003c0003t0002g0007 a0003c0003t0002g0214 a0003c0003t0002g0242 |
4 | HG01106.hp2 HG02257.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5723C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298292 | |||||||
| chr3:44298608 | C | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3798-5407C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298608 | |||||||
| chr3:44298622 | T | G | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3798-5393T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298622 | |||||||
| chr3:44298739 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-5276C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298739 | |||||||
| chr3:44298800 | G | GAAAAAAT others(299): Show |
1 | a0001c0001t0001g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | ||||||
| chr3:44298800 | G | GAAAAAAT others(299): Show |
1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | ||||||
| chr3:44298800 | G | GAAAAAAT others(299): Show |
88 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(85): Show |
90 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | ||||||
| chr3:44298800 | G | GAAAAAAT others(300): Show |
11 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0081 others(8): Show |
11 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.3798-5203_3798-520 others(311): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | ||||||
| chr3:44298800 | G | GAAAAAAT others(301): Show |
1 | a0001c0001t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(312): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | ||||||
| chr3:44298800 | G | GAAAAAAT others(299): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 |
4 | HG01074.hp1 HG01099.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5203_3798-520 others(310): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | ||||||
| chr3:44298800 | G | GAAAAAAT others(298): Show |
1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(309): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298800 | ||||||
| chr3:44298807 | T | TAGGGGCC others(298): Show |
1 | a0001c0001t0001g0044 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3798-5203_3798-520 others(309): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298807 | ||||||
| chr3:44298882 | G | A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3798-5133G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298882 | |||||||
| chr3:44298882 | G | GTATATAT others(10): Show |
1 | a0001c0001t0001g0025 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3798-5126_3798-512 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298882 | ||||||
| chr3:44298882 | G | GTATATAT others(16): Show |
1 | a0017c0014t0001g0020 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3798-5126_3798-512 others(27): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298882 | ||||||
| chr3:44298890 | A | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.3798-5125A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298890 | |||||||
| chr3:44298891 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3798-5124T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298891 | |||||||
| chr3:44298891 | T | TA | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0017c0014t0001g0020 |
3 | HG03490.hp2 NA18975.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3798-5124_3798-512 others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298891 | |||||||
| chr3:44298891 | T | TTA | 5 | a0002c0002t0001g0138 a0002c0002t0001g0141 a0002c0002t0001g0143 others(2): Show |
5 | HG01261.hp1 HG01346.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5106_3798-510 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATA | 4 | a0002c0002t0001g0151 a0002c0002t0001g0157 a0002c0002t0001g0182 others(1): Show |
4 | HG01123.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5108_3798-510 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATA | 3 | a0002c0006t0001g0010 a0003c0003t0002g0189 a0003c0003t0002g0201 |
3 | HG02451.hp1 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3798-5110_3798-510 others(10): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(1): Show |
14 | a0003c0003t0002g0007 a0003c0003t0002g0199 a0003c0003t0002g0204 others(11): Show |
15 | HG00408.hp2 HG01106.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.3798-5112_3798-510 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(3): Show |
3 | a0003c0003t0002g0202 a0003c0003t0002g0210 a0015c0019t0002g0236 |
3 | HG01975.hp2 HG03041.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3798-5114_3798-510 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(5): Show |
3 | a0002c0006t0001g0247 a0003c0003t0002g0187 a0003c0003t0002g0226 |
3 | HG02280.hp1 HG02809.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3798-5116_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(11): Show |
1 | a0003c0003t0002g0217 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3798-5122_3798-510 others(22): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(15): Show |
13 | a0001c0001t0001g0021 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
13 | HG00609.hp1 HG02698.hp1 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(17): Show |
8 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG00423.hp1 HG00558.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(28): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(19): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01358.hp2 HG02135.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(30): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(21): Show |
6 | a0001c0001t0001g0029 a0001c0001t0001g0075 a0001c0001t0001g0082 others(3): Show |
6 | HG01123.hp1 HG02004.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(32): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0074 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(34): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0073 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(36): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(38): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298891 | T | TTTTATAT others(19): Show |
1 | a0001c0001t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3798-5123_3798-512 others(30): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298891 | ||||||
| chr3:44298909 | A | ATATATAT others(2): Show |
5 | a0001c0001t0001g0037 a0003c0003t0002g0192 a0003c0003t0002g0222 others(2): Show |
5 | HG00558.hp2 HG01516.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0086 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(37): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(26): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATAT others(5): Show |
3 | a0003c0003t0002g0224 a0003c0003t0002g0225 a0003c0003t0002g0238 |
3 | NA18986.hp1 NA19056.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATAT others(3): Show |
2 | a0003c0003t0002g0162 a0003c0003t0002g0195 |
2 | HG02615.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(14): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATAT others(7): Show |
1 | a0016c0020t0002g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATAT others(2): Show |
4 | a0003c0004t0002g0001 a0003c0004t0002g0188 a0003c0004t0002g0196 others(1): Show |
7 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATAT others(8): Show |
1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATATTT others(5): Show |
1 | a0005c0008t0002g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | A | ATATTTTT others(5): Show |
1 | a0005c0008t0002g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | ATT | A | 3 | a0002c0002t0001g0002 a0002c0002t0001g0161 a0002c0002t0001g0164 |
5 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5082_3798-508 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | ATTT | A | 5 | a0002c0002t0001g0121 a0002c0002t0001g0122 a0002c0002t0001g0131 others(2): Show |
5 | HG02145.hp1 HG03669.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5083_3798-508 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298909 | ATTTT | A | 24 | a0002c0002t0001g0116 a0002c0002t0001g0117 a0002c0002t0001g0118 others(21): Show |
25 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.3798-5084_3798-508 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298909 | ||||||
| chr3:44298910 | T | TA | 11 | a0002c0002t0001g0144 a0002c0002t0001g0145 a0002c0002t0001g0150 others(8): Show |
11 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATA | 7 | a0002c0002t0001g0147 a0002c0002t0001g0149 a0002c0002t0001g0156 others(4): Show |
7 | HG01361.hp2 HG02055.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATA | 13 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0002c0002t0001g0140 others(10): Show |
13 | HG01934.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA | 9 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0101 others(6): Show |
9 | HG00609.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(2): Show |
15 | a0001c0001t0001g0024 a0001c0001t0001g0032 a0001c0001t0001g0033 others(12): Show |
15 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(13): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(4): Show |
12 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0001t0001g0049 others(9): Show |
12 | HG00738.hp1 HG01175.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(15): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(6): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(17): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(8): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0106 |
2 | HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(19): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(10): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0065 others(2): Show |
5 | HG00140.hp2 HG00741.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(21): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(12): Show |
6 | a0001c0001t0001g0042 a0001c0001t0001g0068 a0001c0001t0001g0076 others(3): Show |
6 | HG00140.hp1 HG00673.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(23): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(14): Show |
3 | a0001c0001t0001g0057 a0001c0001t0001g0112 a0002c0006t0001g0009 |
3 | HG01261.hp2 HG02129.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(25): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0087 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(27): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0077 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(29): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(20): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0011c0018t0001g0083 |
3 | HG01167.hp1 HG02109.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(31): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(22): Show |
2 | a0001c0001t0001g0067 a0002c0006t0001g0245 |
2 | HG02109.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.3798-5105_3798-510 others(33): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298910 | T | TATATATA others(28): Show |
1 | a0002c0006t0001g0244 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3798-5105_3798-510 others(39): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298910 | |||||||
| chr3:44298911 | T | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(60): Show |
65 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.3798-5104T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298911 | |||||||
| chr3:44298912 | T | A | 80 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0031 others(77): Show |
80 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.3798-5103T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298912 | |||||||
| chr3:44298913 | T | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(53): Show |
60 | HG00558.hp1 HG00609.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.3798-5102T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298913 | |||||||
| chr3:44298914 | T | A | 77 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0031 others(74): Show |
77 | HG00140.hp2 HG00642.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.3798-5101T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298914 | |||||||
| chr3:44298915 | T | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(62): Show |
70 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.3798-5100T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298915 | |||||||
| chr3:44298916 | T | A | 64 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0034 others(61): Show |
64 | HG00140.hp2 HG00642.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.3798-5099T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298916 | |||||||
| chr3:44298917 | T | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(49): Show |
56 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.3798-5098T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298917 | |||||||
| chr3:44298918 | T | A | 47 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0040 others(44): Show |
47 | HG00738.hp1 HG01074.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.3798-5097T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298918 | |||||||
| chr3:44298919 | T | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(40): Show |
47 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.3798-5096T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298919 | |||||||
| chr3:44298920 | T | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0089 others(12): Show |
15 | HG00738.hp1 HG01891.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.3798-5095T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298920 | |||||||
| chr3:44298921 | T | A | 9 | a0001c0001t0001g0016 a0001c0017t0001g0095 a0002c0002t0001g0002 others(6): Show |
11 | HG00423.hp2 HG01123.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3798-5094T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298921 | |||||||
| chr3:44298922 | T | A | 2 | a0002c0002t0001g0148 a0004c0007t0001g0173 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3798-5093T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298922 | |||||||
| chr3:44298923 | T | A | 3 | a0002c0002t0001g0002 a0002c0002t0001g0158 a0002c0002t0001g0161 |
5 | HG00423.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5092T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298923 | |||||||
| chr3:44298924 | T | A | 1 | a0002c0002t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3798-5091T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298924 | |||||||
| chr3:44298925 | T | A | 1 | a0002c0002t0001g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3798-5090T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298925 | |||||||
| chr3:44298925 | T | G | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3798-5090T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298925 | |||||||
| chr3:44298929 | T | G | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5086T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298929 | |||||||
| chr3:44298929 | T | TTTTTTTT others(7): Show |
1 | a0005c0008t0002g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3798-5081_3798-508 others(18): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44298929 | ||||||
| chr3:44298930 | TTTTTC | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
6 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3798-5084_3798-508 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298930 | |||||||
| chr3:44298933 | TTCC | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG01074.hp1 HG01099.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-5081_3798-507 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298933 | |||||||
| chr3:44298934 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3798-5081T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298934 | |||||||
| chr3:44298935 | C | T | 26 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
27 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.3798-5080C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298935 | |||||||
| chr3:44298936 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0037 others(2): Show |
5 | HG00639.hp2 HG01106.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-5079C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298936 | |||||||
| chr3:44298938 | CCT | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0021 others(68): Show |
71 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.3798-5076_3798-507 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298938 | |||||||
| chr3:44298939 | CT | C | 21 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0040 others(18): Show |
22 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.3798-5075delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298939 | |||||||
| chr3:44298940 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(12): Show |
17 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.3798-5075T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44298940 | |||||||
| chr3:44299003 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3798-5012A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299003 | |||||||
| chr3:44299070 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3798-4945G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299070 | |||||||
| chr3:44299115 | G | T | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3798-4900G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299115 | |||||||
| chr3:44299392 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-4623C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299392 | |||||||
| chr3:44299447 | AAAC | A | 3 | a0003c0003t0002g0007 a0003c0003t0002g0214 a0003c0003t0002g0242 |
4 | HG01106.hp2 HG02257.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-4563_3798-456 others(7): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44299447 | ||||||
| chr3:44299466 | G | A | 1 | a0003c0003t0002g0211 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3798-4549G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299466 | |||||||
| chr3:44299545 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3798-4470G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299545 | |||||||
| chr3:44299574 | C | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0039 others(13): Show |
16 | HG00738.hp1 HG01074.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3798-4441C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299574 | |||||||
| chr3:44299744 | C | T | 1 | a0002c0002t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3798-4271C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299744 | |||||||
| chr3:44299766 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3798-4249G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44299766 | |||||||
| chr3:44299957 | T | TG | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
105 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.3798-4052dupG | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44299957 | ||||||
| chr3:44300039 | A | T | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3798-3976A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300039 | |||||||
| chr3:44300121 | TAAATAAA | T | 2 | a0002c0002t0001g0002 a0002c0002t0001g0161 |
4 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-3883_3798-387 others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44300121 | ||||||
| chr3:44300129 | A | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-3886A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300129 | |||||||
| chr3:44300249 | A | G | 18 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0120 others(15): Show |
19 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.3798-3766A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300249 | |||||||
| chr3:44300314 | G | A | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3798-3701G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300314 | |||||||
| chr3:44300430 | AAAAG | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3798-3577_3798-357 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44300430 | ||||||
| chr3:44300477 | A | G | 5 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG01074.hp2 HG01243.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3798-3538A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300477 | |||||||
| chr3:44300654 | A | T | 1 | a0001c0001t0001g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3798-3361A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300654 | |||||||
| chr3:44300852 | G | A | 82 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.3798-3163G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44300852 | |||||||
| chr3:44301028 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0098 |
3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3798-2987C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301028 | |||||||
| chr3:44301068 | T | C | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3798-2947T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301068 | |||||||
| chr3:44301115 | A | C | 1 | a0002c0002t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3798-2900A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301115 | |||||||
| chr3:44301162 | A | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(92): Show |
96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.3798-2853A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301162 | |||||||
| chr3:44301228 | T | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.3798-2787T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301228 | |||||||
| chr3:44301611 | T | C | 4 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3798-2404T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301611 | |||||||
| chr3:44301770 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-2245A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301770 | |||||||
| chr3:44301870 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3798-2145T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44301870 | |||||||
| chr3:44302069 | T | A | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.3798-1946T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302069 | |||||||
| chr3:44302091 | A | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.3798-1924A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302091 | |||||||
| chr3:44302192 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3798-1823C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302192 | |||||||
| chr3:44302209 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3798-1806G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302209 | |||||||
| chr3:44302360 | A | G | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3798-1655A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302360 | |||||||
| chr3:44302374 | C | T | 1 | a0002c0002t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3798-1641C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302374 | |||||||
| chr3:44302440 | A | G | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-1575A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302440 | |||||||
| chr3:44302530 | C | G | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3798-1485C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302530 | |||||||
| chr3:44302602 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3798-1413T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302602 | |||||||
| chr3:44302789 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3798-1226G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302789 | |||||||
| chr3:44302969 | C | T | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-1046C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302969 | |||||||
| chr3:44302985 | G | C | 1 | a0002c0006t0001g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3798-1030G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44302985 | |||||||
| chr3:44303022 | T | C | 1 | a0003c0004t0002g0223 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3798-993T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303022 | |||||||
| chr3:44303182 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3798-833G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303182 | |||||||
| chr3:44303193 | T | C | 1 | a0003c0003t0002g0189 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3798-822T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303193 | |||||||
| chr3:44303299 | A | G | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3798-716A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303299 | |||||||
| chr3:44303342 | T | C | 1 | a0003c0003t0002g0227 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3798-673T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303342 | |||||||
| chr3:44303479 | C | CT | 7 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0182 others(4): Show |
7 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3798-514dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | ||||||
| chr3:44303479 | CT | C | 52 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0116 others(49): Show |
55 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.3798-514delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | ||||||
| chr3:44303479 | CTT | C | 46 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0037 others(43): Show |
46 | HG00597.hp1 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.3798-515_3798-514d others(4): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | ||||||
| chr3:44303479 | CTTT | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.3798-516_3798-514d others(5): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 44303479 | ||||||
| chr3:44303536 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-479C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303536 | |||||||
| chr3:44303587 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(94): Show |
99 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.3798-428A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303587 | |||||||
| chr3:44303689 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3798-326A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303689 | |||||||
| chr3:44303847 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3798-168G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303847 | |||||||
| chr3:44303974 | G | A | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3798-41G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 12/19 | chr3 | 44303974 | |||||||
| chr3:44304154 | A | T | 83 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(80): Show |
86 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.3864+73A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304154 | |||||||
| chr3:44304194 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3864+113A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304194 | |||||||
| chr3:44304470 | A | T | 1 | a0001c0001t0001g0087 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3864+389A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304470 | |||||||
| chr3:44304687 | G | A | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.3865-460G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44304687 | |||||||
| chr3:44305088 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3865-59A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 13/19 | chr3 | 44305088 | |||||||
| chr3:44305529 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(242): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.4039+208T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305529 | |||||||
| chr3:44305664 | G | A | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4039+343G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305664 | |||||||
| chr3:44305687 | A | G | 1 | a0004c0007t0001g0170 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4039+366A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305687 | |||||||
| chr3:44305803 | T | G | 7 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0132 others(4): Show |
7 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.4039+482T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305803 | |||||||
| chr3:44305974 | A | G | 2 | a0003c0003t0002g0225 a0003c0003t0002g0226 |
2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4040-352A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44305974 | |||||||
| chr3:44306168 | C | T | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.4040-158C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44306168 | |||||||
| chr3:44306234 | T | C | 2 | a0003c0003t0002g0007 a0003c0003t0002g0242 |
3 | HG02257.hp1 HG04199.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4040-92T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 14/19 | chr3 | 44306234 | |||||||
| chr3:44306631 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4140+205A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44306631 | |||||||
| chr3:44306971 | A | G | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4140+545A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44306971 | |||||||
| chr3:44307108 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4140+682C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307108 | |||||||
| chr3:44307170 | G | A | 5 | a0003c0003t0002g0215 a0003c0003t0002g0219 a0003c0003t0002g0221 others(2): Show |
5 | HG01928.hp2 NA18947.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.4140+744G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307170 | |||||||
| chr3:44307331 | T | G | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4140+905T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307331 | |||||||
| chr3:44307608 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4140+1182A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307608 | |||||||
| chr3:44307609 | G | A | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4140+1183G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44307609 | |||||||
| chr3:44308026 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4140+1600T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308026 | |||||||
| chr3:44308090 | A | G | 1 | a0003c0003t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4140+1664A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308090 | |||||||
| chr3:44308144 | G | A | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.4141-1681G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308144 | |||||||
| chr3:44308287 | C | A | 1 | a0004c0007t0001g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4141-1538C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308287 | |||||||
| chr3:44308373 | C | T | 83 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(80): Show |
86 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.4141-1452C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308373 | |||||||
| chr3:44308424 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.4141-1401A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308424 | |||||||
| chr3:44308594 | G | T | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4141-1231G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308594 | |||||||
| chr3:44308610 | A | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4141-1215A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308610 | |||||||
| chr3:44308640 | T | TTTTTAAT others(21): Show |
1 | a0003c0003t0002g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1185_4141-118 others(32): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308640 | |||||||
| chr3:44308641 | C | G | 1 | a0003c0003t0002g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1184C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308641 | |||||||
| chr3:44308646 | T | A | 1 | a0003c0003t0002g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1179T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308646 | |||||||
| chr3:44308647 | G | A | 1 | a0003c0003t0002g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4141-1178G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308647 | |||||||
| chr3:44308772 | A | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.4141-1053A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308772 | |||||||
| chr3:44308795 | C | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4141-1030C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308795 | |||||||
| chr3:44308831 | C | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4141-994C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308831 | |||||||
| chr3:44308902 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4141-923A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308902 | |||||||
| chr3:44308959 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4141-866C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44308959 | |||||||
| chr3:44309126 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4141-699G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309126 | |||||||
| chr3:44309202 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4141-623T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309202 | |||||||
| chr3:44309229 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4141-596C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309229 | |||||||
| chr3:44309428 | T | TCTCC | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0098 |
3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4141-392_4141-389d others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr3 | 44309428 | ||||||
| chr3:44309478 | A | T | 2 | a0003c0003t0002g0195 a0003c0003t0002g0238 |
2 | NA19056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4141-347A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309478 | |||||||
| chr3:44309589 | G | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.4141-236G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309589 | |||||||
| chr3:44309628 | C | T | 1 | a0015c0019t0002g0236 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4141-197C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309628 | |||||||
| chr3:44309789 | T | C | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4141-36T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 15/19 | chr3 | 44309789 | |||||||
| chr3:44310188 | C | T | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4306+198C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310188 | |||||||
| chr3:44310236 | A | T | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4306+246A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310236 | |||||||
| chr3:44310243 | T | A | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4306+253T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310243 | |||||||
| chr3:44310294 | T | A | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4306+304T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310294 | |||||||
| chr3:44310319 | C | T | 1 | a0003c0004t0002g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4306+329C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310319 | |||||||
| chr3:44310413 | C | T | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4306+423C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310413 | |||||||
| chr3:44310424 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4306+434G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310424 | |||||||
| chr3:44310671 | A | G | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4306+681A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310671 | |||||||
| chr3:44310675 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4306+685T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310675 | |||||||
| chr3:44310937 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4306+947A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310937 | |||||||
| chr3:44310946 | C | T | 1 | a0003c0003t0002g0226 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4306+956C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44310946 | |||||||
| chr3:44311023 | C | T | 36 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(33): Show |
39 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.4306+1033C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311023 | |||||||
| chr3:44311045 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.4306+1055G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311045 | |||||||
| chr3:44311214 | A | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4306+1224A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311214 | |||||||
| chr3:44311653 | T | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4306+1663T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311653 | |||||||
| chr3:44311843 | C | G | 1 | a0009c0009t0001g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4306+1853C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44311843 | |||||||
| chr3:44312231 | C | CA | 7 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0002c0002t0001g0182 others(4): Show |
7 | HG02040.hp1 HG02615.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.4306+2258dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44312231 | ||||||
| chr3:44312231 | CA | C | 4 | a0001c0001t0001g0025 a0002c0002t0001g0002 a0002c0002t0001g0140 others(1): Show |
6 | HG02895.hp1 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.4306+2258delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44312231 | ||||||
| chr3:44312248 | A | C | 1 | a0001c0001t0001g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4306+2258A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312248 | |||||||
| chr3:44312528 | C | T | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4306+2538C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312528 | |||||||
| chr3:44312536 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4306+2546C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312536 | |||||||
| chr3:44312697 | A | T | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4306+2707A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312697 | |||||||
| chr3:44312735 | A | G | 3 | a0002c0002t0001g0140 a0002c0002t0001g0142 a0002c0002t0001g0166 |
3 | HG02970.hp1 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4306+2745A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312735 | |||||||
| chr3:44312894 | T | C | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4306+2904T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312894 | |||||||
| chr3:44312945 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4306+2955A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44312945 | |||||||
| chr3:44313042 | C | T | 1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4306+3052C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313042 | |||||||
| chr3:44313212 | C | T | 3 | a0003c0003t0002g0189 a0003c0003t0002g0201 a0003c0003t0002g0237 |
3 | HG02818.hp1 HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4306+3222C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313212 | |||||||
| chr3:44313452 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4306+3462A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313452 | |||||||
| chr3:44313556 | G | T | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4306+3566G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313556 | |||||||
| chr3:44313617 | C | CA | 10 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0067 others(7): Show |
10 | HG01106.hp2 HG01109.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.4306+3644dupA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44313617 | ||||||
| chr3:44313617 | CA | C | 57 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0002c0002t0001g0002 others(54): Show |
61 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.4306+3644delA | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44313617 | ||||||
| chr3:44313617 | CAA | C | 29 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(26): Show |
29 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.4306+3643_4306+364 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44313617 | ||||||
| chr3:44313694 | A | C | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4306+3704A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44313694 | |||||||
| chr3:44314180 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4306+4190G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44314180 | |||||||
| chr3:44314368 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4306+4378T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44314368 | |||||||
| chr3:44314833 | A | G | 1 | a0003c0003t0002g0187 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4306+4843A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44314833 | |||||||
| chr3:44315105 | G | GTGGA | 16 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0132 others(13): Show |
16 | HG00408.hp2 HG00639.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.4306+5146_4306+514 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | ||||||
| chr3:44315105 | G | GTGGATGG others(1): Show |
11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(8): Show |
13 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4306+5142_4306+514 others(12): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | ||||||
| chr3:44315105 | G | GTGGATGG others(5): Show |
82 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0024 others(79): Show |
83 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.4306+5138_4306+514 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | ||||||
| chr3:44315105 | G | GTGGATGG others(9): Show |
12 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0065 others(9): Show |
12 | HG01074.hp2 HG01243.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.4306+5134_4306+514 others(20): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | ||||||
| chr3:44315105 | G | GTGGATGG others(13): Show |
1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4306+5130_4306+514 others(24): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | ||||||
| chr3:44315105 | GTGGA | G | 3 | a0002c0002t0001g0145 a0002c0002t0001g0233 a0003c0003t0002g0227 |
3 | HG06807.hp2 NA18991.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4306+5146_4306+514 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315105 | ||||||
| chr3:44315200 | C | CGT | 4 | a0003c0003t0002g0194 a0003c0003t0002g0199 a0003c0003t0002g0203 others(1): Show |
4 | HG02132.hp1 HG02135.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4306+5237_4306+523 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315200 | ||||||
| chr3:44315200 | CGT | C | 84 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(81): Show |
87 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.4306+5237_4306+523 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315200 | ||||||
| chr3:44315200 | CGTGTGTG others(5): Show |
C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4306+5227_4306+523 others(16): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315200 | ||||||
| chr3:44315278 | G | A | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4306+5288G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315278 | |||||||
| chr3:44315282 | G | A | 1 | a0013c0021t0001g0181 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4306+5292G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315282 | |||||||
| chr3:44315343 | A | T | 2 | a0003c0003t0002g0225 a0003c0003t0002g0226 |
2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4306+5353A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315343 | |||||||
| chr3:44315533 | A | AT | 11 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0069 others(8): Show |
11 | HG00423.hp1 HG00642.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.4307-5475dupT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315533 | ||||||
| chr3:44315533 | A | ATT | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(90): Show |
96 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.4307-5476_4307-547 others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44315533 | ||||||
| chr3:44315651 | C | T | 31 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(28): Show |
31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4307-5376C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315651 | |||||||
| chr3:44315668 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
6 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4307-5359G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315668 | |||||||
| chr3:44315854 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0017 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.4307-5173T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44315854 | |||||||
| chr3:44316078 | T | A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4307-4949T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316078 | |||||||
| chr3:44316119 | G | A | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4307-4908G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316119 | |||||||
| chr3:44316192 | G | T | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4307-4835G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316192 | |||||||
| chr3:44316250 | A | T | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4307-4777A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316250 | |||||||
| chr3:44316275 | AAAGT | A | 3 | a0002c0002t0001g0117 a0002c0002t0001g0124 a0002c0002t0001g0165 |
3 | HG02486.hp1 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4307-4749_4307-474 others(8): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44316275 | ||||||
| chr3:44316877 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4307-4150G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44316877 | |||||||
| chr3:44317020 | C | T | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4307-4007C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317020 | |||||||
| chr3:44317033 | C | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0037 |
3 | HG00639.hp2 HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.4307-3994C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317033 | |||||||
| chr3:44317042 | G | T | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4307-3985G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317042 | |||||||
| chr3:44317142 | T | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.4307-3885T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317142 | |||||||
| chr3:44317156 | C | T | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.4307-3871C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317156 | |||||||
| chr3:44317314 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.4307-3713A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317314 | |||||||
| chr3:44317346 | G | A | 1 | a0002c0002t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4307-3681G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317346 | |||||||
| chr3:44317376 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.4307-3651G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317376 | |||||||
| chr3:44317389 | T | G | 1 | a0002c0002t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4307-3638T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317389 | |||||||
| chr3:44317730 | A | G | 1 | a0002c0026t0001g0230 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4307-3297A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317730 | |||||||
| chr3:44317775 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4307-3252G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317775 | |||||||
| chr3:44317873 | T | C | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4307-3154T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44317873 | |||||||
| chr3:44318155 | C | CTTAAA | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4307-2872_4307-287 others(9): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318155 | |||||||
| chr3:44318169 | C | T | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4307-2858C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318169 | |||||||
| chr3:44318213 | C | T | 1 | a0003c0003t0002g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4307-2814C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318213 | |||||||
| chr3:44318229 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.4307-2798A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318229 | |||||||
| chr3:44318282 | T | C | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4307-2745T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318282 | |||||||
| chr3:44318377 | G | A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4307-2650G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318377 | |||||||
| chr3:44318698 | C | A | 83 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(80): Show |
86 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.4307-2329C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318698 | |||||||
| chr3:44318767 | A | T | 1 | a0003c0004t0002g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4307-2260A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44318767 | |||||||
| chr3:44319103 | G | A | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4307-1924G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319103 | |||||||
| chr3:44319343 | C | G | 4 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0135 others(1): Show |
4 | HG00639.hp1 HG00741.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.4307-1684C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319343 | |||||||
| chr3:44319609 | A | G | 8 | a0002c0002t0001g0148 a0003c0003t0002g0222 a0003c0004t0002g0001 others(5): Show |
11 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(8): Show |
intron_variant | MODIFIER | c.4307-1418A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319609 | |||||||
| chr3:44319879 | G | A | 1 | a0005c0008t0002g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4307-1148G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44319879 | |||||||
| chr3:44320283 | T | C | 1 | a0002c0002t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4307-744T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320283 | |||||||
| chr3:44320288 | T | TAGAC | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(191): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.4307-736_4307-735i others(6): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr3 | 44320288 | ||||||
| chr3:44320318 | T | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4307-709T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320318 | |||||||
| chr3:44320326 | A | G | 5 | a0005c0008t0002g0183 a0005c0008t0002g0184 a0005c0008t0002g0185 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4307-701A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320326 | |||||||
| chr3:44320394 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4307-633G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320394 | |||||||
| chr3:44320520 | C | T | 1 | a0006c0010t0001g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4307-507C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320520 | |||||||
| chr3:44320916 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.4307-111G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 16/19 | chr3 | 44320916 | |||||||
| chr3:44321211 | A | G | 2 | a0003c0003t0002g0187 a0003c0003t0002g0224 |
2 | NA18986.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.4471+20A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44321211 | |||||||
| chr3:44321781 | G | C | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4471+590G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44321781 | |||||||
| chr3:44322039 | G | C | 1 | a0019c0027t0001g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4471+848G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322039 | |||||||
| chr3:44322072 | G | T | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4471+881G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322072 | |||||||
| chr3:44322129 | A | T | 7 | a0002c0002t0001g0120 a0002c0005t0001g0006 a0002c0005t0001g0125 others(4): Show |
8 | HG00099.hp1 HG00733.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.4471+938A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322129 | |||||||
| chr3:44322357 | T | C | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4472-735T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322357 | |||||||
| chr3:44322570 | T | C | 1 | a0002c0002t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4472-522T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322570 | |||||||
| chr3:44322647 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
7 | HG01884.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4472-445G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 17/19 | chr3 | 44322647 | |||||||
| chr3:44323311 | A | G | 1 | a0002c0002t0001g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4675+16A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323311 | |||||||
| chr3:44323333 | T | C | 30 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(27): Show |
30 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.4675+38T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323333 | |||||||
| chr3:44323652 | T | A | 1 | a0003c0003t0002g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4675+357T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323652 | |||||||
| chr3:44323722 | A | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0098 |
3 | HG02735.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4675+427A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323722 | |||||||
| chr3:44323916 | C | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4675+621C>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44323916 | |||||||
| chr3:44324091 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0006c0010t0001g0050 others(1): Show |
4 | HG00642.hp2 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.4675+796A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324091 | |||||||
| chr3:44324316 | G | T | 2 | a0002c0002t0001g0167 a0002c0002t0001g0168 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.4675+1021G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324316 | |||||||
| chr3:44324678 | C | G | 1 | a0002c0005t0001g0127 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4675+1383C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324678 | |||||||
| chr3:44324780 | A | T | 1 | a0002c0002t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4675+1485A>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324780 | |||||||
| chr3:44324888 | G | A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4675+1593G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44324888 | |||||||
| chr3:44325082 | G | A | 1 | a0010c0023t0001g0152 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4675+1787G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325082 | |||||||
| chr3:44325315 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
106 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.4675+2020T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325315 | |||||||
| chr3:44325471 | C | T | 1 | a0003c0003t0002g0219 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4675+2176C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325471 | |||||||
| chr3:44325498 | T | G | 2 | a0003c0003t0002g0207 a0003c0003t0002g0217 |
2 | HG00738.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.4675+2203T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325498 | |||||||
| chr3:44325643 | CT | C | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4675+2362delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 44325643 | ||||||
| chr3:44325876 | C | T | 1 | a0003c0003t0002g0203 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4676-2374C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44325876 | |||||||
| chr3:44326401 | C | T | 2 | a0008c0012t0001g0022 a0008c0012t0001g0023 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4676-1849C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44326401 | |||||||
| chr3:44327016 | G | C | 1 | a0007c0011t0001g0005 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4676-1234G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327016 | |||||||
| chr3:44327219 | A | G | 84 | a0001c0001t0001g0012 a0002c0002t0001g0002 a0002c0002t0001g0114 others(81): Show |
87 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.4676-1031A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327219 | |||||||
| chr3:44327377 | TGTTCTAG others(2): Show |
T | 31 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(28): Show |
31 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4676-869_4676-861d others(11): Show |
TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr3 | 44327377 | ||||||
| chr3:44327688 | T | C | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4676-562T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327688 | |||||||
| chr3:44327784 | G | A | 1 | a0011c0018t0001g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4676-466G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327784 | |||||||
| chr3:44327820 | C | T | 1 | a0002c0002t0001g0182 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4676-430C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327820 | |||||||
| chr3:44327951 | C | T | 1 | a0002c0002t0001g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4676-299C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44327951 | |||||||
| chr3:44328115 | T | A | 1 | a0008c0012t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4676-135T>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 18/19 | chr3 | 44328115 | |||||||
| chr3:44328497 | G | T | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4859+64G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328497 | |||||||
| chr3:44328517 | T | C | 1 | a0002c0002t0001g0145 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4859+84T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328517 | |||||||
| chr3:44328557 | G | T | 1 | a0002c0002t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4859+124G>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328557 | |||||||
| chr3:44328665 | T | C | 34 | a0002c0002t0001g0002 a0002c0002t0001g0114 a0002c0002t0001g0115 others(31): Show |
37 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.4859+232T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328665 | |||||||
| chr3:44328814 | G | A | 1 | a0002c0024t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4859+381G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328814 | |||||||
| chr3:44328852 | G | A | 1 | a0002c0002t0001g0233 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4859+419G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44328852 | |||||||
| chr3:44329080 | A | C | 7 | a0002c0006t0001g0009 a0002c0006t0001g0010 a0002c0006t0001g0244 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4859+647A>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329080 | |||||||
| chr3:44329298 | A | G | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4859+865A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329298 | |||||||
| chr3:44329359 | G | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.4859+926G>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329359 | |||||||
| chr3:44329437 | T | C | 1 | a0003c0004t0002g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4859+1004T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329437 | |||||||
| chr3:44329523 | T | C | 3 | a0002c0002t0001g0131 a0002c0002t0001g0135 a0002c0002t0001g0136 |
3 | HG00639.hp1 HG00741.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.4859+1090T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329523 | |||||||
| chr3:44329652 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(242): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.4859+1219C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329652 | |||||||
| chr3:44329880 | C | T | 1 | a0003c0003t0002g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4859+1447C>T | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44329880 | |||||||
| chr3:44330315 | G | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4860-1477G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44330315 | |||||||
| chr3:44330654 | T | C | 40 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0140 others(37): Show |
40 | HG01123.hp2 HG01192.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.4860-1138T>C | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44330654 | |||||||
| chr3:44330810 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4860-982A>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44330810 | |||||||
| chr3:44331186 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4860-606G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331186 | |||||||
| chr3:44331334 | CT | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.4860-448delT | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr3 | 44331334 | ||||||
| chr3:44331377 | G | A | 1 | a0002c0002t0001g0147 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4860-415G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331377 | |||||||
| chr3:44331402 | T | G | 1 | a0008c0012t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4860-390T>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331402 | |||||||
| chr3:44331421 | G | A | 5 | a0004c0007t0001g0170 a0004c0007t0001g0171 a0004c0007t0001g0172 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.4860-371G>A | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331421 | |||||||
| chr3:44331749 | C | G | 3 | a0003c0003t0002g0219 a0003c0003t0002g0221 a0003c0003t0002g0228 |
3 | NA18947.hp2 NA18957.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.4860-43C>G | TOPAZ1 | ENSG00000173769.4 | transcript | ENST00000309765.4 | protein_coding | 19/19 | chr3 | 44331749 |