Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91646 |
| ensemblid | ENSG00000173809.18 |
| hgncid | 25044 |
| symbol | TDRD12 |
| name | tudor domain containing 12 |
| refseq_nuc | NM_001366102.1 |
| refseq_prot | NP_001353031.1 |
| ensembl_nuc | ENST00000639142.2 |
| ensembl_prot | ENSP00000492643.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 32719767 |
| end | 32829580 |
| strand | + |
| ver | v1.2 |
| region | chr19:32719767-32829580 |
| region5000 | chr19:32714767-32834580 |
| regionname0 | TDRD12_chr19_32719767_32829580 |
| regionname5000 | TDRD12_chr19_32714767_32834580 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1330 | 128 | 26 | 11 | 78 | 4 | 9 | 58 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0002 | 0/0 | 1330 | 89 | 13 | 12 | 57 | 0 | 7 | 50 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0003 | 1/1 | 1330 | 85 | 18 | 18 | 29 | 4 | 14 | 17 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0004 | 0/0 | 1330 | 24 | 19 | 0 | 0 | 0 | 5 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0005 | 0/0 | 1330 | 11 | 0 | 1 | 10 | 0 | 0 | 7 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0006 | 0/0 | 1330 | 8 | 1 | 1 | 1 | 1 | 4 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0007 | 0/0 | 1330 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0008 | 0/0 | 1330 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0009 | 0/0 | 1330 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0010 | 0/0 | 1330 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0011 | 0/0 | 1330 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0012 | 0/0 | 1330 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0013 | 0/0 | 1330 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0014 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0015 | 0/0 | 1330 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0016 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0017 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0018 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0019 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0020 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0021 | 0/0 | 1330 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0022 | 0/0 | 1330 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0023 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0024 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0025 | 0/0 | 800 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(795): Show |
chr19 | 32714767 | 32834580 |
| a0026 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| a0027 | 0/0 | 1330 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | MLQLL others(1325): Show |
chr19 | 32714767 | 32834580 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3990 | 112 | 17 | 10 | 72 | 4 | 9 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0001c0007 | 0/0 | 3990 | 7 | 7 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0001c0008 | 0/0 | 3990 | 5 | 0 | 0 | 5 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0001c0017 | 0/0 | 3990 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0001c0019 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0001c0031 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0002c0003 | 0/0 | 3990 | 85 | 13 | 9 | 57 | 0 | 6 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0002c0010 | 0/0 | 3990 | 4 | 0 | 3 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0003c0002 | 1/1 | 3990 | 85 | 18 | 18 | 29 | 4 | 14 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0004c0004 | 0/0 | 3990 | 24 | 19 | 0 | 0 | 0 | 5 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0005c0005 | 0/0 | 3990 | 11 | 0 | 1 | 10 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0006c0006 | 0/0 | 3990 | 8 | 1 | 1 | 1 | 1 | 4 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0007c0011 | 0/0 | 3990 | 4 | 0 | 0 | 4 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0008c0012 | 0/0 | 3990 | 4 | 0 | 0 | 4 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0009c0009 | 0/0 | 3990 | 4 | 0 | 2 | 0 | 1 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0010c0013 | 0/0 | 3990 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0011c0016 | 0/0 | 3990 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0012c0015 | 0/0 | 3990 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0013c0014 | 0/0 | 3990 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0014c0026 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0015c0028 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0016c0027 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0017c0032 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0018c0033 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0019c0022 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0020c0021 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0021c0024 | 0/0 | 3990 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0022c0018 | 0/0 | 3990 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0023c0020 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0024c0025 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0025c0029 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(4005): Show |
chr19 | 32714767 | 32834580 | ||
| a0026c0030 | 0/0 | 3990 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 | ||
| a0027c0023 | 0/0 | 3990 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | ATGCT others(3985): Show |
chr19 | 32714767 | 32834580 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003 | 0/0 | 6622 | 47 | 0 | 5 | 35 | 2 | 5 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0004 | 0/0 | 6626 | 28 | 0 | 1 | 25 | 0 | 2 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6621): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0005 | 0/0 | 6623 | 10 | 7 | 1 | 2 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0007 | 0/0 | 6624 | 3 | 2 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6619): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0010 | 0/0 | 6627 | 7 | 1 | 1 | 5 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6622): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0012 | 0/0 | 6612 | 5 | 1 | 0 | 2 | 0 | 2 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0018 | 0/0 | 6626 | 2 | 1 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6621): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0020 | 0/0 | 6613 | 2 | 0 | 0 | 1 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6608): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0022 | 0/0 | 6623 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0025 | 0/0 | 6624 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6619): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0026 | 0/0 | 6612 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0029 | 0/0 | 6625 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6620): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0030 | 0/0 | 6626 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6621): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0031 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6620): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0032 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6621): Show |
chr19 | 32714767 | 32834580 |
| a0001c0001t0044 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0001c0007t0009 | 0/0 | 6613 | 7 | 7 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6608): Show |
chr19 | 32714767 | 32834580 |
| a0001c0008t0003 | 0/0 | 6622 | 4 | 0 | 0 | 4 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0001c0008t0005 | 0/0 | 6623 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0001c0017t0021 | 0/0 | 6612 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0001c0019t0004 | 0/0 | 6626 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6621): Show |
chr19 | 32714767 | 32834580 |
| a0001c0031t0003 | 0/0 | 6622 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0001 | 0/0 | 6605 | 71 | 13 | 9 | 44 | 0 | 5 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0002 | 0/0 | 6612 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0011 | 0/0 | 6605 | 6 | 0 | 0 | 6 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0033 | 0/0 | 6605 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0034 | 0/0 | 6605 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0035 | 0/0 | 6605 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0036 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6604): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0037 | 0/0 | 6605 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0040 | 0/0 | 6608 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6603): Show |
chr19 | 32714767 | 32834580 |
| a0002c0003t0041 | 0/0 | 6608 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6603): Show |
chr19 | 32714767 | 32834580 |
| a0002c0010t0001 | 0/0 | 6605 | 3 | 0 | 2 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0002c0010t0039 | 0/0 | 6608 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6603): Show |
chr19 | 32714767 | 32834580 |
| a0003c0002t0002 | 1/1 | 6612 | 63 | 5 | 17 | 25 | 2 | 12 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0003c0002t0008 | 0/0 | 6613 | 7 | 2 | 1 | 3 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6608): Show |
chr19 | 32714767 | 32834580 |
| a0003c0002t0013 | 0/0 | 6613 | 5 | 5 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6608): Show |
chr19 | 32714767 | 32834580 |
| a0003c0002t0015 | 0/0 | 6611 | 5 | 1 | 0 | 1 | 1 | 2 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6606): Show |
chr19 | 32714767 | 32834580 |
| a0003c0002t0019 | 0/0 | 6612 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0003c0002t0023 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0003c0002t0043 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0004c0004t0005 | 0/0 | 6623 | 16 | 11 | 0 | 0 | 0 | 5 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0004c0004t0007 | 0/0 | 6624 | 5 | 5 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6619): Show |
chr19 | 32714767 | 32834580 |
| a0004c0004t0016 | 0/0 | 6623 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0005c0005t0006 | 0/0 | 6621 | 8 | 0 | 0 | 8 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6616): Show |
chr19 | 32714767 | 32834580 |
| a0005c0005t0014 | 0/0 | 6622 | 2 | 0 | 1 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0005c0005t0027 | 0/0 | 6623 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0006c0006t0006 | 0/0 | 6621 | 4 | 0 | 1 | 1 | 0 | 2 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6616): Show |
chr19 | 32714767 | 32834580 |
| a0006c0006t0014 | 0/0 | 6622 | 3 | 1 | 0 | 0 | 1 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0006c0006t0028 | 0/0 | 6623 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0007c0011t0004 | 0/0 | 6626 | 4 | 0 | 0 | 4 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6621): Show |
chr19 | 32714767 | 32834580 |
| a0008c0012t0002 | 0/0 | 6612 | 3 | 0 | 0 | 3 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0008c0012t0008 | 0/0 | 6613 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6608): Show |
chr19 | 32714767 | 32834580 |
| a0009c0009t0001 | 0/0 | 6605 | 4 | 0 | 2 | 0 | 1 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0010c0013t0002 | 0/0 | 6612 | 3 | 3 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0011c0016t0003 | 0/0 | 6622 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0012c0015t0017 | 0/0 | 6625 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6620): Show |
chr19 | 32714767 | 32834580 |
| a0013c0014t0003 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0013c0014t0012 | 0/0 | 6612 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0014c0026t0003 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0015c0028t0024 | 0/0 | 6612 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0016c0027t0038 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0017c0032t0005 | 0/0 | 6623 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6618): Show |
chr19 | 32714767 | 32834580 |
| a0018c0033t0007 | 0/0 | 6624 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6619): Show |
chr19 | 32714767 | 32834580 |
| a0019c0022t0001 | 0/0 | 6605 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0020c0021t0018 | 0/0 | 6626 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6621): Show |
chr19 | 32714767 | 32834580 |
| a0021c0024t0001 | 0/0 | 6605 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0022c0018t0042 | 0/0 | 6612 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6607): Show |
chr19 | 32714767 | 32834580 |
| a0023c0020t0001 | 0/0 | 6605 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0024c0025t0003 | 0/0 | 6622 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6617): Show |
chr19 | 32714767 | 32834580 |
| a0025c0029t0004 | 0/0 | 6646 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6641): Show |
chr19 | 32714767 | 32834580 |
| a0026c0030t0001 | 0/0 | 6605 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6600): Show |
chr19 | 32714767 | 32834580 |
| a0027c0023t0017 | 0/0 | 6625 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | CTGCT others(6620): Show |
chr19 | 32714767 | 32834580 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0010g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0010g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0010g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0012g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0012g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0012g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0012g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0018g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0018g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0020g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0020g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0022g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0025g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0026g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0029g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0030g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0031g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0032g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0001t0044g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0007t0009g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0007t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0007t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0007t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0007t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0007t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0008t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0008t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0008t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0008t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0008t0005g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0017t0021g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0017t0021g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0019t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0001c0031t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0011g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0011g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0033g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0034g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0035g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0036g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0037g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0040g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0003t0041g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0010t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0010t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0010t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0002c0010t0039g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0080 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0008g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0013g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0015g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0015g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0015g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0015g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0019g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0019g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0023g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0003c0002t0043g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0005g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0004c0004t0016g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0014g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0014g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0005c0005t0027g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0006g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0006g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0014g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0014g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0006c0006t0028g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0007c0011t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0007c0011t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0007c0011t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0007c0011t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0008c0012t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0008c0012t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0008c0012t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0008c0012t0008g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0009c0009t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0009c0009t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0009c0009t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0009c0009t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0010c0013t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0010c0013t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0010c0013t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0011c0016t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0011c0016t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0012c0015t0017g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0012c0015t0017g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0013c0014t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0013c0014t0012g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0014c0026t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0015c0028t0024g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0016c0027t0038g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0017c0032t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0018c0033t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0019c0022t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0020c0021t0018g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0021c0024t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0022c0018t0042g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0023c0020t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0024c0025t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0025c0029t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0026c0030t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| a0027c0023t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0002 | t0002 | g0051 | EUR | GBR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00099 | hp2 | a0006 | c0006 | t0014 | g0259 | EUR | GBR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00140 | hp1 | a0003 | c0002 | t0002 | g0083 | EUR | GBR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0309 | EUR | GBR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0341 | EUR | FIN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00323 | hp2 | a0001 | c0001 | t0020 | g0156 | EUR | FIN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00408 | hp1 | a0003 | c0002 | t0002 | g0025 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00423 | hp1 | a0003 | c0002 | t0008 | g0067 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00423 | hp2 | a0007 | c0011 | t0004 | g0153 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00438 | hp2 | a0001 | c0008 | t0005 | g0363 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00544 | hp1 | a0014 | c0026 | t0003 | g0352 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00544 | hp2 | a0003 | c0002 | t0002 | g0027 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00558 | hp1 | a0002 | c0003 | t0011 | g0241 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0183 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00597 | hp2 | a0007 | c0011 | t0004 | g0199 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00609 | hp1 | a0008 | c0012 | t0002 | g0019 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0376 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00639 | hp1 | a0003 | c0002 | t0002 | g0073 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00639 | hp2 | a0002 | c0010 | t0039 | g0256 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0257 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00673 | hp1 | a0003 | c0002 | t0002 | g0081 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | CHS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00735 | hp1 | a0003 | c0002 | t0008 | g0072 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG00735 | hp2 | a0002 | c0010 | t0001 | g0251 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0254 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01069 | hp2 | a0009 | c0009 | t0001 | g0225 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01070 | hp1 | a0011 | c0016 | t0003 | g0350 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01070 | hp2 | a0003 | c0002 | t0002 | g0046 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01071 | hp1 | a0011 | c0016 | t0003 | g0347 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01071 | hp2 | a0009 | c0009 | t0001 | g0226 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0330 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01074 | hp2 | a0006 | c0006 | t0006 | g0246 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01109 | hp1 | a0003 | c0002 | t0002 | g0041 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01109 | hp2 | a0015 | c0028 | t0024 | g0096 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0267 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01168 | hp2 | a0003 | c0002 | t0002 | g0084 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01169 | hp1 | a0003 | c0002 | t0002 | g0074 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0266 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01175 | hp1 | a0001 | c0001 | t0018 | g0099 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01175 | hp2 | a0003 | c0002 | t0002 | g0058 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01243 | hp1 | a0002 | c0010 | t0001 | g0218 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01243 | hp2 | a0003 | c0002 | t0002 | g0048 | AMR | PUR | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0346 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01257 | hp2 | a0003 | c0002 | t0002 | g0001 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01258 | hp1 | a0003 | c0002 | t0002 | g0001 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0336 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01261 | hp1 | a0003 | c0002 | t0002 | g0008 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0265 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01358 | hp2 | a0003 | c0002 | t0002 | g0044 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0191 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0146 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01496 | hp1 | a0003 | c0002 | t0002 | g0060 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0311 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01516 | hp1 | a0003 | c0002 | t0008 | g0082 | EUR | IBS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0317 | EUR | IBS | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01884 | hp1 | a0016 | c0027 | t0038 | g0110 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01884 | hp2 | a0017 | c0032 | t0005 | g0323 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01891 | hp1 | a0004 | c0004 | t0005 | g0128 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0281 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0205 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01952 | hp2 | a0003 | c0002 | t0002 | g0068 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0291 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01975 | hp2 | a0003 | c0002 | t0002 | g0071 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01978 | hp1 | a0003 | c0002 | t0002 | g0075 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01978 | hp2 | a0001 | c0031 | t0003 | g0338 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0211 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01981 | hp2 | a0003 | c0002 | t0002 | g0022 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0138 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02027 | hp2 | a0003 | c0002 | t0002 | g0012 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0263 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02055 | hp1 | a0018 | c0033 | t0007 | g0095 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02055 | hp2 | a0004 | c0004 | t0005 | g0127 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02056 | hp1 | a0003 | c0002 | t0002 | g0061 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02056 | hp2 | a0005 | c0005 | t0006 | g0112 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02071 | hp1 | a0003 | c0002 | t0002 | g0079 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02074 | hp1 | a0006 | c0006 | t0006 | g0119 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02074 | hp2 | a0001 | c0001 | t0010 | g0171 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02080 | hp2 | a0019 | c0022 | t0001 | g0247 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02083 | hp1 | a0001 | c0008 | t0003 | g0299 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02083 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0222 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02129 | hp2 | a0003 | c0002 | t0002 | g0076 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02132 | hp2 | a0005 | c0005 | t0006 | g0292 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0361 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02145 | hp1 | a0004 | c0004 | t0007 | g0097 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02145 | hp2 | a0002 | c0003 | t0001 | g0283 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | CDX | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02155 | hp2 | a0003 | c0002 | t0002 | g0028 | EAS | CDX | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02165 | hp1 | a0005 | c0005 | t0006 | g0111 | EAS | CDX | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0293 | EAS | CDX | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0296 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02257 | hp2 | a0001 | c0001 | t0044 | g0103 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0277 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0252 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02280 | hp2 | a0003 | c0002 | t0002 | g0035 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02293 | hp1 | a0003 | c0002 | t0002 | g0049 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0327 | AMR | PEL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02523 | hp1 | a0003 | c0002 | t0002 | g0085 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02523 | hp2 | a0003 | c0002 | t0002 | g0026 | EAS | KHV | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0302 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02572 | hp2 | a0001 | c0007 | t0009 | g0107 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02602 | hp1 | a0003 | c0002 | t0002 | g0093 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0295 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02615 | hp2 | a0003 | c0002 | t0002 | g0020 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02622 | hp1 | a0004 | c0004 | t0016 | g0185 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02622 | hp2 | a0020 | c0021 | t0018 | g0189 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02630 | hp1 | a0012 | c0015 | t0017 | g0142 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02630 | hp2 | a0010 | c0013 | t0002 | g0029 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02647 | hp1 | a0001 | c0001 | t0022 | g0318 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02647 | hp2 | a0010 | c0013 | t0002 | g0033 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02698 | hp1 | a0004 | c0004 | t0005 | g0270 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02698 | hp2 | a0003 | c0002 | t0002 | g0054 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02717 | hp1 | a0001 | c0007 | t0009 | g0002 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02717 | hp2 | a0004 | c0004 | t0007 | g0214 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02735 | hp1 | a0009 | c0009 | t0001 | g0275 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02735 | hp2 | a0003 | c0002 | t0002 | g0037 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02738 | hp1 | a0006 | c0006 | t0014 | g0118 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0314 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02809 | hp1 | a0012 | c0015 | t0017 | g0173 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02809 | hp2 | a0004 | c0004 | t0016 | g0213 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02818 | hp1 | a0004 | c0004 | t0005 | g0124 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02818 | hp2 | a0001 | c0007 | t0009 | g0002 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0303 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02886 | hp2 | a0001 | c0001 | t0025 | g0289 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02896 | hp1 | a0003 | c0002 | t0019 | g0057 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02896 | hp2 | a0001 | c0007 | t0009 | g0109 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02897 | hp1 | a0004 | c0004 | t0005 | g0123 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02897 | hp2 | a0001 | c0007 | t0009 | g0108 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02922 | hp1 | a0003 | c0002 | t0013 | g0088 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02922 | hp2 | a0003 | c0002 | t0008 | g0045 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02965 | hp1 | a0003 | c0002 | t0013 | g0091 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02965 | hp2 | a0004 | c0004 | t0005 | g0129 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02970 | hp1 | a0003 | c0002 | t0013 | g0018 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0154 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02976 | hp1 | a0003 | c0002 | t0015 | g0090 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02976 | hp2 | a0001 | c0001 | t0031 | g0181 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03017 | hp1 | a0001 | c0001 | t0012 | g0342 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03017 | hp2 | a0002 | c0003 | t0001 | g0187 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03041 | hp1 | a0003 | c0002 | t0023 | g0017 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03041 | hp2 | a0001 | c0001 | t0018 | g0100 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0286 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0316 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0276 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03130 | hp2 | a0001 | c0017 | t0021 | g0137 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0280 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03139 | hp2 | a0004 | c0004 | t0005 | g0375 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0319 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03209 | hp1 | a0003 | c0002 | t0043 | g0034 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03209 | hp2 | a0003 | c0002 | t0013 | g0016 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03225 | hp1 | a0004 | c0004 | t0005 | g0304 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03225 | hp2 | a0004 | c0004 | t0007 | g0288 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03239 | hp1 | a0004 | c0004 | t0005 | g0271 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03239 | hp2 | a0003 | c0002 | t0002 | g0064 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03453 | hp2 | a0004 | c0004 | t0007 | g0215 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0098 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03486 | hp2 | a0004 | c0004 | t0005 | g0125 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03491 | hp1 | a0006 | c0006 | t0006 | g0238 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03491 | hp2 | a0003 | c0002 | t0015 | g0043 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03516 | hp1 | a0003 | c0002 | t0019 | g0055 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03516 | hp2 | a0003 | c0002 | t0013 | g0015 | AFR | ESN | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03540 | hp1 | a0004 | c0004 | t0005 | g0130 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0356 | AFR | GWD | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03654 | hp1 | a0003 | c0002 | t0002 | g0062 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03654 | hp2 | a0006 | c0006 | t0028 | g0261 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03669 | hp1 | a0003 | c0002 | t0002 | g0092 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03669 | hp2 | a0002 | c0010 | t0001 | g0255 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03688 | hp1 | a0003 | c0002 | t0002 | g0053 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0325 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0351 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0141 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03710 | hp1 | a0004 | c0004 | t0005 | g0272 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03710 | hp2 | a0021 | c0024 | t0001 | g0253 | SAS | PJL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0348 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03831 | hp2 | a0004 | c0004 | t0005 | g0269 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03834 | hp1 | a0002 | c0003 | t0037 | g0207 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03834 | hp2 | a0003 | c0002 | t0002 | g0050 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0332 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03927 | hp2 | a0003 | c0002 | t0002 | g0014 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0208 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04115 | hp2 | a0003 | c0002 | t0002 | g0078 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0182 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04184 | hp2 | a0003 | c0002 | t0015 | g0009 | SAS | BEB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04199 | hp1 | a0022 | c0018 | t0042 | g0021 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04199 | hp2 | a0003 | c0002 | t0002 | g0180 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04204 | hp1 | a0006 | c0006 | t0006 | g0113 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04204 | hp2 | a0004 | c0004 | t0005 | g0268 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0287 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0188 | SAS | STU | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18522 | hp1 | a0003 | c0002 | t0008 | g0011 | AFR | YRI | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | YRI | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18612 | hp1 | a0001 | c0001 | t0029 | g0163 | EAS | CHB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | CHB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | CHB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18747 | hp2 | a0001 | c0001 | t0020 | g0133 | EAS | CHB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18939 | hp1 | a0003 | c0002 | t0002 | g0038 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0344 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18941 | hp1 | a0003 | c0002 | t0002 | g0047 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0374 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18942 | hp2 | a0002 | c0003 | t0040 | g0227 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0237 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18944 | hp2 | a0005 | c0005 | t0006 | g0116 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18945 | hp1 | a0003 | c0002 | t0002 | g0042 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18946 | hp2 | a0002 | c0003 | t0001 | g0229 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0219 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18948 | hp1 | a0002 | c0003 | t0011 | g0198 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18949 | hp1 | a0008 | c0012 | t0002 | g0023 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18949 | hp2 | a0005 | c0005 | t0006 | g0117 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18950 | hp1 | a0007 | c0011 | t0004 | g0151 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18951 | hp1 | a0002 | c0003 | t0034 | g0210 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18951 | hp2 | a0001 | c0008 | t0003 | g0358 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0232 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18956 | hp2 | a0002 | c0003 | t0001 | g0230 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18960 | hp2 | a0001 | c0001 | t0030 | g0166 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18961 | hp1 | a0003 | c0002 | t0015 | g0024 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0200 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18963 | hp1 | a0001 | c0008 | t0003 | g0315 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18963 | hp2 | a0002 | c0003 | t0041 | g0236 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18966 | hp1 | a0024 | c0025 | t0003 | g0343 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0201 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18967 | hp1 | a0008 | c0012 | t0002 | g0077 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18967 | hp2 | a0002 | c0003 | t0011 | g0190 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18969 | hp1 | a0013 | c0014 | t0012 | g0334 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0258 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18972 | hp1 | a0002 | c0003 | t0011 | g0104 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18972 | hp2 | a0001 | c0008 | t0003 | g0359 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18973 | hp2 | a0005 | c0005 | t0006 | g0120 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18974 | hp1 | a0003 | c0002 | t0002 | g0087 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0294 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18978 | hp1 | a0003 | c0002 | t0002 | g0005 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18978 | hp2 | a0025 | c0029 | t0004 | g0140 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18979 | hp1 | a0001 | c0001 | t0012 | g0132 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18979 | hp2 | a0002 | c0003 | t0002 | g0235 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18980 | hp1 | a0005 | c0005 | t0014 | g0115 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18981 | hp1 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18982 | hp2 | a0003 | c0002 | t0002 | g0007 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18983 | hp2 | a0003 | c0002 | t0002 | g0065 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18986 | hp1 | a0001 | c0001 | t0012 | g0362 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18989 | hp1 | a0003 | c0002 | t0002 | g0066 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18989 | hp2 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18990 | hp1 | a0001 | c0019 | t0004 | g0144 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18990 | hp2 | a0002 | c0003 | t0033 | g0203 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0366 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18998 | hp1 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18998 | hp2 | a0001 | c0001 | t0010 | g0179 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18999 | hp1 | a0003 | c0002 | t0008 | g0069 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19000 | hp1 | a0008 | c0012 | t0008 | g0364 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19002 | hp1 | a0003 | c0002 | t0002 | g0039 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0360 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19005 | hp2 | a0002 | c0003 | t0011 | g0010 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19007 | hp1 | a0007 | c0011 | t0004 | g0158 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19007 | hp2 | a0002 | c0003 | t0035 | g0242 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0168 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19011 | hp1 | a0026 | c0030 | t0001 | g0216 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19012 | hp2 | a0005 | c0005 | t0006 | g0114 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19030 | hp1 | a0004 | c0004 | t0005 | g0301 | AFR | LWK | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19030 | hp2 | a0003 | c0002 | t0019 | g0056 | AFR | LWK | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19043 | hp1 | a0027 | c0023 | t0017 | g0186 | AFR | LWK | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19043 | hp2 | a0004 | c0004 | t0007 | g0212 | AFR | LWK | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19055 | hp1 | a0003 | c0002 | t0002 | g0089 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19055 | hp2 | a0002 | c0003 | t0001 | g0194 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0231 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0273 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19057 | hp2 | a0003 | c0002 | t0002 | g0052 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19060 | hp1 | a0003 | c0002 | t0002 | g0040 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19062 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0204 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0250 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19068 | hp2 | a0002 | c0003 | t0001 | g0209 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19074 | hp1 | a0003 | c0002 | t0002 | g0031 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0370 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19079 | hp1 | a0002 | c0003 | t0036 | g0202 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19081 | hp1 | a0003 | c0002 | t0002 | g0070 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0233 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19082 | hp2 | a0002 | c0003 | t0011 | g0274 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19083 | hp1 | a0005 | c0005 | t0027 | g0122 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19083 | hp2 | a0001 | c0001 | t0010 | g0162 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0365 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19087 | hp1 | a0002 | c0003 | t0001 | g0228 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19087 | hp2 | a0003 | c0002 | t0008 | g0006 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0234 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0371 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19089 | hp1 | a0002 | c0003 | t0001 | g0243 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0206 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19091 | hp2 | a0013 | c0014 | t0003 | g0298 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0278 | AFR | YRI | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA19240 | hp2 | a0003 | c0002 | t0002 | g0086 | AFR | YRI | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA20805 | hp1 | a0009 | c0009 | t0001 | g0224 | EUR | TSI | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA20805 | hp2 | a0003 | c0002 | t0015 | g0063 | EUR | TSI | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0155 | SAS | GIH | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA20905 | hp2 | a0003 | c0002 | t0002 | g0030 | SAS | GIH | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01123 | hp1 | a0005 | c0005 | t0014 | g0262 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG01123 | hp2 | a0001 | c0001 | t0026 | g0290 | AMR | CLM | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02109 | hp2 | a0010 | c0013 | t0002 | g0032 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02486 | hp1 | a0003 | c0002 | t0002 | g0059 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0285 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02559 | hp1 | a0006 | c0006 | t0014 | g0260 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG02559 | hp2 | a0001 | c0017 | t0021 | g0136 | AFR | ACB | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03471 | hp1 | a0004 | c0004 | t0005 | g0126 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0282 | AFR | MSL | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG06807 | hp1 | a0023 | c0020 | t0001 | g0264 | AFR | USA | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| HG06807 | hp2 | a0001 | c0007 | t0009 | g0105 | AFR | USA | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18955 | hp1 | a0005 | c0005 | t0006 | g0121 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA18955 | hp2 | a0002 | c0003 | t0001 | g0223 | EAS | JPT | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA20300 | hp1 | a0004 | c0004 | t0016 | g0184 | AFR | USA | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA20300 | hp2 | a0001 | c0007 | t0009 | g0106 | AFR | USA | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA21309 | hp1 | a0003 | c0002 | t0002 | g0036 | AFR | LWK | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| NA21309 | hp2 | a0001 | c0001 | t0032 | g0174 | AFR | LWK | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| homoSapiens | chm13v2 | a0003 | c0002 | t0002 | g0094 | REF | REF | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| homoSapiens | grch38p0 | a0003 | c0002 | t0002 | g0080 | REF | REF | TDRD12_chr19_32714767_32834580 | TDRD12 | chr19 | 32714767 | 32834580 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32742882 | G | A | 1 | a0013 | 2 | NA18969.hp1 NA19091.hp2 |
missense_variant | MODERATE | c.422G>A | p.Arg141Gln | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/33 | 728/6612 | 422/3993 | 141/1330 | chr19 | 32742882 | |||
| chr19:32749828 | A | G | 2 | a0010 a0018 |
4 | HG02055.hp1 HG02109.hp2 HG02630.hp2 others(1): Show |
missense_variant | MODERATE | c.541A>G | p.Thr181Ala | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/33 | 847/6612 | 541/3993 | 181/1330 | chr19 | 32749828 | |||
| chr19:32757059 | C | T | 2 | a0008 a0017 |
5 | HG00609.hp1 HG01884.hp2 NA18949.hp1 others(2): Show |
missense_variant | MODERATE | c.794C>T | p.Pro265Leu | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/33 | 1100/6612 | 794/3993 | 265/1330 | chr19 | 32757059 | |||
| chr19:32791018 | A | G | 23 | a0001 a0002 a0004 others(20): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
missense_variant | MODERATE | c.1237A>G | p.Lys413Glu | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/33 | 1543/6612 | 1237/3993 | 413/1330 | chr19 | 32791018 | |||
| chr19:32794778 | G | A | 1 | a0009 | 4 | HG01069.hp2 HG01071.hp2 HG02735.hp1 others(1): Show |
missense_variant | MODERATE | c.1438G>A | p.Gly480Arg | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/33 | 1744/6612 | 1438/3993 | 480/1330 | chr19 | 32794778 | |||
| chr19:32798362 | G | A | 1 | a0012 | 2 | HG02630.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.1685G>A | p.Ser562Asn | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/33 | 1991/6612 | 1685/3993 | 562/1330 | chr19 | 32798362 | |||
| chr19:32800278 | C | T | 1 | a0007 | 4 | HG00423.hp2 HG00597.hp2 NA18950.hp1 others(1): Show |
missense_variant | MODERATE | c.1870C>T | p.Leu624Phe | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 17/33 | 2176/6612 | 1870/3993 | 624/1330 | chr19 | 32800278 | |||
| chr19:32800769 | T | G | 1 | a0023 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.2076T>G | p.Cys692Trp | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/33 | 2382/6612 | 2076/3993 | 692/1330 | chr19 | 32800769 | |||
| chr19:32801774 | A | G | 1 | a0026 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.2098A>G | p.Ile700Val | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/33 | 2404/6612 | 2098/3993 | 700/1330 | chr19 | 32801774 | |||
| chr19:32802701 | C | T | 2 | a0005 a0006 |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
missense_variant | MODERATE | c.2243C>T | p.Thr748Met | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 20/33 | 2549/6612 | 2243/3993 | 748/1330 | chr19 | 32802701 | |||
| chr19:32803042 | G | A | 8 | a0002 a0009 a0019 others(5): Show |
99 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(96): Show |
missense_variant | MODERATE | c.2452G>A | p.Ala818Thr | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/33 | 2758/6612 | 2452/3993 | 818/1330 | chr19 | 32803042 | |||
| chr19:32807593 | C | A | 1 | a0011 | 2 | HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.2597C>A | p.Thr866Lys | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/33 | 2903/6612 | 2597/3993 | 866/1330 | chr19 | 32807593 | |||
| chr19:32807593 | C | T | 1 | a0015 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2597C>T | p.Thr866Met | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/33 | 2903/6612 | 2597/3993 | 866/1330 | chr19 | 32807593 | |||
| chr19:32810139 | T | C | 1 | a0020 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.2699T>C | p.Ile900Thr | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/33 | 3005/6612 | 2699/3993 | 900/1330 | chr19 | 32810139 | |||
| chr19:32811346 | C | T | 2 | a0015 a0016 |
2 | HG01109.hp2 HG01884.hp1 |
missense_variant | MODERATE | c.2974C>T | p.Leu992Phe | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/33 | 3280/6612 | 2974/3993 | 992/1330 | chr19 | 32811346 | |||
| chr19:32811415 | C | A | 1 | a0024 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.3043C>A | p.Pro1015Thr | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/33 | 3349/6612 | 3043/3993 | 1015/1330 | chr19 | 32811415 | |||
| chr19:32813703 | A | G | 1 | a0021 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.3068A>G | p.His1023Arg | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/33 | 3374/6612 | 3068/3993 | 1023/1330 | chr19 | 32813703 | |||
| chr19:32818124 | A | T | 2 | a0005 a0006 |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
missense_variant | MODERATE | c.3350A>T | p.Gln1117Leu | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/33 | 3656/6612 | 3350/3993 | 1117/1330 | chr19 | 32818124 | |||
| chr19:32821086 | C | T | 2 | a0004 a0022 |
25 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(22): Show |
missense_variant | MODERATE | c.3437C>T | p.Thr1146Met | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/33 | 3743/6612 | 3437/3993 | 1146/1330 | chr19 | 32821086 | |||
| chr19:32826495 | A | G | 1 | a0018 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.3719A>G | p.Asn1240Ser | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 31/33 | 4025/6612 | 3719/3993 | 1240/1330 | chr19 | 32826495 | |||
| chr19:32826515 | C | A | 6 | a0005 a0014 a0018 others(3): Show |
16 | HG00544.hp1 HG01123.hp1 HG02055.hp1 others(13): Show |
missense_variant | MODERATE | c.3739C>A | p.Gln1247Lys | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 31/33 | 4045/6612 | 3739/3993 | 1247/1330 | chr19 | 32826515 | |||
| chr19:32826530 | A | G | 2 | a0020 a0027 |
2 | HG02622.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.3754A>G | p.Asn1252Asp | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 31/33 | 4060/6612 | 3754/3993 | 1252/1330 | chr19 | 32826530 | |||
| chr19:32827166 | G | C | 2 | a0015 a0016 |
2 | HG01109.hp2 HG01884.hp1 |
missense_variant&splice_region_variant | MODERATE | c.3892G>C | p.Val1298Leu | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 4198/6612 | 3892/3993 | 1298/1330 | chr19 | 32827166 | |||
| chr19:32827185 | C | T | 1 | a0007 | 4 | HG00423.hp2 HG00597.hp2 NA18950.hp1 others(1): Show |
missense_variant | MODERATE | c.3911C>T | p.Pro1304Leu | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 4217/6612 | 3911/3993 | 1304/1330 | chr19 | 32827185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32756042 | A | G | 1 | a0001c0008 | 5 | HG00438.hp2 HG02083.hp1 NA18951.hp2 others(2): Show |
synonymous_variant | LOW | c.633A>G | p.Ser211Ser | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 7/33 | 939/6612 | 633/3993 | 211/1330 | chr19 | 32756042 | |||
| chr19:32794645 | G | A | 1 | a0001c0019 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.1305G>A | p.Lys435Lys | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/33 | 1611/6612 | 1305/3993 | 435/1330 | chr19 | 32794645 | |||
| chr19:32794750 | C | T | 1 | a0001c0031 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.1410C>T | p.Leu470Leu | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/33 | 1716/6612 | 1410/3993 | 470/1330 | chr19 | 32794750 | |||
| chr19:32800172 | T | C | 1 | a0001c0007 | 7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
synonymous_variant | LOW | c.1764T>C | p.Phe588Phe | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 17/33 | 2070/6612 | 1764/3993 | 588/1330 | chr19 | 32800172 | |||
| chr19:32800304 | C | T | 1 | a0018c0033 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1896C>T | p.Pro632Pro | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 17/33 | 2202/6612 | 1896/3993 | 632/1330 | chr19 | 32800304 | |||
| chr19:32803002 | C | T | 1 | a0001c0017 | 2 | HG02559.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.2412C>T | p.Gly804Gly | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/33 | 2718/6612 | 2412/3993 | 804/1330 | chr19 | 32803002 | |||
| chr19:32811279 | C | T | 1 | a0002c0010 | 4 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(1): Show |
synonymous_variant | LOW | c.2907C>T | p.Ile969Ile | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/33 | 3213/6612 | 2907/3993 | 969/1330 | chr19 | 32811279 | |||
| chr19:32818137 | C | T | 1 | a0018c0033 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.3363C>T | p.Ser1121Ser | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/33 | 3669/6612 | 3363/3993 | 1121/1330 | chr19 | 32818137 | |||
| chr19:32826500 | A | C | 1 | a0018c0033 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.3724A>C | p.Arg1242Arg | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 31/33 | 4030/6612 | 3724/3993 | 1242/1330 | chr19 | 32826500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32719843 | T | C | 1 | a0001c0001t0022 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-230T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/33 | 230 | chr19 | 32719843 | ||||||
| chr19:32719963 | G | A | 2 | a0003c0002t0013 a0003c0002t0023 |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-110G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/33 | 110 | chr19 | 32719963 | ||||||
| chr19:32719996 | G | A | 2 | a0001c0007t0009 a0015c0028t0024 |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/33 | 77 | chr19 | 32719996 | ||||||
| chr19:32720018 | G | A | 2 | a0001c0007t0009 a0015c0028t0024 |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-55G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/33 | 55 | chr19 | 32720018 | ||||||
| chr19:32720026 | G | A | 2 | a0001c0001t0025 a0001c0001t0026 |
2 | HG01123.hp2 HG02886.hp2 |
5_prime_UTR_variant | MODIFIER | c.-47G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/33 | 47 | chr19 | 32720026 | ||||||
| chr19:32827357 | T | TTTTTCTT others(3): Show |
7 | a0001c0001t0003 a0001c0008t0003 a0001c0031t0003 others(4): Show |
57 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*100_*109dupCTTTTC others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827357 | |||||
| chr19:32827368 | T | TTTTCTTT others(2): Show |
2 | a0005c0005t0006 a0006c0006t0006 |
12 | HG01074.hp2 HG02056.hp2 HG02074.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*110insCTTTCT others(3): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827368 | |||||
| chr19:32827372 | C | CT | 3 | a0001c0007t0009 a0003c0002t0008 a0008c0012t0008 |
15 | HG00423.hp1 HG00735.hp1 HG01516.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*130dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 131 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | C | CTTTTCTT others(3): Show |
3 | a0005c0005t0014 a0005c0005t0027 a0006c0006t0014 |
6 | HG00099.hp2 HG01123.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*110insCTTTCT others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | C | CTTTTCTT others(4): Show |
1 | a0006c0006t0028 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109_*110insCTTTCT others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | C | CTTTTCTT others(4): Show |
6 | a0001c0001t0005 a0001c0001t0022 a0001c0008t0005 others(3): Show |
32 | HG00438.hp2 HG01257.hp1 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*110insCTTTTC others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | C | CTTTTCTT others(5): Show |
5 | a0001c0001t0007 a0001c0001t0025 a0001c0001t0029 others(2): Show |
11 | HG01516.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*110insCTTTTC others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | C | CTTTTCTT others(6): Show |
8 | a0001c0001t0004 a0001c0001t0030 a0001c0001t0031 others(5): Show |
39 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*110insCTTTTC others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | C | CTTTTCTT others(7): Show |
4 | a0001c0001t0010 a0001c0001t0018 a0001c0001t0032 others(1): Show |
11 | HG01175.hp1 HG01361.hp2 HG02027.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*109_*110insCTTTTC others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 110 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | C | T | 1 | a0001c0001t0026 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 105 | chr19 | 32827372 | ||||||
| chr19:32827372 | CT | C | 2 | a0003c0002t0015 a0003c0002t0023 |
6 | HG02976.hp1 HG03041.hp1 HG03491.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*130delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 130 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827372 | CTTT | C | 13 | a0002c0003t0001 a0002c0003t0011 a0002c0003t0033 others(10): Show |
93 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*128_*130delTTT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 128 | INFO_REALIGN_3_PRIME | chr19 | 32827372 | |||||
| chr19:32827378 | T | C | 2 | a0015c0028t0024 a0016c0027t0038 |
2 | HG01109.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 111 | chr19 | 32827378 | ||||||
| chr19:32827379 | T | C | 1 | a0002c0010t0039 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 112 | chr19 | 32827379 | ||||||
| chr19:32827380 | T | C | 13 | a0002c0003t0001 a0002c0003t0011 a0002c0003t0033 others(10): Show |
93 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*113T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 113 | chr19 | 32827380 | ||||||
| chr19:32827381 | T | C | 2 | a0002c0003t0040 a0002c0003t0041 |
2 | NA18942.hp2 NA18963.hp2 |
3_prime_UTR_variant | MODIFIER | c.*114T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 114 | chr19 | 32827381 | ||||||
| chr19:32827419 | G | A | 3 | a0003c0002t0013 a0003c0002t0023 a0022c0018t0042 |
7 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*152G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 152 | chr19 | 32827419 | ||||||
| chr19:32827587 | A | C | 2 | a0015c0028t0024 a0016c0027t0038 |
2 | HG01109.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*320A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 320 | chr19 | 32827587 | ||||||
| chr19:32828144 | C | T | 1 | a0001c0007t0009 | 7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*877C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 877 | chr19 | 32828144 | ||||||
| chr19:32828202 | C | T | 1 | a0001c0007t0009 | 7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*935C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 935 | chr19 | 32828202 | ||||||
| chr19:32828239 | C | T | 1 | a0002c0003t0037 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 972 | chr19 | 32828239 | ||||||
| chr19:32828388 | T | TG | 11 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0020 others(8): Show |
52 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1129dupG | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1130 | INFO_REALIGN_3_PRIME | chr19 | 32828388 | |||||
| chr19:32828389 | G | C | 1 | a0002c0003t0033 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1122 | chr19 | 32828389 | ||||||
| chr19:32828390 | G | C | 2 | a0015c0028t0024 a0016c0027t0038 |
2 | HG01109.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1123G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1123 | chr19 | 32828390 | ||||||
| chr19:32828394 | G | T | 2 | a0001c0001t0031 a0002c0003t0011 |
7 | HG00558.hp1 HG02976.hp2 NA18948.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1127G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1127 | chr19 | 32828394 | ||||||
| chr19:32828534 | CTTGT | C | 15 | a0002c0003t0001 a0002c0003t0011 a0002c0003t0033 others(12): Show |
95 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1270_*1273delGTTT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1270 | INFO_REALIGN_3_PRIME | chr19 | 32828534 | |||||
| chr19:32828596 | C | T | 1 | a0003c0002t0019 | 3 | HG02896.hp1 HG03516.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1329C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1329 | chr19 | 32828596 | ||||||
| chr19:32828638 | A | G | 60 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(57): Show |
285 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1371A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1371 | chr19 | 32828638 | ||||||
| chr19:32828640 | T | C | 1 | a0001c0001t0030 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1373T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1373 | chr19 | 32828640 | ||||||
| chr19:32828732 | A | G | 2 | a0002c0003t0035 a0002c0003t0041 |
2 | NA18963.hp2 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1465A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1465 | chr19 | 32828732 | ||||||
| chr19:32828812 | G | A | 1 | a0002c0003t0034 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1545G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1545 | chr19 | 32828812 | ||||||
| chr19:32829177 | C | T | 1 | a0001c0001t0044 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1910C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1910 | chr19 | 32829177 | ||||||
| chr19:32829222 | G | A | 1 | a0003c0002t0043 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1955G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 1955 | chr19 | 32829222 | ||||||
| chr19:32829412 | G | A | 1 | a0004c0004t0016 | 3 | HG02622.hp1 HG02809.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2145G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 2145 | chr19 | 32829412 | ||||||
| chr19:32829497 | G | A | 2 | a0001c0001t0032 a0001c0017t0021 |
3 | HG02559.hp2 HG03130.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2230G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 2230 | chr19 | 32829497 | ||||||
| chr19:32829562 | T | C | 2 | a0015c0028t0024 a0016c0027t0038 |
2 | HG01109.hp2 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2295T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 33/33 | 2295 | chr19 | 32829562 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:32720143 | A | C | 1 | a0002c0003t0001g0376 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.24+47A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720143 | |||||||
| chr19:32720163 | C | T | 197 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0300 others(194): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.24+67C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720163 | |||||||
| chr19:32720169 | C | T | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.24+73C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720169 | |||||||
| chr19:32720319 | C | T | 1 | a0003c0002t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.24+223C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720319 | |||||||
| chr19:32720326 | A | G | 81 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0300 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.24+230A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720326 | |||||||
| chr19:32720440 | A | C | 1 | a0002c0003t0001g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.24+344A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720440 | |||||||
| chr19:32720504 | C | A | 1 | a0002c0003t0001g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.24+408C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720504 | |||||||
| chr19:32720544 | A | C | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.24+448A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720544 | |||||||
| chr19:32720591 | C | G | 1 | a0004c0004t0005g0375 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.24+495C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720591 | |||||||
| chr19:32720651 | C | T | 1 | a0001c0001t0010g0179 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.24+555C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720651 | |||||||
| chr19:32720653 | A | C | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.24+557A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720653 | |||||||
| chr19:32720670 | A | AC | 16 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0300 others(13): Show |
16 | HG00597.hp1 HG00642.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.24+576dupC | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32720670 | ||||||
| chr19:32720673 | G | C | 287 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(284): Show |
290 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.24+577G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720673 | |||||||
| chr19:32720737 | C | T | 50 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(47): Show |
50 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.24+641C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720737 | |||||||
| chr19:32720823 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.24+727C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720823 | |||||||
| chr19:32720905 | C | T | 1 | a0001c0001t0004g0176 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.24+809C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720905 | |||||||
| chr19:32720950 | C | A | 1 | a0002c0003t0001g0294 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.24+854C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720950 | |||||||
| chr19:32720974 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.24+878A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720974 | |||||||
| chr19:32720977 | G | A | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.24+881G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32720977 | |||||||
| chr19:32721049 | G | C | 2 | a0004c0004t0016g0184 a0004c0004t0016g0185 |
2 | HG02622.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.24+953G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721049 | |||||||
| chr19:32721082 | G | A | 8 | a0001c0001t0005g0302 a0001c0001t0005g0305 a0001c0001t0005g0306 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.24+986G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721082 | |||||||
| chr19:32721367 | T | A | 3 | a0003c0002t0002g0005 a0003c0002t0002g0007 a0003c0002t0008g0006 |
3 | NA18978.hp1 NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.24+1271T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721367 | |||||||
| chr19:32721395 | A | AT | 82 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.24+1306dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721395 | ||||||
| chr19:32721424 | T | C | 2 | a0003c0002t0002g0008 a0003c0002t0015g0009 |
2 | HG01261.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.24+1328T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721424 | |||||||
| chr19:32721468 | C | T | 1 | a0002c0003t0001g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.24+1372C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721468 | |||||||
| chr19:32721614 | A | C | 1 | a0005c0005t0006g0292 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.24+1518A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721614 | |||||||
| chr19:32721614 | A | G | 64 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(61): Show |
64 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.24+1518A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721614 | |||||||
| chr19:32721679 | C | CTATTT | 36 | a0001c0001t0004g0134 a0001c0001t0004g0135 a0001c0001t0012g0132 others(33): Show |
36 | HG01168.hp1 HG01169.hp2 HG01358.hp1 others(33): Show |
intron_variant | MODIFIER | c.24+1625_24+1629dup others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721679 | C | CTATTTTA others(3): Show |
66 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(63): Show |
67 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.24+1620_24+1629dup others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721679 | C | CTATTTTA others(8): Show |
25 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(22): Show |
27 | HG00597.hp2 HG01109.hp2 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.24+1615_24+1629dup others(15): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721679 | C | CTATTTTA others(13): Show |
3 | a0002c0003t0001g0187 a0002c0003t0001g0188 a0020c0021t0018g0189 |
3 | HG02622.hp2 HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.24+1610_24+1629dup others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721679 | C | CTATTTTA others(18): Show |
1 | a0027c0023t0017g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.24+1605_24+1629dup others(25): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721679 | CTATTT | C | 81 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(78): Show |
81 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.24+1625_24+1629del others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721679 | CTATTTTA others(3): Show |
C | 16 | a0003c0002t0002g0092 a0003c0002t0002g0093 a0003c0002t0013g0091 others(13): Show |
16 | HG02055.hp1 HG02056.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.24+1620_24+1629del others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721679 | CTATTTTA others(8): Show |
C | 2 | a0001c0001t0003g0373 a0001c0001t0003g0374 |
2 | NA18942.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.24+1615_24+1629del others(15): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721679 | ||||||
| chr19:32721701 | A | ATTTTATT others(116): Show |
1 | a0004c0004t0005g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.24+1629_24+1630ins others(123): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721701 | ||||||
| chr19:32721718 | T | TTTATTTT others(72): Show |
1 | a0004c0004t0005g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.24+1629_24+1630ins others(79): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721718 | ||||||
| chr19:32721718 | T | TTTATTTT others(82): Show |
1 | a0004c0004t0007g0097 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.24+1629_24+1630ins others(89): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721718 | ||||||
| chr19:32721718 | T | TTTATTTT others(77): Show |
2 | a0004c0004t0005g0125 a0004c0004t0005g0126 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.24+1629_24+1630ins others(84): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721718 | ||||||
| chr19:32721718 | T | TTTATTTT others(67): Show |
1 | a0004c0004t0005g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.24+1629_24+1630ins others(74): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721718 | ||||||
| chr19:32721718 | T | TTTATTTT others(72): Show |
2 | a0004c0004t0005g0128 a0004c0004t0005g0129 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.24+1629_24+1630ins others(79): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721718 | ||||||
| chr19:32721718 | T | TTTATTTT others(77): Show |
1 | a0004c0004t0005g0130 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.24+1629_24+1630ins others(84): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721718 | ||||||
| chr19:32721721 | A | G | 7 | a0001c0001t0003g0300 a0001c0001t0003g0367 a0001c0001t0003g0368 others(4): Show |
7 | NA18944.hp1 NA18948.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.24+1625A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721721 | |||||||
| chr19:32721726 | G | A | 1 | a0004c0004t0005g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.24+1630G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721726 | |||||||
| chr19:32721727 | A | T | 1 | a0004c0004t0005g0123 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.24+1631A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721727 | |||||||
| chr19:32721842 | G | C | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.24+1746G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721842 | |||||||
| chr19:32721864 | C | G | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.24+1768C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32721864 | |||||||
| chr19:32721874 | A | AT | 13 | a0001c0001t0003g0365 a0001c0001t0003g0366 a0001c0001t0004g0178 others(10): Show |
13 | HG00099.hp2 HG01123.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.24+1793dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32721874 | ||||||
| chr19:32722125 | G | A | 1 | a0003c0002t0015g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.24+2029G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722125 | |||||||
| chr19:32722225 | A | G | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.24+2129A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722225 | |||||||
| chr19:32722293 | T | C | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.24+2197T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722293 | |||||||
| chr19:32722324 | G | A | 1 | a0005c0005t0006g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.24+2228G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722324 | |||||||
| chr19:32722462 | T | C | 1 | a0003c0002t0002g0014 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.24+2366T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722462 | |||||||
| chr19:32722469 | G | A | 1 | a0001c0001t0010g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.24+2373G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722469 | |||||||
| chr19:32722513 | A | C | 1 | a0004c0004t0007g0288 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.24+2417A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722513 | |||||||
| chr19:32722597 | C | T | 1 | a0002c0003t0037g0207 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.24+2501C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722597 | |||||||
| chr19:32722620 | T | C | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.24+2524T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722620 | |||||||
| chr19:32722671 | TA | T | 14 | a0001c0007t0009g0109 a0002c0003t0001g0205 a0002c0003t0001g0206 others(11): Show |
14 | HG01952.hp1 HG02074.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.24+2583delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32722671 | ||||||
| chr19:32722678 | AAT | A | 98 | a0001c0001t0031g0181 a0001c0007t0009g0002 a0001c0007t0009g0105 others(95): Show |
101 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.24+2583_24+2584del others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722678 | |||||||
| chr19:32722679 | A | T | 2 | a0005c0005t0006g0112 a0005c0005t0027g0122 |
2 | HG02056.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.24+2583A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722679 | |||||||
| chr19:32722679 | AT | A | 94 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(91): Show |
94 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.24+2601delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32722679 | ||||||
| chr19:32722679 | ATT | A | 80 | a0001c0001t0003g0341 a0001c0001t0003g0370 a0001c0001t0003g0374 others(77): Show |
80 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.24+2600_24+2601del others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32722679 | ||||||
| chr19:32722681 | T | A | 3 | a0001c0001t0004g0101 a0001c0001t0004g0139 a0001c0001t0012g0132 |
3 | HG02135.hp2 NA18979.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.24+2585T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722681 | |||||||
| chr19:32722682 | T | A | 47 | a0001c0001t0004g0102 a0001c0001t0004g0134 a0001c0001t0004g0135 others(44): Show |
47 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.24+2586T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722682 | |||||||
| chr19:32722826 | C | T | 2 | a0020c0021t0018g0189 a0027c0023t0017g0186 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.24+2730C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32722826 | |||||||
| chr19:32723076 | A | G | 1 | a0002c0003t0001g0204 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.24+2980A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32723076 | |||||||
| chr19:32723218 | C | T | 1 | a0003c0002t0013g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.24+3122C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32723218 | |||||||
| chr19:32723260 | T | G | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.24+3164T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32723260 | |||||||
| chr19:32723557 | A | G | 1 | a0015c0028t0024g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.24+3461A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32723557 | |||||||
| chr19:32723667 | C | CA | 67 | a0001c0001t0003g0295 a0001c0001t0003g0300 a0001c0001t0003g0367 others(64): Show |
67 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.24+3587dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32723667 | ||||||
| chr19:32723667 | C | CAA | 7 | a0001c0001t0003g0313 a0001c0001t0004g0141 a0001c0001t0018g0099 others(4): Show |
7 | HG01175.hp1 HG03041.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.24+3586_24+3587dup others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32723667 | ||||||
| chr19:32723667 | CA | C | 17 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(14): Show |
18 | HG00140.hp1 HG01109.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.24+3587delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32723667 | ||||||
| chr19:32723743 | A | G | 1 | a0003c0002t0015g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.24+3647A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32723743 | |||||||
| chr19:32723923 | T | C | 216 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(213): Show |
219 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.24+3827T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32723923 | |||||||
| chr19:32724019 | G | T | 21 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(18): Show |
21 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.24+3923G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32724019 | |||||||
| chr19:32724103 | G | A | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.24+4007G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32724103 | |||||||
| chr19:32724310 | G | C | 2 | a0004c0004t0007g0212 a0004c0004t0007g0288 |
2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.24+4214G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32724310 | |||||||
| chr19:32724393 | T | C | 2 | a0002c0003t0001g0191 a0002c0003t0001g0205 |
2 | HG01361.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.24+4297T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32724393 | |||||||
| chr19:32724706 | A | T | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.24+4610A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32724706 | |||||||
| chr19:32725319 | T | C | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.24+5223T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32725319 | |||||||
| chr19:32725424 | T | A | 4 | a0001c0001t0007g0296 a0001c0001t0007g0316 a0001c0001t0007g0317 others(1): Show |
4 | HG01516.hp2 HG02257.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.24+5328T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32725424 | |||||||
| chr19:32725614 | G | T | 1 | a0002c0003t0001g0258 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.24+5518G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32725614 | |||||||
| chr19:32725686 | G | A | 73 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(70): Show |
75 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.24+5590G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32725686 | |||||||
| chr19:32725761 | G | T | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.24+5665G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32725761 | |||||||
| chr19:32725774 | A | G | 289 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(286): Show |
292 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.24+5678A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32725774 | |||||||
| chr19:32725923 | A | G | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.25-5802A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32725923 | |||||||
| chr19:32726024 | G | A | 2 | a0002c0003t0001g0192 a0002c0003t0001g0219 |
2 | NA18947.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.25-5701G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726024 | |||||||
| chr19:32726083 | AT | A | 8 | a0003c0002t0002g0083 a0003c0002t0013g0015 a0003c0002t0013g0016 others(5): Show |
8 | HG00140.hp1 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.25-5627delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32726083 | ||||||
| chr19:32726103 | C | T | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0002c0003t0001g0098 |
3 | HG01175.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.25-5622C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726103 | |||||||
| chr19:32726182 | G | A | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.25-5543G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726182 | |||||||
| chr19:32726293 | G | A | 2 | a0003c0002t0002g0025 a0003c0002t0002g0026 |
2 | HG00408.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.25-5432G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726293 | |||||||
| chr19:32726395 | T | G | 1 | a0003c0002t0002g0005 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.25-5330T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726395 | |||||||
| chr19:32726445 | A | G | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25-5280A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726445 | |||||||
| chr19:32726461 | T | C | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.25-5264T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726461 | |||||||
| chr19:32726476 | A | T | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.25-5249A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726476 | |||||||
| chr19:32726658 | GGAGGATT others(9): Show |
G | 82 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.25-5030_25-5015del others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32726658 | ||||||
| chr19:32726764 | T | A | 9 | a0001c0001t0005g0302 a0001c0001t0005g0305 a0001c0001t0005g0306 others(6): Show |
9 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.25-4961T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32726764 | |||||||
| chr19:32727035 | C | T | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.25-4690C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727035 | |||||||
| chr19:32727105 | T | C | 214 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(211): Show |
217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.25-4620T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727105 | |||||||
| chr19:32727141 | G | GT | 6 | a0001c0001t0004g0101 a0001c0001t0004g0169 a0001c0001t0004g0170 others(3): Show |
6 | HG00438.hp1 HG02074.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.25-4576dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32727141 | ||||||
| chr19:32727142 | T | G | 1 | a0002c0003t0001g0220 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.25-4583T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727142 | |||||||
| chr19:32727231 | C | T | 1 | a0003c0002t0008g0082 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.25-4494C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727231 | |||||||
| chr19:32727409 | C | T | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-4316C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727409 | |||||||
| chr19:32727717 | G | A | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0002c0003t0001g0098 |
3 | HG01175.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.25-4008G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727717 | |||||||
| chr19:32727740 | C | T | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.25-3985C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727740 | |||||||
| chr19:32727783 | C | T | 1 | a0002c0003t0001g0257 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.25-3942C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727783 | |||||||
| chr19:32727928 | G | A | 372 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(369): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.25-3797G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32727928 | |||||||
| chr19:32728443 | G | A | 1 | a0006c0006t0006g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.25-3282G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32728443 | |||||||
| chr19:32728503 | G | A | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-3222G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32728503 | |||||||
| chr19:32728514 | T | A | 1 | a0006c0006t0014g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.25-3211T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32728514 | |||||||
| chr19:32728530 | C | G | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.25-3195C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32728530 | |||||||
| chr19:32728570 | T | C | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.25-3155T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32728570 | |||||||
| chr19:32728594 | G | A | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.25-3131G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32728594 | |||||||
| chr19:32728645 | C | CT | 125 | a0001c0001t0003g0313 a0001c0001t0003g0372 a0001c0001t0004g0175 others(122): Show |
128 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.25-3063dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32728645 | ||||||
| chr19:32728645 | C | CTT | 7 | a0002c0003t0001g0182 a0002c0003t0001g0248 a0002c0003t0001g0249 others(4): Show |
7 | HG01168.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.25-3064_25-3063dup others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32728645 | ||||||
| chr19:32728811 | AT | A | 259 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(256): Show |
262 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.25-2896delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32728811 | ||||||
| chr19:32728811 | ATT | A | 22 | a0001c0001t0004g0134 a0002c0003t0001g0276 a0002c0003t0001g0277 others(19): Show |
22 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.25-2897_25-2896del others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32728811 | ||||||
| chr19:32728893 | C | T | 1 | a0002c0003t0001g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.25-2832C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32728893 | |||||||
| chr19:32729093 | C | T | 50 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(47): Show |
50 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.25-2632C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729093 | |||||||
| chr19:32729104 | A | G | 7 | a0003c0002t0002g0022 a0003c0002t0002g0070 a0003c0002t0002g0071 others(4): Show |
7 | HG00639.hp1 HG00735.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-2621A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729104 | |||||||
| chr19:32729195 | G | A | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.25-2530G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729195 | |||||||
| chr19:32729214 | T | C | 1 | a0003c0002t0002g0027 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.25-2511T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729214 | |||||||
| chr19:32729221 | G | GT | 9 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0360 others(6): Show |
9 | HG02080.hp2 HG02647.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.25-2492dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729221 | ||||||
| chr19:32729221 | G | T | 16 | a0003c0002t0002g0022 a0003c0002t0002g0025 a0003c0002t0002g0026 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.25-2504G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729221 | |||||||
| chr19:32729264 | C | A | 1 | a0004c0004t0005g0269 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.25-2461C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729264 | |||||||
| chr19:32729278 | C | T | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.25-2447C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729278 | |||||||
| chr19:32729359 | G | GGGTATCT others(566): Show |
3 | a0003c0002t0002g0001 a0003c0002t0002g0008 a0003c0002t0015g0063 |
4 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.25-2261_25-1689dup others(573): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729359 | ||||||
| chr19:32729359 | GGGTATCT others(566): Show |
G | 1 | a0001c0001t0004g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.25-2261_25-1689del | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729359 | ||||||
| chr19:32729377 | C | T | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.25-2348C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729377 | |||||||
| chr19:32729406 | A | C | 12 | a0001c0001t0004g0102 a0001c0001t0004g0139 a0001c0001t0004g0160 others(9): Show |
12 | NA18612.hp1 NA18946.hp1 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.25-2319A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729406 | |||||||
| chr19:32729546 | A | G | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.25-2179A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729546 | |||||||
| chr19:32729718 | C | T | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.25-2007C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729718 | |||||||
| chr19:32729765 | ACTTTTT | A | 7 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0120 others(4): Show |
7 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.25-1947_25-1942del others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729765 | ||||||
| chr19:32729778 | C | CT | 78 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0335 others(75): Show |
78 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.25-1919dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729778 | C | CTT | 12 | a0001c0001t0003g0297 a0001c0001t0004g0101 a0001c0001t0004g0102 others(9): Show |
12 | HG00408.hp2 HG00642.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.25-1920_25-1919dup others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729778 | C | CTTTTTTT others(567): Show |
1 | a0003c0002t0002g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.25-1689_25-1688ins others(574): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729778 | C | CTTTTTTT others(569): Show |
1 | a0003c0002t0015g0009 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.25-1919_25-1918ins others(576): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729778 | CT | C | 115 | a0001c0001t0003g0367 a0001c0001t0003g0374 a0001c0001t0005g0302 others(112): Show |
117 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.25-1919delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729778 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0339 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.25-1928_25-1919del others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729778 | CTTTTTTT others(6): Show |
C | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.25-1931_25-1919del others(13): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729778 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.25-1934_25-1919del others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32729778 | ||||||
| chr19:32729789 | T | C | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.25-1936T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729789 | |||||||
| chr19:32729794 | T | G | 1 | a0002c0003t0001g0263 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.25-1931T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32729794 | |||||||
| chr19:32730018 | C | T | 4 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0031g0181 others(1): Show |
4 | HG01175.hp1 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.25-1707C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730018 | |||||||
| chr19:32730067 | G | A | 82 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.25-1658G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730067 | |||||||
| chr19:32730197 | T | C | 1 | a0001c0019t0004g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.25-1528T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730197 | |||||||
| chr19:32730255 | C | A | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25-1470C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730255 | |||||||
| chr19:32730322 | T | C | 1 | a0003c0002t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.25-1403T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730322 | |||||||
| chr19:32730345 | T | C | 3 | a0002c0003t0001g0193 a0002c0003t0001g0222 a0002c0003t0001g0223 |
3 | HG02129.hp1 NA18955.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.25-1380T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730345 | |||||||
| chr19:32730356 | G | A | 50 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(47): Show |
50 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.25-1369G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730356 | |||||||
| chr19:32730366 | G | T | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.25-1359G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730366 | |||||||
| chr19:32730420 | T | C | 317 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(314): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.25-1305T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730420 | |||||||
| chr19:32730484 | A | G | 1 | a0003c0002t0002g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.25-1241A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730484 | |||||||
| chr19:32730496 | T | C | 1 | a0001c0001t0004g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.25-1229T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730496 | |||||||
| chr19:32730577 | A | G | 1 | a0001c0001t0004g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.25-1148A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730577 | |||||||
| chr19:32730653 | G | A | 216 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(213): Show |
219 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.25-1072G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730653 | |||||||
| chr19:32730701 | TTAGG | T | 82 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.25-1021_25-1018del others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32730701 | ||||||
| chr19:32730854 | A | G | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.25-871A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730854 | |||||||
| chr19:32730861 | C | T | 82 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.25-864C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730861 | |||||||
| chr19:32730876 | A | G | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.25-849A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32730876 | |||||||
| chr19:32731250 | C | T | 1 | a0015c0028t0024g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.25-475C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32731250 | |||||||
| chr19:32731339 | G | A | 1 | a0003c0002t0015g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.25-386G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32731339 | |||||||
| chr19:32731346 | G | A | 1 | a0002c0003t0001g0273 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.25-379G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32731346 | |||||||
| chr19:32731375 | C | T | 3 | a0001c0008t0003g0315 a0001c0008t0003g0358 a0001c0008t0003g0359 |
3 | NA18951.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.25-350C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32731375 | |||||||
| chr19:32731391 | T | A | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.25-334T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32731391 | |||||||
| chr19:32731411 | A | T | 1 | a0003c0002t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.25-314A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32731411 | |||||||
| chr19:32731411 | AT | A | 5 | a0001c0001t0004g0178 a0004c0004t0007g0212 a0004c0004t0007g0214 others(2): Show |
5 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.25-306delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr19 | 32731411 | ||||||
| chr19:32731655 | T | C | 1 | a0002c0003t0001g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.25-70T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 1/32 | chr19 | 32731655 | |||||||
| chr19:32731976 | G | A | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.183+93G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32731976 | |||||||
| chr19:32732090 | G | A | 1 | a0005c0005t0006g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.183+207G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32732090 | |||||||
| chr19:32732099 | G | T | 214 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(211): Show |
217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.183+216G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32732099 | |||||||
| chr19:32732144 | C | T | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.183+261C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32732144 | |||||||
| chr19:32732840 | A | C | 1 | a0002c0003t0037g0207 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.183+957A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32732840 | |||||||
| chr19:32732860 | T | C | 82 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.183+977T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32732860 | |||||||
| chr19:32732996 | A | C | 1 | a0003c0002t0002g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.183+1113A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32732996 | |||||||
| chr19:32733008 | TACAAAAG others(8): Show |
T | 1 | a0008c0012t0002g0023 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.183+1127_183+1141d others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32733008 | ||||||
| chr19:32733015 | G | A | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.183+1132G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733015 | |||||||
| chr19:32733053 | G | A | 1 | a0001c0001t0005g0319 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.183+1170G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733053 | |||||||
| chr19:32733062 | A | G | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.183+1179A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733062 | |||||||
| chr19:32733092 | A | C | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.183+1209A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733092 | |||||||
| chr19:32733260 | G | A | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.183+1377G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733260 | |||||||
| chr19:32733468 | C | G | 1 | a0001c0001t0004g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.183+1585C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733468 | |||||||
| chr19:32733470 | C | CA | 272 | a0001c0001t0003g0131 a0001c0001t0003g0297 a0001c0001t0003g0300 others(269): Show |
275 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.183+1601dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32733470 | ||||||
| chr19:32733470 | C | CAA | 8 | a0001c0001t0003g0295 a0002c0003t0001g0265 a0002c0003t0001g0266 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.183+1600_183+1601d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32733470 | ||||||
| chr19:32733592 | A | G | 8 | a0004c0004t0005g0268 a0004c0004t0005g0269 a0004c0004t0005g0270 others(5): Show |
8 | HG02622.hp1 HG02698.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+1709A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733592 | |||||||
| chr19:32733610 | A | G | 1 | a0001c0001t0003g0357 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.183+1727A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733610 | |||||||
| chr19:32733829 | T | A | 3 | a0009c0009t0001g0224 a0009c0009t0001g0225 a0009c0009t0001g0226 |
3 | HG01069.hp2 HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.183+1946T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733829 | |||||||
| chr19:32733838 | C | A | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.183+1955C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733838 | |||||||
| chr19:32733863 | A | T | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.183+1980A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733863 | |||||||
| chr19:32733866 | T | A | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.183+1983T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32733866 | |||||||
| chr19:32733895 | A | AT | 25 | a0001c0001t0004g0178 a0001c0001t0018g0099 a0001c0001t0018g0100 others(22): Show |
25 | HG01175.hp1 HG01981.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.183+2026dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32733895 | ||||||
| chr19:32733895 | A | ATT | 50 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(47): Show |
50 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.183+2025_183+2026d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32733895 | ||||||
| chr19:32734268 | T | C | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.183+2385T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734268 | |||||||
| chr19:32734353 | C | A | 1 | a0001c0001t0003g0320 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.183+2470C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734353 | |||||||
| chr19:32734374 | CT | C | 6 | a0001c0001t0004g0178 a0001c0001t0031g0181 a0002c0003t0011g0104 others(3): Show |
6 | HG02735.hp2 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+2503delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32734374 | ||||||
| chr19:32734457 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2574G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734457 | |||||||
| chr19:32734469 | C | T | 3 | a0003c0002t0002g0020 a0003c0002t0002g0035 a0003c0002t0043g0034 |
3 | HG02280.hp2 HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.183+2586C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734469 | |||||||
| chr19:32734537 | A | AT | 17 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(14): Show |
17 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.183+2661dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32734537 | ||||||
| chr19:32734620 | G | A | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.183+2737G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734620 | |||||||
| chr19:32734641 | G | A | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.183+2758G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734641 | |||||||
| chr19:32734827 | A | T | 3 | a0003c0002t0002g0020 a0003c0002t0002g0035 a0003c0002t0043g0034 |
3 | HG02280.hp2 HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.183+2944A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734827 | |||||||
| chr19:32734876 | T | C | 1 | a0002c0003t0033g0203 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.183+2993T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32734876 | |||||||
| chr19:32735131 | T | C | 1 | a0001c0001t0005g0319 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.183+3248T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735131 | |||||||
| chr19:32735274 | G | GA | 104 | a0001c0001t0003g0295 a0002c0003t0001g0003 a0002c0003t0001g0004 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.183+3401dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32735274 | ||||||
| chr19:32735274 | G | GAA | 13 | a0002c0003t0001g0183 a0002c0003t0001g0194 a0002c0003t0001g0204 others(10): Show |
13 | HG00597.hp1 NA18942.hp2 NA18946.hp2 others(10): Show |
intron_variant | MODIFIER | c.183+3400_183+3401d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32735274 | ||||||
| chr19:32735323 | T | C | 103 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.183+3440T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735323 | |||||||
| chr19:32735466 | C | T | 5 | a0004c0004t0005g0268 a0004c0004t0005g0269 a0004c0004t0005g0270 others(2): Show |
5 | HG02698.hp1 HG03239.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-3390C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735466 | |||||||
| chr19:32735498 | G | A | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.184-3358G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735498 | |||||||
| chr19:32735579 | A | G | 1 | a0003c0002t0002g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.184-3277A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735579 | |||||||
| chr19:32735719 | C | T | 1 | a0009c0009t0001g0275 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.184-3137C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735719 | |||||||
| chr19:32735767 | C | T | 50 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(47): Show |
50 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.184-3089C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735767 | |||||||
| chr19:32735839 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-3017G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32735839 | |||||||
| chr19:32736150 | A | C | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.184-2706A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736150 | |||||||
| chr19:32736189 | G | A | 1 | a0002c0003t0034g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.184-2667G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736189 | |||||||
| chr19:32736286 | C | T | 1 | a0004c0004t0016g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.184-2570C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736286 | |||||||
| chr19:32736295 | A | G | 1 | a0003c0002t0002g0075 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.184-2561A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736295 | |||||||
| chr19:32736429 | C | T | 8 | a0004c0004t0005g0268 a0004c0004t0005g0269 a0004c0004t0005g0270 others(5): Show |
8 | HG02622.hp1 HG02698.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-2427C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736429 | |||||||
| chr19:32736518 | A | G | 1 | a0001c0001t0005g0356 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.184-2338A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736518 | |||||||
| chr19:32736611 | C | T | 1 | a0001c0001t0010g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.184-2245C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736611 | |||||||
| chr19:32736678 | A | G | 1 | a0004c0004t0016g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.184-2178A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736678 | |||||||
| chr19:32736803 | T | C | 1 | a0010c0013t0002g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.184-2053T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736803 | |||||||
| chr19:32736934 | A | T | 1 | a0001c0001t0003g0355 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.184-1922A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736934 | |||||||
| chr19:32736951 | C | T | 1 | a0001c0001t0003g0313 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.184-1905C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736951 | |||||||
| chr19:32736980 | C | T | 1 | a0003c0002t0002g0008 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.184-1876C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32736980 | |||||||
| chr19:32737010 | TA | T | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.184-1844delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32737010 | ||||||
| chr19:32737100 | A | G | 2 | a0010c0013t0002g0029 a0010c0013t0002g0033 |
2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.184-1756A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737100 | |||||||
| chr19:32737150 | G | C | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.184-1706G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737150 | |||||||
| chr19:32737212 | T | A | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.184-1644T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737212 | |||||||
| chr19:32737258 | T | C | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.184-1598T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737258 | |||||||
| chr19:32737457 | G | A | 46 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(43): Show |
46 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.184-1399G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737457 | |||||||
| chr19:32737533 | T | A | 3 | a0002c0003t0001g0233 a0002c0003t0001g0234 a0002c0003t0002g0235 |
3 | NA18979.hp2 NA19081.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.184-1323T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737533 | |||||||
| chr19:32737796 | G | A | 1 | a0003c0002t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.184-1060G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737796 | |||||||
| chr19:32737934 | G | A | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.184-922G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737934 | |||||||
| chr19:32737935 | C | T | 215 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(212): Show |
218 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.184-921C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32737935 | |||||||
| chr19:32738051 | C | T | 1 | a0002c0003t0034g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.184-805C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32738051 | |||||||
| chr19:32738149 | A | C | 1 | a0004c0004t0005g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.184-707A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32738149 | |||||||
| chr19:32738186 | G | A | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.184-670G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32738186 | |||||||
| chr19:32738278 | T | C | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.184-578T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32738278 | |||||||
| chr19:32738590 | C | T | 1 | a0002c0003t0001g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.184-266C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32738590 | |||||||
| chr19:32738678 | C | T | 1 | a0001c0001t0004g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.184-178C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | chr19 | 32738678 | |||||||
| chr19:32738836 | ACT | A | 8 | a0004c0004t0005g0268 a0004c0004t0005g0269 a0004c0004t0005g0270 others(5): Show |
8 | HG02622.hp1 HG02698.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-15_184-14delCT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr19 | 32738836 | ||||||
| chr19:32739025 | T | G | 1 | a0001c0001t0003g0367 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.320+33T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739025 | |||||||
| chr19:32739274 | C | G | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.320+282C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739274 | |||||||
| chr19:32739296 | ACT | A | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+309_320+310del others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739296 | ||||||
| chr19:32739336 | A | ACT | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.320+347_320+348dup others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739336 | ||||||
| chr19:32739410 | TTCTC | T | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.320+424_320+427del others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739410 | ||||||
| chr19:32739504 | C | T | 1 | a0006c0006t0014g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.320+512C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739504 | |||||||
| chr19:32739518 | C | CTGCATCT others(14): Show |
1 | a0004c0004t0005g0269 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.320+560_320+580dup others(21): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739518 | ||||||
| chr19:32739560 | TTGCATCT others(13): Show |
T | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+601_320+620del others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739560 | ||||||
| chr19:32739675 | GCTCTCTG others(13): Show |
G | 26 | a0002c0003t0001g0182 a0002c0003t0001g0252 a0002c0003t0001g0254 others(23): Show |
26 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.320+723_320+742del others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739675 | ||||||
| chr19:32739693 | G | C | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.320+701G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739693 | |||||||
| chr19:32739695 | A | G | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.320+703A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739695 | |||||||
| chr19:32739695 | ACTCTCTG others(15): Show |
A | 4 | a0002c0003t0001g0211 a0002c0003t0001g0265 a0002c0003t0001g0266 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+708_320+729del others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739695 | ||||||
| chr19:32739698 | C | G | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.320+706C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739698 | |||||||
| chr19:32739715 | A | G | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+723A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739715 | |||||||
| chr19:32739718 | C | CTCTGCAT others(13): Show |
1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.320+746_320+765dup others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739718 | ||||||
| chr19:32739718 | C | G | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+726C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739718 | |||||||
| chr19:32739738 | G | C | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+746G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739738 | |||||||
| chr19:32739749 | C | T | 1 | a0009c0009t0001g0275 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.320+757C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739749 | |||||||
| chr19:32739754 | T | C | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+762T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739754 | |||||||
| chr19:32739755 | G | T | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+763G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739755 | |||||||
| chr19:32739775 | C | T | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+783C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739775 | |||||||
| chr19:32739776 | T | G | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+784T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739776 | |||||||
| chr19:32739815 | T | C | 10 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.320+823T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739815 | |||||||
| chr19:32739816 | G | A | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.320+824G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739816 | |||||||
| chr19:32739836 | A | ACTCTCTG others(14): Show |
1 | a0002c0003t0034g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.320+864_320+884dup others(21): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739836 | ||||||
| chr19:32739860 | C | CTCTGCAT others(14): Show |
49 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(46): Show |
49 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.320+883_320+903dup others(21): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739860 | ||||||
| chr19:32739889 | C | CTCCTGGT others(12): Show |
1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.320+903_320+904ins others(19): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32739889 | ||||||
| chr19:32739954 | A | G | 1 | a0001c0001t0003g0295 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.320+962A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739954 | |||||||
| chr19:32739963 | A | C | 1 | a0007c0011t0004g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.320+971A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739963 | |||||||
| chr19:32739981 | G | C | 271 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(268): Show |
274 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.320+989G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32739981 | |||||||
| chr19:32740078 | T | C | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.320+1086T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740078 | |||||||
| chr19:32740119 | A | G | 73 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(70): Show |
75 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.320+1127A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740119 | |||||||
| chr19:32740122 | C | G | 73 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(70): Show |
75 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.320+1130C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740122 | |||||||
| chr19:32740159 | A | ACTCTCTG others(33): Show |
2 | a0001c0017t0021g0136 a0001c0017t0021g0137 |
2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.320+1187_320+1226d others(42): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32740159 | ||||||
| chr19:32740182 | G | C | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.320+1190G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740182 | |||||||
| chr19:32740182 | GTCTGCAT others(13): Show |
G | 1 | a0001c0001t0003g0321 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.320+1207_320+1226d others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32740182 | ||||||
| chr19:32740202 | C | G | 3 | a0003c0002t0013g0018 a0003c0002t0013g0091 a0015c0028t0024g0096 |
3 | HG01109.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.320+1210C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740202 | |||||||
| chr19:32740256 | G | T | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.320+1264G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740256 | |||||||
| chr19:32740260 | T | TCTCTCTG others(13): Show |
1 | a0002c0003t0034g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.320+1286_320+1287i others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32740260 | ||||||
| chr19:32740279 | C | T | 264 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(261): Show |
266 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.320+1287C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740279 | |||||||
| chr19:32740300 | A | G | 1 | a0001c0001t0003g0354 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.320+1308A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740300 | |||||||
| chr19:32740320 | ACTCTCTG others(13): Show |
A | 2 | a0001c0001t0030g0166 a0002c0003t0001g0187 |
2 | HG03017.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.320+1351_320+1370d others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32740320 | ||||||
| chr19:32740344 | T | C | 8 | a0004c0004t0005g0124 a0004c0004t0005g0125 a0004c0004t0005g0126 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.320+1352T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740344 | |||||||
| chr19:32740378 | G | A | 6 | a0002c0003t0001g0211 a0002c0003t0001g0265 a0002c0003t0001g0266 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+1386G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740378 | |||||||
| chr19:32740573 | G | A | 2 | a0001c0001t0010g0179 a0002c0003t0001g0277 |
2 | HG02258.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.320+1581G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740573 | |||||||
| chr19:32740713 | C | T | 65 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(62): Show |
65 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.320+1721C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740713 | |||||||
| chr19:32740716 | T | C | 2 | a0001c0001t0003g0324 a0001c0001t0003g0354 |
2 | NA18973.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.320+1724T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740716 | |||||||
| chr19:32740722 | CA | C | 4 | a0001c0001t0003g0353 a0001c0001t0003g0355 a0001c0001t0012g0362 others(1): Show |
4 | HG00544.hp1 HG02080.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.320+1731delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740722 | |||||||
| chr19:32740788 | C | A | 9 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.320+1796C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740788 | |||||||
| chr19:32740880 | T | C | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.320+1888T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32740880 | |||||||
| chr19:32741560 | G | A | 1 | a0006c0006t0006g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.321-1221G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32741560 | |||||||
| chr19:32741648 | G | A | 1 | a0003c0002t0002g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.321-1133G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32741648 | |||||||
| chr19:32741749 | C | T | 1 | a0002c0003t0001g0232 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.321-1032C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32741749 | |||||||
| chr19:32742040 | C | G | 1 | a0003c0002t0002g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.321-741C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32742040 | |||||||
| chr19:32742056 | G | A | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.321-725G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32742056 | |||||||
| chr19:32742159 | C | CT | 108 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(105): Show |
108 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.321-608dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32742159 | ||||||
| chr19:32742159 | C | CTT | 109 | a0001c0001t0005g0361 a0001c0007t0009g0002 a0001c0007t0009g0107 others(106): Show |
112 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.321-609_321-608dup others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr19 | 32742159 | ||||||
| chr19:32742280 | C | T | 1 | a0015c0028t0024g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.321-501C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32742280 | |||||||
| chr19:32742384 | T | C | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.321-397T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32742384 | |||||||
| chr19:32742518 | A | G | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.321-263A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32742518 | |||||||
| chr19:32742524 | C | G | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.321-257C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 3/32 | chr19 | 32742524 | |||||||
| chr19:32742982 | T | C | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.440+82T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32742982 | |||||||
| chr19:32742993 | G | A | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.440+93G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32742993 | |||||||
| chr19:32743112 | A | G | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.440+212A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743112 | |||||||
| chr19:32743186 | T | C | 1 | a0001c0001t0005g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.440+286T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743186 | |||||||
| chr19:32743202 | C | T | 1 | a0001c0001t0003g0351 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.440+302C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743202 | |||||||
| chr19:32743203 | G | A | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.440+303G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743203 | |||||||
| chr19:32743411 | C | T | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.440+511C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743411 | |||||||
| chr19:32743693 | G | A | 11 | a0002c0003t0001g0252 a0002c0003t0001g0276 a0002c0003t0001g0277 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+793G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743693 | |||||||
| chr19:32743790 | A | C | 1 | a0001c0001t0004g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.440+890A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743790 | |||||||
| chr19:32743920 | C | G | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+1020C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743920 | |||||||
| chr19:32743953 | G | A | 1 | a0002c0003t0001g0280 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.440+1053G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32743953 | |||||||
| chr19:32744028 | C | CA | 6 | a0001c0001t0004g0169 a0002c0003t0001g0208 a0002c0003t0011g0104 others(3): Show |
6 | HG00099.hp2 HG00544.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+1146dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32744028 | ||||||
| chr19:32744122 | A | T | 1 | a0002c0003t0001g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.440+1222A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744122 | |||||||
| chr19:32744206 | T | C | 1 | a0003c0002t0002g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.440+1306T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744206 | |||||||
| chr19:32744222 | C | T | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.440+1322C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744222 | |||||||
| chr19:32744499 | C | CA | 70 | a0001c0001t0003g0348 a0001c0001t0003g0349 a0001c0001t0004g0102 others(67): Show |
71 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.440+1624dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32744499 | ||||||
| chr19:32744499 | C | CAA | 117 | a0001c0001t0003g0131 a0001c0001t0003g0297 a0001c0001t0003g0300 others(114): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.440+1623_440+1624d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32744499 | ||||||
| chr19:32744499 | C | CAAA | 55 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0327 others(52): Show |
56 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.440+1622_440+1624d others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32744499 | ||||||
| chr19:32744499 | C | CAAAA | 8 | a0001c0001t0003g0325 a0001c0001t0003g0326 a0001c0001t0003g0355 others(5): Show |
8 | HG02080.hp1 HG02257.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.440+1621_440+1624d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32744499 | ||||||
| chr19:32744499 | CAAAAAAA others(1): Show |
C | 6 | a0004c0004t0005g0268 a0004c0004t0005g0269 a0004c0004t0005g0272 others(3): Show |
6 | HG02622.hp1 HG02809.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+1617_440+1624d others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32744499 | ||||||
| chr19:32744499 | CAAAAAAA others(7): Show |
C | 1 | a0003c0002t0002g0061 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.440+1611_440+1624d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32744499 | ||||||
| chr19:32744510 | A | AC | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0116 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.440+1610_440+1611i others(3): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744510 | |||||||
| chr19:32744525 | C | A | 81 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.440+1625C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744525 | |||||||
| chr19:32744574 | T | C | 33 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0191 others(30): Show |
35 | HG00558.hp1 HG00597.hp2 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.440+1674T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744574 | |||||||
| chr19:32744583 | G | A | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.440+1683G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744583 | |||||||
| chr19:32744686 | C | G | 1 | a0003c0002t0002g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.440+1786C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744686 | |||||||
| chr19:32744687 | G | A | 3 | a0001c0001t0003g0297 a0001c0001t0003g0327 a0001c0001t0005g0346 |
3 | HG00642.hp1 HG01257.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.440+1787G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744687 | |||||||
| chr19:32744824 | A | C | 4 | a0002c0003t0001g0209 a0002c0003t0001g0217 a0002c0003t0001g0237 others(1): Show |
4 | NA18943.hp2 NA18964.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.440+1924A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32744824 | |||||||
| chr19:32745049 | C | T | 2 | a0001c0001t0004g0134 a0001c0001t0010g0168 |
2 | NA18954.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.440+2149C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745049 | |||||||
| chr19:32745064 | C | T | 1 | a0006c0006t0014g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.440+2164C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745064 | |||||||
| chr19:32745079 | C | A | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.440+2179C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745079 | |||||||
| chr19:32745079 | C | G | 1 | a0005c0005t0006g0117 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.440+2179C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745079 | |||||||
| chr19:32745079 | C | T | 1 | a0003c0002t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440+2179C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745079 | |||||||
| chr19:32745100 | G | A | 1 | a0005c0005t0006g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.440+2200G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745100 | |||||||
| chr19:32745181 | A | G | 1 | a0004c0004t0005g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.440+2281A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745181 | |||||||
| chr19:32745287 | C | T | 45 | a0001c0001t0003g0344 a0001c0001t0003g0345 a0001c0001t0004g0101 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.440+2387C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745287 | |||||||
| chr19:32745643 | A | ATGGCTGA others(141): Show |
19 | a0002c0003t0001g0252 a0002c0003t0001g0276 a0002c0003t0001g0277 others(16): Show |
19 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.440+2769_440+2770i others(150): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745643 | ||||||
| chr19:32745669 | G | C | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.440+2769G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745669 | |||||||
| chr19:32745762 | T | TGA | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-2703_441-2702d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745762 | ||||||
| chr19:32745783 | T | TGTG | 288 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0300 others(285): Show |
291 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.441-2691_441-2690i others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745783 | ||||||
| chr19:32745787 | A | G | 1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.441-2689A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745787 | |||||||
| chr19:32745788 | T | G | 1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.441-2688T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745788 | |||||||
| chr19:32745790 | C | CTG | 58 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(55): Show |
58 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.441-2663_441-2662d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745790 | ||||||
| chr19:32745790 | C | CTGTG | 12 | a0001c0001t0004g0159 a0001c0001t0004g0175 a0001c0019t0004g0144 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.441-2665_441-2662d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745790 | ||||||
| chr19:32745791 | T | A | 1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.441-2685T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745791 | |||||||
| chr19:32745792 | G | T | 1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.441-2684G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745792 | |||||||
| chr19:32745813 | T | A | 16 | a0002c0003t0001g0182 a0002c0003t0001g0211 a0002c0003t0001g0254 others(13): Show |
16 | HG00642.hp2 HG01069.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.441-2663T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745813 | |||||||
| chr19:32745813 | T | TGA | 5 | a0002c0003t0001g0265 a0002c0010t0001g0218 a0002c0010t0001g0251 others(2): Show |
5 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.441-2656_441-2655d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745813 | ||||||
| chr19:32745813 | T | TGTGTGA | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-2662_441-2661i others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745813 | ||||||
| chr19:32745831 | ACTGGCTG others(33): Show |
A | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.441-2617_441-2578d others(42): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745831 | ||||||
| chr19:32745909 | GGAGAGAG others(39): Show |
G | 3 | a0003c0002t0002g0020 a0003c0002t0002g0035 a0003c0002t0043g0034 |
3 | HG02280.hp2 HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.441-2544_441-2499d others(48): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745909 | ||||||
| chr19:32745949 | TGAGAGAG others(45): Show |
T | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.441-2518_441-2467d others(54): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745949 | ||||||
| chr19:32745982 | C | CTGTG | 6 | a0002c0003t0001g0276 a0002c0003t0001g0277 a0002c0003t0001g0280 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-2479_441-2476d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745982 | ||||||
| chr19:32745982 | C | CTGTGTGT others(1): Show |
4 | a0002c0003t0001g0278 a0002c0003t0001g0283 a0002c0003t0001g0284 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-2483_441-2476d others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745982 | ||||||
| chr19:32745984 | G | GTGTGTGT others(183): Show |
1 | a0002c0003t0001g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.441-2476_441-2475i others(192): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745984 | ||||||
| chr19:32745999 | T | A | 2 | a0003c0002t0002g0041 a0003c0002t0002g0064 |
2 | HG01109.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.441-2477T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32745999 | |||||||
| chr19:32745999 | TGA | T | 212 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(209): Show |
215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.441-2468_441-2467d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32745999 | ||||||
| chr19:32746001 | A | AGAGAGAG others(179): Show |
10 | a0002c0003t0001g0276 a0002c0003t0001g0277 a0002c0003t0001g0278 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-2384_441-2383i others(188): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746001 | ||||||
| chr19:32746001 | A | T | 13 | a0001c0001t0003g0333 a0001c0001t0003g0360 a0001c0001t0018g0099 others(10): Show |
13 | HG01175.hp1 HG02257.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.441-2475A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746001 | |||||||
| chr19:32746050 | G | A | 3 | a0003c0002t0002g0005 a0003c0002t0002g0007 a0003c0002t0008g0006 |
3 | NA18978.hp1 NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.441-2426G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746050 | |||||||
| chr19:32746093 | G | C | 81 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.441-2383G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746093 | |||||||
| chr19:32746095 | G | A | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.441-2381G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746095 | |||||||
| chr19:32746238 | G | A | 1 | a0005c0005t0006g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441-2238G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746238 | |||||||
| chr19:32746261 | A | T | 1 | a0001c0001t0003g0311 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.441-2215A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746261 | |||||||
| chr19:32746302 | CAGAGGGG others(39): Show |
C | 2 | a0001c0001t0004g0141 a0001c0001t0004g0155 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.441-1986_441-1941d others(48): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746302 | ||||||
| chr19:32746392 | C | G | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.441-2084C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746392 | |||||||
| chr19:32746398 | G | C | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.441-2078G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746398 | |||||||
| chr19:32746438 | CAG | C | 3 | a0001c0001t0003g0324 a0001c0001t0003g0354 a0001c0001t0003g0357 |
3 | NA18954.hp2 NA18973.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.441-2033_441-2032d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746438 | ||||||
| chr19:32746440 | G | GAGAGGGG others(209): Show |
1 | a0001c0019t0004g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.441-1895_441-1894i others(218): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746440 | ||||||
| chr19:32746474 | C | G | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.441-2002C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746474 | |||||||
| chr19:32746484 | CAG | C | 23 | a0001c0001t0003g0131 a0001c0001t0003g0312 a0001c0001t0003g0313 others(20): Show |
23 | HG00323.hp1 HG00438.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.441-1987_441-1986d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746484 | ||||||
| chr19:32746564 | T | A | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-1912T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746564 | |||||||
| chr19:32746575 | TGA | T | 44 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(41): Show |
44 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.441-1889_441-1888d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746575 | ||||||
| chr19:32746582 | G | A | 232 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(229): Show |
234 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.441-1894G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746582 | |||||||
| chr19:32746584 | G | A | 44 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(41): Show |
44 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.441-1892G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746584 | |||||||
| chr19:32746617 | T | A | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.441-1859T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746617 | |||||||
| chr19:32746767 | T | C | 4 | a0005c0005t0014g0262 a0006c0006t0014g0259 a0006c0006t0014g0260 others(1): Show |
4 | HG00099.hp2 HG01123.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-1709T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746767 | |||||||
| chr19:32746889 | T | A | 4 | a0002c0003t0001g0193 a0002c0003t0001g0222 a0002c0003t0001g0223 others(1): Show |
4 | HG01243.hp1 HG02129.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-1587T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746889 | |||||||
| chr19:32746889 | TGAGA | T | 3 | a0004c0004t0016g0184 a0004c0004t0016g0185 a0004c0004t0016g0213 |
3 | HG02622.hp1 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.441-1571_441-1568d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746889 | ||||||
| chr19:32746908 | G | A | 103 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(100): Show |
105 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.441-1568G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746908 | |||||||
| chr19:32746937 | T | TGA | 282 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(279): Show |
285 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.441-1527_441-1526d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746937 | ||||||
| chr19:32746965 | T | C | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.441-1511T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32746965 | |||||||
| chr19:32746983 | AGAGAGAG others(33): Show |
A | 1 | a0001c0001t0012g0342 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.441-1451_441-1412d others(42): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32746983 | ||||||
| chr19:32747023 | T | TGA | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.441-1447_441-1446d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32747023 | ||||||
| chr19:32747023 | T | TGAGAGAG others(37): Show |
2 | a0002c0003t0001g0195 a0002c0003t0001g0196 |
2 | NA18960.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.441-1446_441-1445i others(46): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr19 | 32747023 | ||||||
| chr19:32747125 | A | G | 2 | a0002c0003t0001g0287 a0002c0003t0001g0291 |
2 | HG01975.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.441-1351A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32747125 | |||||||
| chr19:32747179 | T | A | 1 | a0003c0002t0002g0008 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.441-1297T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32747179 | |||||||
| chr19:32747183 | T | C | 289 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(286): Show |
292 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.441-1293T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32747183 | |||||||
| chr19:32747433 | G | A | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-1043G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32747433 | |||||||
| chr19:32747500 | G | A | 1 | a0001c0001t0032g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441-976G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32747500 | |||||||
| chr19:32747763 | C | A | 1 | a0001c0001t0018g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441-713C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32747763 | |||||||
| chr19:32747939 | C | T | 1 | a0001c0001t0018g0099 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.441-537C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32747939 | |||||||
| chr19:32748043 | T | C | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-433T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32748043 | |||||||
| chr19:32748072 | T | A | 1 | a0004c0004t0005g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.441-404T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32748072 | |||||||
| chr19:32748075 | C | T | 1 | a0003c0002t0002g0060 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.441-401C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32748075 | |||||||
| chr19:32748093 | C | T | 275 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(272): Show |
277 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.441-383C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32748093 | |||||||
| chr19:32748154 | C | T | 1 | a0004c0004t0005g0269 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.441-322C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32748154 | |||||||
| chr19:32748199 | G | T | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.441-277G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32748199 | |||||||
| chr19:32748294 | C | T | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.441-182C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 4/32 | chr19 | 32748294 | |||||||
| chr19:32748544 | C | G | 273 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(270): Show |
275 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.496+13C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32748544 | |||||||
| chr19:32748633 | C | T | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.496+102C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32748633 | |||||||
| chr19:32748706 | C | T | 1 | a0002c0003t0001g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.496+175C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32748706 | |||||||
| chr19:32748818 | G | A | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.496+287G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32748818 | |||||||
| chr19:32748860 | A | G | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+329A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32748860 | |||||||
| chr19:32748904 | T | C | 1 | a0001c0001t0004g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.496+373T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32748904 | |||||||
| chr19:32748940 | T | G | 81 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.496+409T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32748940 | |||||||
| chr19:32749029 | G | A | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.496+498G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749029 | |||||||
| chr19:32749044 | G | C | 1 | a0015c0028t0024g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.496+513G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749044 | |||||||
| chr19:32749054 | T | G | 372 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(369): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.496+523T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749054 | |||||||
| chr19:32749058 | G | A | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.496+527G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749058 | |||||||
| chr19:32749082 | G | A | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.496+551G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749082 | |||||||
| chr19:32749094 | G | A | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.496+563G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749094 | |||||||
| chr19:32749187 | G | C | 1 | a0001c0001t0005g0356 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.497-597G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749187 | |||||||
| chr19:32749348 | TA | T | 275 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(272): Show |
277 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.497-434delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr19 | 32749348 | ||||||
| chr19:32749402 | G | A | 2 | a0013c0014t0003g0298 a0013c0014t0012g0334 |
2 | NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.497-382G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749402 | |||||||
| chr19:32749467 | C | T | 1 | a0001c0001t0004g0102 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.497-317C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749467 | |||||||
| chr19:32749541 | T | C | 81 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.497-243T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749541 | |||||||
| chr19:32749587 | G | A | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.497-197G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749587 | |||||||
| chr19:32749648 | C | A | 1 | a0004c0004t0005g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.497-136C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749648 | |||||||
| chr19:32749664 | G | A | 208 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(205): Show |
210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.497-120G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749664 | |||||||
| chr19:32749704 | T | A | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.497-80T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 5/32 | chr19 | 32749704 | |||||||
| chr19:32750008 | C | T | 1 | a0006c0006t0006g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.582+139C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750008 | |||||||
| chr19:32750083 | CAAGAAAT others(4): Show |
C | 4 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0031g0181 others(1): Show |
4 | HG01175.hp1 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+215_582+225del others(11): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750083 | |||||||
| chr19:32750166 | G | C | 1 | a0004c0004t0005g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.582+297G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750166 | |||||||
| chr19:32750291 | AG | A | 3 | a0001c0001t0003g0332 a0001c0001t0003g0341 a0001c0001t0012g0342 |
3 | HG00323.hp1 HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.582+424delG | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32750291 | ||||||
| chr19:32750322 | C | T | 2 | a0003c0002t0002g0059 a0003c0002t0002g0060 |
2 | HG01496.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.582+453C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750322 | |||||||
| chr19:32750436 | A | T | 2 | a0005c0005t0006g0111 a0005c0005t0006g0120 |
2 | HG02165.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.582+567A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750436 | |||||||
| chr19:32750453 | A | G | 1 | a0001c0001t0005g0307 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.582+584A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750453 | |||||||
| chr19:32750493 | T | G | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+624T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750493 | |||||||
| chr19:32750676 | G | A | 1 | a0002c0003t0001g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.582+807G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750676 | |||||||
| chr19:32750776 | G | C | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.582+907G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750776 | |||||||
| chr19:32750820 | T | C | 8 | a0002c0003t0001g0204 a0002c0003t0001g0221 a0002c0003t0001g0228 others(5): Show |
8 | NA18946.hp2 NA18956.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.582+951T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750820 | |||||||
| chr19:32750826 | T | C | 206 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(203): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.582+957T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32750826 | |||||||
| chr19:32751101 | T | TC | 9 | a0001c0001t0003g0313 a0001c0001t0003g0351 a0001c0001t0004g0175 others(6): Show |
9 | HG01261.hp2 HG02055.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.582+1238dupC | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32751101 | ||||||
| chr19:32751117 | C | T | 2 | a0002c0003t0001g0188 a0002c0003t0001g0208 |
2 | HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.582+1248C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751117 | |||||||
| chr19:32751171 | T | A | 1 | a0003c0002t0002g0042 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.582+1302T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751171 | |||||||
| chr19:32751223 | A | G | 1 | a0003c0002t0002g0022 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.582+1354A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751223 | |||||||
| chr19:32751240 | A | G | 276 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(273): Show |
278 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.582+1371A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751240 | |||||||
| chr19:32751393 | G | A | 1 | a0002c0003t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.582+1524G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751393 | |||||||
| chr19:32751472 | A | G | 2 | a0020c0021t0018g0189 a0027c0023t0017g0186 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.582+1603A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751472 | |||||||
| chr19:32751526 | C | G | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.582+1657C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751526 | |||||||
| chr19:32751568 | C | T | 1 | a0022c0018t0042g0021 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.582+1699C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751568 | |||||||
| chr19:32751577 | C | T | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0002c0003t0001g0098 |
3 | HG01175.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.582+1708C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751577 | |||||||
| chr19:32751746 | T | A | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.582+1877T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751746 | |||||||
| chr19:32751778 | C | G | 1 | a0004c0004t0016g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.582+1909C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751778 | |||||||
| chr19:32751795 | G | A | 102 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.582+1926G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751795 | |||||||
| chr19:32751849 | C | T | 102 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.582+1980C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751849 | |||||||
| chr19:32751884 | A | T | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.582+2015A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32751884 | |||||||
| chr19:32752020 | A | G | 44 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(41): Show |
44 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.582+2151A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752020 | |||||||
| chr19:32752332 | A | G | 1 | a0003c0002t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.582+2463A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752332 | |||||||
| chr19:32752341 | G | A | 1 | a0001c0001t0003g0357 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.582+2472G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752341 | |||||||
| chr19:32752426 | C | T | 2 | a0001c0001t0004g0141 a0001c0001t0004g0155 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.582+2557C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752426 | |||||||
| chr19:32752460 | G | A | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.582+2591G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752460 | |||||||
| chr19:32752592 | G | T | 1 | a0003c0002t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.582+2723G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752592 | |||||||
| chr19:32752593 | G | T | 1 | a0003c0002t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.582+2724G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752593 | |||||||
| chr19:32752790 | C | CT | 16 | a0001c0001t0003g0330 a0001c0001t0004g0101 a0001c0001t0004g0178 others(13): Show |
16 | HG00438.hp2 HG01074.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.582+2941dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32752790 | ||||||
| chr19:32752790 | CT | C | 19 | a0001c0001t0003g0295 a0001c0001t0003g0308 a0001c0001t0005g0346 others(16): Show |
19 | HG00099.hp2 HG01175.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.582+2941delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32752790 | ||||||
| chr19:32752941 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.583-3051C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752941 | |||||||
| chr19:32752949 | C | T | 102 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.583-3043C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752949 | |||||||
| chr19:32752997 | C | T | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.583-2995C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32752997 | |||||||
| chr19:32753083 | C | T | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.583-2909C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753083 | |||||||
| chr19:32753084 | G | A | 208 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(205): Show |
210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.583-2908G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753084 | |||||||
| chr19:32753096 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.583-2896G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753096 | |||||||
| chr19:32753211 | C | G | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.583-2781C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753211 | |||||||
| chr19:32753289 | T | A | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.583-2703T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753289 | |||||||
| chr19:32753404 | T | G | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.583-2588T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753404 | |||||||
| chr19:32753565 | G | A | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.583-2427G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753565 | |||||||
| chr19:32753651 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.583-2341C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753651 | |||||||
| chr19:32753653 | G | A | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.583-2339G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753653 | |||||||
| chr19:32753670 | A | AT | 11 | a0001c0001t0003g0357 a0001c0001t0003g0373 a0001c0001t0003g0374 others(8): Show |
11 | HG00544.hp2 HG01123.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.583-2302dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32753670 | ||||||
| chr19:32753670 | AT | A | 91 | a0001c0001t0004g0102 a0001c0001t0004g0134 a0001c0001t0004g0135 others(88): Show |
91 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.583-2302delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32753670 | ||||||
| chr19:32753670 | ATT | A | 11 | a0001c0001t0010g0146 a0001c0007t0009g0002 a0001c0007t0009g0105 others(8): Show |
12 | HG01109.hp2 HG01361.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.583-2303_583-2302d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32753670 | ||||||
| chr19:32753670 | ATTT | A | 97 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(94): Show |
99 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.583-2304_583-2302d others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32753670 | ||||||
| chr19:32753672 | T | A | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.583-2320T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753672 | |||||||
| chr19:32753688 | T | G | 1 | a0002c0003t0001g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.583-2304T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753688 | |||||||
| chr19:32753738 | C | T | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.583-2254C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753738 | |||||||
| chr19:32753752 | C | T | 54 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(51): Show |
54 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.583-2240C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753752 | |||||||
| chr19:32753794 | G | A | 2 | a0002c0003t0001g0188 a0002c0003t0001g0208 |
2 | HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.583-2198G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753794 | |||||||
| chr19:32753806 | C | T | 1 | a0001c0001t0003g0326 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.583-2186C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753806 | |||||||
| chr19:32753808 | C | T | 3 | a0002c0003t0001g0220 a0002c0003t0001g0232 a0002c0003t0040g0227 |
3 | NA18942.hp2 NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.583-2184C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32753808 | |||||||
| chr19:32754115 | T | C | 282 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(279): Show |
285 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.583-1877T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754115 | |||||||
| chr19:32754224 | T | C | 1 | a0001c0001t0004g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.583-1768T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754224 | |||||||
| chr19:32754359 | C | G | 1 | a0009c0009t0001g0275 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.583-1633C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754359 | |||||||
| chr19:32754469 | C | CA | 16 | a0001c0001t0004g0176 a0001c0001t0004g0178 a0001c0001t0007g0316 others(13): Show |
16 | HG01981.hp2 HG02027.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.583-1515dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32754469 | ||||||
| chr19:32754478 | C | A | 7 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(4): Show |
7 | HG01884.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.583-1514C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754478 | |||||||
| chr19:32754479 | C | T | 2 | a0002c0003t0001g0282 a0002c0003t0001g0286 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.583-1513C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754479 | |||||||
| chr19:32754510 | T | C | 2 | a0002c0003t0001g0192 a0002c0003t0001g0219 |
2 | NA18947.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.583-1482T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754510 | |||||||
| chr19:32754604 | C | A | 1 | a0003c0002t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.583-1388C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754604 | |||||||
| chr19:32754669 | CT | C | 246 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(243): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.583-1299delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32754669 | ||||||
| chr19:32754669 | CTT | C | 22 | a0001c0001t0003g0341 a0001c0001t0003g0367 a0001c0001t0004g0135 others(19): Show |
22 | HG00323.hp1 HG00323.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-1300_583-1299d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr19 | 32754669 | ||||||
| chr19:32754671 | T | C | 1 | a0001c0001t0003g0330 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.583-1321T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754671 | |||||||
| chr19:32754727 | A | C | 3 | a0001c0001t0003g0324 a0001c0001t0003g0354 a0001c0001t0003g0357 |
3 | NA18954.hp2 NA18973.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.583-1265A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754727 | |||||||
| chr19:32754769 | T | C | 1 | a0001c0001t0004g0176 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.583-1223T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754769 | |||||||
| chr19:32754918 | G | A | 1 | a0001c0001t0003g0349 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.583-1074G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754918 | |||||||
| chr19:32754925 | G | A | 1 | a0006c0006t0006g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.583-1067G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754925 | |||||||
| chr19:32754962 | T | A | 1 | a0009c0009t0001g0275 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.583-1030T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754962 | |||||||
| chr19:32754972 | C | T | 44 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(41): Show |
44 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.583-1020C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754972 | |||||||
| chr19:32754981 | A | T | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.583-1011A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754981 | |||||||
| chr19:32754985 | G | A | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.583-1007G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32754985 | |||||||
| chr19:32755126 | C | CAT | 102 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.583-866_583-865ins others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755126 | |||||||
| chr19:32755127 | C | T | 102 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.583-865C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755127 | |||||||
| chr19:32755128 | A | T | 102 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.583-864A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755128 | |||||||
| chr19:32755139 | A | G | 1 | a0003c0002t0008g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583-853A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755139 | |||||||
| chr19:32755411 | A | G | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.583-581A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755411 | |||||||
| chr19:32755416 | C | G | 4 | a0003c0002t0008g0045 a0003c0002t0019g0055 a0003c0002t0019g0056 others(1): Show |
4 | HG02896.hp1 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-576C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755416 | |||||||
| chr19:32755469 | G | A | 1 | a0003c0002t0002g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.583-523G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755469 | |||||||
| chr19:32755693 | G | A | 206 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(203): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.583-299G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755693 | |||||||
| chr19:32755804 | T | C | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.583-188T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755804 | |||||||
| chr19:32755847 | A | C | 1 | a0002c0003t0001g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-145A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755847 | |||||||
| chr19:32755943 | G | A | 1 | a0001c0001t0004g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.583-49G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 6/32 | chr19 | 32755943 | |||||||
| chr19:32756325 | C | T | 53 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(50): Show |
53 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.772+144C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 7/32 | chr19 | 32756325 | |||||||
| chr19:32756395 | G | GT | 81 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.772+224dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr19 | 32756395 | ||||||
| chr19:32756480 | C | T | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.772+299C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 7/32 | chr19 | 32756480 | |||||||
| chr19:32756624 | A | G | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.773-414A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 7/32 | chr19 | 32756624 | |||||||
| chr19:32756677 | C | T | 1 | a0012c0015t0017g0173 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.773-361C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 7/32 | chr19 | 32756677 | |||||||
| chr19:32756746 | T | C | 1 | a0001c0001t0012g0362 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.773-292T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 7/32 | chr19 | 32756746 | |||||||
| chr19:32757152 | T | C | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.865+22T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757152 | |||||||
| chr19:32757278 | A | T | 9 | a0002c0003t0001g0254 a0002c0003t0001g0257 a0002c0003t0001g0287 others(6): Show |
9 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.865+148A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757278 | |||||||
| chr19:32757421 | A | C | 3 | a0009c0009t0001g0224 a0009c0009t0001g0225 a0009c0009t0001g0226 |
3 | HG01069.hp2 HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.865+291A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757421 | |||||||
| chr19:32757485 | T | C | 3 | a0001c0001t0012g0132 a0001c0001t0020g0133 a0001c0001t0020g0156 |
3 | HG00323.hp2 NA18747.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.865+355T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757485 | |||||||
| chr19:32757629 | G | A | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.865+499G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757629 | |||||||
| chr19:32757708 | C | T | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.865+578C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757708 | |||||||
| chr19:32757737 | T | C | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.865+607T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757737 | |||||||
| chr19:32757780 | C | G | 2 | a0001c0001t0003g0312 a0001c0001t0003g0349 |
2 | NA19012.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.865+650C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32757780 | |||||||
| chr19:32758202 | G | A | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.865+1072G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32758202 | |||||||
| chr19:32758220 | G | T | 1 | a0003c0002t0002g0044 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.865+1090G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32758220 | |||||||
| chr19:32758472 | C | A | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.865+1342C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32758472 | |||||||
| chr19:32758561 | G | C | 50 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(47): Show |
50 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.865+1431G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32758561 | |||||||
| chr19:32758699 | T | G | 1 | a0003c0002t0023g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.865+1569T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32758699 | |||||||
| chr19:32758905 | G | C | 103 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(100): Show |
105 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.865+1775G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32758905 | |||||||
| chr19:32759008 | G | C | 206 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(203): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.865+1878G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759008 | |||||||
| chr19:32759446 | G | A | 5 | a0001c0001t0004g0145 a0001c0001t0004g0157 a0001c0017t0021g0136 others(2): Show |
5 | HG02559.hp2 HG03130.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+2316G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759446 | |||||||
| chr19:32759505 | G | T | 2 | a0001c0001t0003g0312 a0001c0001t0003g0349 |
2 | NA19012.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.865+2375G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759505 | |||||||
| chr19:32759522 | G | A | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.865+2392G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759522 | |||||||
| chr19:32759777 | A | G | 31 | a0002c0003t0001g0182 a0002c0003t0001g0211 a0002c0003t0001g0252 others(28): Show |
31 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.865+2647A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759777 | |||||||
| chr19:32759784 | C | T | 102 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.865+2654C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759784 | |||||||
| chr19:32759873 | C | T | 1 | a0001c0001t0022g0318 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.865+2743C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759873 | |||||||
| chr19:32759898 | G | A | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.865+2768G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759898 | |||||||
| chr19:32759947 | C | T | 1 | a0001c0001t0032g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.865+2817C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32759947 | |||||||
| chr19:32760000 | G | A | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.865+2870G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760000 | |||||||
| chr19:32760120 | C | G | 3 | a0003c0002t0002g0001 a0003c0002t0002g0041 a0003c0002t0015g0063 |
4 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.865+2990C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760120 | |||||||
| chr19:32760121 | G | T | 1 | a0001c0019t0004g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.865+2991G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760121 | |||||||
| chr19:32760248 | T | G | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0002c0003t0001g0098 |
3 | HG01175.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.865+3118T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760248 | |||||||
| chr19:32760452 | GGCTAATA others(8): Show |
G | 3 | a0002c0003t0001g0220 a0002c0003t0001g0232 a0002c0003t0040g0227 |
3 | NA18942.hp2 NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.865+3337_865+3351d others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32760452 | ||||||
| chr19:32760582 | A | G | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.865+3452A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760582 | |||||||
| chr19:32760692 | C | G | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.865+3562C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760692 | |||||||
| chr19:32760737 | C | T | 1 | a0005c0005t0006g0112 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.865+3607C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760737 | |||||||
| chr19:32760823 | T | A | 1 | a0001c0001t0004g0178 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.865+3693T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760823 | |||||||
| chr19:32760898 | C | G | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.865+3768C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32760898 | |||||||
| chr19:32761070 | C | T | 1 | a0004c0004t0016g0185 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.865+3940C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761070 | |||||||
| chr19:32761106 | G | A | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.865+3976G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761106 | |||||||
| chr19:32761130 | T | C | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+4000T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761130 | |||||||
| chr19:32761139 | C | T | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.865+4009C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761139 | |||||||
| chr19:32761155 | C | T | 1 | a0003c0002t0002g0074 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.865+4025C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761155 | |||||||
| chr19:32761223 | C | G | 3 | a0003c0002t0002g0020 a0003c0002t0002g0035 a0003c0002t0043g0034 |
3 | HG02280.hp2 HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.865+4093C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761223 | |||||||
| chr19:32761269 | C | T | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+4139C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761269 | |||||||
| chr19:32761372 | C | T | 21 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(18): Show |
21 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.865+4242C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761372 | |||||||
| chr19:32761472 | G | A | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+4342G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761472 | |||||||
| chr19:32761607 | G | A | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.865+4477G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761607 | |||||||
| chr19:32761684 | C | CTTAT | 4 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0002c0003t0001g0098 others(1): Show |
4 | HG01175.hp1 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+4574_865+4577d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32761684 | ||||||
| chr19:32761790 | A | G | 1 | a0002c0003t0001g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.865+4660A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761790 | |||||||
| chr19:32761947 | G | A | 1 | a0003c0002t0002g0061 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.865+4817G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761947 | |||||||
| chr19:32761955 | C | T | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.865+4825C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761955 | |||||||
| chr19:32761956 | G | A | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.865+4826G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32761956 | |||||||
| chr19:32762066 | CT | C | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.865+4939delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32762066 | ||||||
| chr19:32762662 | G | A | 4 | a0001c0001t0004g0135 a0001c0001t0004g0145 a0001c0001t0004g0157 others(1): Show |
4 | NA18962.hp2 NA18978.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+5532G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32762662 | |||||||
| chr19:32762705 | T | C | 1 | a0001c0007t0009g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.865+5575T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32762705 | |||||||
| chr19:32762771 | A | G | 1 | a0003c0002t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.865+5641A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32762771 | |||||||
| chr19:32762782 | T | C | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.865+5652T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32762782 | |||||||
| chr19:32762801 | A | G | 104 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.865+5671A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32762801 | |||||||
| chr19:32763016 | G | A | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.865+5886G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763016 | |||||||
| chr19:32763052 | G | A | 3 | a0001c0001t0003g0333 a0001c0001t0003g0360 a0024c0025t0003g0343 |
3 | NA18964.hp2 NA18966.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.865+5922G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763052 | |||||||
| chr19:32763212 | C | T | 1 | a0001c0001t0003g0330 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.865+6082C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763212 | |||||||
| chr19:32763218 | T | C | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.865+6088T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763218 | |||||||
| chr19:32763371 | T | C | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.865+6241T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763371 | |||||||
| chr19:32763398 | C | G | 12 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(9): Show |
12 | HG02056.hp2 HG02074.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.865+6268C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763398 | |||||||
| chr19:32763612 | TC | T | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.865+6486delC | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32763612 | ||||||
| chr19:32763614 | C | T | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.865+6484C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763614 | |||||||
| chr19:32763682 | G | A | 2 | a0011c0016t0003g0347 a0011c0016t0003g0350 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.865+6552G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763682 | |||||||
| chr19:32763851 | C | G | 2 | a0001c0001t0003g0332 a0001c0001t0012g0342 |
2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.865+6721C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763851 | |||||||
| chr19:32763862 | T | C | 289 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(286): Show |
292 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.865+6732T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763862 | |||||||
| chr19:32763972 | A | G | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.865+6842A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763972 | |||||||
| chr19:32763998 | T | C | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.865+6868T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32763998 | |||||||
| chr19:32764103 | C | CT | 27 | a0001c0001t0003g0324 a0001c0001t0003g0341 a0001c0001t0003g0370 others(24): Show |
27 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.865+6998dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32764103 | ||||||
| chr19:32764103 | C | CTT | 179 | a0001c0001t0003g0300 a0001c0001t0003g0308 a0001c0001t0003g0309 others(176): Show |
181 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.865+6997_865+6998d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32764103 | ||||||
| chr19:32764103 | C | CTTT | 78 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(75): Show |
78 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.865+6996_865+6998d others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32764103 | ||||||
| chr19:32764103 | C | CTTTT | 8 | a0001c0001t0004g0145 a0001c0001t0004g0152 a0001c0001t0004g0172 others(5): Show |
8 | HG00438.hp1 HG02027.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.865+6995_865+6998d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32764103 | ||||||
| chr19:32764195 | C | T | 50 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(47): Show |
50 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.865+7065C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32764195 | |||||||
| chr19:32764240 | A | T | 2 | a0004c0004t0005g0125 a0004c0004t0005g0126 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.865+7110A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32764240 | |||||||
| chr19:32764464 | C | T | 1 | a0004c0004t0005g0304 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.865+7334C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32764464 | |||||||
| chr19:32764682 | C | A | 9 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0007t0009g0002 others(6): Show |
10 | HG01109.hp2 HG01175.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.865+7552C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32764682 | |||||||
| chr19:32764774 | G | A | 1 | a0001c0001t0004g0135 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.865+7644G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32764774 | |||||||
| chr19:32764897 | TTAAAC | T | 23 | a0001c0001t0003g0131 a0001c0001t0003g0312 a0001c0001t0003g0313 others(20): Show |
23 | HG00323.hp1 HG00438.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.865+7772_865+7776d others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32764897 | ||||||
| chr19:32765411 | G | A | 1 | a0006c0006t0006g0246 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.866-7342G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765411 | |||||||
| chr19:32765452 | C | T | 2 | a0003c0002t0002g0027 a0003c0002t0002g0089 |
2 | HG00544.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.866-7301C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765452 | |||||||
| chr19:32765500 | A | C | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.866-7253A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765500 | |||||||
| chr19:32765503 | T | C | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.866-7250T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765503 | |||||||
| chr19:32765504 | G | A | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.866-7249G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765504 | |||||||
| chr19:32765552 | C | T | 3 | a0005c0005t0006g0114 a0005c0005t0006g0116 a0005c0005t0014g0115 |
3 | NA18944.hp2 NA18980.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.866-7201C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765552 | |||||||
| chr19:32765597 | A | T | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.866-7156A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765597 | |||||||
| chr19:32765727 | G | A | 2 | a0020c0021t0018g0189 a0027c0023t0017g0186 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.866-7026G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765727 | |||||||
| chr19:32765805 | G | A | 1 | a0001c0001t0003g0326 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.866-6948G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765805 | |||||||
| chr19:32765805 | G | T | 3 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 |
3 | HG00438.hp1 NA19002.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.866-6948G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765805 | |||||||
| chr19:32765887 | A | T | 1 | a0003c0002t0002g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.866-6866A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765887 | |||||||
| chr19:32765929 | G | T | 282 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(279): Show |
285 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.866-6824G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32765929 | |||||||
| chr19:32766146 | T | TTGTGTCC others(32): Show |
1 | a0003c0002t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.866-6605_866-6567d others(41): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32766146 | ||||||
| chr19:32766252 | A | G | 2 | a0002c0003t0001g0233 a0002c0003t0001g0234 |
2 | NA19081.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.866-6501A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32766252 | |||||||
| chr19:32766276 | G | A | 1 | a0006c0006t0028g0261 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.866-6477G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32766276 | |||||||
| chr19:32766621 | A | AT | 105 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(102): Show |
107 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.866-6121dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32766621 | ||||||
| chr19:32766667 | C | T | 289 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(286): Show |
292 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.866-6086C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32766667 | |||||||
| chr19:32766670 | G | A | 1 | a0003c0002t0008g0082 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.866-6083G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32766670 | |||||||
| chr19:32766771 | C | T | 1 | a0001c0001t0005g0319 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.866-5982C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32766771 | |||||||
| chr19:32766858 | G | A | 2 | a0002c0003t0001g0217 a0002c0003t0001g0244 |
2 | NA18964.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.866-5895G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32766858 | |||||||
| chr19:32767092 | T | TTTTA | 4 | a0001c0001t0020g0156 a0003c0002t0002g0062 a0003c0002t0008g0011 others(1): Show |
4 | HG00323.hp2 HG02630.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-5613_866-5610d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32767092 | ||||||
| chr19:32767092 | TTTTA | T | 73 | a0001c0001t0003g0335 a0001c0001t0003g0344 a0001c0001t0003g0345 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.866-5613_866-5610d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32767092 | ||||||
| chr19:32767092 | TTTTATTT others(1): Show |
T | 174 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(171): Show |
177 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.866-5617_866-5610d others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32767092 | ||||||
| chr19:32767092 | TTTTATTT others(5): Show |
T | 7 | a0001c0001t0004g0143 a0002c0003t0001g0222 a0002c0003t0001g0257 others(4): Show |
7 | HG00642.hp2 HG02129.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.866-5621_866-5610d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32767092 | ||||||
| chr19:32767092 | TTTTATTT others(9): Show |
T | 23 | a0002c0003t0001g0098 a0002c0003t0001g0182 a0002c0003t0001g0252 others(20): Show |
23 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.866-5625_866-5610d others(18): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32767092 | ||||||
| chr19:32767092 | TTTTATTT others(13): Show |
T | 2 | a0001c0001t0032g0174 a0001c0007t0009g0107 |
2 | HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.866-5629_866-5610d others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32767092 | ||||||
| chr19:32767102 | T | G | 1 | a0003c0002t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.866-5651T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767102 | |||||||
| chr19:32767177 | G | A | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.866-5576G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767177 | |||||||
| chr19:32767182 | G | A | 2 | a0001c0001t0005g0319 a0001c0001t0005g0322 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.866-5571G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767182 | |||||||
| chr19:32767221 | T | C | 9 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.866-5532T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767221 | |||||||
| chr19:32767447 | T | C | 3 | a0001c0001t0003g0335 a0001c0001t0005g0328 a0001c0001t0005g0361 |
3 | HG00621.hp1 HG02135.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.866-5306T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767447 | |||||||
| chr19:32767623 | C | T | 1 | a0001c0019t0004g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.866-5130C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767623 | |||||||
| chr19:32767762 | G | C | 2 | a0011c0016t0003g0347 a0011c0016t0003g0350 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.866-4991G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767762 | |||||||
| chr19:32767844 | G | T | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG01109.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.866-4909G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767844 | |||||||
| chr19:32767911 | G | A | 282 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(279): Show |
285 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.866-4842G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767911 | |||||||
| chr19:32767940 | A | G | 1 | a0003c0002t0002g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.866-4813A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767940 | |||||||
| chr19:32767982 | G | C | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.866-4771G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32767982 | |||||||
| chr19:32768069 | T | C | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.866-4684T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32768069 | |||||||
| chr19:32768089 | A | G | 289 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(286): Show |
292 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.866-4664A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32768089 | |||||||
| chr19:32768113 | C | T | 3 | a0003c0002t0002g0005 a0003c0002t0002g0007 a0003c0002t0008g0006 |
3 | NA18978.hp1 NA18982.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.866-4640C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32768113 | |||||||
| chr19:32768385 | CT | C | 9 | a0003c0002t0002g0084 a0004c0004t0005g0123 a0004c0004t0005g0124 others(6): Show |
9 | HG01168.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.866-4353delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32768385 | ||||||
| chr19:32768385 | CTTTTTTT | C | 80 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(77): Show |
80 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.866-4359_866-4353d others(9): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32768385 | ||||||
| chr19:32768497 | G | T | 5 | a0001c0008t0003g0299 a0001c0008t0003g0315 a0001c0008t0003g0358 others(2): Show |
5 | HG00438.hp2 HG02083.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.866-4256G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32768497 | |||||||
| chr19:32768506 | A | G | 1 | a0003c0002t0002g0058 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.866-4247A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32768506 | |||||||
| chr19:32768697 | G | A | 2 | a0001c0001t0025g0289 a0001c0001t0026g0290 |
2 | HG01123.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.866-4056G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32768697 | |||||||
| chr19:32768885 | G | A | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.866-3868G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32768885 | |||||||
| chr19:32769068 | C | T | 5 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(2): Show |
6 | HG02717.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.866-3685C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769068 | |||||||
| chr19:32769114 | A | G | 3 | a0001c0001t0004g0102 a0001c0001t0004g0139 a0001c0001t0004g0165 |
3 | NA18977.hp2 NA19064.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.866-3639A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769114 | |||||||
| chr19:32769219 | TTCTC | T | 15 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(12): Show |
15 | HG01123.hp1 HG02056.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.866-3532_866-3529d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32769219 | ||||||
| chr19:32769640 | AT | A | 105 | a0001c0001t0003g0344 a0001c0007t0009g0002 a0001c0007t0009g0105 others(102): Show |
108 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.866-3100delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32769640 | ||||||
| chr19:32769750 | C | T | 16 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0031g0181 others(13): Show |
16 | HG01175.hp1 HG02257.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.866-3003C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769750 | |||||||
| chr19:32769786 | G | A | 65 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(62): Show |
67 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.866-2967G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769786 | |||||||
| chr19:32769856 | G | A | 200 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(197): Show |
202 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.866-2897G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769856 | |||||||
| chr19:32769951 | A | T | 1 | a0001c0001t0018g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.866-2802A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769951 | |||||||
| chr19:32769963 | G | A | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.866-2790G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769963 | |||||||
| chr19:32769978 | C | T | 1 | a0003c0002t0002g0089 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.866-2775C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32769978 | |||||||
| chr19:32769997 | C | CT | 233 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(230): Show |
236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.866-2743dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32769997 | ||||||
| chr19:32769997 | C | CTT | 56 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(53): Show |
56 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.866-2744_866-2743d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32769997 | ||||||
| chr19:32770230 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.866-2523C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32770230 | |||||||
| chr19:32770323 | A | G | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.866-2430A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32770323 | |||||||
| chr19:32770554 | G | A | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.866-2199G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32770554 | |||||||
| chr19:32770577 | T | C | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.866-2176T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32770577 | |||||||
| chr19:32770627 | G | A | 1 | a0001c0001t0004g0157 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.866-2126G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32770627 | |||||||
| chr19:32770804 | A | G | 1 | a0003c0002t0019g0057 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.866-1949A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32770804 | |||||||
| chr19:32771319 | C | T | 1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.866-1434C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32771319 | |||||||
| chr19:32771429 | G | T | 1 | a0003c0002t0002g0075 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.866-1324G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32771429 | |||||||
| chr19:32771587 | C | CT | 7 | a0002c0003t0035g0242 a0002c0003t0041g0236 a0003c0002t0002g0092 others(4): Show |
7 | HG02145.hp1 HG02602.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.866-1152dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32771587 | ||||||
| chr19:32771587 | CT | C | 22 | a0001c0001t0003g0297 a0001c0007t0009g0002 a0001c0007t0009g0105 others(19): Show |
23 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.866-1152delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | INFO_REALIGN_3_PRIME | chr19 | 32771587 | ||||||
| chr19:32771699 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.866-1054A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32771699 | |||||||
| chr19:32771988 | G | A | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.866-765G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32771988 | |||||||
| chr19:32772104 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.866-649C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772104 | |||||||
| chr19:32772126 | G | A | 4 | a0008c0012t0002g0019 a0008c0012t0002g0023 a0008c0012t0002g0077 others(1): Show |
4 | HG00609.hp1 NA18949.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-627G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772126 | |||||||
| chr19:32772217 | C | T | 2 | a0001c0001t0005g0319 a0001c0001t0005g0322 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.866-536C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772217 | |||||||
| chr19:32772314 | C | T | 1 | a0005c0005t0006g0112 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.866-439C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772314 | |||||||
| chr19:32772323 | A | G | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.866-430A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772323 | |||||||
| chr19:32772385 | A | G | 1 | a0023c0020t0001g0264 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.866-368A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772385 | |||||||
| chr19:32772601 | C | T | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.866-152C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772601 | |||||||
| chr19:32772619 | A | G | 1 | a0002c0003t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.866-134A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772619 | |||||||
| chr19:32772715 | T | C | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.866-38T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 8/32 | chr19 | 32772715 | |||||||
| chr19:32772905 | A | G | 1 | a0001c0001t0022g0318 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.963+55A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 9/32 | chr19 | 32772905 | |||||||
| chr19:32773175 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.964-281C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 9/32 | chr19 | 32773175 | |||||||
| chr19:32773273 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.964-183G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 9/32 | chr19 | 32773273 | |||||||
| chr19:32773388 | GTTCCAAA others(32): Show |
G | 1 | a0022c0018t0042g0021 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.964-67_964-29delTT others(37): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 9/32 | chr19 | 32773388 | |||||||
| chr19:32773442 | G | T | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.964-14G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 9/32 | chr19 | 32773442 | |||||||
| chr19:32773566 | C | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1040+34C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32773566 | |||||||
| chr19:32773567 | G | A | 1 | a0003c0002t0002g0046 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1040+35G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32773567 | |||||||
| chr19:32773572 | C | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1040+40C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32773572 | |||||||
| chr19:32773776 | G | C | 1 | a0002c0003t0001g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1040+244G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32773776 | |||||||
| chr19:32774107 | A | G | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1040+575A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774107 | |||||||
| chr19:32774295 | G | T | 1 | a0002c0003t0001g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1040+763G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774295 | |||||||
| chr19:32774330 | G | A | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.1040+798G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774330 | |||||||
| chr19:32774468 | T | G | 1 | a0002c0003t0001g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1040+936T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774468 | |||||||
| chr19:32774473 | A | T | 99 | a0001c0001t0005g0306 a0001c0001t0044g0103 a0002c0003t0001g0003 others(96): Show |
101 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.1040+941A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774473 | |||||||
| chr19:32774808 | C | G | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1040+1276C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774808 | |||||||
| chr19:32774877 | C | T | 2 | a0001c0001t0003g0333 a0001c0001t0003g0360 |
2 | NA18964.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1040+1345C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774877 | |||||||
| chr19:32774913 | A | G | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+1381A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774913 | |||||||
| chr19:32774970 | A | G | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1040+1438A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774970 | |||||||
| chr19:32774972 | A | G | 1 | a0014c0026t0003g0352 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1040+1440A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774972 | |||||||
| chr19:32774979 | C | T | 6 | a0001c0001t0032g0174 a0001c0001t0044g0103 a0001c0017t0021g0136 others(3): Show |
6 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+1447C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32774979 | |||||||
| chr19:32775254 | T | C | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1040+1722T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32775254 | |||||||
| chr19:32775644 | T | C | 1 | a0001c0001t0004g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1041-1505T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32775644 | |||||||
| chr19:32775777 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1041-1372C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32775777 | |||||||
| chr19:32775838 | G | A | 1 | a0001c0001t0004g0176 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1041-1311G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32775838 | |||||||
| chr19:32775838 | G | T | 2 | a0001c0001t0018g0099 a0001c0001t0018g0100 |
2 | HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1041-1311G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32775838 | |||||||
| chr19:32776044 | G | A | 1 | a0002c0003t0001g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1041-1105G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776044 | |||||||
| chr19:32776061 | G | A | 1 | a0001c0001t0003g0312 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1041-1088G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776061 | |||||||
| chr19:32776174 | G | A | 103 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1041-975G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776174 | |||||||
| chr19:32776230 | T | C | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-919T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776230 | |||||||
| chr19:32776271 | G | A | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1041-878G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776271 | |||||||
| chr19:32776287 | C | T | 10 | a0001c0001t0010g0154 a0001c0001t0018g0099 a0001c0001t0018g0100 others(7): Show |
10 | HG01175.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041-862C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776287 | |||||||
| chr19:32776481 | G | A | 1 | a0001c0001t0003g0300 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1041-668G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776481 | |||||||
| chr19:32776533 | G | T | 1 | a0001c0001t0005g0356 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1041-616G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776533 | |||||||
| chr19:32776593 | A | G | 1 | a0001c0001t0005g0302 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1041-556A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776593 | |||||||
| chr19:32776613 | C | A | 1 | a0002c0003t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1041-536C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776613 | |||||||
| chr19:32776616 | T | G | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041-533T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776616 | |||||||
| chr19:32776629 | T | G | 7 | a0002c0003t0001g0252 a0002c0003t0001g0276 a0002c0003t0001g0277 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041-520T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776629 | |||||||
| chr19:32776753 | T | C | 1 | a0001c0001t0010g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1041-396T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776753 | |||||||
| chr19:32776905 | A | G | 1 | a0004c0004t0016g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1041-244A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776905 | |||||||
| chr19:32776993 | A | G | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1041-156A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32776993 | |||||||
| chr19:32777019 | G | C | 2 | a0011c0016t0003g0347 a0011c0016t0003g0350 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1041-130G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 10/32 | chr19 | 32777019 | |||||||
| chr19:32777302 | C | T | 1 | a0002c0003t0001g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1121+73C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777302 | |||||||
| chr19:32777304 | C | T | 1 | a0002c0003t0001g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1121+75C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777304 | |||||||
| chr19:32777406 | G | A | 1 | a0004c0004t0005g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1121+177G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777406 | |||||||
| chr19:32777455 | A | G | 13 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(10): Show |
13 | HG02056.hp2 HG02074.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1121+226A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777455 | |||||||
| chr19:32777519 | T | A | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121+290T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777519 | |||||||
| chr19:32777531 | G | A | 7 | a0001c0001t0031g0181 a0002c0003t0001g0211 a0002c0003t0001g0265 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+302G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777531 | |||||||
| chr19:32777770 | A | C | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121+541A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777770 | |||||||
| chr19:32777773 | T | C | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121+544T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777773 | |||||||
| chr19:32777774 | A | T | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121+545A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777774 | |||||||
| chr19:32777775 | G | A | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121+546G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777775 | |||||||
| chr19:32777777 | T | TTGG | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121+548_1121+549i others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777777 | |||||||
| chr19:32777809 | T | G | 1 | a0017c0032t0005g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1121+580T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777809 | |||||||
| chr19:32777812 | C | CAT | 6 | a0003c0002t0002g0030 a0003c0002t0002g0031 a0003c0002t0002g0048 others(3): Show |
6 | HG01243.hp2 HG02129.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+628_1121+629d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | C | CATAT | 3 | a0003c0002t0002g0044 a0003c0002t0002g0047 a0003c0002t0008g0072 |
3 | HG00735.hp1 HG01358.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1121+626_1121+629d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | C | CATATAT | 5 | a0003c0002t0002g0012 a0003c0002t0002g0092 a0003c0002t0002g0093 others(2): Show |
5 | HG02027.hp2 HG02602.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+624_1121+629d others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | C | CATATATA others(1): Show |
3 | a0003c0002t0002g0027 a0003c0002t0002g0059 a0003c0002t0019g0057 |
3 | HG00544.hp2 HG02486.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1121+622_1121+629d others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | C | CATATATA others(5): Show |
2 | a0003c0002t0002g0001 a0003c0002t0013g0091 |
3 | HG01257.hp2 HG01258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1121+618_1121+629d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | C | CATATATA others(7): Show |
1 | a0003c0002t0002g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1121+616_1121+629d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | C | CATATATA others(9): Show |
1 | a0003c0002t0002g0060 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1121+614_1121+629d others(18): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | CATATATA others(5): Show |
C | 4 | a0001c0001t0031g0181 a0001c0017t0021g0137 a0003c0002t0002g0028 others(1): Show |
4 | HG02056.hp1 HG02155.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+618_1121+629d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | CATATATA others(7): Show |
C | 1 | a0003c0002t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1121+616_1121+629d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | CATATATA others(9): Show |
C | 1 | a0012c0015t0017g0142 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1121+614_1121+629d others(18): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | CATATATA others(11): Show |
C | 1 | a0001c0001t0004g0164 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1121+612_1121+629d others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | CATATATA others(17): Show |
C | 1 | a0003c0002t0002g0068 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1121+606_1121+629d others(26): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777812 | CATATATA others(19): Show |
C | 4 | a0002c0003t0001g0285 a0003c0002t0002g0008 a0003c0002t0002g0037 others(1): Show |
4 | HG01261.hp1 HG02486.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+604_1121+629d others(28): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777812 | ||||||
| chr19:32777828 | TATATATA others(20): Show |
T | 2 | a0003c0002t0002g0180 a0016c0027t0038g0110 |
2 | HG01884.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1121+600_1121+626d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777828 | |||||||
| chr19:32777830 | TATATATA others(20): Show |
T | 1 | a0001c0001t0005g0361 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1121+602_1121+628d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777830 | |||||||
| chr19:32777831 | ATATATAT others(20): Show |
A | 5 | a0001c0001t0003g0131 a0001c0001t0012g0314 a0001c0008t0005g0363 others(2): Show |
5 | HG00438.hp2 HG01109.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+604_1121+630d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777831 | ||||||
| chr19:32777831 | ATATATAT others(21): Show |
A | 12 | a0001c0001t0003g0324 a0001c0001t0003g0325 a0001c0001t0003g0336 others(9): Show |
12 | HG01258.hp2 HG02083.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+604_1121+631d others(30): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777831 | ||||||
| chr19:32777831 | ATATATAT others(22): Show |
A | 1 | a0002c0003t0002g0235 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1121+604_1121+632d others(31): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777831 | ||||||
| chr19:32777831 | ATATATAT others(23): Show |
A | 3 | a0002c0003t0001g0245 a0002c0003t0001g0294 a0002c0003t0034g0210 |
3 | NA18951.hp1 NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1121+604_1121+633d others(32): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777831 | ||||||
| chr19:32777831 | ATATATAT others(24): Show |
A | 1 | a0002c0003t0001g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1121+604_1121+634d others(33): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777831 | ||||||
| chr19:32777833 | ATATATAT others(19): Show |
A | 1 | a0002c0003t0001g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1121+606_1121+631d others(28): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777833 | ||||||
| chr19:32777833 | ATATATAT others(20): Show |
A | 12 | a0001c0001t0003g0295 a0001c0001t0003g0326 a0001c0001t0003g0335 others(9): Show |
12 | HG00621.hp1 HG00642.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.1121+606_1121+632d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777833 | ||||||
| chr19:32777833 | ATATATAT others(21): Show |
A | 31 | a0001c0001t0003g0300 a0001c0001t0003g0309 a0001c0001t0003g0310 others(28): Show |
31 | HG00140.hp2 HG01071.hp2 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.1121+606_1121+633d others(30): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777833 | ||||||
| chr19:32777833 | ATATATAT others(22): Show |
A | 16 | a0001c0001t0003g0308 a0001c0001t0003g0330 a0001c0001t0003g0341 others(13): Show |
16 | HG00323.hp1 HG01074.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1121+606_1121+634d others(31): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777833 | ||||||
| chr19:32777833 | ATATATAT others(23): Show |
A | 2 | a0001c0001t0003g0367 a0002c0003t0001g0233 |
2 | NA18948.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1121+606_1121+635d others(32): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777833 | ||||||
| chr19:32777835 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0004g0135 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1121+608_1121+630d others(25): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777835 | ATATATAT others(17): Show |
A | 1 | a0007c0011t0004g0199 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1121+608_1121+631d others(26): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777835 | ATATATAT others(18): Show |
A | 2 | a0001c0001t0026g0290 a0002c0003t0001g0197 |
2 | HG01123.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1121+608_1121+632d others(27): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777835 | ATATATAT others(19): Show |
A | 7 | a0001c0001t0025g0289 a0002c0003t0001g0004 a0002c0003t0001g0194 others(4): Show |
8 | HG01169.hp2 HG02886.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121+608_1121+633d others(28): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777835 | ATATATAT others(20): Show |
A | 21 | a0001c0001t0003g0332 a0001c0001t0012g0303 a0002c0003t0001g0211 others(18): Show |
21 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1121+608_1121+634d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777835 | ATATATAT others(21): Show |
A | 31 | a0001c0001t0003g0333 a0001c0001t0003g0344 a0001c0001t0003g0345 others(28): Show |
31 | HG00597.hp1 HG00621.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1121+608_1121+635d others(30): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777835 | ATATATAT others(22): Show |
A | 5 | a0001c0001t0003g0320 a0001c0001t0003g0331 a0001c0001t0005g0356 others(2): Show |
5 | HG00673.hp2 HG03017.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+608_1121+636d others(31): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777835 | ATATATAT others(23): Show |
A | 1 | a0004c0004t0005g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1121+608_1121+637d others(32): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777835 | ||||||
| chr19:32777836 | TATATATA others(14): Show |
T | 1 | a0007c0011t0004g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1121+608_1121+628d others(23): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777836 | |||||||
| chr19:32777837 | ATATATAT others(14): Show |
A | 6 | a0001c0001t0004g0134 a0001c0001t0004g0141 a0001c0001t0004g0155 others(3): Show |
6 | HG00609.hp2 HG03704.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+610_1121+630d others(23): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0004g0145 a0007c0011t0004g0153 |
2 | HG00423.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1121+610_1121+631d others(24): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(16): Show |
A | 4 | a0001c0001t0004g0147 a0001c0001t0004g0148 a0001c0001t0004g0150 others(1): Show |
4 | HG02071.hp2 NA18970.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+610_1121+632d others(25): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0004g0149 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1121+610_1121+633d others(26): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(18): Show |
A | 4 | a0002c0003t0001g0191 a0002c0003t0011g0104 a0002c0003t0011g0190 others(1): Show |
4 | HG01361.hp1 NA18967.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+610_1121+634d others(27): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(19): Show |
A | 14 | a0001c0001t0003g0313 a0001c0001t0003g0321 a0001c0001t0003g0351 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1121+610_1121+635d others(28): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(20): Show |
A | 9 | a0001c0001t0007g0317 a0002c0003t0001g0188 a0002c0003t0001g0196 others(6): Show |
9 | HG01516.hp2 HG03130.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121+610_1121+636d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(21): Show |
A | 11 | a0001c0001t0003g0327 a0001c0001t0003g0348 a0001c0001t0005g0346 others(8): Show |
11 | HG01257.hp1 HG02129.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121+610_1121+637d others(30): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777837 | ATATATAT others(22): Show |
A | 1 | a0004c0004t0016g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1121+610_1121+638d others(31): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777837 | ||||||
| chr19:32777839 | ATATATAT others(12): Show |
A | 4 | a0001c0001t0004g0102 a0001c0001t0004g0139 a0001c0001t0004g0178 others(1): Show |
4 | NA18977.hp2 NA18998.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+612_1121+630d others(21): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(13): Show |
A | 3 | a0001c0001t0004g0161 a0001c0001t0004g0165 a0001c0001t0004g0167 |
3 | NA18946.hp1 NA19009.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1121+612_1121+631d others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(14): Show |
A | 7 | a0001c0001t0004g0101 a0001c0001t0004g0157 a0001c0001t0004g0169 others(4): Show |
7 | HG00323.hp2 HG00438.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121+612_1121+632d others(23): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(15): Show |
A | 4 | a0001c0001t0004g0143 a0001c0001t0004g0170 a0001c0001t0004g0175 others(1): Show |
4 | HG01261.hp2 NA18956.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+612_1121+633d others(24): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0004g0159 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1121+612_1121+634d others(25): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(17): Show |
A | 3 | a0002c0003t0001g0182 a0002c0003t0001g0240 a0020c0021t0018g0189 |
3 | HG02622.hp2 HG04184.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1121+612_1121+635d others(26): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0007g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1121+612_1121+638d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(21): Show |
A | 1 | a0001c0001t0003g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1121+612_1121+639d others(30): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(23): Show |
A | 1 | a0005c0005t0014g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1121+612_1121+641d others(32): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777839 | ATATATAT others(24): Show |
A | 1 | a0006c0006t0014g0259 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1121+612_1121+642d others(33): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777839 | ||||||
| chr19:32777841 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0010g0162 a0001c0001t0020g0133 |
2 | NA18747.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1121+614_1121+631d others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777841 | ||||||
| chr19:32777841 | ATATATAT others(12): Show |
A | 3 | a0001c0001t0004g0160 a0001c0001t0004g0176 a0001c0001t0012g0132 |
3 | NA18979.hp1 NA18986.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1121+614_1121+632d others(21): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777841 | ||||||
| chr19:32777841 | ATATATAT others(13): Show |
A | 3 | a0001c0001t0010g0138 a0001c0001t0029g0163 a0007c0011t0004g0151 |
3 | HG02027.hp1 NA18612.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1121+614_1121+633d others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777841 | ||||||
| chr19:32777841 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0010g0146 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1121+614_1121+634d others(23): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777841 | ||||||
| chr19:32777841 | ATATATAT others(15): Show |
A | 1 | a0002c0003t0001g0003 | 2 | NA18969.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1121+614_1121+635d others(24): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777841 | ||||||
| chr19:32777841 | ATATATAT others(16): Show |
A | 1 | a0002c0003t0036g0202 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1121+614_1121+636d others(25): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777841 | ||||||
| chr19:32777843 | ATATATAT others(8): Show |
A | 2 | a0003c0002t0002g0038 a0012c0015t0017g0173 |
2 | HG02809.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1121+616_1121+630d others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777843 | ||||||
| chr19:32777843 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1121+616_1121+633d others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777843 | ||||||
| chr19:32777843 | ATATATAT others(14): Show |
A | 1 | a0004c0004t0007g0288 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1121+616_1121+636d others(23): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777843 | ||||||
| chr19:32777843 | ATATATAT others(16): Show |
A | 2 | a0004c0004t0007g0214 a0004c0004t0007g0215 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1121+616_1121+638d others(25): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777843 | ||||||
| chr19:32777843 | ATATATAT others(18): Show |
A | 1 | a0006c0006t0014g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+616_1121+640d others(27): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777843 | ||||||
| chr19:32777843 | ATATATAT others(19): Show |
A | 3 | a0005c0005t0006g0121 a0006c0006t0006g0238 a0006c0006t0028g0261 |
3 | HG03491.hp1 HG03654.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1121+616_1121+641d others(28): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777843 | ||||||
| chr19:32777843 | ATATATAT others(20): Show |
A | 2 | a0005c0005t0006g0112 a0006c0006t0006g0246 |
2 | HG01074.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1121+616_1121+642d others(29): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777843 | ||||||
| chr19:32777845 | ATATATAT others(9): Show |
A | 1 | a0001c0017t0021g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1121+618_1121+633d others(18): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777845 | ||||||
| chr19:32777845 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0032g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1121+618_1121+634d others(19): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777845 | ||||||
| chr19:32777845 | ATATATAT others(17): Show |
A | 2 | a0005c0005t0006g0111 a0005c0005t0006g0120 |
2 | HG02165.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1121+618_1121+641d others(26): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777845 | ||||||
| chr19:32777845 | ATATATAT others(19): Show |
A | 7 | a0005c0005t0006g0114 a0005c0005t0006g0116 a0005c0005t0006g0292 others(4): Show |
7 | HG02074.hp1 HG02132.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+618_1121+643d others(28): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777845 | ||||||
| chr19:32777847 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0018g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1121+620_1121+631d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777847 | ||||||
| chr19:32777847 | ATATATAT others(7): Show |
A | 1 | a0001c0007t0009g0002 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1121+620_1121+633d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777847 | ||||||
| chr19:32777847 | ATATATAT others(8): Show |
A | 1 | a0001c0007t0009g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1121+620_1121+634d others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777847 | ||||||
| chr19:32777847 | ATATATAT others(13): Show |
A | 1 | a0004c0004t0007g0212 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1121+620_1121+639d others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777847 | ||||||
| chr19:32777847 | ATATATAT others(19): Show |
A | 1 | a0005c0005t0006g0117 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1121+620_1121+645d others(28): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777847 | ||||||
| chr19:32777849 | ATATATAT others(5): Show |
A | 1 | a0001c0007t0009g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1121+622_1121+633d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777849 | ||||||
| chr19:32777849 | ATATATAT others(7): Show |
A | 3 | a0001c0007t0009g0002 a0001c0007t0009g0107 a0001c0007t0009g0109 |
3 | HG02572.hp2 HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1121+622_1121+635d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777849 | ||||||
| chr19:32777849 | ATATATAT others(8): Show |
A | 1 | a0001c0007t0009g0108 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1121+622_1121+636d others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777849 | ||||||
| chr19:32777849 | ATATATAT others(13): Show |
A | 2 | a0001c0001t0018g0099 a0006c0006t0006g0113 |
2 | HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1121+622_1121+641d others(22): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777849 | ||||||
| chr19:32777853 | A | T | 1 | a0003c0002t0002g0035 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1121+624A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777853 | |||||||
| chr19:32777855 | A | T | 4 | a0003c0002t0002g0035 a0003c0002t0002g0066 a0003c0002t0002g0071 others(1): Show |
4 | HG01516.hp1 HG01975.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+626A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777855 | |||||||
| chr19:32777855 | ATATTTTT others(10): Show |
A | 1 | a0003c0002t0002g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1121+628_1121+644d others(19): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777855 | ||||||
| chr19:32777856 | TA | T | 3 | a0003c0002t0002g0013 a0003c0002t0015g0024 a0018c0033t0007g0095 |
3 | HG02055.hp1 HG02083.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1121+628delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777856 | |||||||
| chr19:32777857 | A | ATATATAT others(7): Show |
1 | a0003c0002t0013g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1121+629_1121+630i others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777857 | ||||||
| chr19:32777857 | A | ATATATAT others(5): Show |
1 | a0022c0018t0042g0021 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1121+629_1121+630i others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32777857 | ||||||
| chr19:32777857 | A | T | 20 | a0003c0002t0002g0008 a0003c0002t0002g0025 a0003c0002t0002g0028 others(17): Show |
20 | HG00099.hp1 HG00408.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1121+628A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777857 | |||||||
| chr19:32777858 | T | TATATA | 3 | a0003c0002t0002g0036 a0003c0002t0023g0017 a0008c0012t0002g0023 |
3 | HG03041.hp1 NA18949.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1121+629_1121+630i others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777858 | |||||||
| chr19:32777858 | T | TATATATA others(8): Show |
1 | a0003c0002t0002g0014 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1121+629_1121+630i others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777858 | |||||||
| chr19:32777859 | T | A | 6 | a0003c0002t0002g0005 a0003c0002t0002g0030 a0003c0002t0002g0031 others(3): Show |
6 | HG01496.hp1 HG02698.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+630T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777859 | |||||||
| chr19:32777860 | T | A | 5 | a0003c0002t0002g0036 a0003c0002t0002g0086 a0003c0002t0008g0045 others(2): Show |
5 | HG02922.hp2 NA18949.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+631T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777860 | |||||||
| chr19:32777861 | T | A | 2 | a0003c0002t0002g0005 a0003c0002t0002g0060 |
2 | HG01496.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1121+632T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777861 | |||||||
| chr19:32777862 | T | A | 3 | a0003c0002t0002g0036 a0003c0002t0008g0006 a0008c0012t0002g0023 |
3 | NA18949.hp1 NA19087.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1121+633T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777862 | |||||||
| chr19:32777894 | A | G | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+665A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32777894 | |||||||
| chr19:32778079 | C | T | 7 | a0001c0001t0003g0300 a0001c0001t0003g0367 a0001c0001t0003g0368 others(4): Show |
7 | NA18944.hp1 NA18948.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121+850C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778079 | |||||||
| chr19:32778167 | A | C | 1 | a0001c0001t0003g0320 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1121+938A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778167 | |||||||
| chr19:32778293 | C | T | 51 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(48): Show |
51 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1121+1064C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778293 | |||||||
| chr19:32778389 | A | G | 12 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+1160A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778389 | |||||||
| chr19:32778510 | T | A | 5 | a0002c0003t0001g0211 a0002c0003t0001g0265 a0002c0003t0001g0266 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+1281T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778510 | |||||||
| chr19:32778556 | A | G | 1 | a0002c0003t0034g0210 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1121+1327A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778556 | |||||||
| chr19:32778823 | T | C | 2 | a0001c0001t0018g0099 a0001c0001t0018g0100 |
2 | HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1121+1594T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778823 | |||||||
| chr19:32778878 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1121+1649T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32778878 | |||||||
| chr19:32778977 | CTT | C | 6 | a0003c0002t0002g0022 a0003c0002t0002g0071 a0003c0002t0002g0073 others(3): Show |
6 | HG00639.hp1 HG00735.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+1750_1121+175 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32778977 | ||||||
| chr19:32779207 | C | T | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1121+1978C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32779207 | |||||||
| chr19:32779250 | A | C | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+2021A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32779250 | |||||||
| chr19:32779250 | A | G | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1121+2021A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32779250 | |||||||
| chr19:32779363 | G | A | 1 | a0002c0003t0001g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1121+2134G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32779363 | |||||||
| chr19:32779799 | T | C | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1121+2570T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32779799 | |||||||
| chr19:32779985 | T | C | 247 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(244): Show |
249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1121+2756T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32779985 | |||||||
| chr19:32779986 | G | A | 1 | a0004c0004t0005g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1121+2757G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32779986 | |||||||
| chr19:32780084 | C | CT | 236 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(233): Show |
238 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1121+2872dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780084 | ||||||
| chr19:32780084 | C | CTT | 18 | a0001c0001t0003g0300 a0001c0001t0003g0353 a0001c0001t0003g0355 others(15): Show |
18 | HG00423.hp2 HG00597.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.1121+2871_1121+287 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780084 | ||||||
| chr19:32780084 | CTTT | C | 6 | a0001c0001t0010g0154 a0001c0001t0032g0174 a0001c0017t0021g0136 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+2870_1121+287 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780084 | ||||||
| chr19:32780084 | CTTTTTTT others(4): Show |
C | 1 | a0003c0002t0002g0093 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1121+2862_1121+287 others(15): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780084 | ||||||
| chr19:32780115 | G | A | 1 | a0006c0006t0014g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1121+2886G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780115 | |||||||
| chr19:32780153 | G | A | 266 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(263): Show |
268 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.1121+2924G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780153 | |||||||
| chr19:32780179 | G | A | 4 | a0002c0010t0001g0218 a0002c0010t0001g0251 a0002c0010t0001g0255 others(1): Show |
4 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+2950G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780179 | |||||||
| chr19:32780355 | G | A | 1 | a0003c0002t0002g0049 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1121+3126G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780355 | |||||||
| chr19:32780445 | G | C | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1121+3216G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780445 | |||||||
| chr19:32780473 | C | T | 1 | a0003c0002t0002g0070 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1121+3244C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780473 | |||||||
| chr19:32780485 | A | T | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0031g0181 |
3 | HG01175.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1121+3256A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780485 | |||||||
| chr19:32780537 | C | G | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1121+3308C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780537 | |||||||
| chr19:32780554 | G | A | 4 | a0002c0003t0001g0277 a0002c0003t0001g0281 a0002c0003t0001g0282 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+3325G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780554 | |||||||
| chr19:32780604 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+3375C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780604 | |||||||
| chr19:32780664 | AT | A | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+3437delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780664 | ||||||
| chr19:32780795 | G | GT | 276 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0300 others(273): Show |
279 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1121+3579dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780795 | ||||||
| chr19:32780795 | G | GTT | 7 | a0001c0001t0003g0131 a0001c0001t0012g0132 a0001c0001t0018g0099 others(4): Show |
7 | HG01109.hp2 HG01175.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+3578_1121+357 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780795 | ||||||
| chr19:32780926 | C | A | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1121+3697C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32780926 | |||||||
| chr19:32780944 | C | CT | 225 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1121+3731dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780944 | ||||||
| chr19:32780944 | C | CTT | 49 | a0001c0001t0003g0348 a0001c0001t0003g0355 a0001c0001t0004g0101 others(46): Show |
49 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1121+3730_1121+373 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32780944 | ||||||
| chr19:32781086 | G | T | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1121+3857G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32781086 | |||||||
| chr19:32781512 | A | AGGG | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1121+4284_1121+428 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32781512 | ||||||
| chr19:32781589 | T | C | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+4360T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32781589 | |||||||
| chr19:32781591 | G | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121+4362G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32781591 | |||||||
| chr19:32781658 | C | T | 6 | a0001c0001t0010g0154 a0001c0001t0032g0174 a0001c0017t0021g0136 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+4429C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32781658 | |||||||
| chr19:32781687 | T | TTC | 96 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(93): Show |
98 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.1121+4482_1121+448 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32781687 | ||||||
| chr19:32781734 | T | G | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1121+4505T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32781734 | |||||||
| chr19:32781946 | A | C | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1121+4717A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32781946 | |||||||
| chr19:32781967 | T | TTTC | 265 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(262): Show |
268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.1121+4741_1121+474 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32781967 | ||||||
| chr19:32781971 | T | TTC | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1121+4743_1121+474 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32781971 | ||||||
| chr19:32782007 | G | A | 1 | a0001c0001t0005g0306 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1121+4778G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782007 | |||||||
| chr19:32782124 | C | G | 1 | a0001c0001t0003g0351 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1121+4895C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782124 | |||||||
| chr19:32782279 | C | T | 44 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(41): Show |
44 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1121+5050C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782279 | |||||||
| chr19:32782291 | T | C | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121+5062T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782291 | |||||||
| chr19:32782292 | G | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+5063G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782292 | |||||||
| chr19:32782333 | A | C | 1 | a0003c0002t0002g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1121+5104A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782333 | |||||||
| chr19:32782472 | G | A | 1 | a0001c0001t0003g0331 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1121+5243G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782472 | |||||||
| chr19:32782652 | C | T | 1 | a0003c0002t0015g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1121+5423C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782652 | |||||||
| chr19:32782740 | T | A | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1121+5511T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782740 | |||||||
| chr19:32782947 | C | T | 1 | a0001c0001t0003g0348 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1121+5718C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32782947 | |||||||
| chr19:32783059 | A | G | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.1121+5830A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783059 | |||||||
| chr19:32783066 | T | A | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1121+5837T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783066 | |||||||
| chr19:32783103 | T | G | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1121+5874T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783103 | |||||||
| chr19:32783306 | C | G | 1 | a0003c0002t0002g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1121+6077C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783306 | |||||||
| chr19:32783554 | C | T | 96 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(93): Show |
98 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.1121+6325C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783554 | |||||||
| chr19:32783593 | T | TG | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1121+6365dupG | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32783593 | ||||||
| chr19:32783722 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+6493A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783722 | |||||||
| chr19:32783726 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+6497A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783726 | |||||||
| chr19:32783921 | G | A | 1 | a0003c0002t0002g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1122-6610G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783921 | |||||||
| chr19:32783948 | T | C | 1 | a0003c0002t0002g0007 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1122-6583T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32783948 | |||||||
| chr19:32784166 | C | T | 1 | a0003c0002t0008g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1122-6365C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32784166 | |||||||
| chr19:32784340 | C | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122-6191C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32784340 | |||||||
| chr19:32784341 | G | C | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1122-6190G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32784341 | |||||||
| chr19:32784351 | T | C | 2 | a0002c0003t0001g0266 a0002c0003t0001g0267 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1122-6180T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32784351 | |||||||
| chr19:32784385 | G | A | 1 | a0001c0001t0025g0289 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1122-6146G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32784385 | |||||||
| chr19:32784643 | A | G | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1122-5888A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32784643 | |||||||
| chr19:32785112 | G | A | 1 | a0001c0019t0004g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1122-5419G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785112 | |||||||
| chr19:32785124 | T | C | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-5407T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785124 | |||||||
| chr19:32785254 | A | G | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1122-5277A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785254 | |||||||
| chr19:32785471 | T | C | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1122-5060T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785471 | |||||||
| chr19:32785505 | C | T | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1122-5026C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785505 | |||||||
| chr19:32785600 | C | A | 221 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(218): Show |
223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1122-4931C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785600 | |||||||
| chr19:32785638 | A | G | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1122-4893A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785638 | |||||||
| chr19:32785734 | A | G | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1122-4797A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785734 | |||||||
| chr19:32785830 | C | T | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1122-4701C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32785830 | |||||||
| chr19:32786273 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1122-4258A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32786273 | |||||||
| chr19:32786691 | A | G | 1 | a0003c0002t0002g0070 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1122-3840A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32786691 | |||||||
| chr19:32786742 | C | T | 6 | a0005c0005t0014g0262 a0006c0006t0006g0238 a0006c0006t0006g0246 others(3): Show |
6 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-3789C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32786742 | |||||||
| chr19:32786949 | A | G | 1 | a0001c0001t0003g0330 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1122-3582A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32786949 | |||||||
| chr19:32786973 | G | A | 1 | a0001c0001t0004g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1122-3558G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32786973 | |||||||
| chr19:32787371 | A | G | 2 | a0001c0001t0003g0353 a0001c0001t0012g0362 |
2 | NA18612.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1122-3160A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32787371 | |||||||
| chr19:32787438 | A | G | 1 | a0003c0002t0002g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1122-3093A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32787438 | |||||||
| chr19:32787501 | T | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1122-3030T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32787501 | |||||||
| chr19:32787714 | G | A | 1 | a0003c0002t0002g0046 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1122-2817G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32787714 | |||||||
| chr19:32787855 | C | T | 2 | a0002c0003t0001g0191 a0002c0003t0001g0205 |
2 | HG01361.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1122-2676C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32787855 | |||||||
| chr19:32787935 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122-2596G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32787935 | |||||||
| chr19:32788185 | C | G | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1122-2346C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32788185 | |||||||
| chr19:32788482 | T | C | 1 | a0001c0001t0018g0099 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1122-2049T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32788482 | |||||||
| chr19:32788692 | A | G | 2 | a0006c0006t0014g0260 a0006c0006t0028g0261 |
2 | HG02559.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1122-1839A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32788692 | |||||||
| chr19:32788712 | G | C | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1122-1819G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32788712 | |||||||
| chr19:32788916 | A | T | 1 | a0001c0007t0009g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1122-1615A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32788916 | |||||||
| chr19:32789004 | C | T | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1122-1527C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32789004 | |||||||
| chr19:32789109 | AG | A | 18 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(15): Show |
18 | HG00099.hp2 HG01123.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.1122-1420delG | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32789109 | ||||||
| chr19:32789114 | C | T | 18 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(15): Show |
18 | HG00099.hp2 HG01123.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.1122-1417C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32789114 | |||||||
| chr19:32789178 | G | A | 78 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(75): Show |
78 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1122-1353G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32789178 | |||||||
| chr19:32789193 | G | T | 1 | a0005c0005t0006g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1122-1338G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32789193 | |||||||
| chr19:32789345 | G | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1122-1186G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32789345 | |||||||
| chr19:32789613 | G | T | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0031g0181 |
3 | HG01175.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1122-918G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32789613 | |||||||
| chr19:32789837 | A | G | 201 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(198): Show |
203 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.1122-694A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32789837 | |||||||
| chr19:32790027 | C | T | 1 | a0002c0003t0001g0201 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1122-504C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32790027 | |||||||
| chr19:32790081 | C | T | 1 | a0003c0002t0015g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1122-450C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32790081 | |||||||
| chr19:32790176 | TAGAGG | T | 3 | a0004c0004t0016g0184 a0004c0004t0016g0185 a0004c0004t0016g0213 |
3 | HG02622.hp1 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1122-353_1122-349d others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr19 | 32790176 | ||||||
| chr19:32790221 | C | T | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1122-310C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 11/32 | chr19 | 32790221 | |||||||
| chr19:32790817 | G | GT | 11 | a0001c0001t0004g0102 a0001c0001t0004g0139 a0001c0001t0004g0160 others(8): Show |
11 | NA18612.hp1 NA18946.hp1 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183-137dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr19 | 32790817 | ||||||
| chr19:32791203 | C | T | 219 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(216): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1287+135C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791203 | |||||||
| chr19:32791239 | T | G | 1 | a0003c0002t0002g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1287+171T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791239 | |||||||
| chr19:32791338 | A | G | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1287+270A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791338 | |||||||
| chr19:32791343 | G | A | 1 | a0001c0001t0003g0335 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1287+275G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791343 | |||||||
| chr19:32791430 | A | G | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1287+362A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791430 | |||||||
| chr19:32791462 | A | T | 3 | a0001c0001t0004g0145 a0001c0001t0004g0157 a0025c0029t0004g0140 |
3 | NA18962.hp2 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1287+394A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791462 | |||||||
| chr19:32791601 | C | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1287+533C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791601 | |||||||
| chr19:32791717 | G | C | 219 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(216): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1287+649G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791717 | |||||||
| chr19:32791718 | G | A | 1 | a0004c0004t0005g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1287+650G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791718 | |||||||
| chr19:32791809 | C | A | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1287+741C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791809 | |||||||
| chr19:32791810 | T | G | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1287+742T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791810 | |||||||
| chr19:32791881 | G | C | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1287+813G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791881 | |||||||
| chr19:32791891 | G | A | 103 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1287+823G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32791891 | |||||||
| chr19:32791945 | TA | T | 213 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(210): Show |
214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1287+892delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32791945 | ||||||
| chr19:32791945 | TAA | T | 67 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(64): Show |
69 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1287+891_1287+892d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32791945 | ||||||
| chr19:32792012 | G | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1287+944G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792012 | |||||||
| chr19:32792112 | G | A | 97 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(94): Show |
99 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.1287+1044G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792112 | |||||||
| chr19:32792222 | G | A | 20 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(17): Show |
20 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1287+1154G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792222 | |||||||
| chr19:32792260 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1287+1192C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792260 | |||||||
| chr19:32792347 | G | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1287+1279G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792347 | |||||||
| chr19:32792434 | A | T | 1 | a0001c0001t0032g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1287+1366A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792434 | |||||||
| chr19:32792560 | G | A | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1287+1492G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792560 | |||||||
| chr19:32792670 | A | G | 1 | a0003c0002t0002g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1287+1602A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792670 | |||||||
| chr19:32792808 | A | G | 14 | a0001c0001t0005g0302 a0001c0001t0005g0305 a0001c0001t0005g0306 others(11): Show |
14 | HG01516.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1287+1740A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32792808 | |||||||
| chr19:32793118 | G | A | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1288-1510G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793118 | |||||||
| chr19:32793185 | C | CAAT | 5 | a0003c0002t0002g0039 a0003c0002t0002g0047 a0003c0002t0002g0048 others(2): Show |
5 | HG01243.hp2 HG01516.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288-1418_1288-141 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32793185 | ||||||
| chr19:32793185 | C | CAATAATA others(8): Show |
1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1288-1430_1288-141 others(19): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32793185 | ||||||
| chr19:32793185 | CAAT | C | 306 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(303): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1288-1418_1288-141 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32793185 | ||||||
| chr19:32793244 | C | G | 8 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(5): Show |
9 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288-1384C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793244 | |||||||
| chr19:32793344 | G | A | 11 | a0003c0002t0002g0044 a0003c0002t0002g0046 a0003c0002t0002g0048 others(8): Show |
11 | HG00099.hp1 HG01070.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1288-1284G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793344 | |||||||
| chr19:32793475 | G | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1288-1153G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793475 | |||||||
| chr19:32793505 | C | T | 1 | a0022c0018t0042g0021 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1288-1123C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793505 | |||||||
| chr19:32793543 | G | A | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.1288-1085G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793543 | |||||||
| chr19:32793636 | G | A | 2 | a0002c0003t0001g0188 a0002c0003t0001g0208 |
2 | HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1288-992G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793636 | |||||||
| chr19:32793698 | G | A | 1 | a0001c0001t0012g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1288-930G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793698 | |||||||
| chr19:32793723 | A | G | 2 | a0003c0002t0002g0040 a0003c0002t0002g0052 |
2 | NA19057.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1288-905A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793723 | |||||||
| chr19:32793793 | C | CT | 77 | a0001c0001t0003g0312 a0001c0001t0004g0101 a0001c0001t0004g0102 others(74): Show |
78 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1288-817dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32793793 | ||||||
| chr19:32793793 | C | CTT | 205 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(202): Show |
207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1288-818_1288-817d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32793793 | ||||||
| chr19:32793793 | C | CTTT | 9 | a0001c0001t0003g0300 a0001c0001t0012g0362 a0001c0001t0044g0103 others(6): Show |
9 | HG01981.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288-819_1288-817d others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32793793 | ||||||
| chr19:32793844 | G | A | 79 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(76): Show |
79 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1288-784G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793844 | |||||||
| chr19:32793900 | T | G | 1 | a0005c0005t0027g0122 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1288-728T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793900 | |||||||
| chr19:32793939 | T | C | 1 | a0001c0001t0005g0356 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1288-689T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793939 | |||||||
| chr19:32793955 | C | T | 2 | a0001c0001t0003g0349 a0018c0033t0007g0095 |
2 | HG02055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1288-673C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32793955 | |||||||
| chr19:32793982 | C | CG | 199 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(196): Show |
201 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.1288-642dupG | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32793982 | ||||||
| chr19:32794092 | C | CT | 24 | a0003c0002t0002g0022 a0003c0002t0002g0027 a0003c0002t0002g0040 others(21): Show |
24 | HG00099.hp1 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1288-505dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32794092 | ||||||
| chr19:32794092 | CT | C | 19 | a0003c0002t0002g0005 a0003c0002t0002g0007 a0003c0002t0002g0013 others(16): Show |
19 | HG00140.hp1 HG00609.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1288-505delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32794092 | ||||||
| chr19:32794092 | CTTT | C | 15 | a0004c0004t0005g0124 a0004c0004t0005g0127 a0004c0004t0005g0128 others(12): Show |
15 | HG01891.hp1 HG02055.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1288-507_1288-505d others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32794092 | ||||||
| chr19:32794092 | CTTTT | C | 56 | a0001c0001t0003g0300 a0001c0001t0003g0326 a0001c0001t0003g0335 others(53): Show |
56 | HG00099.hp2 HG00621.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1288-508_1288-505d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32794092 | ||||||
| chr19:32794092 | CTTTTT | C | 104 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(101): Show |
104 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1288-509_1288-505d others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32794092 | ||||||
| chr19:32794092 | CTTTTTT | C | 34 | a0001c0001t0003g0367 a0001c0001t0020g0133 a0001c0001t0026g0290 others(31): Show |
34 | HG00597.hp1 HG00621.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1288-510_1288-505d others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32794092 | ||||||
| chr19:32794092 | CTTTTTTT | C | 71 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0031g0181 others(68): Show |
74 | HG00558.hp1 HG01069.hp2 HG01071.hp2 others(71): Show |
intron_variant | MODIFIER | c.1288-511_1288-505d others(9): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr19 | 32794092 | ||||||
| chr19:32794125 | A | G | 195 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(192): Show |
197 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.1288-503A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32794125 | |||||||
| chr19:32794136 | C | T | 1 | a0003c0002t0002g0070 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1288-492C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32794136 | |||||||
| chr19:32794182 | C | T | 1 | a0004c0004t0005g0269 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1288-446C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32794182 | |||||||
| chr19:32794192 | G | A | 1 | a0002c0003t0001g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1288-436G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32794192 | |||||||
| chr19:32794285 | G | T | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1288-343G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 13/32 | chr19 | 32794285 | |||||||
| chr19:32794829 | T | G | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1473+16T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32794829 | |||||||
| chr19:32794894 | G | T | 1 | a0003c0002t0015g0024 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1473+81G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32794894 | |||||||
| chr19:32795062 | C | T | 7 | a0001c0001t0003g0313 a0001c0001t0003g0339 a0001c0001t0003g0340 others(4): Show |
7 | NA18939.hp2 NA18942.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.1473+249C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32795062 | |||||||
| chr19:32795117 | C | G | 7 | a0001c0001t0003g0300 a0001c0001t0003g0367 a0001c0001t0003g0368 others(4): Show |
7 | NA18944.hp1 NA18948.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1473+304C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32795117 | |||||||
| chr19:32795205 | T | C | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+392T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32795205 | |||||||
| chr19:32795335 | GA | G | 275 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(272): Show |
278 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.1473+539delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr19 | 32795335 | ||||||
| chr19:32795335 | GAA | G | 6 | a0001c0001t0003g0326 a0001c0001t0004g0160 a0001c0001t0010g0154 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+538_1473+539d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr19 | 32795335 | ||||||
| chr19:32795339 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1473+526A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32795339 | |||||||
| chr19:32795419 | A | G | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1473+606A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32795419 | |||||||
| chr19:32795533 | G | A | 1 | a0001c0001t0003g0336 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1473+720G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32795533 | |||||||
| chr19:32795660 | C | T | 1 | a0001c0001t0022g0318 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1473+847C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32795660 | |||||||
| chr19:32796067 | G | A | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1473+1254G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796067 | |||||||
| chr19:32796070 | C | T | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1473+1257C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796070 | |||||||
| chr19:32796216 | A | G | 51 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(48): Show |
51 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1473+1403A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796216 | |||||||
| chr19:32796370 | C | T | 26 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(23): Show |
26 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1474-1365C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796370 | |||||||
| chr19:32796406 | G | A | 1 | a0002c0003t0001g0245 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1474-1329G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796406 | |||||||
| chr19:32796407 | A | G | 1 | a0002c0003t0001g0245 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1474-1328A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796407 | |||||||
| chr19:32796427 | A | T | 1 | a0002c0003t0001g0245 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1474-1308A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796427 | |||||||
| chr19:32796428 | T | A | 1 | a0002c0003t0001g0245 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1474-1307T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796428 | |||||||
| chr19:32796585 | C | CA | 21 | a0001c0001t0004g0175 a0003c0002t0043g0034 a0005c0005t0006g0111 others(18): Show |
21 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1474-1136dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr19 | 32796585 | ||||||
| chr19:32796609 | G | A | 97 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(94): Show |
99 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.1474-1126G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796609 | |||||||
| chr19:32796620 | C | T | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1474-1115C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796620 | |||||||
| chr19:32796885 | GGT | G | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1474-843_1474-842d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr19 | 32796885 | ||||||
| chr19:32796909 | G | A | 219 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(216): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1474-826G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796909 | |||||||
| chr19:32796981 | C | CT | 26 | a0001c0001t0012g0314 a0001c0001t0026g0290 a0003c0002t0013g0015 others(23): Show |
26 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1474-737dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr19 | 32796981 | ||||||
| chr19:32796986 | T | TC | 54 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(51): Show |
54 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1474-749_1474-748i others(3): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32796986 | |||||||
| chr19:32797037 | G | T | 1 | a0005c0005t0006g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1474-698G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797037 | |||||||
| chr19:32797085 | A | G | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1474-650A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797085 | |||||||
| chr19:32797103 | C | T | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1474-632C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797103 | |||||||
| chr19:32797127 | C | T | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1474-608C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797127 | |||||||
| chr19:32797170 | GGGGTTTC others(7): Show |
G | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1474-564_1474-551d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797170 | |||||||
| chr19:32797185 | T | A | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1474-550T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797185 | |||||||
| chr19:32797201 | A | G | 57 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(54): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1474-534A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797201 | |||||||
| chr19:32797214 | C | T | 200 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(197): Show |
202 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.1474-521C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797214 | |||||||
| chr19:32797383 | C | T | 1 | a0001c0001t0005g0346 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1474-352C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797383 | |||||||
| chr19:32797478 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1474-257C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 14/32 | chr19 | 32797478 | |||||||
| chr19:32797963 | G | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1630+72G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 15/32 | chr19 | 32797963 | |||||||
| chr19:32797986 | C | CAGTGACA others(67): Show |
1 | a0025c0029t0004g0140 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1630+96_1630+169du others(75): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr19 | 32797986 | ||||||
| chr19:32798049 | C | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1630+158C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 15/32 | chr19 | 32798049 | |||||||
| chr19:32798051 | A | G | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1630+160A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 15/32 | chr19 | 32798051 | |||||||
| chr19:32798112 | A | G | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1631-196A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 15/32 | chr19 | 32798112 | |||||||
| chr19:32798485 | A | G | 1 | a0003c0002t0015g0024 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1758+50A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798485 | |||||||
| chr19:32798514 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1758+79G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798514 | |||||||
| chr19:32798520 | G | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1758+85G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798520 | |||||||
| chr19:32798557 | T | C | 97 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(94): Show |
99 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.1758+122T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798557 | |||||||
| chr19:32798576 | A | G | 1 | a0015c0028t0024g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1758+141A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798576 | |||||||
| chr19:32798642 | T | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1758+207T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798642 | |||||||
| chr19:32798649 | T | G | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1758+214T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798649 | |||||||
| chr19:32798839 | A | G | 1 | a0002c0003t0036g0202 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1758+404A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798839 | |||||||
| chr19:32798905 | A | G | 33 | a0002c0003t0001g0098 a0002c0003t0001g0182 a0002c0003t0001g0211 others(30): Show |
33 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1758+470A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32798905 | |||||||
| chr19:32799057 | G | A | 5 | a0001c0001t0005g0302 a0001c0001t0005g0305 a0001c0001t0005g0306 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1758+622G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799057 | |||||||
| chr19:32799169 | G | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1758+734G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799169 | |||||||
| chr19:32799197 | A | G | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1758+762A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799197 | |||||||
| chr19:32799218 | TACTG | T | 24 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(21): Show |
24 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1758+787_1758+790d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | INFO_REALIGN_3_PRIME | chr19 | 32799218 | ||||||
| chr19:32799346 | T | C | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1759-821T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799346 | |||||||
| chr19:32799459 | C | A | 1 | a0001c0001t0004g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1759-708C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799459 | |||||||
| chr19:32799465 | T | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1759-702T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799465 | |||||||
| chr19:32799527 | A | G | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1759-640A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799527 | |||||||
| chr19:32799728 | C | CT | 100 | a0001c0001t0003g0295 a0001c0001t0003g0374 a0001c0001t0004g0135 others(97): Show |
102 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.1759-416dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | INFO_REALIGN_3_PRIME | chr19 | 32799728 | ||||||
| chr19:32799728 | C | CTT | 107 | a0001c0001t0003g0131 a0001c0001t0003g0297 a0001c0001t0003g0300 others(104): Show |
108 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1759-417_1759-416d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | INFO_REALIGN_3_PRIME | chr19 | 32799728 | ||||||
| chr19:32799728 | C | CTTT | 9 | a0001c0001t0003g0313 a0001c0001t0003g0365 a0001c0001t0005g0322 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1759-418_1759-416d others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | INFO_REALIGN_3_PRIME | chr19 | 32799728 | ||||||
| chr19:32799874 | A | G | 1 | a0006c0006t0014g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1759-293A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799874 | |||||||
| chr19:32799964 | G | A | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1759-203G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 16/32 | chr19 | 32799964 | |||||||
| chr19:32800385 | A | ATG | 8 | a0004c0004t0005g0268 a0004c0004t0005g0269 a0004c0004t0005g0270 others(5): Show |
8 | HG02622.hp1 HG02698.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1950+43_1950+44dup others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr19 | 32800385 | ||||||
| chr19:32800427 | C | T | 1 | a0001c0001t0003g0348 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1950+69C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 17/32 | chr19 | 32800427 | |||||||
| chr19:32800861 | G | C | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2079+89G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32800861 | |||||||
| chr19:32800929 | C | G | 1 | a0002c0003t0001g0291 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2079+157C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32800929 | |||||||
| chr19:32800968 | C | CG | 12 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2079+201dupG | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr19 | 32800968 | ||||||
| chr19:32801016 | T | G | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2079+244T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801016 | |||||||
| chr19:32801051 | T | C | 1 | a0002c0003t0001g0279 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2079+279T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801051 | |||||||
| chr19:32801106 | C | T | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2079+334C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801106 | |||||||
| chr19:32801149 | G | A | 2 | a0001c0001t0018g0099 a0001c0001t0018g0100 |
2 | HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2079+377G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801149 | |||||||
| chr19:32801195 | G | T | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2079+423G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801195 | |||||||
| chr19:32801326 | C | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2080-430C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801326 | |||||||
| chr19:32801390 | G | A | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2080-366G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801390 | |||||||
| chr19:32801424 | A | G | 1 | a0002c0003t0001g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2080-332A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801424 | |||||||
| chr19:32801453 | CTG | C | 3 | a0003c0002t0002g0038 a0015c0028t0024g0096 a0016c0027t0038g0110 |
3 | HG01109.hp2 HG01884.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.2080-291_2080-290d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr19 | 32801453 | ||||||
| chr19:32801467 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2080-289A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801467 | |||||||
| chr19:32801662 | A | T | 278 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(275): Show |
280 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.2080-94A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801662 | |||||||
| chr19:32801697 | C | T | 5 | a0002c0003t0001g0192 a0002c0003t0001g0219 a0002c0003t0001g0250 others(2): Show |
5 | HG00621.hp2 NA18947.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2080-59C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 18/32 | chr19 | 32801697 | |||||||
| chr19:32801991 | C | G | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.2197+118C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | chr19 | 32801991 | |||||||
| chr19:32802110 | A | G | 5 | a0001c0001t0005g0302 a0001c0001t0005g0305 a0001c0001t0005g0306 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2197+237A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | chr19 | 32802110 | |||||||
| chr19:32802115 | T | TTGAGGAT others(73): Show |
3 | a0002c0003t0001g0004 a0002c0003t0001g0197 a0002c0003t0001g0200 |
4 | NA18962.hp1 NA18982.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.2197+244_2197+323d others(82): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802115 | ||||||
| chr19:32802125 | CTATCATA others(39): Show |
C | 2 | a0001c0001t0018g0099 a0001c0001t0018g0100 |
2 | HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2197+269_2197+314d others(48): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802125 | ||||||
| chr19:32802131 | TATATATG others(28): Show |
T | 2 | a0002c0003t0001g0245 a0002c0003t0001g0294 |
2 | NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.2197+265_2197+299d others(37): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802131 | ||||||
| chr19:32802150 | CAT | C | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2197+288_2197+289d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802150 | ||||||
| chr19:32802154 | TATATATA others(14): Show |
T | 1 | a0001c0001t0004g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2197+294_2197+314d others(23): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802154 | ||||||
| chr19:32802190 | GATATATA others(11): Show |
G | 4 | a0001c0001t0003g0341 a0002c0003t0001g0194 a0015c0028t0024g0096 others(1): Show |
4 | HG00323.hp1 HG01109.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.2197+353_2197+370d others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802190 | ||||||
| chr19:32802208 | C | CATATATA others(8): Show |
1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2197+338_2197+352d others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802208 | ||||||
| chr19:32802208 | CATATATA others(26): Show |
C | 1 | a0005c0005t0014g0115 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2197+365_2198-386d others(35): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802208 | ||||||
| chr19:32802210 | TATATATG others(9): Show |
T | 5 | a0001c0001t0026g0290 a0001c0001t0032g0174 a0001c0001t0044g0103 others(2): Show |
5 | HG01123.hp2 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2197+344_2197+359d others(18): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802210 | ||||||
| chr19:32802212 | TATATGAT others(7): Show |
T | 51 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(48): Show |
51 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.2197+344_2197+357d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr19 | 32802212 | ||||||
| chr19:32802261 | T | C | 3 | a0010c0013t0002g0029 a0010c0013t0002g0032 a0010c0013t0002g0033 |
3 | HG02109.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2197+388T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | chr19 | 32802261 | |||||||
| chr19:32802266 | A | G | 3 | a0010c0013t0002g0029 a0010c0013t0002g0032 a0010c0013t0002g0033 |
3 | HG02109.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2198-390A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | chr19 | 32802266 | |||||||
| chr19:32802405 | G | T | 2 | a0001c0001t0003g0308 a0001c0001t0003g0310 |
2 | HG02040.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2198-251G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | chr19 | 32802405 | |||||||
| chr19:32802533 | C | A | 5 | a0001c0001t0005g0302 a0001c0001t0005g0305 a0001c0001t0005g0306 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2198-123C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | chr19 | 32802533 | |||||||
| chr19:32802609 | T | C | 1 | a0002c0003t0001g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2198-47T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 19/32 | chr19 | 32802609 | |||||||
| chr19:32802770 | A | ATCATTTT others(13): Show |
1 | a0025c0029t0004g0140 | 1 | NA18978.hp2 | splice_region_variant&intron_variant | LOW | c.2314_2331+2dupCATT others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 20/32 | INFO_REALIGN_3_PRIME | chr19 | 32802770 | ||||||
| chr19:32803176 | G | A | 200 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(197): Show |
202 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.2552+34G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32803176 | |||||||
| chr19:32803275 | C | T | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2552+133C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32803275 | |||||||
| chr19:32803290 | G | A | 1 | a0005c0005t0006g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2552+148G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32803290 | |||||||
| chr19:32803312 | G | A | 1 | a0001c0001t0018g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2552+170G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32803312 | |||||||
| chr19:32803744 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2552+602C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32803744 | |||||||
| chr19:32804057 | A | G | 5 | a0001c0001t0005g0302 a0001c0001t0005g0305 a0001c0001t0005g0306 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2552+915A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804057 | |||||||
| chr19:32804135 | C | T | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2552+993C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804135 | |||||||
| chr19:32804141 | C | T | 4 | a0003c0002t0002g0038 a0003c0002t0002g0040 a0003c0002t0002g0042 others(1): Show |
4 | NA18939.hp1 NA18945.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.2552+999C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804141 | |||||||
| chr19:32804223 | C | T | 1 | a0006c0006t0014g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2552+1081C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804223 | |||||||
| chr19:32804351 | C | T | 2 | a0002c0003t0001g0182 a0002c0003t0037g0207 |
2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2552+1209C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804351 | |||||||
| chr19:32804500 | T | A | 1 | a0005c0005t0014g0115 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2552+1358T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804500 | |||||||
| chr19:32804551 | G | A | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2552+1409G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804551 | |||||||
| chr19:32804691 | C | CA | 101 | a0001c0001t0003g0309 a0001c0001t0003g0311 a0001c0001t0003g0332 others(98): Show |
103 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.2552+1566dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32804691 | ||||||
| chr19:32804691 | CA | C | 28 | a0001c0001t0003g0351 a0001c0001t0004g0157 a0001c0001t0005g0319 others(25): Show |
28 | HG00099.hp2 HG00323.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.2552+1566delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32804691 | ||||||
| chr19:32804788 | G | A | 7 | a0001c0001t0032g0174 a0001c0007t0009g0002 a0001c0007t0009g0105 others(4): Show |
8 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2552+1646G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804788 | |||||||
| chr19:32804813 | G | A | 1 | a0004c0004t0005g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2552+1671G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804813 | |||||||
| chr19:32804912 | T | C | 1 | a0001c0001t0004g0176 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2552+1770T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804912 | |||||||
| chr19:32804932 | G | C | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2552+1790G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32804932 | |||||||
| chr19:32805190 | T | TATATATA others(29): Show |
1 | a0001c0001t0003g0326 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2552+2056_2552+205 others(40): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805190 | ||||||
| chr19:32805191 | A | C | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2552+2049A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805191 | |||||||
| chr19:32805196 | TATAC | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2552+2056_2552+205 others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805196 | ||||||
| chr19:32805200 | C | T | 21 | a0001c0001t0003g0326 a0001c0001t0010g0154 a0005c0005t0006g0111 others(18): Show |
21 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2552+2058C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805200 | |||||||
| chr19:32805218 | CACAT | C | 102 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(99): Show |
102 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2552+2078_2552+208 others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805218 | ||||||
| chr19:32805220 | CAT | C | 260 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(257): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.2552+2092_2552+209 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805220 | ||||||
| chr19:32805222 | T | C | 10 | a0001c0001t0003g0326 a0001c0001t0003g0357 a0001c0007t0009g0002 others(7): Show |
11 | HG01361.hp1 HG02155.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2552+2080T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805222 | |||||||
| chr19:32805399 | GA | G | 5 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0025g0289 others(2): Show |
5 | HG01168.hp2 HG01175.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.2553-2140delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805399 | ||||||
| chr19:32805412 | T | C | 3 | a0001c0001t0003g0337 a0001c0001t0003g0365 a0001c0001t0003g0366 |
3 | NA18950.hp2 NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2553-2137T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805412 | |||||||
| chr19:32805463 | G | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2553-2086G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805463 | |||||||
| chr19:32805518 | C | T | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2553-2031C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805518 | |||||||
| chr19:32805636 | G | T | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2553-1913G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805636 | |||||||
| chr19:32805679 | T | C | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2553-1870T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805679 | |||||||
| chr19:32805729 | C | CT | 24 | a0001c0001t0003g0312 a0001c0001t0003g0333 a0001c0001t0003g0354 others(21): Show |
24 | HG00597.hp1 HG01109.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.2553-1800dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805729 | ||||||
| chr19:32805729 | CT | C | 39 | a0001c0001t0003g0344 a0001c0001t0005g0356 a0001c0001t0018g0100 others(36): Show |
39 | HG00323.hp2 HG01074.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.2553-1800delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805729 | ||||||
| chr19:32805729 | CTT | C | 13 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(10): Show |
13 | HG00099.hp2 HG02056.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2553-1801_2553-180 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32805729 | ||||||
| chr19:32805750 | G | A | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.2553-1799G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805750 | |||||||
| chr19:32805753 | A | G | 1 | a0002c0003t0001g0192 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2553-1796A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805753 | |||||||
| chr19:32805934 | G | A | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2553-1615G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805934 | |||||||
| chr19:32805938 | G | C | 1 | a0002c0003t0001g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2553-1611G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32805938 | |||||||
| chr19:32806011 | C | T | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2553-1538C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806011 | |||||||
| chr19:32806320 | C | T | 2 | a0020c0021t0018g0189 a0027c0023t0017g0186 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2553-1229C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806320 | |||||||
| chr19:32806337 | G | GT | 107 | a0001c0001t0018g0100 a0002c0003t0001g0003 a0002c0003t0001g0004 others(104): Show |
109 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2553-1193dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32806337 | ||||||
| chr19:32806337 | G | GTT | 13 | a0001c0001t0003g0367 a0001c0001t0012g0362 a0001c0001t0018g0099 others(10): Show |
13 | HG01123.hp1 HG01175.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2553-1194_2553-119 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32806337 | ||||||
| chr19:32806337 | G | GTTT | 139 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(136): Show |
139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2553-1195_2553-119 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32806337 | ||||||
| chr19:32806337 | G | GTTTT | 12 | a0001c0001t0003g0337 a0001c0001t0003g0366 a0001c0001t0003g0370 others(9): Show |
12 | HG01978.hp2 HG03486.hp2 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.2553-1196_2553-119 others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32806337 | ||||||
| chr19:32806342 | T | TTG | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2553-1206_2553-120 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32806342 | ||||||
| chr19:32806403 | C | T | 1 | a0006c0006t0014g0259 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2553-1146C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806403 | |||||||
| chr19:32806471 | A | T | 317 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(314): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.2553-1078A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806471 | |||||||
| chr19:32806585 | G | A | 1 | a0001c0001t0003g0131 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2553-964G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806585 | |||||||
| chr19:32806639 | G | A | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2553-910G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806639 | |||||||
| chr19:32806862 | A | G | 3 | a0003c0002t0002g0039 a0003c0002t0002g0047 a0003c0002t0002g0087 |
3 | NA18941.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2553-687A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806862 | |||||||
| chr19:32806882 | G | A | 1 | a0002c0003t0001g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2553-667G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32806882 | |||||||
| chr19:32807206 | A | G | 1 | a0001c0001t0032g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2553-343A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32807206 | |||||||
| chr19:32807216 | A | G | 6 | a0005c0005t0014g0262 a0006c0006t0006g0238 a0006c0006t0006g0246 others(3): Show |
6 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.2553-333A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32807216 | |||||||
| chr19:32807252 | G | A | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2553-297G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32807252 | |||||||
| chr19:32807264 | T | C | 4 | a0003c0002t0008g0045 a0003c0002t0019g0055 a0003c0002t0019g0056 others(1): Show |
4 | HG02896.hp1 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2553-285T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32807264 | |||||||
| chr19:32807267 | T | TA | 89 | a0001c0001t0003g0295 a0001c0001t0003g0312 a0001c0001t0003g0367 others(86): Show |
91 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.2553-253dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAA | 60 | a0001c0001t0003g0297 a0001c0001t0003g0300 a0001c0001t0003g0308 others(57): Show |
60 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2553-254_2553-253d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAA | 36 | a0001c0001t0003g0131 a0001c0001t0003g0311 a0001c0001t0003g0313 others(33): Show |
37 | HG01258.hp2 HG01496.hp2 HG01516.hp2 others(34): Show |
intron_variant | MODIFIER | c.2553-255_2553-253d others(5): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAAA | 13 | a0001c0001t0005g0305 a0001c0001t0005g0356 a0001c0001t0007g0316 others(10): Show |
13 | HG01891.hp1 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2553-256_2553-253d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAAAA | 8 | a0001c0001t0025g0289 a0001c0001t0026g0290 a0004c0004t0005g0124 others(5): Show |
8 | HG01123.hp2 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2553-257_2553-253d others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAAAAAA others(2): Show |
19 | a0001c0001t0004g0141 a0001c0001t0004g0145 a0001c0001t0004g0148 others(16): Show |
19 | HG00408.hp2 HG02074.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2553-261_2553-253d others(11): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAAAAAA others(3): Show |
16 | a0001c0001t0004g0135 a0001c0001t0004g0152 a0001c0001t0004g0169 others(13): Show |
16 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.2553-262_2553-253d others(12): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAAAAAA others(4): Show |
5 | a0001c0001t0004g0101 a0001c0001t0004g0177 a0001c0001t0010g0154 others(2): Show |
5 | HG00323.hp2 HG00609.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553-263_2553-253d others(13): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0032g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2553-264_2553-253d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0004g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2553-267_2553-253d others(17): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | TA | T | 11 | a0002c0003t0001g0254 a0002c0003t0001g0291 a0003c0002t0002g0007 others(8): Show |
11 | HG01069.hp1 HG01975.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.2553-253delA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | TAAAAAAA others(3): Show |
T | 1 | a0002c0003t0001g0287 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2553-262_2553-253d others(12): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | TAAAAAAA others(4): Show |
T | 20 | a0004c0004t0016g0184 a0005c0005t0006g0111 a0005c0005t0006g0112 others(17): Show |
20 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.2553-263_2553-253d others(13): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807267 | TAAAAAAA others(5): Show |
T | 3 | a0001c0001t0004g0175 a0015c0028t0024g0096 a0016c0027t0038g0110 |
3 | HG01109.hp2 HG01261.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2553-264_2553-253d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr19 | 32807267 | ||||||
| chr19:32807380 | G | A | 282 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(279): Show |
285 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.2553-169G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32807380 | |||||||
| chr19:32807424 | T | G | 1 | a0001c0001t0010g0146 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2553-125T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32807424 | |||||||
| chr19:32807488 | G | A | 2 | a0001c0001t0003g0344 a0001c0001t0003g0345 |
2 | NA18939.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.2553-61G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 21/32 | chr19 | 32807488 | |||||||
| chr19:32808021 | C | T | 1 | a0003c0002t0002g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2652+373C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32808021 | |||||||
| chr19:32808273 | A | G | 201 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(198): Show |
203 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.2652+625A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32808273 | |||||||
| chr19:32808860 | C | A | 65 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(62): Show |
67 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.2652+1212C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32808860 | |||||||
| chr19:32808913 | TCTG | T | 19 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(16): Show |
19 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2653-1177_2653-117 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr19 | 32808913 | ||||||
| chr19:32809039 | G | T | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2653-1054G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809039 | |||||||
| chr19:32809049 | C | T | 2 | a0002c0003t0001g0266 a0002c0003t0001g0267 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2653-1044C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809049 | |||||||
| chr19:32809116 | TGTGCTGT others(14): Show |
T | 1 | a0002c0003t0001g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2653-973_2653-953d others(23): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr19 | 32809116 | ||||||
| chr19:32809298 | C | G | 10 | a0001c0001t0003g0308 a0001c0001t0003g0310 a0001c0001t0003g0329 others(7): Show |
10 | HG00544.hp1 HG00621.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.2653-795C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809298 | |||||||
| chr19:32809435 | G | A | 1 | a0005c0005t0006g0292 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2653-658G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809435 | |||||||
| chr19:32809510 | T | C | 3 | a0001c0001t0003g0337 a0001c0001t0003g0365 a0001c0001t0003g0366 |
3 | NA18950.hp2 NA18995.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2653-583T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809510 | |||||||
| chr19:32809529 | C | T | 1 | a0006c0006t0006g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2653-564C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809529 | |||||||
| chr19:32809679 | C | T | 1 | a0002c0003t0037g0207 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2653-414C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809679 | |||||||
| chr19:32809693 | G | A | 1 | a0003c0002t0002g0061 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2653-400G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809693 | |||||||
| chr19:32809736 | G | A | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2653-357G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809736 | |||||||
| chr19:32809977 | G | A | 3 | a0003c0002t0002g0020 a0003c0002t0002g0035 a0003c0002t0043g0034 |
3 | HG02280.hp2 HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2653-116G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32809977 | |||||||
| chr19:32809986 | CT | C | 5 | a0001c0001t0032g0174 a0001c0017t0021g0136 a0001c0017t0021g0137 others(2): Show |
5 | HG02559.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2653-104delT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr19 | 32809986 | ||||||
| chr19:32810002 | T | G | 1 | a0006c0006t0014g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2653-91T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32810002 | |||||||
| chr19:32810078 | C | A | 3 | a0001c0001t0003g0353 a0001c0001t0003g0355 a0001c0001t0012g0362 |
3 | HG02080.hp1 NA18612.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2653-15C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 22/32 | chr19 | 32810078 | |||||||
| chr19:32810425 | T | A | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2837+148T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | chr19 | 32810425 | |||||||
| chr19:32810471 | G | A | 55 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.2837+194G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | chr19 | 32810471 | |||||||
| chr19:32810600 | G | A | 1 | a0003c0002t0013g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2837+323G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | chr19 | 32810600 | |||||||
| chr19:32810756 | G | A | 2 | a0001c0001t0007g0316 a0001c0001t0007g0317 |
2 | HG01516.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2838-454G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | chr19 | 32810756 | |||||||
| chr19:32810793 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2838-417G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | chr19 | 32810793 | |||||||
| chr19:32810836 | G | A | 2 | a0003c0002t0002g0041 a0003c0002t0015g0063 |
2 | HG01109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2838-374G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | chr19 | 32810836 | |||||||
| chr19:32811089 | T | C | 5 | a0001c0001t0003g0321 a0001c0001t0003g0324 a0001c0001t0003g0326 others(2): Show |
5 | HG00558.hp2 NA18954.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.2838-121T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | chr19 | 32811089 | |||||||
| chr19:32811122 | TTA | T | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2838-84_2838-83del others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr19 | 32811122 | ||||||
| chr19:32811518 | G | A | 20 | a0001c0001t0003g0131 a0001c0001t0003g0312 a0001c0001t0003g0313 others(17): Show |
20 | HG00438.hp2 HG00673.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.3048+98G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811518 | |||||||
| chr19:32811525 | C | T | 61 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(58): Show |
62 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.3048+105C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811525 | |||||||
| chr19:32811527 | G | C | 1 | a0003c0002t0008g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3048+107G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811527 | |||||||
| chr19:32811555 | C | T | 1 | a0003c0002t0002g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3048+135C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811555 | |||||||
| chr19:32811683 | C | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3048+263C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811683 | |||||||
| chr19:32811769 | C | T | 1 | a0001c0001t0010g0179 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3048+349C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811769 | |||||||
| chr19:32811824 | G | A | 1 | a0002c0003t0001g0254 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3048+404G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811824 | |||||||
| chr19:32811917 | C | T | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3048+497C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811917 | |||||||
| chr19:32811969 | T | C | 1 | a0003c0002t0002g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3048+549T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811969 | |||||||
| chr19:32811971 | C | T | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3048+551C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32811971 | |||||||
| chr19:32812200 | G | C | 3 | a0001c0001t0003g0353 a0001c0001t0003g0355 a0001c0001t0012g0362 |
3 | HG02080.hp1 NA18612.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3048+780G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812200 | |||||||
| chr19:32812341 | C | T | 1 | a0005c0005t0006g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3048+921C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812341 | |||||||
| chr19:32812352 | T | TC | 5 | a0004c0004t0005g0268 a0004c0004t0005g0269 a0004c0004t0005g0270 others(2): Show |
5 | HG02698.hp1 HG03239.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.3048+934dupC | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr19 | 32812352 | ||||||
| chr19:32812396 | G | A | 1 | a0006c0006t0006g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3048+976G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812396 | |||||||
| chr19:32812469 | TAAAC | T | 98 | a0001c0001t0026g0290 a0002c0003t0001g0003 a0002c0003t0001g0004 others(95): Show |
100 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.3048+1052_3048+105 others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | INFO_REALIGN_3_PRIME | chr19 | 32812469 | ||||||
| chr19:32812624 | C | T | 1 | a0002c0003t0036g0202 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3049-1060C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812624 | |||||||
| chr19:32812778 | G | T | 103 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3049-906G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812778 | |||||||
| chr19:32812828 | G | A | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3049-856G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812828 | |||||||
| chr19:32812848 | A | G | 99 | a0001c0001t0026g0290 a0002c0003t0001g0003 a0002c0003t0001g0004 others(96): Show |
101 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.3049-836A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812848 | |||||||
| chr19:32812914 | A | G | 51 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(48): Show |
51 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.3049-770A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32812914 | |||||||
| chr19:32813066 | C | T | 1 | a0001c0001t0007g0296 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3049-618C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32813066 | |||||||
| chr19:32813139 | G | T | 1 | a0006c0006t0006g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3049-545G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32813139 | |||||||
| chr19:32813284 | G | A | 5 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3049-400G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32813284 | |||||||
| chr19:32813392 | C | T | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.3049-292C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32813392 | |||||||
| chr19:32813539 | G | C | 1 | a0003c0002t0002g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3049-145G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 24/32 | chr19 | 32813539 | |||||||
| chr19:32813784 | C | T | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
splice_region_variant&intron_variant | LOW | c.3141+8C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32813784 | |||||||
| chr19:32813805 | ATTTG | A | 103 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3141+34_3141+37del others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr19 | 32813805 | ||||||
| chr19:32813807 | T | C | 187 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(184): Show |
190 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.3141+31T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32813807 | |||||||
| chr19:32813811 | T | C | 103 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3141+35T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32813811 | |||||||
| chr19:32813997 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3141+221G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32813997 | |||||||
| chr19:32814020 | C | T | 97 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(94): Show |
99 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.3141+244C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814020 | |||||||
| chr19:32814104 | T | C | 56 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(53): Show |
56 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.3141+328T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814104 | |||||||
| chr19:32814106 | C | T | 2 | a0006c0006t0006g0238 a0006c0006t0006g0246 |
2 | HG01074.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.3141+330C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814106 | |||||||
| chr19:32814111 | C | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3141+335C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814111 | |||||||
| chr19:32814324 | A | G | 1 | a0002c0003t0001g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3141+548A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814324 | |||||||
| chr19:32814341 | C | T | 1 | a0003c0002t0002g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3141+565C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814341 | |||||||
| chr19:32814381 | TACTTACC others(7): Show |
T | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3141+608_3141+621d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr19 | 32814381 | ||||||
| chr19:32814389 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3141+613A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814389 | |||||||
| chr19:32814598 | C | T | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3141+822C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814598 | |||||||
| chr19:32814621 | T | A | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3142-827T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814621 | |||||||
| chr19:32814819 | A | G | 256 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(253): Show |
258 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.3142-629A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814819 | |||||||
| chr19:32814911 | C | T | 1 | a0002c0003t0001g0194 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3142-537C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32814911 | |||||||
| chr19:32815138 | CTGACTAG others(29): Show |
C | 100 | a0001c0001t0003g0339 a0001c0001t0003g0373 a0001c0001t0003g0374 others(97): Show |
102 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.3142-283_3142-248d others(38): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr19 | 32815138 | ||||||
| chr19:32815240 | A | G | 1 | a0016c0027t0038g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3142-208A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32815240 | |||||||
| chr19:32815316 | C | T | 65 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(62): Show |
67 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.3142-132C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32815316 | |||||||
| chr19:32815391 | C | T | 4 | a0001c0001t0005g0305 a0001c0001t0005g0306 a0001c0001t0005g0307 others(1): Show |
4 | HG02258.hp1 HG02886.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3142-57C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 25/32 | chr19 | 32815391 | |||||||
| chr19:32815721 | T | C | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0003c0002t0002g0027 |
3 | HG00544.hp2 HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3314+101T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815721 | |||||||
| chr19:32815722 | G | A | 1 | a0003c0002t0002g0027 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3314+102G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815722 | |||||||
| chr19:32815723 | C | T | 3 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0002c0003t0001g0291 |
3 | HG01175.hp1 HG01975.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3314+103C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815723 | |||||||
| chr19:32815871 | G | T | 4 | a0008c0012t0002g0019 a0008c0012t0002g0023 a0008c0012t0002g0077 others(1): Show |
4 | HG00609.hp1 NA18949.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.3314+251G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815871 | |||||||
| chr19:32815937 | C | T | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3314+317C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815937 | |||||||
| chr19:32815972 | G | A | 67 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(64): Show |
68 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3314+352G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815972 | |||||||
| chr19:32815986 | A | G | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3314+366A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815986 | |||||||
| chr19:32815988 | G | A | 1 | a0002c0003t0001g0229 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3314+368G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32815988 | |||||||
| chr19:32816020 | G | GT | 194 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(191): Show |
196 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.3314+405dupT | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr19 | 32816020 | ||||||
| chr19:32816094 | A | G | 220 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(217): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.3314+474A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816094 | |||||||
| chr19:32816098 | C | A | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3314+478C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816098 | |||||||
| chr19:32816165 | T | C | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.3314+545T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816165 | |||||||
| chr19:32816211 | A | G | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.3314+591A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816211 | |||||||
| chr19:32816227 | G | A | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3314+607G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816227 | |||||||
| chr19:32816313 | C | A | 1 | a0003c0002t0002g0014 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3314+693C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816313 | |||||||
| chr19:32816401 | A | T | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.3314+781A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816401 | |||||||
| chr19:32816516 | T | C | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3314+896T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816516 | |||||||
| chr19:32816536 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3314+916C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816536 | |||||||
| chr19:32816721 | G | A | 1 | a0003c0002t0002g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3314+1101G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32816721 | |||||||
| chr19:32817018 | G | A | 1 | a0006c0006t0006g0246 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3315-1071G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817018 | |||||||
| chr19:32817069 | A | G | 51 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(48): Show |
51 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.3315-1020A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817069 | |||||||
| chr19:32817108 | A | G | 15 | a0001c0001t0003g0131 a0001c0001t0003g0312 a0001c0001t0003g0313 others(12): Show |
15 | HG00673.hp2 NA18939.hp2 NA18942.hp1 others(12): Show |
intron_variant | MODIFIER | c.3315-981A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817108 | |||||||
| chr19:32817215 | A | G | 1 | a0001c0001t0005g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3315-874A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817215 | |||||||
| chr19:32817217 | C | T | 2 | a0001c0001t0003g0344 a0001c0001t0003g0345 |
2 | NA18939.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.3315-872C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817217 | |||||||
| chr19:32817422 | G | A | 1 | a0001c0001t0012g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3315-667G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817422 | |||||||
| chr19:32817700 | C | G | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3315-389C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817700 | |||||||
| chr19:32817722 | C | T | 1 | a0009c0009t0001g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3315-367C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817722 | |||||||
| chr19:32817769 | G | A | 64 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0183 others(61): Show |
66 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.3315-320G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817769 | |||||||
| chr19:32817803 | C | T | 3 | a0002c0003t0001g0263 a0019c0022t0001g0247 a0026c0030t0001g0216 |
3 | HG02040.hp1 HG02080.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3315-286C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817803 | |||||||
| chr19:32817812 | C | T | 1 | a0001c0001t0044g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3315-277C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817812 | |||||||
| chr19:32817843 | G | A | 1 | a0005c0005t0006g0112 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3315-246G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817843 | |||||||
| chr19:32817851 | G | A | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3315-238G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32817851 | |||||||
| chr19:32817918 | AG | A | 103 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.3315-169delG | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr19 | 32817918 | ||||||
| chr19:32818023 | G | A | 1 | a0004c0004t0005g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3315-66G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32818023 | |||||||
| chr19:32818041 | C | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3315-48C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 26/32 | chr19 | 32818041 | |||||||
| chr19:32818261 | C | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3383+104C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32818261 | |||||||
| chr19:32818507 | G | A | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.3383+350G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32818507 | |||||||
| chr19:32818543 | A | T | 1 | a0026c0030t0001g0216 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3383+386A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32818543 | |||||||
| chr19:32818560 | A | T | 1 | a0002c0003t0001g0239 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3383+403A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32818560 | |||||||
| chr19:32818671 | G | C | 1 | a0003c0002t0002g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3383+514G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32818671 | |||||||
| chr19:32818715 | C | A | 1 | a0001c0001t0003g0348 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3383+558C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32818715 | |||||||
| chr19:32819146 | G | A | 32 | a0002c0003t0001g0098 a0002c0003t0001g0182 a0002c0003t0001g0211 others(29): Show |
32 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.3383+989G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819146 | |||||||
| chr19:32819242 | A | G | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.3383+1085A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819242 | |||||||
| chr19:32819314 | C | CA | 132 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.3383+1171dupA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr19 | 32819314 | ||||||
| chr19:32819314 | C | CAA | 125 | a0001c0001t0003g0349 a0001c0001t0005g0302 a0001c0001t0005g0305 others(122): Show |
126 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.3383+1170_3383+117 others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr19 | 32819314 | ||||||
| chr19:32819314 | C | CAAA | 12 | a0001c0001t0005g0319 a0002c0003t0001g0003 a0002c0003t0001g0004 others(9): Show |
14 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.3383+1169_3383+117 others(7): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr19 | 32819314 | ||||||
| chr19:32819424 | C | G | 1 | a0002c0010t0039g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3383+1267C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819424 | |||||||
| chr19:32819445 | T | A | 3 | a0001c0008t0003g0315 a0001c0008t0003g0358 a0001c0008t0003g0359 |
3 | NA18951.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.3383+1288T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819445 | |||||||
| chr19:32819531 | T | C | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3383+1374T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819531 | |||||||
| chr19:32819541 | T | C | 255 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(252): Show |
257 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.3383+1384T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819541 | |||||||
| chr19:32819743 | G | A | 2 | a0003c0002t0002g0012 a0003c0002t0002g0013 |
2 | HG02027.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.3384-1290G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819743 | |||||||
| chr19:32819785 | A | G | 2 | a0001c0001t0018g0099 a0001c0001t0018g0100 |
2 | HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3384-1248A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819785 | |||||||
| chr19:32819860 | C | T | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3384-1173C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32819860 | |||||||
| chr19:32820121 | C | T | 12 | a0004c0004t0005g0123 a0004c0004t0005g0124 a0004c0004t0005g0125 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3384-912C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820121 | |||||||
| chr19:32820259 | C | T | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3384-774C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820259 | |||||||
| chr19:32820279 | G | T | 1 | a0001c0001t0026g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3384-754G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820279 | |||||||
| chr19:32820300 | C | G | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.3384-733C>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820300 | |||||||
| chr19:32820316 | A | G | 1 | a0003c0002t0002g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3384-717A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820316 | |||||||
| chr19:32820332 | T | C | 2 | a0020c0021t0018g0189 a0027c0023t0017g0186 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3384-701T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820332 | |||||||
| chr19:32820483 | T | A | 1 | a0001c0001t0004g0143 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3384-550T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820483 | |||||||
| chr19:32820638 | A | G | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3384-395A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820638 | |||||||
| chr19:32820783 | G | T | 1 | a0004c0004t0016g0185 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3384-250G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820783 | |||||||
| chr19:32820833 | T | C | 57 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(54): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3384-200T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820833 | |||||||
| chr19:32820859 | T | C | 57 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(54): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3384-174T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820859 | |||||||
| chr19:32820951 | G | A | 2 | a0003c0002t0002g0012 a0003c0002t0002g0180 |
2 | HG02027.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3384-82G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820951 | |||||||
| chr19:32820959 | A | G | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3384-74A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 27/32 | chr19 | 32820959 | |||||||
| chr19:32821231 | G | A | 1 | a0003c0002t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3490+92G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32821231 | |||||||
| chr19:32821252 | G | A | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3490+113G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32821252 | |||||||
| chr19:32821369 | A | AGT | 37 | a0002c0003t0002g0235 a0003c0002t0002g0001 a0003c0002t0002g0008 others(34): Show |
38 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.3490+270_3490+271d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821369 | ||||||
| chr19:32821369 | A | AGTGT | 14 | a0003c0002t0002g0030 a0003c0002t0002g0031 a0003c0002t0002g0053 others(11): Show |
14 | HG00423.hp1 HG01496.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3490+268_3490+271d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821369 | ||||||
| chr19:32821369 | AGT | A | 10 | a0003c0002t0002g0005 a0003c0002t0002g0007 a0003c0002t0002g0014 others(7): Show |
10 | HG00140.hp1 HG01952.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3490+270_3490+271d others(4): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821369 | ||||||
| chr19:32821369 | AGTGTGTG others(1): Show |
A | 4 | a0003c0002t0013g0015 a0015c0028t0024g0096 a0016c0027t0038g0110 others(1): Show |
4 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.3490+264_3490+271d others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821369 | ||||||
| chr19:32821369 | AGTGTGTG others(3): Show |
A | 23 | a0003c0002t0013g0016 a0003c0002t0013g0018 a0003c0002t0013g0088 others(20): Show |
23 | HG01074.hp2 HG01123.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.3490+262_3490+271d others(12): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821369 | ||||||
| chr19:32821369 | AGTGTGTG others(5): Show |
A | 7 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(4): Show |
8 | HG00099.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.3490+260_3490+271d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821369 | ||||||
| chr19:32821393 | TGTGTGTG others(11): Show |
T | 1 | a0001c0001t0003g0329 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3490+260_3490+277d others(20): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821393 | ||||||
| chr19:32821395 | TGTGTGTG others(9): Show |
T | 86 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(83): Show |
86 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.3490+262_3490+277d others(18): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821395 | ||||||
| chr19:32821397 | TGTGTGTG others(7): Show |
T | 111 | a0001c0001t0003g0309 a0001c0001t0003g0311 a0001c0001t0005g0356 others(108): Show |
113 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.3490+264_3490+277d others(16): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821397 | ||||||
| chr19:32821399 | TGTGTGTG others(5): Show |
T | 8 | a0001c0001t0010g0154 a0001c0001t0031g0181 a0001c0017t0021g0136 others(5): Show |
8 | HG02109.hp1 HG02559.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.3490+266_3490+277d others(14): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821399 | ||||||
| chr19:32821401 | TGTGTGTG others(3): Show |
T | 2 | a0001c0001t0018g0100 a0001c0001t0044g0103 |
2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3490+268_3490+277d others(12): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821401 | ||||||
| chr19:32821403 | TGTGTGTG others(1): Show |
T | 3 | a0001c0001t0004g0175 a0001c0001t0010g0179 a0001c0001t0020g0156 |
3 | HG00323.hp2 HG01261.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3490+270_3490+277d others(10): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821403 | ||||||
| chr19:32821405 | TGTGTGC | T | 30 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0139 others(27): Show |
30 | HG00423.hp2 HG00597.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.3490+272_3490+277d others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821405 | ||||||
| chr19:32821407 | TGTGC | T | 13 | a0001c0001t0004g0134 a0001c0001t0004g0135 a0001c0001t0004g0147 others(10): Show |
13 | HG00408.hp2 HG00609.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.3490+272_3490+275d others(6): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32821407 | ||||||
| chr19:32821429 | A | G | 3 | a0003c0002t0002g0048 a0003c0002t0002g0062 a0003c0002t0008g0082 |
3 | HG01243.hp2 HG01516.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3490+290A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32821429 | |||||||
| chr19:32821547 | C | A | 1 | a0002c0003t0001g0217 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3490+408C>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32821547 | |||||||
| chr19:32821657 | C | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3490+518C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32821657 | |||||||
| chr19:32821727 | A | C | 5 | a0002c0003t0001g0098 a0002c0003t0001g0278 a0002c0003t0001g0283 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3490+588A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32821727 | |||||||
| chr19:32822060 | G | T | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3490+921G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822060 | |||||||
| chr19:32822172 | A | G | 1 | a0001c0001t0010g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3490+1033A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822172 | |||||||
| chr19:32822192 | G | A | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3490+1053G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822192 | |||||||
| chr19:32822305 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3490+1166G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822305 | |||||||
| chr19:32822418 | T | C | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.3490+1279T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822418 | |||||||
| chr19:32822427 | G | A | 4 | a0004c0004t0007g0212 a0004c0004t0007g0214 a0004c0004t0007g0215 others(1): Show |
4 | HG02717.hp2 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3490+1288G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822427 | |||||||
| chr19:32822703 | C | T | 79 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(76): Show |
79 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.3490+1564C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822703 | |||||||
| chr19:32822746 | C | CAAAA | 261 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(258): Show |
264 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.3490+1615_3490+161 others(8): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32822746 | ||||||
| chr19:32822746 | C | CAAAAA | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.3490+1614_3490+161 others(9): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32822746 | ||||||
| chr19:32822798 | T | G | 283 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(280): Show |
286 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.3490+1659T>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822798 | |||||||
| chr19:32822811 | A | G | 1 | a0001c0001t0003g0310 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3490+1672A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822811 | |||||||
| chr19:32822816 | A | C | 4 | a0001c0001t0018g0099 a0001c0001t0018g0100 a0001c0001t0031g0181 others(1): Show |
4 | HG01175.hp1 HG02257.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3490+1677A>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822816 | |||||||
| chr19:32822900 | A | G | 1 | a0003c0002t0013g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3490+1761A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822900 | |||||||
| chr19:32822943 | T | C | 4 | a0003c0002t0002g0046 a0003c0002t0002g0051 a0013c0014t0003g0298 others(1): Show |
4 | HG00099.hp1 HG01070.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.3490+1804T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32822943 | |||||||
| chr19:32823014 | G | A | 1 | a0001c0001t0031g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3490+1875G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823014 | |||||||
| chr19:32823048 | T | C | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3490+1909T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823048 | |||||||
| chr19:32823057 | G | C | 1 | a0003c0002t0002g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3490+1918G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823057 | |||||||
| chr19:32823115 | T | A | 7 | a0001c0001t0010g0154 a0001c0001t0032g0174 a0001c0001t0044g0103 others(4): Show |
7 | HG02257.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3490+1976T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823115 | |||||||
| chr19:32823274 | C | T | 4 | a0005c0005t0014g0262 a0006c0006t0014g0259 a0006c0006t0014g0260 others(1): Show |
4 | HG00099.hp2 HG01123.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.3490+2135C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823274 | |||||||
| chr19:32823432 | A | T | 1 | a0003c0002t0013g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3490+2293A>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823432 | |||||||
| chr19:32823446 | A | G | 1 | a0003c0002t0002g0066 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3490+2307A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823446 | |||||||
| chr19:32823454 | A | G | 8 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3490+2315A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823454 | |||||||
| chr19:32823478 | C | T | 2 | a0002c0003t0001g0278 a0002c0003t0001g0284 |
2 | HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3490+2339C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823478 | |||||||
| chr19:32823548 | G | A | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3490+2409G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823548 | |||||||
| chr19:32823578 | C | T | 2 | a0003c0002t0002g0046 a0003c0002t0002g0051 |
2 | HG00099.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.3490+2439C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823578 | |||||||
| chr19:32823831 | T | C | 6 | a0001c0001t0010g0154 a0003c0002t0002g0031 a0003c0002t0002g0076 others(3): Show |
6 | HG02129.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3491-2267T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823831 | |||||||
| chr19:32823884 | G | A | 1 | a0003c0002t0002g0086 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3491-2214G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823884 | |||||||
| chr19:32823979 | T | C | 1 | a0018c0033t0007g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3491-2119T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32823979 | |||||||
| chr19:32824007 | A | G | 24 | a0001c0001t0003g0313 a0001c0001t0018g0099 a0002c0003t0001g0240 others(21): Show |
25 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.3491-2091A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824007 | |||||||
| chr19:32824158 | T | C | 1 | a0001c0001t0005g0319 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3491-1940T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824158 | |||||||
| chr19:32824212 | T | C | 291 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(288): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3491-1886T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824212 | |||||||
| chr19:32824313 | G | A | 1 | a0006c0006t0006g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3491-1785G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824313 | |||||||
| chr19:32824449 | T | C | 95 | a0001c0001t0010g0168 a0002c0003t0001g0003 a0002c0003t0001g0004 others(92): Show |
97 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.3491-1649T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824449 | |||||||
| chr19:32824461 | C | T | 1 | a0001c0001t0003g0335 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3491-1637C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824461 | |||||||
| chr19:32824465 | G | A | 30 | a0002c0003t0001g0098 a0002c0003t0001g0182 a0002c0003t0001g0211 others(27): Show |
30 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.3491-1633G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824465 | |||||||
| chr19:32824600 | G | C | 284 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(281): Show |
287 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.3491-1498G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824600 | |||||||
| chr19:32824706 | C | T | 1 | a0003c0002t0002g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3491-1392C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824706 | |||||||
| chr19:32824707 | G | A | 19 | a0005c0005t0006g0111 a0005c0005t0006g0112 a0005c0005t0006g0114 others(16): Show |
19 | HG00099.hp2 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.3491-1391G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32824707 | |||||||
| chr19:32825330 | G | A | 1 | a0001c0001t0004g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3491-768G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825330 | |||||||
| chr19:32825417 | C | T | 225 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(222): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.3491-681C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825417 | |||||||
| chr19:32825575 | G | T | 6 | a0001c0007t0009g0002 a0001c0007t0009g0105 a0001c0007t0009g0106 others(3): Show |
7 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.3491-523G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825575 | |||||||
| chr19:32825647 | C | T | 1 | a0003c0002t0002g0049 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3491-451C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825647 | |||||||
| chr19:32825648 | G | A | 2 | a0012c0015t0017g0142 a0012c0015t0017g0173 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3491-450G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825648 | |||||||
| chr19:32825795 | C | T | 2 | a0015c0028t0024g0096 a0016c0027t0038g0110 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.3491-303C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825795 | |||||||
| chr19:32825836 | T | C | 1 | a0003c0002t0002g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3491-262T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825836 | |||||||
| chr19:32825934 | T | A | 1 | a0001c0001t0010g0179 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3491-164T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32825934 | |||||||
| chr19:32826002 | G | T | 1 | a0001c0001t0004g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3491-96G>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32826002 | |||||||
| chr19:32826022 | G | GTA | 252 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(249): Show |
254 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.3491-66_3491-65dup others(2): Show |
TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr19 | 32826022 | ||||||
| chr19:32826034 | G | A | 1 | a0003c0002t0023g0017 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3491-64G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 28/32 | chr19 | 32826034 | |||||||
| chr19:32826191 | G | A | 4 | a0003c0002t0002g0038 a0003c0002t0002g0040 a0003c0002t0002g0042 others(1): Show |
4 | NA18939.hp1 NA18945.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3554+30G>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 29/32 | chr19 | 32826191 | |||||||
| chr19:32826223 | C | T | 2 | a0020c0021t0018g0189 a0027c0023t0017g0186 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3555-21C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 29/32 | chr19 | 32826223 | |||||||
| chr19:32826401 | T | C | 290 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(287): Show |
293 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.3668+44T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 30/32 | chr19 | 32826401 | |||||||
| chr19:32826637 | C | T | 100 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(97): Show |
100 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.3822+39C>T | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 31/32 | chr19 | 32826637 | |||||||
| chr19:32826678 | AAC | A | 113 | a0002c0003t0001g0003 a0002c0003t0001g0004 a0002c0003t0001g0098 others(110): Show |
115 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(112): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.3823-3_3823-2delCA | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 31/32 | INFO_REALIGN_3_PRIME | chr19 | 32826678 | ||||||
| chr19:32826758 | T | A | 291 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(288): Show |
294 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.3889+9T>A | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32826758 | |||||||
| chr19:32826784 | T | C | 80 | a0001c0001t0003g0353 a0001c0001t0004g0101 a0001c0001t0004g0102 others(77): Show |
80 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.3889+35T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32826784 | |||||||
| chr19:32826842 | A | G | 45 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(42): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.3889+93A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32826842 | |||||||
| chr19:32826884 | T | C | 122 | a0001c0001t0003g0131 a0001c0001t0003g0295 a0001c0001t0003g0297 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.3889+135T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32826884 | |||||||
| chr19:32826922 | T | C | 57 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(54): Show |
57 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.3889+173T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32826922 | |||||||
| chr19:32826938 | T | C | 6 | a0003c0002t0013g0015 a0003c0002t0013g0016 a0003c0002t0013g0018 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3889+189T>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32826938 | |||||||
| chr19:32827006 | A | G | 150 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0134 others(147): Show |
152 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.3890-158A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32827006 | |||||||
| chr19:32827086 | A | G | 1 | a0004c0004t0005g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3890-78A>G | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32827086 | |||||||
| chr19:32827089 | G | C | 3 | a0001c0001t0025g0289 a0020c0021t0018g0189 a0027c0023t0017g0186 |
3 | HG02622.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3890-75G>C | TDRD12 | ENSG00000173809.18 | transcript | ENST00000639142.2 | protein_coding | 32/32 | chr19 | 32827089 |