Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55775 |
| ensemblid | ENSG00000042088.14 |
| hgncid | 18884 |
| symbol | TDP1 |
| name | tyrosyl-DNA phosphodiesterase 1 |
| refseq_nuc | NM_018319.4 |
| refseq_prot | NP_060789.2 |
| ensembl_nuc | ENST00000335725.9 |
| ensembl_prot | ENSP00000337353.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 89955927 |
| end | 90044764 |
| strand | + |
| ver | v1.2 |
| region | chr14:89955927-90044764 |
| region5000 | chr14:89950927-90049764 |
| regionname0 | TDP1_chr14_89955927_90044764 |
| regionname5000 | TDP1_chr14_89950927_90049764 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 608 | 208 | 58 | 44 | 79 | 4 | 21 | 69 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0002 | 0/0 | 608 | 35 | 25 | 3 | 4 | 0 | 3 | 4 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0003 | 0/0 | 608 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0004 | 0/0 | 608 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0005 | 0/0 | 608 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0006 | 0/0 | 608 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0007 | 0/0 | 608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0008 | 0/0 | 608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| a0009 | 0/0 | 608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | MSQEG others(603): Show |
chr14 | 89950927 | 90049764 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1824 | 150 | 15 | 39 | 74 | 3 | 17 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0001c0002 | 0/0 | 1824 | 44 | 29 | 5 | 5 | 1 | 4 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0001c0005 | 0/0 | 1824 | 14 | 14 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0002c0003 | 0/0 | 1824 | 20 | 13 | 0 | 4 | 0 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0002c0004 | 0/0 | 1824 | 14 | 11 | 3 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0002c0011 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0003c0006 | 0/0 | 1824 | 8 | 8 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0004c0007 | 0/0 | 1824 | 6 | 0 | 6 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0005c0008 | 0/0 | 1824 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0006c0010 | 0/0 | 1824 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0007c0012 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0008c0009 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 | ||
| a0009c0013 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | ATGTC others(1819): Show |
chr14 | 89950927 | 90049764 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3722 | 100 | 13 | 29 | 42 | 3 | 12 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0001t0002 | 0/1 | 3722 | 46 | 2 | 8 | 30 | 0 | 5 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0001t0011 | 0/0 | 3722 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0001t0015 | 0/0 | 3722 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0001t0020 | 0/0 | 3722 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0001 | 0/0 | 3722 | 5 | 5 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0003 | 0/0 | 3722 | 2 | 1 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0004 | 0/0 | 3721 | 18 | 5 | 4 | 5 | 1 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3716): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0006 | 0/0 | 3722 | 9 | 8 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0008 | 0/0 | 3722 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0010 | 0/0 | 3721 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3716): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0013 | 0/0 | 3721 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3716): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0014 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0002t0021 | 0/0 | 3721 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3716): Show |
chr14 | 89950927 | 90049764 |
| a0001c0005t0001 | 0/0 | 3722 | 11 | 11 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0005t0016 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0005t0017 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0001c0005t0018 | 0/0 | 3721 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3716): Show |
chr14 | 89950927 | 90049764 |
| a0002c0003t0003 | 0/0 | 3722 | 19 | 12 | 0 | 4 | 0 | 3 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0002c0003t0012 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0002c0004t0005 | 0/0 | 3723 | 11 | 8 | 3 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3718): Show |
chr14 | 89950927 | 90049764 |
| a0002c0004t0009 | 0/0 | 3723 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3718): Show |
chr14 | 89950927 | 90049764 |
| a0002c0011t0019 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0003c0006t0007 | 0/0 | 3721 | 8 | 8 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3716): Show |
chr14 | 89950927 | 90049764 |
| a0004c0007t0002 | 0/0 | 3722 | 6 | 0 | 6 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0005c0008t0001 | 0/0 | 3722 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0006c0010t0003 | 0/0 | 3722 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0007c0012t0012 | 0/0 | 3722 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3717): Show |
chr14 | 89950927 | 90049764 |
| a0008c0009t0005 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3718): Show |
chr14 | 89950927 | 90049764 |
| a0009c0013t0004 | 0/0 | 3721 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | GAAGG others(3716): Show |
chr14 | 89950927 | 90049764 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0001 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0011g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0015g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0001t0020g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0002t0021g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0017g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0001c0005t0018g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0003t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0004t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0002c0011t0019g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0003c0006t0007g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0003c0006t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0003c0006t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0003c0006t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0003c0006t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0003c0006t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0004c0007t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0004c0007t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0004c0007t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0004c0007t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0004c0007t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0005c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0005c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0005c0008t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0006c0010t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0007c0012t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0008c0009t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| a0009c0013t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0217 | EUR | FIN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00735 | hp2 | a0002 | c0004 | t0005 | g0068 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01070 | hp2 | a0006 | c0010 | t0003 | g0185 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01081 | hp1 | a0002 | c0004 | t0005 | g0069 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01109 | hp2 | a0002 | c0004 | t0005 | g0079 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0213 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0218 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01192 | hp1 | a0001 | c0002 | t0006 | g0022 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01255 | hp1 | a0001 | c0001 | t0020 | g0015 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01256 | hp1 | a0001 | c0002 | t0004 | g0219 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01256 | hp2 | a0004 | c0007 | t0002 | g0041 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0204 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01433 | hp2 | a0004 | c0007 | t0002 | g0050 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01884 | hp1 | a0003 | c0006 | t0007 | g0004 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01891 | hp2 | a0003 | c0006 | t0007 | g0082 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01943 | hp2 | a0004 | c0007 | t0002 | g0039 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01981 | hp1 | a0004 | c0007 | t0002 | g0054 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01981 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02055 | hp1 | a0007 | c0012 | t0012 | g0141 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02055 | hp2 | a0002 | c0004 | t0009 | g0074 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0227 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02145 | hp2 | a0002 | c0004 | t0005 | g0075 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CDX | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0028 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0207 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02273 | hp2 | a0004 | c0007 | t0002 | g0014 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0225 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0206 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02451 | hp2 | a0002 | c0003 | t0003 | g0005 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02572 | hp2 | a0001 | c0002 | t0021 | g0192 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02602 | hp2 | a0002 | c0003 | t0003 | g0131 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02615 | hp1 | a0005 | c0008 | t0001 | g0139 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02622 | hp1 | a0001 | c0002 | t0010 | g0229 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02622 | hp2 | a0001 | c0005 | t0018 | g0010 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02630 | hp1 | a0002 | c0004 | t0009 | g0072 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02630 | hp2 | a0001 | c0002 | t0013 | g0199 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02647 | hp2 | a0001 | c0002 | t0014 | g0025 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0223 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02723 | hp2 | a0002 | c0003 | t0012 | g0189 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02738 | hp2 | a0002 | c0003 | t0003 | g0130 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02809 | hp1 | a0002 | c0003 | t0003 | g0132 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02809 | hp2 | a0002 | c0004 | t0005 | g0067 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02886 | hp1 | a0001 | c0002 | t0006 | g0226 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02886 | hp2 | a0005 | c0008 | t0001 | g0138 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02896 | hp1 | a0001 | c0002 | t0004 | g0209 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02896 | hp2 | a0003 | c0006 | t0007 | g0083 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02897 | hp1 | a0003 | c0006 | t0007 | g0084 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0208 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0026 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02965 | hp1 | a0001 | c0002 | t0010 | g0220 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02965 | hp2 | a0001 | c0002 | t0008 | g0197 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02970 | hp1 | a0002 | c0011 | t0019 | g0134 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02970 | hp2 | a0002 | c0004 | t0005 | g0016 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02976 | hp1 | a0008 | c0009 | t0005 | g0076 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02976 | hp2 | a0003 | c0006 | t0007 | g0004 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0193 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0222 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03098 | hp2 | a0005 | c0008 | t0001 | g0140 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03130 | hp1 | a0001 | c0002 | t0010 | g0221 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03130 | hp2 | a0002 | c0004 | t0009 | g0073 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0224 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03195 | hp1 | a0002 | c0003 | t0003 | g0184 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0023 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0188 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0002 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03225 | hp2 | a0002 | c0003 | t0003 | g0005 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03453 | hp1 | a0001 | c0005 | t0016 | g0029 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03453 | hp2 | a0002 | c0004 | t0005 | g0071 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0027 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03516 | hp1 | a0002 | c0004 | t0005 | g0070 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03516 | hp2 | a0002 | c0003 | t0003 | g0024 | AFR | ESN | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0210 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03540 | hp2 | a0002 | c0003 | t0003 | g0137 | AFR | GWD | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03579 | hp1 | a0001 | c0002 | t0008 | g0201 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03579 | hp2 | a0002 | c0003 | t0003 | g0133 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03654 | hp2 | a0002 | c0003 | t0003 | g0136 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03710 | hp1 | a0001 | c0002 | t0004 | g0215 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0216 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG04228 | hp1 | a0001 | c0002 | t0004 | g0214 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0002 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18522 | hp2 | a0002 | c0003 | t0003 | g0182 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18906 | hp1 | a0002 | c0004 | t0005 | g0078 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18944 | hp2 | a0001 | c0002 | t0004 | g0203 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0092 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18957 | hp1 | a0002 | c0003 | t0003 | g0020 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18968 | hp1 | a0002 | c0003 | t0003 | g0020 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18973 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18989 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19009 | hp2 | a0002 | c0003 | t0003 | g0187 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19030 | hp1 | a0002 | c0004 | t0005 | g0077 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19030 | hp2 | a0002 | c0003 | t0003 | g0135 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19043 | hp1 | a0002 | c0003 | t0003 | g0005 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0065 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19056 | hp2 | a0001 | c0002 | t0004 | g0211 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19077 | hp2 | a0001 | c0001 | t0011 | g0145 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19083 | hp2 | a0009 | c0013 | t0004 | g0212 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0205 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19088 | hp1 | a0002 | c0003 | t0003 | g0186 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA19240 | hp2 | a0003 | c0006 | t0007 | g0004 | AFR | YRI | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA20129 | hp2 | a0003 | c0006 | t0007 | g0081 | AFR | ASW | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG01123 | hp2 | a0004 | c0007 | t0002 | g0014 | AMR | CLM | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0002 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02486 | hp1 | a0001 | c0005 | t0017 | g0002 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02486 | hp2 | a0001 | c0002 | t0013 | g0198 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02559 | hp1 | a0002 | c0003 | t0003 | g0183 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03471 | hp1 | a0001 | c0002 | t0006 | g0228 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG03471 | hp2 | a0002 | c0004 | t0005 | g0016 | AFR | MSL | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG06807 | hp1 | a0003 | c0006 | t0007 | g0080 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| HG06807 | hp2 | a0001 | c0002 | t0006 | g0022 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA20300 | hp1 | a0001 | c0002 | t0008 | g0202 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | LWK | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0034 | REF | REF | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0149 | REF | REF | TDP1_chr14_89950927_90049764 | TDP1 | chr14 | 89950927 | 90049764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89963150 | A | G | 1 | a0009 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.36A>G | p.Ile12Met | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 310/3722 | 36/1827 | 12/608 | chr14 | 89963150 | |||
| chr14:89963399 | G | T | 1 | a0005 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.285G>T | p.Glu95Asp | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 559/3722 | 285/1827 | 95/608 | chr14 | 89963399 | |||
| chr14:89963416 | C | T | 1 | a0004 | 6 | HG01123.hp2 HG01256.hp2 HG01433.hp2 others(3): Show |
missense_variant | MODERATE | c.302C>T | p.Pro101Leu | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 576/3722 | 302/1827 | 101/608 | chr14 | 89963416 | |||
| chr14:89963514 | G | A | 4 | a0002 a0003 a0006 others(1): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
missense_variant | MODERATE | c.400G>A | p.Ala134Thr | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 674/3722 | 400/1827 | 134/608 | chr14 | 89963514 | |||
| chr14:89984542 | G | A | 2 | a0003 a0007 |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
missense_variant | MODERATE | c.911G>A | p.Arg304Gln | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/17 | 1185/3722 | 911/1827 | 304/608 | chr14 | 89984542 | |||
| chr14:89988938 | G | A | 1 | a0008 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1165G>A | p.Ala389Thr | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/17 | 1439/3722 | 1165/1827 | 389/608 | chr14 | 89988938 | |||
| chr14:89989085 | T | A | 1 | a0006 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.1312T>A | p.Tyr438Asn | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/17 | 1586/3722 | 1312/1827 | 438/608 | chr14 | 89989085 | |||
| chr14:90033166 | A | G | 1 | a0003 | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
missense_variant | MODERATE | c.1705A>G | p.Thr569Ala | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/17 | 1979/3722 | 1705/1827 | 569/608 | chr14 | 90033166 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89963357 | C | G | 1 | a0007c0012 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.243C>G | p.Ser81Ser | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 517/3722 | 243/1827 | 81/608 | chr14 | 89963357 | |||
| chr14:89963405 | A | G | 10 | a0001c0002 a0001c0005 a0002c0003 others(7): Show |
105 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(102): Show |
synonymous_variant | LOW | c.291A>G | p.Gln97Gln | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 565/3722 | 291/1827 | 97/608 | chr14 | 89963405 | |||
| chr14:89963651 | C | T | 1 | a0005c0008 | 3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
synonymous_variant | LOW | c.537C>T | p.Asn179Asn | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/17 | 811/3722 | 537/1827 | 179/608 | chr14 | 89963651 | |||
| chr14:89985156 | A | G | 3 | a0002c0003 a0002c0011 a0006c0010 |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
synonymous_variant | LOW | c.1077A>G | p.Pro359Pro | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/17 | 1351/3722 | 1077/1827 | 359/608 | chr14 | 89985156 | |||
| chr14:89985177 | A | G | 2 | a0003c0006 a0007c0012 |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
synonymous_variant | LOW | c.1098A>G | p.Gln366Gln | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/17 | 1372/3722 | 1098/1827 | 366/608 | chr14 | 89985177 | |||
| chr14:89985186 | T | C | 1 | a0001c0005 | 14 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
synonymous_variant | LOW | c.1107T>C | p.Asn369Asn | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/17 | 1381/3722 | 1107/1827 | 369/608 | chr14 | 89985186 | |||
| chr14:89993478 | C | T | 1 | a0007c0012 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1536C>T | p.Val512Val | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/17 | 1810/3722 | 1536/1827 | 512/608 | chr14 | 89993478 | |||
| chr14:90043116 | G | A | 1 | a0002c0011 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1800G>A | p.Thr600Thr | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 2074/3722 | 1800/1827 | 600/608 | chr14 | 90043116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89956584 | A | G | 4 | a0001c0002t0004 a0001c0002t0010 a0001c0002t0021 others(1): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-224A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/17 | 6531 | chr14 | 89956584 | ||||||
| chr14:89956631 | C | T | 4 | a0002c0004t0005 a0002c0004t0009 a0003c0006t0007 others(1): Show |
23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-177C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/17 | 6484 | chr14 | 89956631 | ||||||
| chr14:89956787 | C | T | 3 | a0001c0001t0002 a0001c0001t0020 a0004c0007t0002 |
52 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-21C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/17 | 6328 | chr14 | 89956787 | ||||||
| chr14:90043220 | C | T | 18 | a0001c0001t0011 a0001c0002t0003 a0001c0002t0004 others(15): Show |
87 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 77 | chr14 | 90043220 | ||||||
| chr14:90043230 | T | TAA | 3 | a0002c0004t0005 a0002c0004t0009 a0008c0009t0005 |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*89_*90dupAA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 91 | INFO_REALIGN_3_PRIME | chr14 | 90043230 | |||||
| chr14:90043536 | T | C | 3 | a0001c0001t0011 a0001c0002t0004 a0009c0013t0004 |
21 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*393T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 393 | chr14 | 90043536 | ||||||
| chr14:90043682 | G | A | 1 | a0001c0002t0006 | 9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 539 | chr14 | 90043682 | ||||||
| chr14:90043741 | G | A | 1 | a0003c0006t0007 | 8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*598G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 598 | chr14 | 90043741 | ||||||
| chr14:90043748 | CA | C | 10 | a0001c0002t0004 a0001c0002t0010 a0001c0002t0013 others(7): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*608delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 608 | INFO_REALIGN_3_PRIME | chr14 | 90043748 | |||||
| chr14:90043810 | G | T | 1 | a0001c0005t0017 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*667G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 667 | chr14 | 90043810 | ||||||
| chr14:90043942 | A | G | 3 | a0001c0002t0008 a0001c0005t0016 a0002c0004t0009 |
7 | HG02055.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 799 | chr14 | 90043942 | ||||||
| chr14:90044075 | C | T | 1 | a0001c0002t0013 | 2 | HG02486.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*932C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 932 | chr14 | 90044075 | ||||||
| chr14:90044248 | A | G | 1 | a0001c0002t0021 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1105A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1105 | chr14 | 90044248 | ||||||
| chr14:90044293 | G | A | 1 | a0001c0002t0014 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1150G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1150 | chr14 | 90044293 | ||||||
| chr14:90044475 | G | A | 1 | a0002c0011t0019 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1332G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1332 | chr14 | 90044475 | ||||||
| chr14:90044489 | G | A | 1 | a0001c0001t0020 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1346 | chr14 | 90044489 | ||||||
| chr14:90044591 | G | A | 7 | a0001c0002t0004 a0001c0002t0010 a0001c0002t0013 others(4): Show |
27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1448G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1448 | chr14 | 90044591 | ||||||
| chr14:90044595 | C | T | 7 | a0001c0002t0004 a0001c0002t0010 a0001c0002t0013 others(4): Show |
27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1452C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1452 | chr14 | 90044595 | ||||||
| chr14:90044603 | C | G | 7 | a0001c0002t0004 a0001c0002t0010 a0001c0002t0013 others(4): Show |
27 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1460C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1460 | chr14 | 90044603 | ||||||
| chr14:90044733 | C | T | 1 | a0001c0001t0015 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1590 | chr14 | 90044733 | ||||||
| chr14:90044761 | T | C | 1 | a0001c0002t0013 | 2 | HG02486.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1618T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 17/17 | 1618 | chr14 | 90044761 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89955983 | C | A | 1 | a0001c0002t0003g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-231+13C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89955983 | |||||||
| chr14:89956020 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-231+50C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956020 | |||||||
| chr14:89956034 | G | A | 1 | a0002c0003t0003g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-231+64G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956034 | |||||||
| chr14:89956038 | T | G | 55 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0009 others(52): Show |
69 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.-231+68T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956038 | |||||||
| chr14:89956052 | G | A | 20 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(17): Show |
23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-231+82G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956052 | |||||||
| chr14:89956053 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0009 others(112): Show |
134 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(131): Show |
intron_variant | MODIFIER | c.-231+83A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956053 | |||||||
| chr14:89956202 | G | C | 1 | a0001c0002t0021g0192 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-231+232G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956202 | |||||||
| chr14:89956320 | T | C | 47 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0085 others(44): Show |
49 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.-230-258T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956320 | |||||||
| chr14:89956395 | C | G | 1 | a0001c0002t0010g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-230-183C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956395 | |||||||
| chr14:89956470 | A | G | 1 | a0001c0002t0006g0228 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-230-108A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956470 | |||||||
| chr14:89956527 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0009 others(112): Show |
134 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(131): Show |
intron_variant | MODIFIER | c.-230-51C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956527 | |||||||
| chr14:89956564 | C | A | 115 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0009 others(112): Show |
134 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(131): Show |
intron_variant | MODIFIER | c.-230-14C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956564 | |||||||
| chr14:89956574 | G | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.-230-4G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 1/16 | chr14 | 89956574 | |||||||
| chr14:89956828 | CAG | C | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8+33_-8+34delAG | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr14 | 89956828 | ||||||
| chr14:89957064 | C | T | 1 | a0001c0002t0010g0221 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8+264C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957064 | |||||||
| chr14:89957065 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8+265G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957065 | |||||||
| chr14:89957383 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-8+583A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957383 | |||||||
| chr14:89957392 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8+592T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957392 | |||||||
| chr14:89957450 | A | T | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-8+650A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957450 | |||||||
| chr14:89957459 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-8+659C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957459 | |||||||
| chr14:89957515 | G | A | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8+715G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957515 | |||||||
| chr14:89957546 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8+746C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957546 | |||||||
| chr14:89957579 | G | A | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+779G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957579 | |||||||
| chr14:89957837 | C | A | 10 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(7): Show |
12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+1037C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957837 | |||||||
| chr14:89957855 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8+1055C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957855 | |||||||
| chr14:89957946 | C | T | 22 | a0001c0002t0008g0201 a0001c0002t0008g0202 a0002c0004t0005g0016 others(19): Show |
25 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+1146C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957946 | |||||||
| chr14:89957986 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+1186G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957986 | |||||||
| chr14:89957988 | G | A | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-8+1188G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89957988 | |||||||
| chr14:89958124 | G | A | 9 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+1324G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958124 | |||||||
| chr14:89958274 | A | C | 30 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(27): Show |
30 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8+1474A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958274 | |||||||
| chr14:89958306 | A | G | 1 | a0001c0001t0001g0008 | 3 | HG01884.hp2 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-8+1506A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958306 | |||||||
| chr14:89958332 | G | C | 184 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0085 others(181): Show |
208 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.-8+1532G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958332 | |||||||
| chr14:89958361 | G | A | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8+1561G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958361 | |||||||
| chr14:89958369 | G | A | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+1569G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958369 | |||||||
| chr14:89958393 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8+1593C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958393 | |||||||
| chr14:89958510 | T | C | 1 | a0001c0001t0002g0009 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-8+1710T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958510 | |||||||
| chr14:89958557 | T | A | 2 | a0005c0008t0001g0138 a0005c0008t0001g0139 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-8+1757T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958557 | |||||||
| chr14:89958674 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-8+1874A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958674 | |||||||
| chr14:89958703 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-8+1903A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958703 | |||||||
| chr14:89958735 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8+1935C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958735 | |||||||
| chr14:89958820 | C | T | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-8+2020C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958820 | |||||||
| chr14:89958828 | C | T | 2 | a0001c0001t0001g0180 a0001c0005t0001g0065 |
2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-8+2028C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958828 | |||||||
| chr14:89958847 | A | G | 2 | a0001c0002t0003g0193 a0007c0012t0012g0141 |
2 | HG02055.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-8+2047A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89958847 | |||||||
| chr14:89959123 | TC | T | 3 | a0005c0008t0001g0138 a0005c0008t0001g0139 a0005c0008t0001g0140 |
3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-8+2324delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959123 | |||||||
| chr14:89959140 | G | A | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8+2340G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959140 | |||||||
| chr14:89959353 | C | T | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-8+2553C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959353 | |||||||
| chr14:89959504 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8+2704C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959504 | |||||||
| chr14:89959539 | G | A | 1 | a0002c0003t0003g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-8+2739G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959539 | |||||||
| chr14:89959836 | T | C | 6 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG00408.hp2 NA18947.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+3036T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89959836 | |||||||
| chr14:89960023 | G | C | 1 | a0001c0005t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-7-3085G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960023 | |||||||
| chr14:89960259 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-2849A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960259 | |||||||
| chr14:89960276 | T | G | 1 | a0001c0002t0008g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-2832T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960276 | |||||||
| chr14:89960300 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-7-2808A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960300 | |||||||
| chr14:89960421 | T | C | 6 | a0002c0003t0003g0020 a0002c0003t0003g0183 a0002c0003t0003g0184 others(3): Show |
7 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-2687T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960421 | |||||||
| chr14:89960503 | C | T | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-7-2605C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960503 | |||||||
| chr14:89960639 | A | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-2469A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960639 | |||||||
| chr14:89960747 | T | C | 93 | a0001c0002t0001g0031 a0001c0002t0001g0194 a0001c0002t0001g0195 others(90): Show |
104 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(101): Show |
intron_variant | MODIFIER | c.-7-2361T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960747 | |||||||
| chr14:89960863 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-2245C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960863 | |||||||
| chr14:89960872 | C | T | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-7-2236C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960872 | |||||||
| chr14:89960957 | G | A | 2 | a0002c0003t0003g0130 a0002c0003t0003g0131 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-7-2151G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89960957 | |||||||
| chr14:89961074 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-7-2034C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961074 | |||||||
| chr14:89961115 | C | T | 4 | a0001c0005t0001g0010 a0001c0005t0001g0011 a0001c0005t0001g0030 others(1): Show |
5 | HG02258.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-1993C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961115 | |||||||
| chr14:89961124 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-1984G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961124 | |||||||
| chr14:89961157 | G | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-7-1951G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961157 | |||||||
| chr14:89961191 | T | A | 4 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0132 others(1): Show |
6 | HG02451.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-1917T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961191 | |||||||
| chr14:89961478 | A | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-1630A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961478 | |||||||
| chr14:89961551 | A | G | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-7-1557A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961551 | |||||||
| chr14:89961605 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-7-1503G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961605 | |||||||
| chr14:89961648 | C | A | 1 | a0003c0006t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-7-1460C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961648 | |||||||
| chr14:89961763 | T | C | 2 | a0002c0003t0003g0182 a0002c0003t0003g0188 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-7-1345T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961763 | |||||||
| chr14:89961774 | T | A | 63 | a0001c0002t0003g0193 a0001c0002t0004g0021 a0001c0002t0004g0203 others(60): Show |
70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-7-1334T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961774 | |||||||
| chr14:89961879 | C | T | 3 | a0002c0003t0003g0020 a0002c0003t0003g0186 a0002c0003t0003g0187 |
4 | NA18957.hp1 NA18968.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-1229C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961879 | |||||||
| chr14:89961911 | G | A | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-1197G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89961911 | |||||||
| chr14:89962041 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-7-1067A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962041 | |||||||
| chr14:89962074 | G | A | 5 | a0002c0003t0003g0130 a0002c0003t0003g0131 a0002c0003t0003g0135 others(2): Show |
5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-1034G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962074 | |||||||
| chr14:89962090 | A | G | 31 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(28): Show |
32 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-7-1018A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962090 | |||||||
| chr14:89962613 | C | T | 2 | a0001c0002t0010g0220 a0001c0002t0021g0192 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7-495C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962613 | |||||||
| chr14:89962667 | C | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-441C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962667 | |||||||
| chr14:89962712 | G | GA | 32 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(29): Show |
37 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-7-386dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr14 | 89962712 | ||||||
| chr14:89962759 | C | T | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-349C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962759 | |||||||
| chr14:89962773 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-7-335G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962773 | |||||||
| chr14:89962826 | T | C | 71 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(68): Show |
78 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.-7-282T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962826 | |||||||
| chr14:89962884 | A | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-224A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962884 | |||||||
| chr14:89962954 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7-154A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89962954 | |||||||
| chr14:89963016 | G | A | 1 | a0001c0002t0006g0228 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-7-92G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 2/16 | chr14 | 89963016 | |||||||
| chr14:89963771 | C | G | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.559+98C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89963771 | |||||||
| chr14:89963787 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.559+114A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89963787 | |||||||
| chr14:89964020 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.559+347A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964020 | |||||||
| chr14:89964114 | G | C | 1 | a0001c0001t0002g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.559+441G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964114 | |||||||
| chr14:89964207 | AGAAG | A | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.559+535_559+538del others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964207 | |||||||
| chr14:89964226 | T | C | 20 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(17): Show |
23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+553T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964226 | |||||||
| chr14:89964340 | C | T | 1 | a0001c0002t0004g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.559+667C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964340 | |||||||
| chr14:89964782 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.559+1109C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964782 | |||||||
| chr14:89964828 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG00642.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.559+1155A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964828 | |||||||
| chr14:89964894 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.559+1221A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964894 | |||||||
| chr14:89964898 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.559+1225T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964898 | |||||||
| chr14:89964928 | T | C | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.560-1219T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89964928 | |||||||
| chr14:89965010 | G | T | 1 | a0001c0001t0002g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.560-1137G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965010 | |||||||
| chr14:89965165 | A | G | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-982A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965165 | |||||||
| chr14:89965194 | G | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560-953G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965194 | |||||||
| chr14:89965265 | G | GC | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-880dupC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr14 | 89965265 | ||||||
| chr14:89965344 | CTG | C | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.560-801_560-800del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr14 | 89965344 | ||||||
| chr14:89965361 | T | G | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.560-786T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965361 | |||||||
| chr14:89965397 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.560-750C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965397 | |||||||
| chr14:89965504 | A | G | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-643A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965504 | |||||||
| chr14:89965893 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.560-254A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965893 | |||||||
| chr14:89965921 | G | A | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.560-226G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89965921 | |||||||
| chr14:89966082 | G | A | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.560-65G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89966082 | |||||||
| chr14:89966106 | T | C | 1 | a0002c0004t0005g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.560-41T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 3/16 | chr14 | 89966106 | |||||||
| chr14:89966271 | C | T | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.603+81C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966271 | |||||||
| chr14:89966308 | A | G | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.603+118A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966308 | |||||||
| chr14:89966492 | A | T | 2 | a0003c0006t0007g0083 a0003c0006t0007g0084 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.603+302A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966492 | |||||||
| chr14:89966547 | G | A | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.603+357G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966547 | |||||||
| chr14:89966665 | A | G | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.603+475A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966665 | |||||||
| chr14:89966669 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.603+479G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966669 | |||||||
| chr14:89966670 | T | C | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.603+480T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966670 | |||||||
| chr14:89966693 | C | T | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.603+503C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89966693 | |||||||
| chr14:89967259 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.604-108G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 4/16 | chr14 | 89967259 | |||||||
| chr14:89967575 | G | A | 1 | a0002c0004t0005g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.659+153G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89967575 | |||||||
| chr14:89967760 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.659+338G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89967760 | |||||||
| chr14:89967779 | C | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.659+357C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89967779 | |||||||
| chr14:89967954 | C | CAGTG | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.659+534_659+535ins others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89967954 | ||||||
| chr14:89968001 | C | T | 20 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(17): Show |
23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.659+579C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968001 | |||||||
| chr14:89968006 | C | T | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.659+584C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968006 | |||||||
| chr14:89968113 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.659+691T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968113 | |||||||
| chr14:89968160 | C | CT | 10 | a0001c0001t0002g0062 a0001c0002t0006g0022 a0001c0002t0006g0222 others(7): Show |
11 | HG01192.hp1 HG01928.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.659+754dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89968160 | ||||||
| chr14:89968160 | CTT | C | 38 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(35): Show |
44 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.659+753_659+754del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89968160 | ||||||
| chr14:89968195 | T | C | 2 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.659+773T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968195 | |||||||
| chr14:89968264 | G | C | 29 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(26): Show |
32 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.659+842G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968264 | |||||||
| chr14:89968332 | C | T | 25 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(22): Show |
30 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.659+910C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968332 | |||||||
| chr14:89968370 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.659+948A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968370 | |||||||
| chr14:89968424 | A | G | 39 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(36): Show |
45 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.659+1002A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968424 | |||||||
| chr14:89968492 | A | G | 94 | a0001c0002t0001g0031 a0001c0002t0001g0194 a0001c0002t0001g0195 others(91): Show |
105 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(102): Show |
intron_variant | MODIFIER | c.659+1070A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968492 | |||||||
| chr14:89968574 | T | C | 1 | a0001c0001t0002g0009 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.659+1152T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968574 | |||||||
| chr14:89968660 | G | C | 5 | a0002c0003t0003g0130 a0002c0003t0003g0131 a0002c0003t0003g0135 others(2): Show |
5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.659+1238G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968660 | |||||||
| chr14:89968719 | A | G | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.659+1297A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968719 | |||||||
| chr14:89968861 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.659+1439T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89968861 | |||||||
| chr14:89969277 | CCTT | C | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.659+1858_659+1860d others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969277 | ||||||
| chr14:89969304 | A | C | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.660-1871A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969304 | |||||||
| chr14:89969313 | TG | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-1859delG | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969313 | ||||||
| chr14:89969487 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.660-1688A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969487 | |||||||
| chr14:89969580 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.660-1595G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969580 | |||||||
| chr14:89969581 | T | A | 62 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(59): Show |
69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.660-1594T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969581 | |||||||
| chr14:89969714 | A | G | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1461A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969714 | |||||||
| chr14:89969833 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.660-1342A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969833 | |||||||
| chr14:89969876 | C | CT | 150 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.660-1281dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969876 | ||||||
| chr14:89969876 | C | CTT | 38 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0175 others(35): Show |
39 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.660-1282_660-1281d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969876 | ||||||
| chr14:89969876 | CT | C | 15 | a0002c0003t0003g0137 a0002c0004t0005g0016 a0002c0004t0005g0067 others(12): Show |
16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.660-1281delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr14 | 89969876 | ||||||
| chr14:89969881 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.660-1294T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969881 | |||||||
| chr14:89969887 | T | C | 1 | a0003c0006t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.660-1288T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969887 | |||||||
| chr14:89969898 | G | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1277G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969898 | |||||||
| chr14:89969907 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.660-1268C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969907 | |||||||
| chr14:89969915 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.660-1260C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969915 | |||||||
| chr14:89969946 | G | A | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.660-1229G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89969946 | |||||||
| chr14:89970033 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.660-1142C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970033 | |||||||
| chr14:89970078 | G | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.660-1097G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970078 | |||||||
| chr14:89970118 | T | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1057T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970118 | |||||||
| chr14:89970171 | T | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-1004T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970171 | |||||||
| chr14:89970224 | A | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-951A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970224 | |||||||
| chr14:89970235 | A | G | 1 | a0001c0005t0016g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.660-940A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970235 | |||||||
| chr14:89970308 | C | T | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-867C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970308 | |||||||
| chr14:89970313 | C | T | 1 | a0001c0002t0006g0226 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.660-862C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970313 | |||||||
| chr14:89970485 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0098 |
3 | NA18954.hp1 NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.660-690A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970485 | |||||||
| chr14:89970580 | G | A | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.660-595G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970580 | |||||||
| chr14:89970580 | G | C | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.660-595G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970580 | |||||||
| chr14:89970741 | A | G | 2 | a0002c0004t0005g0016 a0002c0004t0005g0079 |
3 | HG01109.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.660-434A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970741 | |||||||
| chr14:89970797 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-378C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970797 | |||||||
| chr14:89970798 | G | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-377G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970798 | |||||||
| chr14:89970821 | A | G | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.660-354A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970821 | |||||||
| chr14:89970834 | T | A | 124 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0001g0101 others(121): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.660-341T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970834 | |||||||
| chr14:89970838 | T | A | 31 | a0001c0001t0002g0035 a0001c0002t0001g0031 a0001c0002t0001g0194 others(28): Show |
34 | HG01074.hp1 HG01433.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.660-337T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970838 | |||||||
| chr14:89970901 | C | A | 5 | a0002c0003t0003g0130 a0002c0003t0003g0131 a0002c0003t0003g0135 others(2): Show |
5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.660-274C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970901 | |||||||
| chr14:89970926 | C | T | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.660-249C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970926 | |||||||
| chr14:89970957 | G | C | 1 | a0001c0001t0002g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.660-218G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970957 | |||||||
| chr14:89970984 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.660-191C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89970984 | |||||||
| chr14:89971013 | A | T | 10 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(7): Show |
12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.660-162A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89971013 | |||||||
| chr14:89971072 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-103G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 5/16 | chr14 | 89971072 | |||||||
| chr14:89971312 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.756+41G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971312 | |||||||
| chr14:89971367 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.756+96T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971367 | |||||||
| chr14:89971399 | T | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+128T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971399 | |||||||
| chr14:89971418 | T | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0057 |
2 | NA19004.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.756+147T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971418 | |||||||
| chr14:89971511 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.756+240T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971511 | |||||||
| chr14:89971536 | G | C | 9 | a0001c0005t0001g0002 a0001c0005t0001g0010 a0001c0005t0001g0011 others(6): Show |
12 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.756+265G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971536 | |||||||
| chr14:89971862 | T | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+591T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971862 | |||||||
| chr14:89971865 | T | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+594T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971865 | |||||||
| chr14:89971911 | CT | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+649delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89971911 | ||||||
| chr14:89971947 | C | T | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.756+676C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971947 | |||||||
| chr14:89971974 | G | T | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.756+703G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971974 | |||||||
| chr14:89971985 | A | G | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+714A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89971985 | |||||||
| chr14:89972041 | T | C | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.756+770T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972041 | |||||||
| chr14:89972232 | A | G | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.756+961A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972232 | |||||||
| chr14:89972252 | G | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+981G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972252 | |||||||
| chr14:89972276 | C | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+1005C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972276 | |||||||
| chr14:89972293 | G | GAA | 186 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0085 others(183): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.756+1023_756+1024i others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89972293 | ||||||
| chr14:89972345 | T | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1074T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972345 | |||||||
| chr14:89972536 | CT | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1268delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89972536 | ||||||
| chr14:89972554 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+1283A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972554 | |||||||
| chr14:89972563 | G | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1292G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972563 | |||||||
| chr14:89972604 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+1333A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972604 | |||||||
| chr14:89972617 | ATCTTCTA others(7): Show |
A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.756+1348_756+1361d others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89972617 | ||||||
| chr14:89972636 | G | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+1365G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972636 | |||||||
| chr14:89972794 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.756+1523T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972794 | |||||||
| chr14:89972841 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.756+1570G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89972841 | |||||||
| chr14:89973042 | A | T | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.756+1771A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973042 | |||||||
| chr14:89973065 | G | GT | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.756+1797dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89973065 | ||||||
| chr14:89973189 | C | A | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.756+1918C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973189 | |||||||
| chr14:89973256 | A | G | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.756+1985A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973256 | |||||||
| chr14:89973282 | G | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+2011G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973282 | |||||||
| chr14:89973364 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.756+2093T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973364 | |||||||
| chr14:89973458 | A | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.756+2187A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973458 | |||||||
| chr14:89973473 | A | T | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.756+2202A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973473 | |||||||
| chr14:89973607 | C | T | 9 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.757-2174C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973607 | |||||||
| chr14:89973706 | G | A | 35 | a0001c0002t0001g0031 a0001c0002t0003g0023 a0001c0002t0004g0021 others(32): Show |
39 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.757-2075G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973706 | |||||||
| chr14:89973736 | G | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-2045G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973736 | |||||||
| chr14:89973821 | T | C | 35 | a0001c0002t0001g0031 a0001c0002t0003g0023 a0001c0002t0004g0021 others(32): Show |
39 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.757-1960T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973821 | |||||||
| chr14:89973880 | C | CTTA | 1 | a0001c0001t0001g0019 | 2 | HG01074.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.757-1899_757-1897d others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89973880 | ||||||
| chr14:89973894 | C | T | 3 | a0002c0003t0003g0130 a0002c0003t0003g0131 a0002c0003t0003g0136 |
3 | HG02602.hp2 HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.757-1887C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973894 | |||||||
| chr14:89973896 | T | C | 9 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.757-1885T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973896 | |||||||
| chr14:89973939 | A | G | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-1842A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973939 | |||||||
| chr14:89973951 | G | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-1830G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973951 | |||||||
| chr14:89973966 | G | A | 3 | a0002c0004t0005g0069 a0002c0004t0005g0070 a0002c0004t0005g0071 |
3 | HG01081.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.757-1815G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973966 | |||||||
| chr14:89973979 | G | A | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-1802G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89973979 | |||||||
| chr14:89974232 | G | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.757-1549G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974232 | |||||||
| chr14:89974246 | A | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-1535A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974246 | |||||||
| chr14:89974316 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01109.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.757-1465C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974316 | |||||||
| chr14:89974317 | G | T | 138 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0009 others(135): Show |
160 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(157): Show |
intron_variant | MODIFIER | c.757-1464G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974317 | |||||||
| chr14:89974584 | G | A | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.757-1197G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974584 | |||||||
| chr14:89974622 | G | A | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-1159G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974622 | |||||||
| chr14:89974637 | ATTGCATG others(10): Show |
A | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.757-1139_757-1123d others(19): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89974637 | ||||||
| chr14:89974799 | A | G | 75 | a0001c0002t0001g0031 a0001c0002t0003g0023 a0001c0002t0004g0021 others(72): Show |
85 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.757-982A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89974799 | |||||||
| chr14:89975015 | A | G | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.757-766A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975015 | |||||||
| chr14:89975098 | C | T | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.757-683C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975098 | |||||||
| chr14:89975106 | C | T | 1 | a0002c0004t0005g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.757-675C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975106 | |||||||
| chr14:89975168 | T | C | 32 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(29): Show |
36 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.757-613T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975168 | |||||||
| chr14:89975200 | T | C | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.757-581T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975200 | |||||||
| chr14:89975240 | A | G | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-541A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975240 | |||||||
| chr14:89975311 | C | T | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.757-470C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975311 | |||||||
| chr14:89975532 | T | TGTA | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.757-245_757-243dup others(3): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975532 | ||||||
| chr14:89975577 | T | TTG | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.757-200_757-199dup others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975577 | ||||||
| chr14:89975581 | G | GT | 9 | a0001c0001t0001g0120 a0001c0001t0002g0055 a0001c0002t0006g0022 others(6): Show |
10 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.757-180dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975581 | ||||||
| chr14:89975581 | GT | G | 42 | a0001c0001t0001g0104 a0001c0001t0002g0037 a0001c0001t0002g0038 others(39): Show |
48 | HG00323.hp1 HG00323.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.757-180delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975581 | ||||||
| chr14:89975581 | GTT | G | 20 | a0001c0002t0004g0213 a0002c0003t0003g0005 a0002c0003t0003g0020 others(17): Show |
23 | HG01070.hp2 HG01168.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.757-181_757-180del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr14 | 89975581 | ||||||
| chr14:89975585 | T | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-196T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975585 | |||||||
| chr14:89975587 | T | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.757-194T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975587 | |||||||
| chr14:89975682 | T | A | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.757-99T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975682 | |||||||
| chr14:89975719 | T | C | 3 | a0001c0001t0001g0105 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01123.hp1 HG01175.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.757-62T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 6/16 | chr14 | 89975719 | |||||||
| chr14:89975853 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+38A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975853 | |||||||
| chr14:89975867 | A | G | 34 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(31): Show |
38 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.791+52A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975867 | |||||||
| chr14:89975873 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+58C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975873 | |||||||
| chr14:89975882 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.791+67T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975882 | |||||||
| chr14:89975970 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+155C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89975970 | |||||||
| chr14:89976117 | A | G | 2 | a0001c0002t0004g0213 a0001c0002t0004g0218 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.791+302A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976117 | |||||||
| chr14:89976210 | A | ATCC | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+399_791+401dup others(3): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976210 | ||||||
| chr14:89976231 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.791+416G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976231 | |||||||
| chr14:89976251 | A | G | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+436A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976251 | |||||||
| chr14:89976255 | G | A | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+440G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976255 | |||||||
| chr14:89976375 | C | T | 5 | a0001c0002t0008g0201 a0001c0002t0008g0202 a0003c0006t0007g0082 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.791+560C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976375 | |||||||
| chr14:89976527 | C | CT | 50 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(47): Show |
54 | HG01081.hp2 HG01109.hp1 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.791+740dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | ||||||
| chr14:89976527 | C | CTT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0129 others(4): Show |
7 | HG01123.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.791+739_791+740dup others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | ||||||
| chr14:89976527 | CT | C | 22 | a0001c0001t0001g0104 a0001c0001t0001g0142 a0001c0001t0001g0177 others(19): Show |
23 | HG00323.hp1 HG01168.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.791+740delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | ||||||
| chr14:89976527 | CTTTTTTT others(3): Show |
C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+731_791+740del others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | ||||||
| chr14:89976527 | CTTTTTTT others(4): Show |
C | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.791+730_791+740del others(11): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976527 | ||||||
| chr14:89976543 | T | A | 1 | a0002c0003t0003g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.791+728T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976543 | |||||||
| chr14:89976543 | T | TA | 7 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(4): Show |
8 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.791+728_791+729ins others(1): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976543 | |||||||
| chr14:89976554 | T | TTTTTTTT others(3): Show |
1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.791+740_791+741ins others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976554 | ||||||
| chr14:89976555 | T | A | 9 | a0001c0001t0001g0106 a0002c0003t0003g0020 a0002c0003t0003g0182 others(6): Show |
10 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.791+740T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976555 | |||||||
| chr14:89976555 | T | TA | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.791+741dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976555 | ||||||
| chr14:89976567 | C | T | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.791+752C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976567 | |||||||
| chr14:89976606 | G | A | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.791+791G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89976606 | |||||||
| chr14:89976704 | CTT | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.791+892_791+893del others(2): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89976704 | ||||||
| chr14:89977128 | T | C | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1313T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977128 | |||||||
| chr14:89977184 | A | G | 1 | a0001c0002t0010g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.791+1369A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977184 | |||||||
| chr14:89977190 | G | A | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.791+1375G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977190 | |||||||
| chr14:89977208 | A | T | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1393A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977208 | |||||||
| chr14:89977304 | A | T | 4 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(1): Show |
4 | HG01891.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.791+1489A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977304 | |||||||
| chr14:89977305 | T | A | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1490T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977305 | |||||||
| chr14:89977339 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.791+1524C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977339 | |||||||
| chr14:89977358 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+1543C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977358 | |||||||
| chr14:89977442 | C | T | 33 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(30): Show |
37 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.791+1627C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977442 | |||||||
| chr14:89977443 | G | A | 1 | a0001c0002t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.791+1628G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977443 | |||||||
| chr14:89977487 | G | A | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.791+1672G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977487 | |||||||
| chr14:89977544 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+1729C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977544 | |||||||
| chr14:89977590 | A | G | 34 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(31): Show |
38 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.791+1775A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977590 | |||||||
| chr14:89977605 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.791+1790A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977605 | |||||||
| chr14:89977634 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.791+1819T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977634 | |||||||
| chr14:89977644 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.791+1829A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977644 | |||||||
| chr14:89977975 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.791+2160G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89977975 | |||||||
| chr14:89978133 | G | A | 1 | a0001c0005t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.791+2318G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978133 | |||||||
| chr14:89978143 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.791+2328C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978143 | |||||||
| chr14:89978148 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.791+2333C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978148 | |||||||
| chr14:89978154 | A | G | 40 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(37): Show |
46 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.791+2339A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978154 | |||||||
| chr14:89978212 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-2328A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978212 | |||||||
| chr14:89978262 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.792-2278C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978262 | |||||||
| chr14:89978310 | A | G | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.792-2230A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978310 | |||||||
| chr14:89978330 | C | A | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.792-2210C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978330 | |||||||
| chr14:89978351 | T | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.792-2189T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978351 | |||||||
| chr14:89978366 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-2174C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978366 | |||||||
| chr14:89978438 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.792-2102T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978438 | |||||||
| chr14:89978464 | A | G | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.792-2076A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978464 | |||||||
| chr14:89978602 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1938C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978602 | |||||||
| chr14:89978671 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-1869C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978671 | |||||||
| chr14:89978961 | CT | C | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1574delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89978961 | ||||||
| chr14:89978968 | T | TCGAACTC others(101): Show |
2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1572_792-1571i others(110): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978968 | |||||||
| chr14:89978975 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1565T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978975 | |||||||
| chr14:89978981 | A | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1559A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978981 | |||||||
| chr14:89978985 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1555T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978985 | |||||||
| chr14:89978988 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1552C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978988 | |||||||
| chr14:89978990 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1550T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978990 | |||||||
| chr14:89978991 | C | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1549C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978991 | |||||||
| chr14:89978993 | T | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1547T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978993 | |||||||
| chr14:89978996 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1544C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89978996 | |||||||
| chr14:89979003 | A | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1537A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979003 | |||||||
| chr14:89979005 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1535G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979005 | |||||||
| chr14:89979009 | A | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1531A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979009 | |||||||
| chr14:89979012 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1528T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979012 | |||||||
| chr14:89979014 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1526G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979014 | |||||||
| chr14:89979018 | A | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1522A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979018 | |||||||
| chr14:89979023 | G | GTGAGAGA others(99): Show |
2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1517_792-1516i others(108): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979023 | |||||||
| chr14:89979025 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.792-1515G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979025 | |||||||
| chr14:89979138 | G | A | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.792-1402G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979138 | |||||||
| chr14:89979186 | A | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-1354A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979186 | |||||||
| chr14:89979219 | G | A | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1321G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979219 | |||||||
| chr14:89979261 | G | A | 1 | a0001c0005t0016g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.792-1279G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979261 | |||||||
| chr14:89979312 | ATT | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1214_792-1213d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr14 | 89979312 | ||||||
| chr14:89979342 | C | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1198C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979342 | |||||||
| chr14:89979403 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1137A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979403 | |||||||
| chr14:89979461 | G | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-1079G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979461 | |||||||
| chr14:89979598 | C | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-942C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979598 | |||||||
| chr14:89979762 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-778C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979762 | |||||||
| chr14:89979835 | G | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.792-705G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89979835 | |||||||
| chr14:89980048 | A | G | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.792-492A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980048 | |||||||
| chr14:89980058 | G | A | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.792-482G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980058 | |||||||
| chr14:89980225 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.792-315G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980225 | |||||||
| chr14:89980245 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-295A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980245 | |||||||
| chr14:89980394 | A | G | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.792-146A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980394 | |||||||
| chr14:89980425 | G | A | 2 | a0003c0006t0007g0083 a0003c0006t0007g0084 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.792-115G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980425 | |||||||
| chr14:89980459 | A | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.792-81A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980459 | |||||||
| chr14:89980488 | A | G | 10 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(7): Show |
12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.792-52A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 7/16 | chr14 | 89980488 | |||||||
| chr14:89980664 | G | C | 1 | a0001c0001t0011g0145 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.884+32G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89980664 | |||||||
| chr14:89980687 | G | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.884+55G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89980687 | |||||||
| chr14:89980716 | A | AT | 27 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(24): Show |
32 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.884+94dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr14 | 89980716 | ||||||
| chr14:89980958 | G | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+326G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89980958 | |||||||
| chr14:89981022 | A | G | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.884+390A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981022 | |||||||
| chr14:89981155 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.884+523A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981155 | |||||||
| chr14:89981184 | G | A | 2 | a0001c0002t0004g0214 a0001c0002t0004g0215 |
2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.884+552G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981184 | |||||||
| chr14:89981292 | A | G | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.884+660A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981292 | |||||||
| chr14:89981406 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+774C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981406 | |||||||
| chr14:89981510 | C | T | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.884+878C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981510 | |||||||
| chr14:89981534 | C | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.884+902C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981534 | |||||||
| chr14:89981784 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1152C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981784 | |||||||
| chr14:89981854 | T | C | 1 | a0001c0002t0008g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.884+1222T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981854 | |||||||
| chr14:89981893 | C | CCAAGGCT others(19): Show |
7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1265_884+1266i others(28): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr14 | 89981893 | ||||||
| chr14:89981909 | C | T | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.884+1277C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981909 | |||||||
| chr14:89981950 | C | T | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.884+1318C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981950 | |||||||
| chr14:89981992 | C | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0191 |
3 | HG01081.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.884+1360C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89981992 | |||||||
| chr14:89982000 | T | C | 48 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(45): Show |
55 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.884+1368T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982000 | |||||||
| chr14:89982047 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1415A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982047 | |||||||
| chr14:89982148 | A | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1516A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982148 | |||||||
| chr14:89982190 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1558C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982190 | |||||||
| chr14:89982197 | A | G | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1565A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982197 | |||||||
| chr14:89982237 | G | A | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.884+1605G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982237 | |||||||
| chr14:89982334 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.884+1702A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982334 | |||||||
| chr14:89982364 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+1732A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982364 | |||||||
| chr14:89982468 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.884+1836A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982468 | |||||||
| chr14:89982654 | T | TA | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.885-1855dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr14 | 89982654 | ||||||
| chr14:89982724 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-1792A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982724 | |||||||
| chr14:89982790 | T | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1726T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982790 | |||||||
| chr14:89982794 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1722C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982794 | |||||||
| chr14:89982880 | A | G | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1636A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982880 | |||||||
| chr14:89982907 | G | T | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.885-1609G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982907 | |||||||
| chr14:89982932 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1584A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89982932 | |||||||
| chr14:89983117 | T | C | 7 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(4): Show |
8 | HG00735.hp2 HG01109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-1399T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983117 | |||||||
| chr14:89983147 | G | C | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1369G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983147 | |||||||
| chr14:89983206 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1310G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983206 | |||||||
| chr14:89983302 | C | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-1214C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983302 | |||||||
| chr14:89983428 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1088C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983428 | |||||||
| chr14:89983549 | C | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-967C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983549 | |||||||
| chr14:89983593 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.885-923T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983593 | |||||||
| chr14:89983765 | A | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.885-751A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983765 | |||||||
| chr14:89983779 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.885-737A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983779 | |||||||
| chr14:89983789 | T | C | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.885-727T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983789 | |||||||
| chr14:89983923 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0125 |
3 | HG00639.hp2 HG00738.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.885-593T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89983923 | |||||||
| chr14:89984022 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0175 |
2 | NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.885-494A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984022 | |||||||
| chr14:89984063 | T | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-453T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984063 | |||||||
| chr14:89984143 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.885-373C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984143 | |||||||
| chr14:89984145 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-371G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984145 | |||||||
| chr14:89984217 | C | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-299C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984217 | |||||||
| chr14:89984280 | G | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0125 |
3 | HG00639.hp2 HG00738.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.885-236G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984280 | |||||||
| chr14:89984298 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.885-218A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984298 | |||||||
| chr14:89984345 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-171A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984345 | |||||||
| chr14:89984365 | T | G | 71 | a0001c0002t0003g0193 a0001c0002t0004g0021 a0001c0002t0004g0203 others(68): Show |
79 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.885-151T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984365 | |||||||
| chr14:89984501 | T | C | 1 | a0001c0002t0008g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.885-15T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 8/16 | chr14 | 89984501 | |||||||
| chr14:89984862 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1052+179A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984862 | |||||||
| chr14:89984863 | G | A | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1052+180G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984863 | |||||||
| chr14:89984885 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1052+202G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984885 | |||||||
| chr14:89984889 | A | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1052+206A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984889 | |||||||
| chr14:89984923 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-209T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | chr14 | 89984923 | |||||||
| chr14:89985069 | A | AT | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1053-55dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr14 | 89985069 | ||||||
| chr14:89985242 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1131+32A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985242 | |||||||
| chr14:89985247 | A | T | 1 | a0005c0008t0001g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1131+37A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985247 | |||||||
| chr14:89985248 | T | A | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1131+38T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985248 | |||||||
| chr14:89985391 | CTT | C | 8 | a0001c0005t0001g0002 a0001c0005t0001g0010 a0001c0005t0001g0011 others(5): Show |
11 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1131+184_1131+185d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89985391 | ||||||
| chr14:89985520 | A | T | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1131+310A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985520 | |||||||
| chr14:89985553 | GA | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+347delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89985553 | ||||||
| chr14:89985571 | C | T | 9 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1131+361C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985571 | |||||||
| chr14:89985722 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+512G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985722 | |||||||
| chr14:89985736 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+526A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985736 | |||||||
| chr14:89985767 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+557G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985767 | |||||||
| chr14:89985780 | GC | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+571delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985780 | |||||||
| chr14:89985825 | A | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+615A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985825 | |||||||
| chr14:89985838 | C | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | NA18989.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1131+628C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985838 | |||||||
| chr14:89985959 | G | A | 3 | a0001c0002t0010g0220 a0001c0002t0010g0229 a0001c0002t0021g0192 |
3 | HG02572.hp2 HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1131+749G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89985959 | |||||||
| chr14:89986223 | A | C | 1 | a0006c0010t0003g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1131+1013A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986223 | |||||||
| chr14:89986232 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1131+1022G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986232 | |||||||
| chr14:89986246 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1131+1036T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986246 | |||||||
| chr14:89986300 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1090G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986300 | |||||||
| chr14:89986309 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1099C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986309 | |||||||
| chr14:89986332 | G | A | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1131+1122G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986332 | |||||||
| chr14:89986399 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1131+1189T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986399 | |||||||
| chr14:89986406 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1131+1196T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986406 | |||||||
| chr14:89986664 | A | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1131+1454A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986664 | |||||||
| chr14:89986669 | C | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1131+1459C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986669 | |||||||
| chr14:89986698 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1131+1488G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986698 | |||||||
| chr14:89986733 | T | A | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1131+1523T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986733 | |||||||
| chr14:89986780 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1131+1570A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986780 | |||||||
| chr14:89986831 | C | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1621C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986831 | |||||||
| chr14:89986848 | A | AATAC | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131+1642_1131+164 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89986848 | ||||||
| chr14:89986909 | T | C | 1 | a0001c0005t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1131+1699T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986909 | |||||||
| chr14:89986993 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1131+1783T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89986993 | |||||||
| chr14:89987297 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132-1608G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987297 | |||||||
| chr14:89987303 | C | T | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1132-1602C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987303 | |||||||
| chr14:89987406 | T | G | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1132-1499T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987406 | |||||||
| chr14:89987475 | C | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1132-1430C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987475 | |||||||
| chr14:89987491 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-1414G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987491 | |||||||
| chr14:89987724 | T | A | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1132-1181T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987724 | |||||||
| chr14:89987847 | T | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-1058T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987847 | |||||||
| chr14:89987876 | AT | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-1021delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr14 | 89987876 | ||||||
| chr14:89987921 | G | A | 3 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0058 |
6 | NA18970.hp1 NA18972.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132-984G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89987921 | |||||||
| chr14:89988251 | T | C | 3 | a0005c0008t0001g0138 a0005c0008t0001g0139 a0005c0008t0001g0140 |
3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1132-654T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988251 | |||||||
| chr14:89988421 | G | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-484G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988421 | |||||||
| chr14:89988459 | T | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1132-446T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988459 | |||||||
| chr14:89988695 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1132-210C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988695 | |||||||
| chr14:89988762 | T | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0094 others(1): Show |
4 | HG02602.hp1 HG02698.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132-143T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 10/16 | chr14 | 89988762 | |||||||
| chr14:89989101 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1317+11G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989101 | |||||||
| chr14:89989116 | G | A | 62 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(59): Show |
69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1317+26G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989116 | |||||||
| chr14:89989154 | T | G | 1 | a0001c0005t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1317+64T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989154 | |||||||
| chr14:89989169 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1317+79A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989169 | |||||||
| chr14:89989195 | C | CT | 15 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(12): Show |
16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1317+118dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr14 | 89989195 | ||||||
| chr14:89989195 | CT | C | 13 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(10): Show |
14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1317+118delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr14 | 89989195 | ||||||
| chr14:89989217 | G | A | 1 | a0001c0002t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1317+127G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989217 | |||||||
| chr14:89989279 | C | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1317+189C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989279 | |||||||
| chr14:89989328 | C | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1317+238C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989328 | |||||||
| chr14:89989444 | A | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-273A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989444 | |||||||
| chr14:89989459 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1318-258T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989459 | |||||||
| chr14:89989510 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1318-207T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989510 | |||||||
| chr14:89989554 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1318-163A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989554 | |||||||
| chr14:89989642 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1318-75C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989642 | |||||||
| chr14:89989687 | C | T | 15 | a0001c0001t0001g0172 a0002c0004t0005g0016 a0002c0004t0005g0067 others(12): Show |
16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1318-30C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 11/16 | chr14 | 89989687 | |||||||
| chr14:89989811 | A | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1366+46A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989811 | |||||||
| chr14:89989843 | C | G | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1366+78C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989843 | |||||||
| chr14:89989844 | G | T | 187 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0085 others(184): Show |
211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1366+79G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989844 | |||||||
| chr14:89989883 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0098 |
3 | NA18954.hp1 NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1366+118A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89989883 | |||||||
| chr14:89990027 | A | G | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1366+262A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990027 | |||||||
| chr14:89990030 | T | C | 9 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1366+265T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990030 | |||||||
| chr14:89990086 | A | G | 4 | a0001c0002t0006g0222 a0001c0002t0006g0223 a0001c0002t0006g0224 others(1): Show |
4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366+321A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990086 | |||||||
| chr14:89990181 | C | T | 6 | a0002c0003t0003g0020 a0002c0003t0003g0183 a0002c0003t0003g0184 others(3): Show |
7 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366+416C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990181 | |||||||
| chr14:89990241 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366+476T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990241 | |||||||
| chr14:89990288 | G | T | 1 | a0001c0001t0002g0040 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1366+523G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990288 | |||||||
| chr14:89990331 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366+566A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990331 | |||||||
| chr14:89990416 | C | T | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1366+651C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990416 | |||||||
| chr14:89990430 | T | C | 82 | a0001c0002t0001g0031 a0001c0002t0001g0194 a0001c0002t0001g0195 others(79): Show |
90 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1366+665T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990430 | |||||||
| chr14:89990451 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366+686C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990451 | |||||||
| chr14:89990547 | C | CT | 7 | a0001c0001t0001g0104 a0001c0002t0001g0194 a0002c0003t0003g0005 others(4): Show |
9 | HG00323.hp1 HG01070.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1366+805dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | ||||||
| chr14:89990547 | CT | C | 30 | a0001c0001t0001g0085 a0001c0001t0001g0095 a0001c0001t0001g0096 others(27): Show |
33 | HG00639.hp1 HG00639.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1366+805delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | ||||||
| chr14:89990547 | CTT | C | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1366+804_1366+805d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | ||||||
| chr14:89990547 | CTTT | C | 13 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(10): Show |
14 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1366+803_1366+805d others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | ||||||
| chr14:89990547 | CTTTTT | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+801_1366+805d others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89990547 | ||||||
| chr14:89990618 | G | T | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1366+853G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990618 | |||||||
| chr14:89990794 | G | C | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1366+1029G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89990794 | |||||||
| chr14:89991435 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1367-482T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991435 | |||||||
| chr14:89991469 | C | CAGG | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367-446_1367-445i others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr14 | 89991469 | ||||||
| chr14:89991632 | A | T | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1367-285A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991632 | |||||||
| chr14:89991716 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1367-201C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991716 | |||||||
| chr14:89991839 | T | A | 16 | a0001c0002t0008g0201 a0001c0002t0008g0202 a0002c0004t0005g0016 others(13): Show |
17 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1367-78T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 12/16 | chr14 | 89991839 | |||||||
| chr14:89992053 | GT | G | 80 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(77): Show |
88 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1433+81delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr14 | 89992053 | ||||||
| chr14:89992216 | G | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1433+233G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992216 | |||||||
| chr14:89992365 | T | A | 82 | a0001c0002t0001g0031 a0001c0002t0001g0194 a0001c0002t0001g0195 others(79): Show |
90 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.1433+382T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992365 | |||||||
| chr14:89992682 | A | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-694A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992682 | |||||||
| chr14:89992876 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-500A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992876 | |||||||
| chr14:89992911 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1434-465G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89992911 | |||||||
| chr14:89993014 | A | G | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1434-362A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993014 | |||||||
| chr14:89993031 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1434-345T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993031 | |||||||
| chr14:89993067 | A | T | 1 | a0001c0002t0013g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1434-309A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993067 | |||||||
| chr14:89993129 | A | G | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1434-247A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993129 | |||||||
| chr14:89993200 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-176C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993200 | |||||||
| chr14:89993225 | T | C | 62 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(59): Show |
69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1434-151T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993225 | |||||||
| chr14:89993226 | G | A | 1 | a0002c0011t0019g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1434-150G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993226 | |||||||
| chr14:89993343 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-33A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 13/16 | chr14 | 89993343 | |||||||
| chr14:89993850 | T | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+367T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89993850 | |||||||
| chr14:89993910 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+427G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89993910 | |||||||
| chr14:89994086 | GA | G | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1541+607delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89994086 | ||||||
| chr14:89994128 | C | G | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+645C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994128 | |||||||
| chr14:89994144 | T | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+661T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994144 | |||||||
| chr14:89994259 | C | T | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+776C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994259 | |||||||
| chr14:89994263 | C | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+780C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994263 | |||||||
| chr14:89994293 | T | G | 1 | a0001c0002t0004g0211 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1541+810T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994293 | |||||||
| chr14:89994305 | C | T | 5 | a0004c0007t0002g0014 a0004c0007t0002g0039 a0004c0007t0002g0041 others(2): Show |
6 | HG01123.hp2 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541+822C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994305 | |||||||
| chr14:89994526 | G | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1043G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994526 | |||||||
| chr14:89994787 | T | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1304T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994787 | |||||||
| chr14:89994879 | A | T | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+1396A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994879 | |||||||
| chr14:89994992 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1541+1509G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89994992 | |||||||
| chr14:89995217 | T | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1734T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995217 | |||||||
| chr14:89995325 | G | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+1842G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995325 | |||||||
| chr14:89995347 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1541+1864G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995347 | |||||||
| chr14:89995392 | GC | G | 83 | a0001c0002t0001g0031 a0001c0002t0001g0194 a0001c0002t0001g0195 others(80): Show |
91 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.1541+1914delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89995392 | ||||||
| chr14:89995485 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2002C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995485 | |||||||
| chr14:89995493 | AAG | A | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1541+2013_1541+201 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89995493 | ||||||
| chr14:89995494 | A | C | 36 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(33): Show |
38 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1541+2011A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995494 | |||||||
| chr14:89995608 | A | C | 36 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(33): Show |
38 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1541+2125A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995608 | |||||||
| chr14:89995629 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2146A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995629 | |||||||
| chr14:89995846 | A | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2363A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995846 | |||||||
| chr14:89995982 | A | C | 54 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(51): Show |
60 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.1541+2499A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89995982 | |||||||
| chr14:89996022 | G | A | 71 | a0001c0002t0003g0193 a0001c0002t0004g0021 a0001c0002t0004g0203 others(68): Show |
79 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.1541+2539G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996022 | |||||||
| chr14:89996053 | A | G | 9 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1541+2570A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996053 | |||||||
| chr14:89996076 | C | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+2593C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996076 | |||||||
| chr14:89996094 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2611C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996094 | |||||||
| chr14:89996241 | G | A | 1 | a0002c0003t0003g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1541+2758G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996241 | |||||||
| chr14:89996242 | T | C | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+2759T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996242 | |||||||
| chr14:89996260 | A | G | 1 | a0003c0006t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1541+2777A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996260 | |||||||
| chr14:89996281 | A | T | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+2798A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996281 | |||||||
| chr14:89996526 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+3043A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996526 | |||||||
| chr14:89996620 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+3137G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996620 | |||||||
| chr14:89996930 | C | T | 3 | a0001c0005t0001g0002 a0001c0005t0001g0027 a0001c0005t0017g0002 |
5 | HG02109.hp2 HG02486.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1541+3447C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996930 | |||||||
| chr14:89996961 | T | C | 4 | a0001c0002t0006g0222 a0001c0002t0006g0223 a0001c0002t0006g0224 others(1): Show |
4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541+3478T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996961 | |||||||
| chr14:89996996 | A | C | 36 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(33): Show |
38 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1541+3513A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89996996 | |||||||
| chr14:89997076 | G | A | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1541+3593G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997076 | |||||||
| chr14:89997278 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0043 |
2 | NA18952.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1541+3795G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997278 | |||||||
| chr14:89997357 | T | C | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1541+3874T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997357 | |||||||
| chr14:89997358 | G | C | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1541+3875G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997358 | |||||||
| chr14:89997394 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+3911A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997394 | |||||||
| chr14:89997598 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0150 |
3 | HG02698.hp1 HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1541+4115G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997598 | |||||||
| chr14:89997812 | TTA | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4339_1541+434 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89997812 | ||||||
| chr14:89997882 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4399A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997882 | |||||||
| chr14:89997938 | CT | C | 63 | a0001c0002t0003g0193 a0001c0002t0004g0021 a0001c0002t0004g0203 others(60): Show |
70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1541+4459delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89997938 | ||||||
| chr14:89997982 | G | A | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+4499G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997982 | |||||||
| chr14:89997990 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4507G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89997990 | |||||||
| chr14:89998157 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4674C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998157 | |||||||
| chr14:89998200 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4717C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998200 | |||||||
| chr14:89998201 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4718C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998201 | |||||||
| chr14:89998370 | CAT | C | 5 | a0001c0002t0004g0204 a0001c0002t0004g0206 a0001c0002t0004g0213 others(2): Show |
5 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541+4888_1541+488 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | |||||||
| chr14:89998370 | CATTA | C | 3 | a0001c0002t0004g0205 a0001c0002t0004g0207 a0001c0002t0004g0208 |
3 | HG02258.hp1 HG02897.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1541+4888_1541+489 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | |||||||
| chr14:89998370 | CATTATA | C | 3 | a0001c0002t0004g0209 a0001c0002t0004g0210 a0001c0002t0004g0219 |
3 | HG01256.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1541+4888_1541+489 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | |||||||
| chr14:89998370 | CATTATAT others(13): Show |
C | 1 | a0001c0002t0021g0192 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1541+4888_1541+490 others(24): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998370 | |||||||
| chr14:89998371 | A | T | 10 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0211 others(7): Show |
11 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541+4888A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998371 | |||||||
| chr14:89998372 | T | A | 10 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0211 others(7): Show |
11 | HG02622.hp1 HG02965.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541+4889T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998372 | |||||||
| chr14:89998372 | T | TTA | 6 | a0001c0001t0001g0018 a0001c0001t0001g0096 a0001c0002t0008g0201 others(3): Show |
7 | HG01081.hp1 HG01255.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+4939_1541+494 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | T | TTATA | 3 | a0001c0001t0002g0048 a0001c0002t0008g0202 a0001c0005t0001g0030 |
3 | HG02165.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1541+4937_1541+494 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | T | TTATATA | 3 | a0001c0001t0001g0100 a0001c0005t0001g0026 a0002c0004t0005g0070 |
3 | HG00280.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1541+4935_1541+494 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | T | TTATATAT others(3): Show |
1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1541+4931_1541+494 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | T | TTTTATAT others(5): Show |
1 | a0001c0002t0006g0224 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1541+4890_1541+489 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTA | T | 8 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0001t0001g0158 others(5): Show |
9 | HG02257.hp1 HG02280.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4939_1541+494 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATA | T | 11 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0102 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541+4937_1541+494 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATA | T | 14 | a0001c0001t0001g0086 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
14 | HG01255.hp1 HG01934.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1541+4935_1541+494 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(1): Show |
T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0091 others(21): Show |
31 | HG00280.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1541+4933_1541+494 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(3): Show |
T | 16 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0119 others(13): Show |
16 | HG00408.hp1 HG00738.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1541+4931_1541+494 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(5): Show |
T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0095 others(14): Show |
19 | HG00408.hp2 HG00735.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1541+4929_1541+494 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(7): Show |
T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0151 a0001c0001t0001g0159 others(5): Show |
9 | HG01981.hp2 HG02280.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4927_1541+494 others(18): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(9): Show |
T | 14 | a0001c0001t0001g0090 a0001c0001t0001g0109 a0001c0001t0001g0142 others(11): Show |
14 | HG01928.hp1 HG02602.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1541+4925_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(11): Show |
T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0152 a0001c0001t0001g0153 others(13): Show |
17 | HG01081.hp2 HG01943.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1541+4923_1541+494 others(22): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(13): Show |
T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0043 others(3): Show |
9 | HG01070.hp2 HG02723.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1541+4921_1541+494 others(24): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(15): Show |
T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1541+4919_1541+494 others(26): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1541+4915_1541+494 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(21): Show |
T | 3 | a0005c0008t0001g0138 a0005c0008t0001g0139 a0005c0008t0001g0140 |
3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1541+4913_1541+494 others(32): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(25): Show |
T | 1 | a0001c0001t0001g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1541+4909_1541+494 others(36): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998372 | TTATATAT others(27): Show |
T | 1 | a0001c0005t0016g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1541+4907_1541+494 others(38): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998372 | ||||||
| chr14:89998374 | A | T | 3 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0228 |
4 | HG01192.hp1 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1541+4891A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998374 | |||||||
| chr14:89998376 | A | T | 1 | a0001c0002t0006g0225 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1541+4893A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998376 | |||||||
| chr14:89998384 | ATATATAT others(37): Show |
A | 2 | a0002c0004t0005g0016 a0002c0004t0005g0079 |
3 | HG01109.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1541+4905_1541+494 others(48): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998384 | ||||||
| chr14:89998388 | A | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+4905A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998388 | |||||||
| chr14:89998396 | A | ATG | 3 | a0001c0002t0004g0021 a0001c0002t0010g0221 a0009c0013t0004g0212 |
3 | HG03130.hp1 NA18989.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1541+4914_1541+491 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998396 | ||||||
| chr14:89998396 | A | G | 1 | a0001c0002t0008g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+4913A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998396 | |||||||
| chr14:89998400 | A | G | 6 | a0001c0002t0004g0021 a0001c0002t0004g0204 a0001c0002t0004g0206 others(3): Show |
6 | HG01433.hp1 HG02451.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1541+4917A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998400 | |||||||
| chr14:89998404 | A | G | 9 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(6): Show |
10 | HG00323.hp2 HG01433.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1541+4921A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998404 | |||||||
| chr14:89998408 | A | G | 26 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(23): Show |
29 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1541+4925A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998408 | |||||||
| chr14:89998408 | ATATATAT others(9): Show |
A | 1 | a0001c0002t0008g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+4929_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998408 | ||||||
| chr14:89998412 | A | G | 31 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(28): Show |
36 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.1541+4929A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998412 | |||||||
| chr14:89998412 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1541+4933_1541+494 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998412 | ||||||
| chr14:89998412 | ATATATAT others(9): Show |
A | 3 | a0002c0004t0009g0072 a0002c0004t0009g0073 a0002c0004t0009g0074 |
3 | HG02055.hp2 HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1541+4933_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998412 | ||||||
| chr14:89998414 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+4931A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998414 | |||||||
| chr14:89998416 | A | ATATATAT others(11): Show |
2 | a0001c0002t0001g0195 a0001c0002t0013g0199 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1541+4940_1541+494 others(22): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | ||||||
| chr14:89998416 | A | ATATATAT others(9): Show |
1 | a0001c0002t0013g0198 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | ||||||
| chr14:89998416 | A | ATATGTAT others(9): Show |
1 | a0002c0003t0003g0183 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1541+4936_1541+493 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | ||||||
| chr14:89998416 | A | ATGTATGT others(3): Show |
1 | a0001c0005t0018g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1541+4934_1541+493 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998416 | ||||||
| chr14:89998416 | A | G | 38 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(35): Show |
44 | HG00323.hp2 HG01070.hp2 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.1541+4933A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998416 | |||||||
| chr14:89998418 | ATATATG | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0011g0092 |
3 | HG02132.hp1 NA18951.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1541+4939_1541+494 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998418 | ||||||
| chr14:89998418 | ATATATGT others(3): Show |
A | 1 | a0002c0004t0005g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1541+4939_1541+494 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998418 | ||||||
| chr14:89998420 | A | ATATATAT others(19): Show |
1 | a0001c0002t0001g0200 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATATAT others(15): Show |
1 | a0001c0005t0017g0002 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(26): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATATAT others(9): Show |
1 | a0001c0005t0001g0002 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATATAT others(9): Show |
1 | a0002c0011t0019g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATATAT others(13): Show |
1 | a0002c0003t0003g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(24): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATATAT others(17): Show |
1 | a0002c0003t0003g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(28): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATATGT others(7): Show |
1 | a0002c0003t0003g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1541+4940_1541+494 others(18): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATGTAT others(5): Show |
1 | a0001c0002t0006g0022 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1541+4949_1541+496 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATATGTAT others(9): Show |
2 | a0001c0002t0006g0228 a0002c0003t0003g0136 |
2 | HG03471.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1541+4945_1541+496 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | ATGTATGT others(3): Show |
1 | a0001c0002t0006g0022 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1541+4938_1541+493 others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998420 | ||||||
| chr14:89998420 | A | G | 59 | a0001c0001t0001g0019 a0001c0001t0001g0097 a0001c0001t0001g0163 others(56): Show |
67 | HG00323.hp2 HG01070.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1541+4937A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998420 | |||||||
| chr14:89998422 | ATG | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0002t0003g0193 others(1): Show |
4 | HG00735.hp2 HG03017.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541+4941_1541+494 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998422 | ||||||
| chr14:89998424 | G | A | 12 | a0001c0002t0001g0195 a0001c0002t0013g0198 a0001c0002t0013g0199 others(9): Show |
12 | HG01081.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1541+4941G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998424 | |||||||
| chr14:89998424 | G | GTATGTAT others(5): Show |
1 | a0001c0002t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1541+4948_1541+494 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998424 | ||||||
| chr14:89998428 | G | A | 11 | a0001c0001t0001g0093 a0001c0002t0001g0196 a0001c0002t0001g0200 others(8): Show |
11 | HG00735.hp2 HG01081.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1541+4945G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998428 | |||||||
| chr14:89998432 | G | A | 7 | a0001c0002t0001g0196 a0001c0002t0001g0200 a0002c0004t0005g0069 others(4): Show |
7 | HG01081.hp1 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+4949G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998432 | |||||||
| chr14:89998435 | T | C | 9 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(6): Show |
10 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1541+4952T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998435 | |||||||
| chr14:89998436 | G | GTATGTAT others(19): Show |
1 | a0002c0003t0003g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1541+4960_1541+496 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998436 | ||||||
| chr14:89998436 | G | GTATGTAT others(31): Show |
1 | a0002c0003t0003g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1541+4960_1541+496 others(42): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998436 | ||||||
| chr14:89998439 | T | C | 5 | a0002c0004t0005g0069 a0002c0004t0005g0070 a0002c0004t0005g0071 others(2): Show |
5 | HG01081.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1541+4956T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998439 | |||||||
| chr14:89998440 | GTA | G | 10 | a0001c0005t0001g0027 a0002c0004t0005g0016 a0002c0004t0005g0067 others(7): Show |
11 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1541+4961_1541+496 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998440 | ||||||
| chr14:89998442 | A | ATG | 7 | a0001c0002t0001g0196 a0001c0002t0001g0200 a0002c0004t0005g0069 others(4): Show |
7 | HG01081.hp1 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+4960_1541+496 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998442 | ||||||
| chr14:89998467 | TATTA | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+4988_1541+499 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89998467 | ||||||
| chr14:89998503 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+5020G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998503 | |||||||
| chr14:89998740 | C | T | 1 | a0002c0003t0003g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1541+5257C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998740 | |||||||
| chr14:89998823 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1541+5340G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998823 | |||||||
| chr14:89998857 | G | T | 1 | a0001c0002t0004g0217 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1541+5374G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998857 | |||||||
| chr14:89998884 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1541+5401C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998884 | |||||||
| chr14:89998901 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+5418C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998901 | |||||||
| chr14:89998927 | G | A | 2 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1541+5444G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89998927 | |||||||
| chr14:89999048 | A | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+5565A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999048 | |||||||
| chr14:89999201 | G | GA | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+5725dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 89999201 | ||||||
| chr14:89999258 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+5775A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999258 | |||||||
| chr14:89999280 | A | G | 41 | a0001c0001t0001g0120 a0001c0001t0002g0001 a0001c0001t0002g0003 others(38): Show |
52 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1541+5797A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999280 | |||||||
| chr14:89999295 | C | T | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1541+5812C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999295 | |||||||
| chr14:89999463 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1541+5980G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999463 | |||||||
| chr14:89999576 | G | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6093G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999576 | |||||||
| chr14:89999658 | A | G | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+6175A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999658 | |||||||
| chr14:89999695 | C | T | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6212C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999695 | |||||||
| chr14:89999707 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6224A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999707 | |||||||
| chr14:89999708 | A | G | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+6225A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999708 | |||||||
| chr14:89999711 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6228G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999711 | |||||||
| chr14:89999786 | C | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+6303C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999786 | |||||||
| chr14:89999811 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6328A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999811 | |||||||
| chr14:89999826 | A | G | 2 | a0001c0002t0006g0222 a0001c0002t0006g0225 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1541+6343A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999826 | |||||||
| chr14:89999852 | C | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+6369C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 89999852 | |||||||
| chr14:90000023 | C | T | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1541+6540C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000023 | |||||||
| chr14:90000058 | A | G | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6575A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000058 | |||||||
| chr14:90000076 | C | T | 1 | a0001c0002t0008g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+6593C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000076 | |||||||
| chr14:90000180 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+6697A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000180 | |||||||
| chr14:90000251 | G | A | 27 | a0001c0002t0006g0222 a0001c0002t0006g0223 a0001c0002t0006g0224 others(24): Show |
30 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1541+6768G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000251 | |||||||
| chr14:90000270 | T | TAGTC | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+6788_1541+678 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90000270 | ||||||
| chr14:90000306 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+6823T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000306 | |||||||
| chr14:90000447 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1541+6964C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000447 | |||||||
| chr14:90000477 | T | C | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+6994T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000477 | |||||||
| chr14:90000530 | A | G | 7 | a0001c0001t0001g0106 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG02132.hp1 NA18951.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1541+7047A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000530 | |||||||
| chr14:90000534 | G | A | 1 | a0001c0002t0004g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1541+7051G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000534 | |||||||
| chr14:90000663 | G | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+7180G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000663 | |||||||
| chr14:90000708 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0190 |
3 | HG02280.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1541+7225G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000708 | |||||||
| chr14:90000780 | T | C | 80 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(77): Show |
88 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1541+7297T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000780 | |||||||
| chr14:90000803 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1541+7320T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000803 | |||||||
| chr14:90000837 | A | T | 1 | a0001c0002t0004g0205 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1541+7354A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000837 | |||||||
| chr14:90000909 | G | A | 1 | a0005c0008t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1541+7426G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90000909 | |||||||
| chr14:90001094 | T | C | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+7611T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001094 | |||||||
| chr14:90001184 | G | C | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+7701G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001184 | |||||||
| chr14:90001248 | C | T | 1 | a0001c0002t0013g0199 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1541+7765C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001248 | |||||||
| chr14:90001423 | A | G | 2 | a0001c0002t0006g0022 a0001c0002t0006g0227 |
3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1541+7940A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001423 | |||||||
| chr14:90001648 | A | C | 62 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(59): Show |
69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1541+8165A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001648 | |||||||
| chr14:90001810 | C | T | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+8327C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001810 | |||||||
| chr14:90001829 | T | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+8346T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001829 | |||||||
| chr14:90001893 | G | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+8410G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90001893 | |||||||
| chr14:90002143 | C | T | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+8660C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002143 | |||||||
| chr14:90002327 | C | A | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+8844C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002327 | |||||||
| chr14:90002354 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1541+8871A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002354 | |||||||
| chr14:90002583 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+9100A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002583 | |||||||
| chr14:90002706 | C | CA | 7 | a0001c0001t0001g0103 a0001c0001t0002g0038 a0001c0002t0004g0207 others(4): Show |
7 | HG01192.hp2 HG01981.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1541+9238dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90002706 | ||||||
| chr14:90002706 | CA | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+9238delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90002706 | ||||||
| chr14:90002717 | A | C | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1541+9234A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002717 | |||||||
| chr14:90002734 | T | A | 1 | a0002c0004t0009g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1541+9251T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002734 | |||||||
| chr14:90002734 | T | G | 20 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(17): Show |
23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1541+9251T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002734 | |||||||
| chr14:90002819 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+9336G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002819 | |||||||
| chr14:90002973 | A | AT | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+9492dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90002973 | ||||||
| chr14:90002974 | T | TG | 7 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(4): Show |
9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+9491_1541+949 others(5): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002974 | |||||||
| chr14:90002999 | A | G | 9 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(6): Show |
11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1541+9516A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90002999 | |||||||
| chr14:90003020 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1541+9537C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003020 | |||||||
| chr14:90003126 | T | C | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+9643T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003126 | |||||||
| chr14:90003128 | A | G | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+9645A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003128 | |||||||
| chr14:90003157 | C | T | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+9674C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003157 | |||||||
| chr14:90003179 | G | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+9696G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003179 | |||||||
| chr14:90003246 | A | G | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+9763A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003246 | |||||||
| chr14:90003292 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1541+9809C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003292 | |||||||
| chr14:90003349 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0011g0092 |
2 | NA18951.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1541+9866T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003349 | |||||||
| chr14:90003482 | G | A | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1541+9999G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003482 | |||||||
| chr14:90003741 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+10258T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003741 | |||||||
| chr14:90003889 | T | C | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1541+10406T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003889 | |||||||
| chr14:90003943 | T | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+10460T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90003943 | |||||||
| chr14:90004019 | G | A | 2 | a0001c0002t0004g0203 a0001c0002t0004g0204 |
2 | HG01433.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1541+10536G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004019 | |||||||
| chr14:90004027 | A | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+10544A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004027 | |||||||
| chr14:90004039 | G | A | 1 | a0001c0002t0008g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1541+10556G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004039 | |||||||
| chr14:90004046 | T | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1541+10563T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004046 | |||||||
| chr14:90004089 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+10606G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004089 | |||||||
| chr14:90004113 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+10630G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004113 | |||||||
| chr14:90004139 | C | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+10656C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004139 | |||||||
| chr14:90004269 | T | C | 1 | a0001c0002t0004g0208 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1541+10786T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004269 | |||||||
| chr14:90004282 | T | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+10799T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004282 | |||||||
| chr14:90004333 | T | C | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+10850T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004333 | |||||||
| chr14:90004433 | G | A | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1541+10950G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004433 | |||||||
| chr14:90004637 | A | G | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1541+11154A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004637 | |||||||
| chr14:90004685 | T | TG | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1541+11203dupG | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90004685 | ||||||
| chr14:90004771 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0107 |
2 | HG00639.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.1541+11288T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004771 | |||||||
| chr14:90004810 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1541+11327C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004810 | |||||||
| chr14:90004929 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1541+11446T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004929 | |||||||
| chr14:90004940 | A | G | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+11457A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004940 | |||||||
| chr14:90004974 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1541+11491A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90004974 | |||||||
| chr14:90005096 | A | G | 2 | a0001c0002t0001g0194 a0001c0002t0001g0195 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1541+11613A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005096 | |||||||
| chr14:90005267 | G | C | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1541+11784G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005267 | |||||||
| chr14:90005414 | A | T | 41 | a0001c0002t0014g0025 a0002c0003t0003g0005 a0002c0003t0003g0020 others(38): Show |
47 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1541+11931A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005414 | |||||||
| chr14:90005422 | A | T | 5 | a0001c0001t0001g0120 a0001c0001t0002g0036 a0001c0001t0002g0048 others(2): Show |
5 | HG02165.hp1 NA18942.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541+11939A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005422 | |||||||
| chr14:90005435 | A | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1541+11952A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90005435 | |||||||
| chr14:90006082 | G | A | 13 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(10): Show |
14 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1541+12599G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006082 | |||||||
| chr14:90006092 | C | T | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1541+12609C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006092 | |||||||
| chr14:90006243 | C | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1541+12760C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006243 | |||||||
| chr14:90006492 | T | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-12824T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006492 | |||||||
| chr14:90006754 | G | C | 1 | a0002c0003t0003g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1542-12562G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006754 | |||||||
| chr14:90006894 | A | G | 3 | a0005c0008t0001g0138 a0005c0008t0001g0139 a0005c0008t0001g0140 |
3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1542-12422A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90006894 | |||||||
| chr14:90007244 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-12072C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007244 | |||||||
| chr14:90007282 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1542-12034G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007282 | |||||||
| chr14:90007326 | T | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11990T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007326 | |||||||
| chr14:90007354 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1542-11962C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007354 | |||||||
| chr14:90007433 | A | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0043 others(1): Show |
7 | NA18952.hp2 NA18970.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542-11883A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007433 | |||||||
| chr14:90007446 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1542-11870G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007446 | |||||||
| chr14:90007526 | T | G | 1 | a0001c0005t0016g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1542-11790T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007526 | |||||||
| chr14:90007568 | A | G | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-11748A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007568 | |||||||
| chr14:90007574 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1542-11742G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007574 | |||||||
| chr14:90007600 | C | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11716C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007600 | |||||||
| chr14:90007626 | A | AT | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11679dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90007626 | ||||||
| chr14:90007626 | A | T | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1542-11690A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007626 | |||||||
| chr14:90007719 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1542-11597C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90007719 | |||||||
| chr14:90008035 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11281G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008035 | |||||||
| chr14:90008052 | C | G | 1 | a0001c0001t0002g0047 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1542-11264C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008052 | |||||||
| chr14:90008096 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1542-11220G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008096 | |||||||
| chr14:90008153 | AT | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11161delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90008153 | ||||||
| chr14:90008219 | A | C | 6 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1542-11097A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008219 | |||||||
| chr14:90008275 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-11041C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008275 | |||||||
| chr14:90008282 | G | A | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1542-11034G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008282 | |||||||
| chr14:90008348 | C | CAT | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-10967_1542-10 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90008348 | ||||||
| chr14:90008420 | C | A | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1542-10896C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008420 | |||||||
| chr14:90008430 | A | G | 2 | a0003c0006t0007g0083 a0003c0006t0007g0084 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-10886A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008430 | |||||||
| chr14:90008485 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-10831C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008485 | |||||||
| chr14:90008491 | G | A | 1 | a0001c0005t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1542-10825G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008491 | |||||||
| chr14:90008514 | A | G | 2 | a0001c0002t0004g0208 a0001c0002t0004g0210 |
2 | HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542-10802A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008514 | |||||||
| chr14:90008580 | G | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-10736G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90008580 | |||||||
| chr14:90009005 | A | G | 21 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(18): Show |
24 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-10311A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009005 | |||||||
| chr14:90009375 | A | G | 2 | a0001c0002t0004g0208 a0001c0002t0004g0210 |
2 | HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542-9941A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009375 | |||||||
| chr14:90009411 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1542-9905A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009411 | |||||||
| chr14:90009664 | A | T | 11 | a0001c0001t0002g0015 a0001c0001t0002g0035 a0001c0001t0002g0056 others(8): Show |
12 | HG01074.hp1 HG01123.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1542-9652A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009664 | |||||||
| chr14:90009705 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1542-9611A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90009705 | |||||||
| chr14:90010014 | C | T | 1 | a0003c0006t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1542-9302C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010014 | |||||||
| chr14:90010085 | A | G | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1542-9231A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010085 | |||||||
| chr14:90010263 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-9053A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010263 | |||||||
| chr14:90010294 | T | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-9022T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010294 | |||||||
| chr14:90010537 | T | C | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1542-8779T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010537 | |||||||
| chr14:90010575 | CGA | C | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-8731_1542-873 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90010575 | ||||||
| chr14:90010629 | G | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8687G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010629 | |||||||
| chr14:90010661 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8655C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010661 | |||||||
| chr14:90010690 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8626G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010690 | |||||||
| chr14:90010905 | A | G | 3 | a0005c0008t0001g0138 a0005c0008t0001g0139 a0005c0008t0001g0140 |
3 | HG02615.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1542-8411A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90010905 | |||||||
| chr14:90011049 | G | C | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-8267G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011049 | |||||||
| chr14:90011154 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-8162C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011154 | |||||||
| chr14:90011162 | G | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | HG00408.hp1 NA18747.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1542-8154G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011162 | |||||||
| chr14:90011279 | A | G | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1542-8037A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011279 | |||||||
| chr14:90011300 | A | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-8016A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011300 | |||||||
| chr14:90011303 | G | C | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-8013G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011303 | |||||||
| chr14:90011542 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-7774G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011542 | |||||||
| chr14:90011548 | A | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-7768A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011548 | |||||||
| chr14:90011663 | T | C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0064 |
3 | HG00738.hp2 HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1542-7653T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011663 | |||||||
| chr14:90011744 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1542-7572C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011744 | |||||||
| chr14:90011811 | G | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7505G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011811 | |||||||
| chr14:90011817 | G | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7499G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011817 | |||||||
| chr14:90011830 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1542-7486G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011830 | |||||||
| chr14:90011855 | A | G | 2 | a0001c0002t0006g0022 a0001c0002t0006g0227 |
3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1542-7461A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011855 | |||||||
| chr14:90011991 | C | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7325C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90011991 | |||||||
| chr14:90012056 | G | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-7260G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012056 | |||||||
| chr14:90012074 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-7242C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012074 | |||||||
| chr14:90012429 | C | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-6887C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012429 | |||||||
| chr14:90012484 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-6832G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012484 | |||||||
| chr14:90012543 | A | T | 1 | a0001c0002t0004g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1542-6773A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012543 | |||||||
| chr14:90012689 | G | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-6627G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012689 | |||||||
| chr14:90012694 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1542-6622C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012694 | |||||||
| chr14:90012810 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-6506A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012810 | |||||||
| chr14:90012927 | C | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-6389C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012927 | |||||||
| chr14:90012951 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-6365G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90012951 | |||||||
| chr14:90013038 | A | G | 1 | a0002c0004t0005g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1542-6278A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013038 | |||||||
| chr14:90013068 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-6248A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013068 | |||||||
| chr14:90013075 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1542-6241A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013075 | |||||||
| chr14:90013180 | G | A | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542-6136G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013180 | |||||||
| chr14:90013190 | A | C | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542-6126A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013190 | |||||||
| chr14:90013289 | T | C | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1542-6027T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013289 | |||||||
| chr14:90013311 | T | C | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-6005T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013311 | |||||||
| chr14:90013477 | C | A | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-5839C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013477 | |||||||
| chr14:90013733 | G | A | 3 | a0001c0002t0001g0031 a0001c0002t0003g0023 a0001c0002t0014g0025 |
3 | HG02559.hp2 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1542-5583G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013733 | |||||||
| chr14:90013761 | A | G | 29 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(26): Show |
33 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1542-5555A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013761 | |||||||
| chr14:90013791 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1542-5525G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013791 | |||||||
| chr14:90013912 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1542-5404T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013912 | |||||||
| chr14:90013928 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | NA18942.hp2 NA18953.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1542-5388A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013928 | |||||||
| chr14:90013960 | T | A | 1 | a0001c0002t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1542-5356T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013960 | |||||||
| chr14:90013978 | T | G | 15 | a0001c0002t0004g0209 a0002c0004t0005g0016 a0002c0004t0005g0067 others(12): Show |
16 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542-5338T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90013978 | |||||||
| chr14:90014032 | C | T | 3 | a0001c0002t0004g0207 a0001c0002t0004g0208 a0001c0002t0004g0210 |
3 | HG02258.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1542-5284C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014032 | |||||||
| chr14:90014119 | C | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-5197C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014119 | |||||||
| chr14:90014168 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1542-5148A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014168 | |||||||
| chr14:90014186 | A | G | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1542-5130A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014186 | |||||||
| chr14:90014287 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-5029A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014287 | |||||||
| chr14:90014351 | A | G | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1542-4965A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014351 | |||||||
| chr14:90014492 | C | G | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-4824C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014492 | |||||||
| chr14:90014751 | C | G | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1542-4565C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014751 | |||||||
| chr14:90014753 | T | A | 42 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(39): Show |
46 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1542-4563T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014753 | |||||||
| chr14:90014795 | G | A | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1542-4521G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014795 | |||||||
| chr14:90014922 | G | T | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1542-4394G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014922 | |||||||
| chr14:90014963 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | NA18942.hp2 NA18953.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1542-4353A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014963 | |||||||
| chr14:90014967 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1542-4349C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90014967 | |||||||
| chr14:90015029 | A | G | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1542-4287A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015029 | |||||||
| chr14:90015235 | T | C | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1542-4081T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015235 | |||||||
| chr14:90015444 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-3872C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015444 | |||||||
| chr14:90015559 | CA | C | 2 | a0001c0002t0006g0022 a0001c0002t0006g0227 |
3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1542-3756delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015559 | |||||||
| chr14:90015612 | A | G | 229 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(226): Show |
259 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.1542-3704A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015612 | |||||||
| chr14:90015806 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1542-3510T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015806 | |||||||
| chr14:90015915 | G | C | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-3401G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015915 | |||||||
| chr14:90015941 | A | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1542-3375A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90015941 | |||||||
| chr14:90016046 | C | CT | 18 | a0001c0001t0001g0162 a0001c0001t0002g0056 a0001c0002t0008g0197 others(15): Show |
19 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1542-3258dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90016046 | ||||||
| chr14:90016193 | T | C | 43 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(40): Show |
47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1542-3123T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016193 | |||||||
| chr14:90016205 | C | T | 44 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0161 others(41): Show |
55 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1542-3111C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016205 | |||||||
| chr14:90016243 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-3073C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016243 | |||||||
| chr14:90016311 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-3005G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016311 | |||||||
| chr14:90016365 | C | T | 1 | a0008c0009t0005g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1542-2951C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016365 | |||||||
| chr14:90016457 | T | C | 1 | a0001c0002t0010g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1542-2859T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016457 | |||||||
| chr14:90016724 | T | TAC | 20 | a0001c0001t0001g0122 a0002c0003t0003g0005 a0002c0003t0003g0020 others(17): Show |
23 | HG01070.hp2 HG01361.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1542-2578_1542-257 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90016724 | ||||||
| chr14:90016743 | G | A | 63 | a0001c0002t0003g0193 a0001c0002t0004g0021 a0001c0002t0004g0203 others(60): Show |
70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1542-2573G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016743 | |||||||
| chr14:90016831 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG00642.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1542-2485G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016831 | |||||||
| chr14:90016919 | C | G | 1 | a0001c0005t0016g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1542-2397C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016919 | |||||||
| chr14:90016927 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1542-2389T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90016927 | |||||||
| chr14:90017090 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1542-2226A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017090 | |||||||
| chr14:90017202 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1542-2114G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017202 | |||||||
| chr14:90017321 | TA | T | 62 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(59): Show |
69 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1542-1993delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90017321 | ||||||
| chr14:90017328 | G | A | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1542-1988G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017328 | |||||||
| chr14:90017331 | T | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18947.hp2 NA18988.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1542-1985T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017331 | |||||||
| chr14:90017365 | T | G | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1542-1951T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017365 | |||||||
| chr14:90017370 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-1946A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017370 | |||||||
| chr14:90017503 | C | G | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-1813C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017503 | |||||||
| chr14:90017527 | A | T | 43 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(40): Show |
47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1542-1789A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017527 | |||||||
| chr14:90017619 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1542-1697G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017619 | |||||||
| chr14:90017904 | T | G | 5 | a0002c0003t0003g0130 a0002c0003t0003g0131 a0002c0003t0003g0135 others(2): Show |
5 | HG02602.hp2 HG02738.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542-1412T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017904 | |||||||
| chr14:90017973 | T | C | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1542-1343T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017973 | |||||||
| chr14:90017977 | C | G | 1 | a0001c0005t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1542-1339C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90017977 | |||||||
| chr14:90018071 | C | CT | 10 | a0001c0001t0001g0148 a0001c0001t0002g0009 a0001c0001t0002g0042 others(7): Show |
11 | HG00738.hp2 HG01891.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1542-1229dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018071 | ||||||
| chr14:90018071 | CT | C | 36 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0002g0036 others(33): Show |
39 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1542-1229delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018071 | ||||||
| chr14:90018071 | CTT | C | 44 | a0001c0002t0003g0193 a0001c0002t0004g0021 a0001c0002t0004g0203 others(41): Show |
49 | HG00323.hp2 HG01070.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.1542-1230_1542-122 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018071 | ||||||
| chr14:90018101 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1542-1215G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018101 | |||||||
| chr14:90018151 | A | C | 13 | a0001c0002t0001g0031 a0001c0002t0003g0023 a0001c0005t0001g0002 others(10): Show |
16 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1542-1165A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018151 | |||||||
| chr14:90018220 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-1096G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018220 | |||||||
| chr14:90018333 | A | G | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1542-983A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018333 | |||||||
| chr14:90018341 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1542-975A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018341 | |||||||
| chr14:90018392 | G | C | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1542-924G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018392 | |||||||
| chr14:90018607 | C | T | 1 | a0001c0002t0010g0221 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1542-709C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018607 | |||||||
| chr14:90018692 | G | A | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1542-624G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018692 | |||||||
| chr14:90018700 | C | T | 1 | a0001c0005t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1542-616C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018700 | |||||||
| chr14:90018750 | C | T | 2 | a0001c0005t0001g0027 a0002c0004t0005g0075 |
2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1542-566C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018750 | |||||||
| chr14:90018795 | C | T | 1 | a0002c0004t0005g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1542-521C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018795 | |||||||
| chr14:90018929 | A | G | 43 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(40): Show |
47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1542-387A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018929 | |||||||
| chr14:90018959 | T | TGCTAGTT others(7): Show |
14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1542-356_1542-343d others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90018959 | ||||||
| chr14:90018995 | C | G | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1542-321C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90018995 | |||||||
| chr14:90019033 | GA | G | 6 | a0001c0001t0001g0109 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG00408.hp2 NA18947.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542-276delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr14 | 90019033 | ||||||
| chr14:90019040 | A | G | 6 | a0001c0001t0001g0109 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG00408.hp2 NA18947.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1542-276A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90019040 | |||||||
| chr14:90019290 | C | G | 1 | a0001c0001t0002g0009 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1542-26C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 14/16 | chr14 | 90019290 | |||||||
| chr14:90019650 | CTG | C | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1644+237_1644+238d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90019650 | ||||||
| chr14:90019719 | C | T | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+301C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019719 | |||||||
| chr14:90019882 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1644+464A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019882 | |||||||
| chr14:90019883 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1644+465C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019883 | |||||||
| chr14:90019912 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644+494C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019912 | |||||||
| chr14:90019965 | C | T | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+547C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90019965 | |||||||
| chr14:90020029 | G | A | 20 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(17): Show |
23 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1644+611G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020029 | |||||||
| chr14:90020188 | T | G | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1644+770T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020188 | |||||||
| chr14:90020285 | T | C | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1644+867T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020285 | |||||||
| chr14:90020285 | TAC | T | 31 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(28): Show |
33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+877_1644+878d others(4): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020285 | ||||||
| chr14:90020309 | G | T | 31 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(28): Show |
33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+891G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020309 | |||||||
| chr14:90020354 | T | TCCTC | 24 | a0001c0001t0001g0006 a0001c0001t0001g0169 a0001c0001t0015g0006 others(21): Show |
28 | HG01891.hp1 HG01981.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1644+956_1644+959d others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020354 | ||||||
| chr14:90020354 | T | TCCTCCCT others(13): Show |
37 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(34): Show |
41 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.1644+955_1644+956i others(22): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020354 | ||||||
| chr14:90020354 | T | TCCTCCCT others(124): Show |
8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+955_1644+956i others(133): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020354 | ||||||
| chr14:90020364 | C | CTCCCTCC others(5): Show |
14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+957_1644+958i others(14): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020364 | ||||||
| chr14:90020374 | C | CCCTT | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644+968_1644+971d others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020374 | ||||||
| chr14:90020374 | C | T | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+956C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020374 | |||||||
| chr14:90020423 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644+1005C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020423 | |||||||
| chr14:90020476 | TTCCC | T | 41 | a0001c0001t0001g0086 a0001c0001t0001g0120 a0001c0001t0001g0163 others(38): Show |
52 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1644+1084_1644+108 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020476 | ||||||
| chr14:90020482 | C | T | 51 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(48): Show |
56 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1644+1064C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020482 | |||||||
| chr14:90020501 | TCCCTTCC others(1): Show |
T | 9 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(6): Show |
11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1084_1644+109 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020501 | |||||||
| chr14:90020509 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644+1091G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020509 | |||||||
| chr14:90020513 | C | T | 9 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(6): Show |
11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1095C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020513 | |||||||
| chr14:90020527 | C | T | 9 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(6): Show |
11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1109C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020527 | |||||||
| chr14:90020530 | T | TTCCG | 2 | a0001c0002t0006g0022 a0001c0002t0006g0227 |
3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1644+1115_1644+111 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020530 | ||||||
| chr14:90020534 | T | C | 2 | a0001c0002t0006g0022 a0001c0002t0006g0227 |
3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1644+1116T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020534 | |||||||
| chr14:90020542 | C | CTCCCTCC others(44): Show |
1 | a0001c0002t0006g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1644+1129_1644+113 others(55): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020542 | ||||||
| chr14:90020543 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1125T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020543 | |||||||
| chr14:90020548 | T | C | 31 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(28): Show |
33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+1130T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020548 | |||||||
| chr14:90020548 | T | TCCTTCCC others(6): Show |
7 | a0001c0001t0001g0100 a0003c0006t0007g0004 a0003c0006t0007g0080 others(4): Show |
9 | HG00280.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1644+1136_1644+113 others(17): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020548 | ||||||
| chr14:90020552 | T | C | 1 | a0001c0002t0006g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1644+1134T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020552 | |||||||
| chr14:90020552 | T | TCCCTCCC others(2): Show |
23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1644+1136_1644+113 others(13): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020552 | ||||||
| chr14:90020552 | T | TCCCTCCC others(19): Show |
3 | a0001c0002t0006g0222 a0001c0002t0006g0224 a0001c0002t0006g0225 |
3 | HG02280.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1644+1136_1644+113 others(30): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020552 | ||||||
| chr14:90020555 | T | C | 9 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(6): Show |
9 | HG01891.hp1 HG02886.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1644+1137T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020555 | |||||||
| chr14:90020559 | C | T | 34 | a0001c0001t0001g0100 a0001c0002t0004g0021 a0001c0002t0004g0203 others(31): Show |
37 | HG00280.hp2 HG00323.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.1644+1141C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020559 | |||||||
| chr14:90020559 | CTCCCTCC others(50): Show |
C | 9 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(6): Show |
11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1155_1644+121 others(61): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020559 | ||||||
| chr14:90020563 | C | CTCCCTTC others(6): Show |
14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1150_1644+115 others(17): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020563 | ||||||
| chr14:90020565 | C | T | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+1147C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020565 | |||||||
| chr14:90020569 | C | T | 18 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(15): Show |
19 | HG01070.hp2 HG01891.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1644+1151C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020569 | |||||||
| chr14:90020572 | T | TCCCTCCC others(34): Show |
2 | a0001c0002t0006g0226 a0001c0002t0006g0228 |
2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1644+1154_1644+115 others(45): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020572 | |||||||
| chr14:90020572 | T | TTCCCTCC others(39): Show |
2 | a0001c0002t0006g0022 a0001c0002t0006g0227 |
3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1644+1157_1644+115 others(50): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020572 | ||||||
| chr14:90020572 | T | TTCCCTCC others(35): Show |
7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+1157_1644+115 others(46): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020572 | ||||||
| chr14:90020573 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1644+1155T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020573 | |||||||
| chr14:90020576 | T | C | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644+1158T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020576 | |||||||
| chr14:90020576 | T | TTCCCTCC others(18): Show |
1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1644+1161_1644+116 others(29): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020576 | ||||||
| chr14:90020576 | T | TTCCTTCC others(5): Show |
53 | a0001c0001t0001g0120 a0001c0001t0001g0163 a0001c0001t0002g0001 others(50): Show |
67 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.1644+1162_1644+117 others(16): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020576 | ||||||
| chr14:90020576 | TTCCTTCC others(1): Show |
T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1644+1162_1644+116 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020576 | ||||||
| chr14:90020579 | CTTCCCTC others(29): Show |
C | 10 | a0002c0003t0003g0020 a0002c0003t0003g0137 a0002c0003t0003g0182 others(7): Show |
11 | HG01070.hp2 HG02559.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1162_1644+119 others(40): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020579 | |||||||
| chr14:90020580 | T | C | 4 | a0001c0002t0006g0022 a0001c0002t0006g0226 a0001c0002t0006g0227 others(1): Show |
5 | HG01192.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+1162T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020580 | |||||||
| chr14:90020580 | T | TTCCCTCC others(9): Show |
21 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(18): Show |
22 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1644+1173_1644+117 others(20): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020580 | ||||||
| chr14:90020580 | TTCCC | T | 39 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0085 others(36): Show |
41 | HG00323.hp1 HG00408.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1644+1184_1644+118 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020580 | ||||||
| chr14:90020582 | C | CCCTCCCT others(4): Show |
1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1644+1173_1644+117 others(15): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020582 | ||||||
| chr14:90020584 | C | CTCCCTCC others(14): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1644+1179_1644+118 others(25): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020584 | ||||||
| chr14:90020584 | C | CTCCCTCC others(1): Show |
14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1173_1644+117 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020584 | ||||||
| chr14:90020584 | C | CTCCCTTC others(6): Show |
6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+1171_1644+117 others(17): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020584 | ||||||
| chr14:90020584 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1644+1166C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020584 | |||||||
| chr14:90020592 | C | T | 5 | a0001c0002t0006g0222 a0001c0002t0006g0223 a0001c0002t0006g0224 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+1174C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020592 | |||||||
| chr14:90020616 | G | C | 10 | a0002c0003t0003g0020 a0002c0003t0003g0137 a0002c0003t0003g0182 others(7): Show |
11 | HG01070.hp2 HG02559.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644+1198G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020616 | |||||||
| chr14:90020800 | C | CTTTTTTT others(282): Show |
3 | a0001c0002t0004g0206 a0001c0002t0004g0209 a0001c0002t0004g0216 |
3 | HG02451.hp1 HG02896.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(282): Show |
1 | a0001c0002t0004g0219 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(283): Show |
2 | a0001c0002t0004g0203 a0001c0002t0004g0204 |
2 | HG01433.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1644+1396_1644+139 others(294): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(282): Show |
1 | a0001c0002t0010g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(283): Show |
12 | a0001c0002t0004g0021 a0001c0002t0004g0207 a0001c0002t0004g0208 others(9): Show |
13 | HG00323.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1644+1396_1644+139 others(294): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(282): Show |
1 | a0001c0002t0004g0213 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(293): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(283): Show |
1 | a0001c0002t0004g0218 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(294): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(284): Show |
1 | a0001c0002t0004g0205 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(295): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020800 | C | CTTTTTTT others(284): Show |
1 | a0001c0002t0010g0221 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1644+1396_1644+139 others(295): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90020800 | ||||||
| chr14:90020826 | C | T | 1 | a0002c0004t0005g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1644+1408C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020826 | |||||||
| chr14:90020834 | C | T | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1644+1416C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020834 | |||||||
| chr14:90020859 | G | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1441G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020859 | |||||||
| chr14:90020988 | G | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+1570G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90020988 | |||||||
| chr14:90021116 | C | T | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644+1698C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021116 | |||||||
| chr14:90021127 | G | A | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+1709G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021127 | |||||||
| chr14:90021177 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+1759C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021177 | |||||||
| chr14:90021352 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+1934C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021352 | |||||||
| chr14:90021628 | T | G | 31 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(28): Show |
33 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1644+2210T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021628 | |||||||
| chr14:90021870 | T | G | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1644+2452T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021870 | |||||||
| chr14:90021892 | CAG | C | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644+2477_1644+247 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90021892 | ||||||
| chr14:90021995 | T | C | 8 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0183 others(5): Show |
9 | HG01070.hp2 HG02559.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+2577T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90021995 | |||||||
| chr14:90022082 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1644+2664C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022082 | |||||||
| chr14:90022114 | G | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+2696G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022114 | |||||||
| chr14:90022179 | TGA | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+2765_1644+276 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90022179 | ||||||
| chr14:90022248 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1644+2830C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022248 | |||||||
| chr14:90022476 | C | G | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1644+3058C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022476 | |||||||
| chr14:90022568 | C | T | 43 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(40): Show |
47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1644+3150C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022568 | |||||||
| chr14:90022742 | G | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+3324G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022742 | |||||||
| chr14:90022770 | C | T | 1 | a0004c0007t0002g0050 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1644+3352C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022770 | |||||||
| chr14:90022804 | A | T | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+3386A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022804 | |||||||
| chr14:90022825 | T | C | 1 | a0001c0002t0010g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1644+3407T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022825 | |||||||
| chr14:90022844 | G | A | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1644+3426G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022844 | |||||||
| chr14:90022913 | C | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1644+3495C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022913 | |||||||
| chr14:90022945 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+3527T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022945 | |||||||
| chr14:90022954 | G | A | 97 | a0001c0001t0001g0018 a0001c0001t0001g0087 a0001c0001t0001g0088 others(94): Show |
109 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(106): Show |
intron_variant | MODIFIER | c.1644+3536G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022954 | |||||||
| chr14:90022986 | A | G | 1 | a0001c0005t0016g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1644+3568A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90022986 | |||||||
| chr14:90023075 | CTGG | C | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1644+3659_1644+366 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90023075 | ||||||
| chr14:90023200 | GC | G | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644+3783delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023200 | |||||||
| chr14:90023254 | A | C | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+3836A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023254 | |||||||
| chr14:90023316 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1644+3898G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023316 | |||||||
| chr14:90023863 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1644+4445C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90023863 | |||||||
| chr14:90024089 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1644+4671A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024089 | |||||||
| chr14:90024095 | C | G | 1 | a0001c0005t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1644+4677C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024095 | |||||||
| chr14:90024130 | G | C | 24 | a0001c0001t0002g0044 a0001c0002t0004g0021 a0001c0002t0004g0203 others(21): Show |
25 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1644+4712G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024130 | |||||||
| chr14:90024204 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+4786C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024204 | |||||||
| chr14:90024341 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+4923A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90024341 | |||||||
| chr14:90025004 | C | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1644+5586C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025004 | |||||||
| chr14:90025013 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1644+5595C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025013 | |||||||
| chr14:90025131 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1644+5713A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025131 | |||||||
| chr14:90025134 | C | T | 2 | a0002c0003t0003g0182 a0002c0003t0003g0188 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1644+5716C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025134 | |||||||
| chr14:90025468 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1644+6050A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025468 | |||||||
| chr14:90025583 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1644+6165G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025583 | |||||||
| chr14:90025594 | G | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1644+6176G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025594 | |||||||
| chr14:90025789 | A | C | 92 | a0001c0002t0001g0031 a0001c0002t0001g0194 a0001c0002t0001g0195 others(89): Show |
103 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(100): Show |
intron_variant | MODIFIER | c.1644+6371A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025789 | |||||||
| chr14:90025903 | A | G | 1 | a0001c0002t0004g0209 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1644+6485A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90025903 | |||||||
| chr14:90026072 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1644+6654G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026072 | |||||||
| chr14:90026377 | C | T | 1 | a0001c0005t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1645-6729C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026377 | |||||||
| chr14:90026567 | C | T | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-6539C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026567 | |||||||
| chr14:90026642 | G | A | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1645-6464G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026642 | |||||||
| chr14:90026698 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1645-6408G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026698 | |||||||
| chr14:90026763 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-6343T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026763 | |||||||
| chr14:90026769 | T | G | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-6337T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026769 | |||||||
| chr14:90026826 | G | C | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-6280G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026826 | |||||||
| chr14:90026908 | T | A | 10 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(7): Show |
12 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1645-6198T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026908 | |||||||
| chr14:90026922 | G | A | 4 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0132 others(1): Show |
6 | HG02451.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1645-6184G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026922 | |||||||
| chr14:90026956 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1645-6150A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90026956 | |||||||
| chr14:90027071 | C | T | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1645-6035C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027071 | |||||||
| chr14:90027192 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1645-5914C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027192 | |||||||
| chr14:90027239 | C | A | 1 | a0001c0001t0002g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1645-5867C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027239 | |||||||
| chr14:90027264 | C | T | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-5842C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027264 | |||||||
| chr14:90027410 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1645-5696G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027410 | |||||||
| chr14:90027431 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-5675A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027431 | |||||||
| chr14:90027466 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-5640G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027466 | |||||||
| chr14:90027479 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1645-5627A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027479 | |||||||
| chr14:90027507 | G | A | 1 | a0001c0005t0001g0065 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1645-5599G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027507 | |||||||
| chr14:90027705 | G | C | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-5401G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027705 | |||||||
| chr14:90027754 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1645-5352G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90027754 | |||||||
| chr14:90028083 | A | G | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1645-5023A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028083 | |||||||
| chr14:90028301 | C | A | 1 | a0001c0002t0003g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1645-4805C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028301 | |||||||
| chr14:90028439 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1645-4667C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028439 | |||||||
| chr14:90028440 | G | A | 1 | a0002c0003t0003g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1645-4666G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028440 | |||||||
| chr14:90028826 | G | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0055 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1645-4280G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028826 | |||||||
| chr14:90028965 | A | G | 1 | a0001c0002t0001g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1645-4141A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90028965 | |||||||
| chr14:90029130 | T | C | 2 | a0002c0003t0003g0182 a0002c0003t0003g0188 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1645-3976T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029130 | |||||||
| chr14:90029194 | A | AT | 23 | a0001c0001t0001g0093 a0001c0001t0001g0102 a0001c0001t0001g0163 others(20): Show |
24 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.1645-3891dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | ||||||
| chr14:90029194 | A | ATT | 4 | a0001c0002t0004g0206 a0001c0002t0004g0209 a0002c0004t0005g0016 others(1): Show |
5 | HG01109.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1645-3892_1645-389 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | ||||||
| chr14:90029194 | A | ATTT | 10 | a0002c0004t0005g0067 a0002c0004t0005g0068 a0002c0004t0005g0069 others(7): Show |
10 | HG00735.hp2 HG01081.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-3893_1645-389 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | ||||||
| chr14:90029194 | AT | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0085 a0001c0001t0001g0107 others(18): Show |
22 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.1645-3891delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | ||||||
| chr14:90029194 | ATT | A | 21 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0224 others(18): Show |
23 | HG01070.hp2 HG01192.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1645-3892_1645-389 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | ||||||
| chr14:90029194 | ATTT | A | 8 | a0002c0003t0003g0005 a0002c0003t0012g0189 a0003c0006t0007g0004 others(5): Show |
10 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-3893_1645-389 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029194 | ||||||
| chr14:90029197 | T | A | 3 | a0001c0001t0001g0099 a0005c0008t0001g0138 a0005c0008t0001g0140 |
3 | HG02723.hp1 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1645-3909T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029197 | |||||||
| chr14:90029198 | T | A | 1 | a0005c0008t0001g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1645-3908T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029198 | |||||||
| chr14:90029199 | T | A | 2 | a0002c0003t0003g0182 a0002c0003t0003g0188 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1645-3907T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029199 | |||||||
| chr14:90029200 | T | A | 1 | a0005c0008t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1645-3906T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029200 | |||||||
| chr14:90029229 | G | A | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1645-3877G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029229 | |||||||
| chr14:90029336 | T | C | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1645-3770T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029336 | |||||||
| chr14:90029345 | G | A | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-3761G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029345 | |||||||
| chr14:90029498 | C | CT | 18 | a0001c0001t0001g0102 a0001c0001t0001g0154 a0001c0001t0001g0158 others(15): Show |
20 | HG02071.hp1 HG02071.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.1645-3591dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | ||||||
| chr14:90029498 | C | CTT | 25 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(22): Show |
26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1645-3592_1645-359 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | ||||||
| chr14:90029498 | C | CTTT | 12 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(9): Show |
13 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1645-3593_1645-359 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | ||||||
| chr14:90029498 | C | CTTTT | 8 | a0001c0002t0013g0198 a0001c0002t0013g0199 a0002c0004t0005g0070 others(5): Show |
10 | HG01884.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-3594_1645-359 others(8): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | ||||||
| chr14:90029498 | CT | C | 7 | a0002c0003t0003g0020 a0002c0003t0003g0182 a0002c0003t0003g0184 others(4): Show |
8 | HG01070.hp2 HG03195.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1645-3591delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90029498 | ||||||
| chr14:90029561 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-3545C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029561 | |||||||
| chr14:90029574 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1645-3532G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029574 | |||||||
| chr14:90029728 | A | G | 1 | a0001c0001t0001g0018 | 2 | NA18968.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1645-3378A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029728 | |||||||
| chr14:90029775 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-3331A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029775 | |||||||
| chr14:90029795 | G | A | 2 | a0001c0002t0004g0208 a0001c0002t0004g0210 |
2 | HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1645-3311G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90029795 | |||||||
| chr14:90030196 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1645-2910C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030196 | |||||||
| chr14:90030204 | C | T | 41 | a0001c0001t0001g0120 a0001c0001t0001g0161 a0001c0001t0001g0162 others(38): Show |
52 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1645-2902C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030204 | |||||||
| chr14:90030266 | C | T | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-2840C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030266 | |||||||
| chr14:90030318 | T | C | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1645-2788T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030318 | |||||||
| chr14:90030403 | C | T | 4 | a0001c0002t0006g0222 a0001c0002t0006g0223 a0001c0002t0006g0224 others(1): Show |
4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1645-2703C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030403 | |||||||
| chr14:90030739 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1645-2367G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030739 | |||||||
| chr14:90030771 | C | CT | 31 | a0001c0001t0001g0118 a0001c0002t0001g0031 a0001c0002t0003g0023 others(28): Show |
37 | HG00741.hp2 HG01192.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1645-2323dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90030771 | ||||||
| chr14:90030771 | C | CTT | 14 | a0001c0005t0001g0065 a0002c0004t0005g0016 a0002c0004t0005g0067 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-2324_1645-232 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90030771 | ||||||
| chr14:90030771 | C | T | 1 | a0001c0002t0008g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1645-2335C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030771 | |||||||
| chr14:90030931 | A | AT | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1645-2164dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90030931 | ||||||
| chr14:90030938 | T | A | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1645-2168T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90030938 | |||||||
| chr14:90031010 | T | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-2096T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031010 | |||||||
| chr14:90031024 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1645-2082C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031024 | |||||||
| chr14:90031121 | ATTATAC | A | 2 | a0001c0002t0006g0022 a0001c0002t0006g0227 |
3 | HG01192.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1645-1982_1645-197 others(10): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90031121 | ||||||
| chr14:90031214 | T | C | 63 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(60): Show |
70 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.1645-1892T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031214 | |||||||
| chr14:90031342 | A | C | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1645-1764A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031342 | |||||||
| chr14:90031438 | C | T | 1 | a0003c0006t0007g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1645-1668C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031438 | |||||||
| chr14:90031495 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-1611A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031495 | |||||||
| chr14:90031664 | C | A | 80 | a0001c0002t0001g0031 a0001c0002t0001g0194 a0001c0002t0001g0195 others(77): Show |
88 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(85): Show |
intron_variant | MODIFIER | c.1645-1442C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031664 | |||||||
| chr14:90031816 | G | A | 43 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(40): Show |
47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1645-1290G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031816 | |||||||
| chr14:90031900 | G | T | 1 | a0002c0004t0005g0079 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1645-1206G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90031900 | |||||||
| chr14:90032079 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-1027T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032079 | |||||||
| chr14:90032183 | G | C | 1 | a0001c0001t0002g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1645-923G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032183 | |||||||
| chr14:90032217 | A | G | 43 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(40): Show |
47 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1645-889A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032217 | |||||||
| chr14:90032248 | C | T | 1 | a0001c0002t0014g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1645-858C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032248 | |||||||
| chr14:90032249 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1645-857G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032249 | |||||||
| chr14:90032259 | T | A | 9 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(6): Show |
11 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1645-847T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032259 | |||||||
| chr14:90032329 | G | T | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1645-777G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032329 | |||||||
| chr14:90032361 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1645-745G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032361 | |||||||
| chr14:90032379 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1645-727A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032379 | |||||||
| chr14:90032456 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-650C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032456 | |||||||
| chr14:90032457 | A | G | 1 | a0007c0012t0012g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1645-649A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032457 | |||||||
| chr14:90032545 | C | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-561C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032545 | |||||||
| chr14:90032590 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1645-516G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032590 | |||||||
| chr14:90032763 | A | G | 1 | a0001c0002t0003g0023 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1645-343A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032763 | |||||||
| chr14:90032938 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0002g0053 |
2 | HG00741.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1645-168C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032938 | |||||||
| chr14:90032962 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1645-144C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032962 | |||||||
| chr14:90032980 | C | A | 3 | a0001c0002t0008g0197 a0001c0002t0008g0201 a0001c0002t0008g0202 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1645-126C>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032980 | |||||||
| chr14:90032980 | C | G | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1645-126C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90032980 | |||||||
| chr14:90033006 | A | T | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1645-100A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033006 | |||||||
| chr14:90033045 | G | GT | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1645-50dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr14 | 90033045 | ||||||
| chr14:90033045 | G | T | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1645-61G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033045 | |||||||
| chr14:90033049 | T | C | 1 | a0002c0003t0012g0189 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1645-57T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033049 | |||||||
| chr14:90033081 | A | T | 2 | a0001c0002t0004g0203 a0001c0002t0004g0204 |
2 | HG01433.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1645-25A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 15/16 | chr14 | 90033081 | |||||||
| chr14:90033451 | T | C | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+237T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033451 | |||||||
| chr14:90033507 | G | A | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1753+293G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033507 | |||||||
| chr14:90033712 | AT | A | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753+500delT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90033712 | ||||||
| chr14:90033739 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1753+525C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033739 | |||||||
| chr14:90033768 | G | A | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1753+554G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033768 | |||||||
| chr14:90033826 | G | A | 7 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(4): Show |
7 | HG01891.hp1 HG02965.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1753+612G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033826 | |||||||
| chr14:90033946 | A | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0118 |
3 | HG00741.hp2 HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1753+732A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033946 | |||||||
| chr14:90033990 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1753+776C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033990 | |||||||
| chr14:90033996 | G | A | 1 | a0001c0005t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1753+782G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90033996 | |||||||
| chr14:90034013 | G | A | 25 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(22): Show |
26 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1753+799G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034013 | |||||||
| chr14:90034208 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+994C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034208 | |||||||
| chr14:90034209 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+995T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034209 | |||||||
| chr14:90034226 | G | A | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1753+1012G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034226 | |||||||
| chr14:90034307 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1753+1093C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034307 | |||||||
| chr14:90034386 | G | T | 1 | a0001c0005t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1753+1172G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034386 | |||||||
| chr14:90034504 | T | G | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1753+1290T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034504 | |||||||
| chr14:90034813 | C | G | 3 | a0001c0002t0008g0197 a0001c0002t0008g0201 a0001c0002t0008g0202 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1753+1599C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034813 | |||||||
| chr14:90034835 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+1621T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034835 | |||||||
| chr14:90034891 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1753+1677C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034891 | |||||||
| chr14:90034931 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1753+1717T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90034931 | |||||||
| chr14:90035039 | CTTCTCAG others(39): Show |
C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0045 |
3 | NA18973.hp1 NA18983.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1753+1864_1753+190 others(50): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035039 | ||||||
| chr14:90035077 | C | G | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1753+1863C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035077 | |||||||
| chr14:90035156 | C | T | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1753+1942C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035156 | |||||||
| chr14:90035215 | C | T | 1 | a0001c0005t0016g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1753+2001C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035215 | |||||||
| chr14:90035332 | AAATCCCC others(10): Show |
A | 1 | a0001c0001t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+2119_1753+213 others(21): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035332 | |||||||
| chr14:90035333 | A | G | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1753+2119A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035333 | |||||||
| chr14:90035461 | C | CA | 19 | a0001c0001t0001g0091 a0001c0001t0001g0159 a0001c0001t0001g0166 others(16): Show |
20 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1753+2260dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035461 | ||||||
| chr14:90035590 | A | G | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1753+2376A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035590 | |||||||
| chr14:90035692 | G | A | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+2478G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035692 | |||||||
| chr14:90035733 | C | CTTTTT | 22 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(19): Show |
23 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1753+2530_1753+253 others(9): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035733 | ||||||
| chr14:90035733 | C | CTTTTTTT | 5 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(2): Show |
7 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1753+2528_1753+253 others(11): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035733 | ||||||
| chr14:90035733 | C | CTTTTTTT others(1): Show |
30 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(27): Show |
34 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1753+2527_1753+253 others(12): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90035733 | ||||||
| chr14:90035983 | C | T | 19 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(16): Show |
22 | HG01070.hp2 HG02451.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1753+2769C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90035983 | |||||||
| chr14:90036173 | A | T | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1753+2959A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036173 | |||||||
| chr14:90036186 | AC | A | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+2973delC | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036186 | |||||||
| chr14:90036637 | T | C | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+3423T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036637 | |||||||
| chr14:90036816 | T | TA | 78 | a0001c0001t0001g0018 a0001c0001t0001g0098 a0001c0002t0001g0031 others(75): Show |
87 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1753+3615dupA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90036816 | ||||||
| chr14:90036816 | T | TAA | 11 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(8): Show |
14 | HG01192.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1753+3614_1753+361 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90036816 | ||||||
| chr14:90036972 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1753+3758C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90036972 | |||||||
| chr14:90037008 | C | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+3794C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037008 | |||||||
| chr14:90037038 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+3824C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037038 | |||||||
| chr14:90037040 | G | A | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+3826G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037040 | |||||||
| chr14:90037047 | A | G | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1753+3833A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037047 | |||||||
| chr14:90037065 | G | A | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1753+3851G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037065 | |||||||
| chr14:90037198 | G | A | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1753+3984G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037198 | |||||||
| chr14:90037316 | G | C | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1753+4102G>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037316 | |||||||
| chr14:90037377 | ATAAAT | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0191 |
3 | HG01081.hp2 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1753+4165_1753+416 others(9): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90037377 | ||||||
| chr14:90037475 | A | T | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+4261A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037475 | |||||||
| chr14:90037501 | A | G | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1753+4287A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037501 | |||||||
| chr14:90037529 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1753+4315G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037529 | |||||||
| chr14:90037560 | A | G | 4 | a0001c0005t0001g0010 a0001c0005t0001g0011 a0001c0005t0001g0030 others(1): Show |
5 | HG02258.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1753+4346A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037560 | |||||||
| chr14:90037581 | G | A | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4367G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037581 | |||||||
| chr14:90037582 | C | T | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4368C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037582 | |||||||
| chr14:90037585 | A | G | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4371A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037585 | |||||||
| chr14:90037650 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1753+4436T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037650 | |||||||
| chr14:90037741 | G | A | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4527G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90037741 | |||||||
| chr14:90038012 | G | A | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1753+4798G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038012 | |||||||
| chr14:90038156 | G | A | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1754-4914G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038156 | |||||||
| chr14:90038186 | T | A | 39 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(36): Show |
41 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1754-4884T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038186 | |||||||
| chr14:90038194 | A | T | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1754-4876A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038194 | |||||||
| chr14:90038217 | A | C | 2 | a0001c0002t0013g0198 a0001c0002t0013g0199 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1754-4853A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038217 | |||||||
| chr14:90038339 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1754-4731C>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038339 | |||||||
| chr14:90038363 | A | C | 1 | a0001c0001t0011g0145 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1754-4707A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038363 | |||||||
| chr14:90038402 | T | A | 79 | a0001c0002t0001g0031 a0001c0002t0003g0023 a0001c0002t0003g0193 others(76): Show |
87 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1754-4668T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038402 | |||||||
| chr14:90038609 | G | A | 4 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(1): Show |
4 | HG01891.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-4461G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038609 | |||||||
| chr14:90038745 | G | A | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1754-4325G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038745 | |||||||
| chr14:90038746 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1754-4324G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038746 | |||||||
| chr14:90038812 | C | T | 45 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(42): Show |
49 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1754-4258C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038812 | |||||||
| chr14:90038904 | G | GT | 22 | a0002c0003t0003g0005 a0002c0003t0003g0020 a0002c0003t0003g0024 others(19): Show |
25 | HG01070.hp2 HG02145.hp2 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.1754-4154dupT | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90038904 | ||||||
| chr14:90038904 | G | GTT | 42 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(39): Show |
46 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1754-4155_1754-415 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90038904 | ||||||
| chr14:90038972 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1754-4098A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90038972 | |||||||
| chr14:90039016 | T | G | 1 | a0001c0001t0002g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1754-4054T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039016 | |||||||
| chr14:90039135 | A | G | 23 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(20): Show |
24 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.1754-3935A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039135 | |||||||
| chr14:90039206 | A | C | 19 | a0001c0002t0004g0021 a0001c0002t0004g0203 a0001c0002t0004g0204 others(16): Show |
20 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1754-3864A>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039206 | |||||||
| chr14:90039316 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1754-3754T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039316 | |||||||
| chr14:90039352 | G | A | 2 | a0001c0002t0008g0201 a0001c0002t0008g0202 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1754-3718G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039352 | |||||||
| chr14:90039495 | C | T | 4 | a0001c0002t0001g0194 a0001c0002t0001g0195 a0001c0002t0001g0196 others(1): Show |
4 | HG01891.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-3575C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039495 | |||||||
| chr14:90039512 | A | G | 15 | a0001c0001t0001g0104 a0001c0001t0001g0113 a0001c0001t0001g0114 others(12): Show |
15 | HG00323.hp1 HG00735.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1754-3558A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039512 | |||||||
| chr14:90039549 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0003g0023 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1754-3521G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039549 | |||||||
| chr14:90039586 | C | T | 1 | a0002c0004t0005g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1754-3484C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039586 | |||||||
| chr14:90039673 | T | TTA | 3 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 |
5 | HG01884.hp1 HG02976.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1754-3397_1754-339 others(6): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039673 | |||||||
| chr14:90039673 | T | TTAA | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1754-3397_1754-339 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039673 | |||||||
| chr14:90039673 | TA | T | 24 | a0001c0001t0001g0157 a0001c0001t0002g0033 a0001c0002t0004g0021 others(21): Show |
25 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1754-3383delA | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90039673 | ||||||
| chr14:90039673 | TAAA | T | 11 | a0002c0003t0003g0005 a0002c0003t0003g0024 a0002c0003t0003g0130 others(8): Show |
13 | HG02451.hp2 HG02602.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1754-3385_1754-338 others(7): Show |
TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr14 | 90039673 | ||||||
| chr14:90039706 | A | G | 1 | a0002c0003t0003g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1754-3364A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039706 | |||||||
| chr14:90039933 | A | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0086 a0001c0001t0001g0090 others(6): Show |
10 | HG00639.hp2 HG01109.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1754-3137A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039933 | |||||||
| chr14:90039978 | G | A | 1 | a0001c0002t0008g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1754-3092G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90039978 | |||||||
| chr14:90040744 | A | G | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1754-2326A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90040744 | |||||||
| chr14:90040919 | A | G | 1 | a0002c0003t0003g0187 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1754-2151A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90040919 | |||||||
| chr14:90040948 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG01109.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1754-2122A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90040948 | |||||||
| chr14:90041166 | C | T | 14 | a0002c0004t0005g0016 a0002c0004t0005g0067 a0002c0004t0005g0068 others(11): Show |
15 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1754-1904C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041166 | |||||||
| chr14:90041246 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1754-1824A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041246 | |||||||
| chr14:90041255 | A | G | 3 | a0003c0006t0007g0082 a0003c0006t0007g0083 a0003c0006t0007g0084 |
3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1754-1815A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041255 | |||||||
| chr14:90041515 | C | T | 1 | a0002c0003t0003g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1754-1555C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041515 | |||||||
| chr14:90041612 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1754-1458G>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041612 | |||||||
| chr14:90041661 | G | A | 12 | a0001c0002t0001g0031 a0001c0002t0003g0023 a0001c0005t0001g0002 others(9): Show |
15 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1754-1409G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041661 | |||||||
| chr14:90041731 | T | C | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-1339T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041731 | |||||||
| chr14:90041757 | T | C | 41 | a0001c0001t0001g0120 a0001c0001t0001g0161 a0001c0001t0001g0162 others(38): Show |
52 | HG00408.hp1 HG00738.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1754-1313T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041757 | |||||||
| chr14:90041776 | T | C | 1 | a0001c0002t0004g0214 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1754-1294T>C | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041776 | |||||||
| chr14:90041899 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1754-1171C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041899 | |||||||
| chr14:90041942 | A | G | 6 | a0003c0006t0007g0004 a0003c0006t0007g0080 a0003c0006t0007g0081 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1754-1128A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041942 | |||||||
| chr14:90041980 | A | T | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-1090A>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90041980 | |||||||
| chr14:90042103 | G | A | 1 | a0001c0002t0004g0205 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1754-967G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042103 | |||||||
| chr14:90042410 | T | A | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-660T>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042410 | |||||||
| chr14:90042422 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1754-648T>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042422 | |||||||
| chr14:90042466 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1754-604A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042466 | |||||||
| chr14:90042624 | G | A | 8 | a0001c0002t0006g0022 a0001c0002t0006g0222 a0001c0002t0006g0223 others(5): Show |
9 | HG01192.hp1 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-446G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042624 | |||||||
| chr14:90042734 | G | A | 3 | a0001c0002t0008g0197 a0001c0002t0008g0201 a0001c0002t0008g0202 |
3 | HG02965.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1754-336G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042734 | |||||||
| chr14:90042886 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1754-184G>A | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042886 | |||||||
| chr14:90042921 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1754-149C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042921 | |||||||
| chr14:90042966 | C | T | 1 | a0001c0001t0002g0013 | 2 | NA18944.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1754-104C>T | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042966 | |||||||
| chr14:90042988 | A | G | 2 | a0001c0002t0004g0206 a0001c0002t0004g0209 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1754-82A>G | TDP1 | ENSG00000042088.14 | transcript | ENST00000335725.9 | protein_coding | 16/16 | chr14 | 90042988 |