Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5965 |
| ensemblid | ENSG00000004700.16 |
| hgncid | 9948 |
| symbol | RECQL |
| name | RecQ like helicase |
| refseq_nuc | NM_002907.4 |
| refseq_prot | NP_002898.2 |
| ensembl_nuc | ENST00000444129.7 |
| ensembl_prot | ENSP00000416739.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 21468910 |
| end | 21501635 |
| strand | - |
| ver | v1.2 |
| region | chr12:21468910-21501635 |
| region5000 | chr12:21463910-21506635 |
| regionname0 | RECQL_chr12_21468910_21501635 |
| regionname5000 | RECQL_chr12_21463910_21506635 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 649 | 379 | 83 | 58 | 187 | 14 | 37 | 149 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| a0002 | 0/0 | 649 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| a0003 | 0/0 | 649 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| a0004 | 0/0 | 649 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| a0005 | 0/0 | 649 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| a0006 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| a0007 | 0/0 | 649 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| a0008 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | MASVS others(644): Show |
chr12 | 21463910 | 21506635 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1947 | 284 | 64 | 52 | 126 | 13 | 29 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0001c0002 | 0/0 | 1947 | 91 | 15 | 6 | 61 | 1 | 8 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0001c0005 | 0/0 | 1947 | 3 | 3 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0001c0009 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0002c0004 | 0/0 | 1947 | 7 | 7 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0002c0006 | 0/0 | 1947 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0003c0003 | 0/0 | 1947 | 8 | 7 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0004c0007 | 0/0 | 1947 | 2 | 0 | 0 | 0 | 2 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0005c0010 | 0/0 | 1947 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0006c0008 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0007c0012 | 0/0 | 1947 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 | ||
| a0008c0011 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | ATGGC others(1942): Show |
chr12 | 21463910 | 21506635 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3745 | 89 | 1 | 15 | 57 | 5 | 11 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0002 | 0/0 | 3745 | 71 | 6 | 14 | 39 | 4 | 8 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0004 | 0/0 | 3745 | 24 | 0 | 3 | 19 | 0 | 2 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0005 | 0/0 | 3745 | 23 | 14 | 7 | 0 | 1 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0006 | 0/0 | 3745 | 14 | 13 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0007 | 0/0 | 3745 | 11 | 6 | 2 | 0 | 1 | 2 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0009 | 0/0 | 3745 | 8 | 7 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0010 | 0/0 | 3742 | 7 | 0 | 1 | 6 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3737): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0013 | 0/0 | 3744 | 3 | 0 | 1 | 0 | 1 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0014 | 0/0 | 3745 | 4 | 4 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0016 | 0/0 | 3745 | 3 | 2 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0017 | 0/0 | 3744 | 3 | 0 | 0 | 2 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0021 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0023 | 0/0 | 3745 | 2 | 1 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0026 | 0/0 | 3745 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0028 | 0/0 | 3744 | 2 | 0 | 2 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0030 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0032 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0033 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0035 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0036 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0039 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0041 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0042 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0043 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0044 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0045 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0046 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0047 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3431): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0050 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0051 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0001t0052 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0003 | 0/0 | 3745 | 61 | 0 | 5 | 51 | 1 | 4 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0008 | 0/0 | 3744 | 9 | 9 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0011 | 0/0 | 3744 | 5 | 1 | 0 | 3 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0015 | 0/0 | 3744 | 3 | 0 | 0 | 1 | 0 | 2 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0020 | 0/0 | 3744 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0024 | 0/0 | 3744 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0025 | 0/0 | 3744 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0027 | 0/0 | 3744 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0029 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3755): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0034 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0037 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0048 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0002t0053 | 0/0 | 3729 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3724): Show |
chr12 | 21463910 | 21506635 |
| a0001c0005t0018 | 0/0 | 3745 | 3 | 3 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0001c0009t0049 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0002c0004t0012 | 0/0 | 3730 | 4 | 4 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3725): Show |
chr12 | 21463910 | 21506635 |
| a0002c0004t0019 | 0/0 | 3745 | 3 | 3 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0002c0006t0022 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0003c0003t0002 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0003c0003t0006 | 0/0 | 3745 | 3 | 2 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0003c0003t0007 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0003c0003t0031 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0003c0003t0038 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0003c0003t0040 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3739): Show |
chr12 | 21463910 | 21506635 |
| a0004c0007t0002 | 0/0 | 3745 | 2 | 0 | 0 | 0 | 2 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0005c0010t0002 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0006c0008t0012 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3725): Show |
chr12 | 21463910 | 21506635 |
| a0007c0012t0001 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| a0008c0011t0002 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | GTGGA others(3740): Show |
chr12 | 21463910 | 21506635 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 35 | 1 | 4 | 28 | 2 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0002 | 0/0 | 19 | 1 | 4 | 8 | 3 | 3 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0009g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0009g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0009g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0010g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0010g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0010g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0013g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0014g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0014g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0016g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0016g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0016g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0017g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0017g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0017g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0021g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0023g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0026g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0026g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0028g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0028g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0030g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0032g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0033g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0035g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0036g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0039g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0041g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0042g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0043g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0044g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0045g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0046g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0047g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0050g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0051g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0001t0052g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0003 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0004 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0007 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0011g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0011g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0015g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0015g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0015g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0020g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0020g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0024g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0024g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0025g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0025g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0027g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0027g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0029g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0034g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0037g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0048g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0002t0053g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0005t0018g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0005t0018g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0005t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0001c0009t0049g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0004t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0004t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0004t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0004t0012g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0004t0019g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0004t0019g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0004t0019g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0002c0006t0022g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0003c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0003c0003t0006g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0003c0003t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0003c0003t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0003c0003t0031g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0003c0003t0038g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0003c0003t0040g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0004c0007t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0004c0007t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0005c0010t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0006c0008t0012g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0007c0012t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| a0008c0011t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0046 | EUR | GBR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0013 | EUR | FIN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00323 | hp1 | a0001 | c0001 | t0044 | g0196 | EUR | FIN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00408 | hp2 | a0001 | c0002 | t0027 | g0098 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0187 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00639 | hp2 | a0001 | c0001 | t0050 | g0216 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00733 | hp2 | a0001 | c0001 | t0051 | g0254 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00735 | hp2 | a0001 | c0001 | t0028 | g0202 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0208 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01069 | hp1 | a0001 | c0001 | t0043 | g0104 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0226 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0013 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01099 | hp2 | a0001 | c0002 | t0048 | g0214 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0013 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0219 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01243 | hp1 | a0003 | c0003 | t0006 | g0047 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01243 | hp2 | a0001 | c0001 | t0023 | g0021 | AMR | PUR | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01346 | hp2 | a0001 | c0001 | t0028 | g0227 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01361 | hp1 | a0001 | c0001 | t0013 | g0012 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01361 | hp2 | a0005 | c0010 | t0002 | g0178 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0237 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01496 | hp2 | a0001 | c0001 | t0041 | g0127 | AMR | CLM | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0012 | EUR | IBS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01516 | hp2 | a0004 | c0007 | t0002 | g0082 | EUR | IBS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01517 | hp2 | a0004 | c0007 | t0002 | g0081 | EUR | IBS | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0247 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01884 | hp2 | a0001 | c0002 | t0008 | g0236 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01891 | hp2 | a0001 | c0005 | t0018 | g0242 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01952 | hp2 | a0001 | c0001 | t0010 | g0033 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0207 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02055 | hp2 | a0001 | c0002 | t0008 | g0211 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0107 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02145 | hp1 | a0002 | c0004 | t0012 | g0261 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CDX | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | CDX | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02165 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | CDX | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0180 | EAS | CDX | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02258 | hp1 | a0001 | c0005 | t0018 | g0241 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02258 | hp2 | a0002 | c0004 | t0019 | g0263 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | PEL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02451 | hp1 | a0001 | c0001 | t0042 | g0173 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02451 | hp2 | a0001 | c0001 | t0035 | g0167 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02523 | hp1 | a0001 | c0002 | t0029 | g0053 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02622 | hp1 | a0001 | c0001 | t0023 | g0021 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02630 | hp1 | a0001 | c0002 | t0011 | g0069 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02630 | hp2 | a0002 | c0004 | t0012 | g0258 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02647 | hp1 | a0001 | c0001 | t0047 | g0243 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02647 | hp2 | a0003 | c0003 | t0007 | g0064 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02717 | hp1 | a0001 | c0001 | t0030 | g0066 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0203 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02723 | hp1 | a0003 | c0003 | t0031 | g0063 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02809 | hp2 | a0001 | c0001 | t0032 | g0061 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02818 | hp1 | a0001 | c0001 | t0052 | g0255 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0244 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02886 | hp2 | a0001 | c0001 | t0046 | g0222 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0224 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02895 | hp2 | a0002 | c0006 | t0022 | g0022 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02896 | hp1 | a0001 | c0002 | t0020 | g0057 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02896 | hp2 | a0001 | c0002 | t0008 | g0232 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02897 | hp1 | a0002 | c0006 | t0022 | g0022 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02897 | hp2 | a0001 | c0002 | t0020 | g0056 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02965 | hp2 | a0001 | c0002 | t0024 | g0060 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02970 | hp1 | a0001 | c0001 | t0014 | g0251 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02970 | hp2 | a0003 | c0003 | t0040 | g0120 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02976 | hp1 | a0006 | c0008 | t0012 | g0259 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02976 | hp2 | a0001 | c0001 | t0014 | g0051 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03017 | hp1 | a0007 | c0012 | t0001 | g0149 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03041 | hp2 | a0001 | c0002 | t0008 | g0245 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03098 | hp1 | a0001 | c0001 | t0039 | g0194 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0065 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03130 | hp2 | a0001 | c0002 | t0024 | g0059 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0051 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0118 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03209 | hp1 | a0001 | c0009 | t0049 | g0229 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03209 | hp2 | a0001 | c0005 | t0018 | g0240 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0253 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03225 | hp2 | a0001 | c0002 | t0008 | g0050 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03239 | hp2 | a0001 | c0001 | t0017 | g0148 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0233 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03486 | hp2 | a0001 | c0001 | t0021 | g0023 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03490 | hp1 | a0001 | c0001 | t0033 | g0072 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03490 | hp2 | a0001 | c0001 | t0045 | g0197 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03491 | hp1 | a0001 | c0002 | t0015 | g0099 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0193 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03516 | hp1 | a0002 | c0004 | t0012 | g0256 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0228 | AFR | ESN | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03540 | hp2 | a0001 | c0001 | t0016 | g0154 | AFR | GWD | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03579 | hp1 | a0002 | c0004 | t0012 | g0257 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03579 | hp2 | a0003 | c0003 | t0006 | g0249 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03669 | hp2 | a0001 | c0001 | t0016 | g0191 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0174 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0020 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03710 | hp1 | a0001 | c0001 | t0007 | g0020 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0172 | SAS | PJL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0213 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0052 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0003 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04184 | hp1 | a0001 | c0002 | t0011 | g0019 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04184 | hp2 | a0001 | c0002 | t0015 | g0177 | SAS | BEB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0171 | SAS | STU | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18522 | hp1 | a0001 | c0001 | t0021 | g0023 | AFR | YRI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18522 | hp2 | a0003 | c0003 | t0038 | g0119 | AFR | YRI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | CHB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | CHB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0248 | AFR | YRI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | YRI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18941 | hp1 | a0001 | c0001 | t0010 | g0151 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18962 | hp2 | a0001 | c0002 | t0011 | g0054 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18970 | hp1 | a0001 | c0002 | t0011 | g0055 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18972 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18972 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18977 | hp1 | a0001 | c0001 | t0026 | g0101 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18983 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18987 | hp2 | a0001 | c0001 | t0010 | g0153 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18989 | hp1 | a0001 | c0001 | t0010 | g0033 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18992 | hp2 | a0008 | c0011 | t0002 | g0103 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | LWK | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19030 | hp2 | a0003 | c0003 | t0006 | g0047 | AFR | LWK | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | LWK | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | LWK | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19055 | hp2 | a0001 | c0001 | t0026 | g0077 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19059 | hp1 | a0001 | c0002 | t0025 | g0097 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19066 | hp2 | a0001 | c0001 | t0017 | g0138 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19067 | hp2 | a0001 | c0002 | t0011 | g0019 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19072 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19075 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19076 | hp1 | a0001 | c0002 | t0037 | g0091 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19078 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19081 | hp1 | a0001 | c0002 | t0027 | g0109 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19082 | hp2 | a0001 | c0002 | t0015 | g0095 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19087 | hp2 | a0001 | c0001 | t0036 | g0078 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19088 | hp1 | a0001 | c0001 | t0010 | g0157 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19089 | hp1 | a0001 | c0002 | t0025 | g0094 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19089 | hp2 | a0001 | c0001 | t0017 | g0134 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19091 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | YRI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | YRI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ASW | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20129 | hp2 | a0001 | c0002 | t0008 | g0050 | AFR | ASW | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0007 | EUR | TSI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | TSI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | GIH | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20905 | hp2 | a0001 | c0002 | t0034 | g0183 | SAS | GIH | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0252 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02559 | hp1 | a0002 | c0004 | t0019 | g0262 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0210 | AFR | ACB | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03471 | hp1 | a0001 | c0002 | t0008 | g0198 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0209 | AFR | MSL | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG06807 | hp1 | a0002 | c0004 | t0019 | g0264 | AFR | USA | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | USA | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20300 | hp1 | a0001 | c0002 | t0053 | g0260 | AFR | USA | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | USA | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA21309 | hp1 | a0003 | c0003 | t0002 | g0195 | AFR | LWK | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | LWK | RECQL_chr12_21463910_21506635 | RECQL | chr12 | 21463910 | 21506635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21471630 | T | C | 1 | a0005 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1465A>G | p.Ile489Val | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/15 | 1976/3745 | 1465/1950 | 489/649 | chr12 | 21471630 | |||
| chr12:21471635 | T | G | 1 | a0003 | 8 | HG01243.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.1460A>C | p.Lys487Thr | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/15 | 1971/3745 | 1460/1950 | 487/649 | chr12 | 21471635 | |||
| chr12:21473562 | C | T | 1 | a0006 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1436G>A | p.Cys479Tyr | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/15 | 1947/3745 | 1436/1950 | 479/649 | chr12 | 21473562 | |||
| chr12:21473616 | T | C | 1 | a0008 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.1382A>G | p.His461Arg | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/15 | 1893/3745 | 1382/1950 | 461/649 | chr12 | 21473616 | |||
| chr12:21477837 | G | C | 1 | a0007 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.833C>G | p.Thr278Arg | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/15 | 1344/3745 | 833/1950 | 278/649 | chr12 | 21477837 | |||
| chr12:21490207 | C | T | 1 | a0004 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.386G>A | p.Cys129Tyr | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/15 | 897/3745 | 386/1950 | 129/649 | chr12 | 21490207 | |||
| chr12:21490289 | C | T | 2 | a0002 a0006 |
10 | HG02145.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
missense_variant | MODERATE | c.304G>A | p.Val102Ile | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/15 | 815/3745 | 304/1950 | 102/649 | chr12 | 21490289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21470245 | T | C | 3 | a0001c0002 a0001c0009 a0002c0006 |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
synonymous_variant | LOW | c.1899A>G | p.Gln633Gln | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 2410/3745 | 1899/1950 | 633/649 | chr12 | 21470245 | |||
| chr12:21471035 | A | G | 3 | a0001c0002 a0001c0009 a0002c0006 |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
synonymous_variant | LOW | c.1731T>C | p.Asn577Asn | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/15 | 2242/3745 | 1731/1950 | 577/649 | chr12 | 21471035 | |||
| chr12:21471565 | G | C | 1 | a0001c0009 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1530C>G | p.Leu510Leu | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/15 | 2041/3745 | 1530/1950 | 510/649 | chr12 | 21471565 | |||
| chr12:21491655 | T | C | 1 | a0001c0005 | 3 | HG01891.hp2 HG02258.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.78A>G | p.Gln26Gln | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/15 | 589/3745 | 78/1950 | 26/649 | chr12 | 21491655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21468957 | T | C | 8 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0033 others(5): Show |
98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1237A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 1237 | chr12 | 21468957 | ||||||
| chr12:21469096 | A | C | 1 | a0001c0001t0035 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1098T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 1098 | chr12 | 21469096 | ||||||
| chr12:21469117 | A | C | 8 | a0001c0002t0003 a0001c0002t0025 a0001c0002t0027 others(5): Show |
71 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1077T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 1077 | chr12 | 21469117 | ||||||
| chr12:21469163 | T | C | 1 | a0001c0001t0043 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1031A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 1031 | chr12 | 21469163 | ||||||
| chr12:21469168 | A | G | 1 | a0001c0001t0042 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1026T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 1026 | chr12 | 21469168 | ||||||
| chr12:21469286 | C | T | 5 | a0001c0001t0009 a0001c0001t0032 a0001c0001t0039 others(2): Show |
14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*908G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 908 | chr12 | 21469286 | ||||||
| chr12:21469374 | AT | A | 5 | a0001c0001t0017 a0001c0001t0036 a0001c0002t0025 others(2): Show |
8 | HG02970.hp2 HG03239.hp2 NA18522.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*819delA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 819 | chr12 | 21469374 | ||||||
| chr12:21469409 | T | C | 1 | a0001c0001t0026 | 2 | NA18977.hp1 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*785A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 785 | chr12 | 21469409 | ||||||
| chr12:21469435 | A | C | 1 | a0001c0001t0050 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*759T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 759 | chr12 | 21469435 | ||||||
| chr12:21469440 | ATTC | A | 1 | a0001c0001t0010 | 7 | HG01952.hp2 NA18941.hp1 NA18987.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*751_*753delGAA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 751 | chr12 | 21469440 | ||||||
| chr12:21469443 | C | A | 1 | a0001c0001t0047 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 751 | chr12 | 21469443 | ||||||
| chr12:21469493 | A | G | 1 | a0001c0002t0034 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*701T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 701 | chr12 | 21469493 | ||||||
| chr12:21469514 | AC | A | 7 | a0001c0002t0008 a0001c0002t0011 a0001c0002t0015 others(4): Show |
23 | HG01884.hp2 HG02055.hp2 HG02630.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*679delG | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 679 | chr12 | 21469514 | ||||||
| chr12:21469557 | GGTTATGT others(302): Show |
G | 1 | a0001c0001t0047 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328_*636del | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 328 | chr12 | 21469557 | ||||||
| chr12:21469561 | A | C | 1 | a0003c0003t0031 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*633T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 633 | chr12 | 21469561 | ||||||
| chr12:21469621 | T | A | 1 | a0001c0002t0037 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 573 | chr12 | 21469621 | ||||||
| chr12:21469651 | T | A | 1 | a0001c0002t0037 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*543A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 543 | chr12 | 21469651 | ||||||
| chr12:21469686 | AT | A | 3 | a0001c0001t0013 a0001c0001t0028 a0001c0002t0027 |
8 | HG00408.hp2 HG00735.hp2 HG01346.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*507delA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 507 | chr12 | 21469686 | ||||||
| chr12:21469761 | A | G | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0021 others(1): Show |
50 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*433T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 433 | chr12 | 21469761 | ||||||
| chr12:21469812 | C | T | 1 | a0003c0003t0038 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 382 | chr12 | 21469812 | ||||||
| chr12:21469888 | T | C | 2 | a0001c0001t0013 a0001c0001t0028 |
6 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*306A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 306 | chr12 | 21469888 | ||||||
| chr12:21469917 | T | G | 1 | a0001c0009t0049 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 277 | chr12 | 21469917 | ||||||
| chr12:21469993 | T | C | 6 | a0001c0001t0009 a0001c0001t0032 a0001c0001t0039 others(3): Show |
13 | HG00741.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*201A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 201 | chr12 | 21469993 | ||||||
| chr12:21470050 | A | G | 1 | a0001c0001t0041 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 144 | chr12 | 21470050 | ||||||
| chr12:21470073 | A | C | 1 | a0001c0001t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 121 | chr12 | 21470073 | ||||||
| chr12:21470175 | A | C | 1 | a0001c0002t0020 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*19T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 19 | chr12 | 21470175 | ||||||
| chr12:21470188 | T | G | 14 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0014 others(11): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*6A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 6 | chr12 | 21470188 | ||||||
| chr12:21470193 | A | C | 1 | a0001c0001t0046 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 15/15 | 1 | chr12 | 21470193 | ||||||
| chr12:21499605 | C | A | 1 | a0001c0002t0024 | 2 | HG02965.hp2 HG03130.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-35G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/15 | chr12 | 21499605 | |||||||
| chr12:21501222 | G | A | 1 | a0001c0001t0044 | 1 | HG00323.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1652 | chr12 | 21501222 | ||||||
| chr12:21501370 | G | T | 1 | a0001c0001t0033 | 1 | HG03490.hp1 | 5_prime_UTR_variant | MODIFIER | c.-246C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1800 | chr12 | 21501370 | ||||||
| chr12:21501473 | G | A | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(28): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-349C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | chr12 | 21501473 | |||||||
| chr12:21501491 | T | C | 1 | a0001c0001t0052 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-367A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1921 | chr12 | 21501491 | ||||||
| chr12:21501497 | G | A | 1 | a0001c0001t0045 | 1 | HG03490.hp2 | 5_prime_UTR_variant | MODIFIER | c.-373C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1927 | chr12 | 21501497 | ||||||
| chr12:21501501 | G | GGTGTCCG others(8): Show |
1 | a0001c0002t0029 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-392_-378dupAGGACA others(9): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1932 | chr12 | 21501501 | ||||||
| chr12:21501530 | CGATCTCC others(8): Show |
C | 3 | a0001c0002t0053 a0002c0004t0012 a0006c0008t0012 |
6 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-421_-407delCGAGAG others(9): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1961 | chr12 | 21501530 | ||||||
| chr12:21501535 | T | G | 15 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(12): Show |
73 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
5_prime_UTR_variant | MODIFIER | c.-411A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1965 | chr12 | 21501535 | ||||||
| chr12:21501558 | C | T | 1 | a0001c0001t0013 | 4 | HG01361.hp1 HG01516.hp1 HG03927.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-434G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 1988 | chr12 | 21501558 | ||||||
| chr12:21501600 | G | C | 1 | a0002c0004t0019 | 3 | HG02258.hp2 HG02559.hp1 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-476C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/15 | 2030 | chr12 | 21501600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:21470350 | C | CA | 18 | a0001c0001t0002g0096 a0001c0001t0002g0102 a0001c0001t0005g0219 others(15): Show |
18 | HG01175.hp1 HG01261.hp2 HG02145.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.1798-5dupT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/14 | chr12 | 21470350 | |||||||
| chr12:21470350 | C | CAA | 7 | a0001c0001t0006g0206 a0001c0001t0006g0246 a0001c0001t0006g0247 others(4): Show |
10 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1798-6_1798-5dupTT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/14 | chr12 | 21470350 | |||||||
| chr12:21470350 | C | CAAA | 63 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(60): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
splice_region_variant&intron_variant | LOW | c.1798-7_1798-5dupTT others(1): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/14 | chr12 | 21470350 | |||||||
| chr12:21470350 | CA | C | 54 | a0001c0002t0003g0003 a0001c0002t0003g0004 a0001c0002t0003g0005 others(51): Show |
90 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(87): Show |
splice_region_variant&intron_variant | LOW | c.1798-5delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/14 | chr12 | 21470350 | |||||||
| chr12:21470577 | A | G | 17 | a0001c0001t0009g0018 a0001c0001t0009g0207 a0001c0001t0009g0208 others(14): Show |
21 | HG00735.hp2 HG00741.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.1798-231T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/14 | chr12 | 21470577 | |||||||
| chr12:21470581 | CACTTG | C | 8 | a0001c0001t0009g0018 a0001c0001t0009g0207 a0001c0001t0009g0208 others(5): Show |
10 | HG00741.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1798-240_1798-236d others(7): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/14 | chr12 | 21470581 | |||||||
| chr12:21470951 | AAATT | A | 4 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(1): Show |
6 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1797+14_1797+17del others(4): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 14/14 | chr12 | 21470951 | |||||||
| chr12:21471165 | G | T | 1 | a0001c0001t0046g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1668-67C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/14 | chr12 | 21471165 | |||||||
| chr12:21471179 | C | T | 7 | a0003c0003t0002g0195 a0003c0003t0006g0047 a0003c0003t0006g0249 others(4): Show |
8 | HG01243.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668-81G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/14 | chr12 | 21471179 | |||||||
| chr12:21471258 | G | A | 1 | a0001c0001t0005g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1668-160C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/14 | chr12 | 21471258 | |||||||
| chr12:21471298 | T | C | 2 | a0001c0002t0011g0069 a0001c0002t0053g0260 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1667+130A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/14 | chr12 | 21471298 | |||||||
| chr12:21471374 | TA | T | 91 | a0001c0001t0001g0136 a0001c0001t0002g0002 a0001c0001t0002g0008 others(88): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1667+53delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/14 | chr12 | 21471374 | |||||||
| chr12:21471375 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(63): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1667+53T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 13/14 | chr12 | 21471375 | |||||||
| chr12:21471739 | G | A | 1 | a0001c0001t0006g0247 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1448-92C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21471739 | |||||||
| chr12:21471760 | TA | T | 58 | a0001c0002t0003g0003 a0001c0002t0003g0004 a0001c0002t0003g0005 others(55): Show |
94 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1448-114delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21471760 | |||||||
| chr12:21471798 | GGCTATT | G | 28 | a0001c0001t0004g0017 a0001c0001t0004g0030 a0001c0001t0004g0043 others(25): Show |
36 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1448-157_1448-152d others(8): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21471798 | |||||||
| chr12:21471874 | A | G | 1 | a0001c0001t0009g0253 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1448-227T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21471874 | |||||||
| chr12:21471875 | A | T | 1 | a0001c0001t0006g0250 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1448-228T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21471875 | |||||||
| chr12:21472075 | T | G | 3 | a0001c0001t0004g0011 a0001c0001t0004g0040 a0001c0001t0004g0170 |
7 | NA18965.hp1 NA18970.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.1448-428A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472075 | |||||||
| chr12:21472089 | CTT | C | 1 | a0001c0001t0004g0017 | 3 | NA18951.hp2 NA18964.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1448-444_1448-443d others(4): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472089 | |||||||
| chr12:21472130 | T | G | 3 | a0001c0001t0007g0013 a0001c0001t0007g0020 a0001c0001t0007g0058 |
6 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1448-483A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472130 | |||||||
| chr12:21472180 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1448-533T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472180 | |||||||
| chr12:21472197 | C | CT | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(4): Show |
10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1448-551_1448-550i others(3): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472197 | |||||||
| chr12:21472200 | T | TGGTAA | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(4): Show |
10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1448-554_1448-553i others(7): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472200 | |||||||
| chr12:21472207 | C | G | 5 | a0001c0001t0004g0011 a0001c0001t0004g0040 a0001c0001t0004g0128 others(2): Show |
9 | HG02300.hp2 HG04228.hp2 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1448-560G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472207 | |||||||
| chr12:21472348 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0017g0134 a0001c0001t0017g0138 |
3 | NA19066.hp2 NA19081.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1448-701C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472348 | |||||||
| chr12:21472473 | A | T | 1 | a0001c0001t0002g0008 | 5 | HG02132.hp2 NA18980.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1448-826T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472473 | |||||||
| chr12:21472552 | TA | T | 12 | a0001c0001t0009g0018 a0001c0001t0009g0207 a0001c0001t0009g0208 others(9): Show |
14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1448-906delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472552 | |||||||
| chr12:21472554 | G | C | 12 | a0001c0001t0009g0018 a0001c0001t0009g0207 a0001c0001t0009g0208 others(9): Show |
14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1448-907C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472554 | |||||||
| chr12:21472555 | A | T | 12 | a0001c0001t0009g0018 a0001c0001t0009g0207 a0001c0001t0009g0208 others(9): Show |
14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1448-908T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472555 | |||||||
| chr12:21472563 | A | G | 40 | a0001c0001t0014g0228 a0001c0001t0023g0021 a0001c0001t0042g0173 others(37): Show |
75 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1448-916T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472563 | |||||||
| chr12:21472617 | T | A | 1 | a0001c0001t0002g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1447+934A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472617 | |||||||
| chr12:21472633 | T | C | 4 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(1): Show |
6 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447+918A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472633 | |||||||
| chr12:21472692 | G | T | 1 | a0001c0001t0002g0166 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1447+859C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472692 | |||||||
| chr12:21472700 | C | T | 1 | a0003c0003t0002g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1447+851G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472700 | |||||||
| chr12:21472711 | C | T | 1 | a0001c0001t0032g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1447+840G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472711 | |||||||
| chr12:21472754 | C | T | 9 | a0001c0001t0009g0018 a0001c0001t0009g0207 a0001c0001t0009g0208 others(6): Show |
11 | HG00741.hp2 HG02055.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1447+797G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21472754 | |||||||
| chr12:21473218 | A | T | 95 | a0001c0001t0001g0100 a0001c0001t0002g0002 a0001c0001t0002g0008 others(92): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.1447+333T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21473218 | |||||||
| chr12:21473234 | C | T | 57 | a0001c0001t0005g0234 a0001c0001t0006g0204 a0001c0002t0003g0003 others(54): Show |
93 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1447+317G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21473234 | |||||||
| chr12:21473353 | G | A | 38 | a0001c0001t0004g0011 a0001c0001t0004g0017 a0001c0001t0004g0030 others(35): Show |
52 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1447+198C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21473353 | |||||||
| chr12:21473355 | T | C | 1 | a0002c0006t0022g0022 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1447+196A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21473355 | |||||||
| chr12:21473390 | A | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(256): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1447+161T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21473390 | |||||||
| chr12:21473396 | C | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(260): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1447+155G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 12/14 | chr12 | 21473396 | |||||||
| chr12:21473880 | C | A | 1 | a0001c0001t0002g0092 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1356-238G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21473880 | |||||||
| chr12:21473969 | T | C | 1 | a0003c0003t0006g0047 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1356-327A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21473969 | |||||||
| chr12:21474010 | T | C | 169 | a0001c0001t0001g0100 a0001c0001t0001g0160 a0001c0001t0002g0002 others(166): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1356-368A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474010 | |||||||
| chr12:21474120 | ATTC | A | 9 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0201 others(6): Show |
11 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1356-481_1356-479d others(5): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474120 | |||||||
| chr12:21474227 | C | T | 1 | a0001c0001t0005g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1356-585G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474227 | |||||||
| chr12:21474248 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1355+593A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474248 | |||||||
| chr12:21474259 | A | T | 136 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1355+582T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474259 | |||||||
| chr12:21474331 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1355+510G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474331 | |||||||
| chr12:21474353 | A | G | 172 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(169): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1355+488T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474353 | |||||||
| chr12:21474591 | C | T | 4 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(1): Show |
6 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1355+250G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474591 | |||||||
| chr12:21474623 | A | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(56): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1355+218T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474623 | |||||||
| chr12:21474647 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1355+194T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474647 | |||||||
| chr12:21474658 | A | G | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1355+183T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474658 | |||||||
| chr12:21474738 | C | G | 136 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1355+103G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474738 | |||||||
| chr12:21474778 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1355+63G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474778 | |||||||
| chr12:21474811 | A | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(58): Show |
110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1355+30T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 11/14 | chr12 | 21474811 | |||||||
| chr12:21475044 | CAT | C | 3 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0007g0070 |
3 | HG01884.hp1 HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1217-67_1217-66del others(2): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 10/14 | chr12 | 21475044 | |||||||
| chr12:21475221 | C | G | 1 | a0003c0003t0006g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1217-242G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 10/14 | chr12 | 21475221 | |||||||
| chr12:21475321 | A | G | 1 | a0001c0001t0005g0226 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1216+147T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 10/14 | chr12 | 21475321 | |||||||
| chr12:21475386 | C | T | 154 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(151): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1216+82G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 10/14 | chr12 | 21475386 | |||||||
| chr12:21475402 | G | A | 154 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(151): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1216+66C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 10/14 | chr12 | 21475402 | |||||||
| chr12:21475857 | T | C | 154 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(151): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.950-33A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21475857 | |||||||
| chr12:21475878 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(256): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.950-54C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21475878 | |||||||
| chr12:21475904 | T | C | 1 | a0001c0001t0030g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.950-80A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21475904 | |||||||
| chr12:21475963 | CAT | C | 1 | a0001c0002t0003g0006 | 5 | HG00558.hp2 HG00597.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-141_950-140del others(2): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21475963 | |||||||
| chr12:21476026 | G | C | 1 | a0001c0002t0003g0029 | 2 | NA18986.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.950-202C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476026 | |||||||
| chr12:21476125 | C | T | 1 | a0001c0001t0010g0153 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.950-301G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476125 | |||||||
| chr12:21476151 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0145 |
2 | NA19007.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.950-327G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476151 | |||||||
| chr12:21476178 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.950-354A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476178 | |||||||
| chr12:21476273 | G | A | 3 | a0001c0001t0005g0223 a0001c0001t0005g0225 a0001c0001t0046g0222 |
3 | HG02109.hp2 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.950-449C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476273 | |||||||
| chr12:21476298 | G | A | 12 | a0001c0001t0006g0206 a0001c0001t0009g0018 a0001c0001t0009g0207 others(9): Show |
14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.950-474C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476298 | |||||||
| chr12:21476379 | T | C | 73 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(70): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.949+532A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476379 | |||||||
| chr12:21476721 | T | C | 66 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(63): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.949+190A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476721 | |||||||
| chr12:21476742 | C | A | 16 | a0001c0001t0006g0206 a0001c0001t0009g0018 a0001c0001t0009g0207 others(13): Show |
20 | HG00735.hp2 HG00741.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.949+169G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476742 | |||||||
| chr12:21476785 | A | C | 1 | a0003c0003t0002g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.949+126T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476785 | |||||||
| chr12:21476796 | G | A | 1 | a0001c0001t0044g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.949+115C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476796 | |||||||
| chr12:21476798 | T | C | 17 | a0001c0001t0005g0234 a0001c0002t0008g0050 a0001c0002t0008g0232 others(14): Show |
19 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(16): Show |
intron_variant | MODIFIER | c.949+113A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476798 | |||||||
| chr12:21476835 | T | C | 3 | a0001c0001t0007g0013 a0001c0001t0007g0020 a0001c0001t0007g0058 |
6 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.949+76A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 8/14 | chr12 | 21476835 | |||||||
| chr12:21477053 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(253): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.868-61A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477053 | |||||||
| chr12:21477059 | A | AC | 154 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(151): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.868-68dupG | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477059 | |||||||
| chr12:21477081 | A | G | 17 | a0001c0001t0005g0234 a0001c0002t0008g0050 a0001c0002t0008g0232 others(14): Show |
19 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(16): Show |
intron_variant | MODIFIER | c.868-89T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477081 | |||||||
| chr12:21477092 | G | GT | 1 | a0001c0002t0003g0006 | 5 | HG00558.hp2 HG00597.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.868-101dupA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477092 | |||||||
| chr12:21477110 | C | T | 2 | a0003c0003t0038g0119 a0003c0003t0040g0120 |
2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.868-118G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477110 | |||||||
| chr12:21477212 | A | G | 154 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(151): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.868-220T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477212 | |||||||
| chr12:21477408 | T | C | 1 | a0001c0001t0007g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.867+395A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477408 | |||||||
| chr12:21477515 | T | C | 16 | a0001c0001t0006g0206 a0001c0001t0009g0018 a0001c0001t0009g0207 others(13): Show |
20 | HG00735.hp2 HG00741.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.867+288A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 7/14 | chr12 | 21477515 | |||||||
| chr12:21478051 | C | T | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.701-82G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21478051 | |||||||
| chr12:21478301 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.701-332C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21478301 | |||||||
| chr12:21478480 | G | A | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.701-511C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21478480 | |||||||
| chr12:21479000 | G | A | 114 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0160 others(111): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.701-1031C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479000 | |||||||
| chr12:21479350 | A | AT | 14 | a0001c0001t0002g0121 a0001c0001t0002g0162 a0001c0001t0004g0164 others(11): Show |
16 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.701-1382dupA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479350 | |||||||
| chr12:21479350 | A | ATT | 6 | a0001c0001t0006g0206 a0001c0001t0009g0208 a0001c0001t0013g0012 others(3): Show |
8 | HG00741.hp2 HG01346.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-1383_701-1382d others(4): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479350 | |||||||
| chr12:21479350 | AT | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(131): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.701-1382delA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479350 | |||||||
| chr12:21479350 | ATT | A | 10 | a0001c0001t0001g0152 a0001c0001t0002g0105 a0001c0001t0006g0230 others(7): Show |
10 | HG01257.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.701-1383_701-1382d others(4): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479350 | |||||||
| chr12:21479454 | G | A | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.701-1485C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479454 | |||||||
| chr12:21479505 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(258): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.701-1536C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479505 | |||||||
| chr12:21479511 | C | A | 5 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(2): Show |
7 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-1542G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479511 | |||||||
| chr12:21479512 | C | G | 1 | a0001c0001t0006g0246 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.701-1543G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479512 | |||||||
| chr12:21479541 | C | T | 6 | a0001c0001t0002g0121 a0001c0001t0013g0012 a0001c0001t0013g0052 others(3): Show |
8 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.701-1572G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479541 | |||||||
| chr12:21479605 | G | A | 5 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(2): Show |
7 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-1636C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479605 | |||||||
| chr12:21479632 | C | T | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.701-1663G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479632 | |||||||
| chr12:21479647 | C | T | 2 | a0001c0002t0008g0244 a0001c0002t0008g0245 |
2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.701-1678G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479647 | |||||||
| chr12:21479648 | G | A | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.701-1679C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479648 | |||||||
| chr12:21479703 | A | T | 6 | a0001c0001t0007g0062 a0001c0002t0003g0089 a0001c0002t0025g0094 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.701-1734T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479703 | |||||||
| chr12:21479781 | A | G | 3 | a0001c0001t0007g0062 a0002c0004t0019g0262 a0002c0004t0019g0264 |
3 | HG02559.hp1 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.701-1812T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479781 | |||||||
| chr12:21479805 | C | T | 14 | a0001c0001t0002g0121 a0001c0001t0006g0206 a0001c0001t0006g0209 others(11): Show |
16 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.701-1836G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479805 | |||||||
| chr12:21479823 | T | C | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.701-1854A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479823 | |||||||
| chr12:21479872 | T | A | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.701-1903A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21479872 | |||||||
| chr12:21480102 | C | T | 42 | a0001c0001t0001g0169 a0001c0001t0002g0162 a0001c0001t0002g0163 others(39): Show |
73 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.701-2133G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480102 | |||||||
| chr12:21480193 | T | C | 2 | a0001c0001t0007g0013 a0001c0001t0007g0020 |
5 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.701-2224A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480193 | |||||||
| chr12:21480201 | A | G | 1 | a0001c0002t0008g0233 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.701-2232T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480201 | |||||||
| chr12:21480256 | T | C | 1 | a0003c0003t0040g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.701-2287A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480256 | |||||||
| chr12:21480377 | G | T | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.701-2408C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480377 | |||||||
| chr12:21480413 | C | G | 3 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 |
3 | HG01884.hp1 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.701-2444G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480413 | |||||||
| chr12:21480452 | G | A | 1 | a0001c0001t0005g0048 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.701-2483C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480452 | |||||||
| chr12:21480752 | T | C | 1 | a0001c0001t0005g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.700+2624A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480752 | |||||||
| chr12:21480881 | T | C | 1 | a0001c0001t0006g0235 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.700+2495A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480881 | |||||||
| chr12:21480913 | C | G | 1 | a0001c0001t0002g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.700+2463G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21480913 | |||||||
| chr12:21481094 | T | G | 1 | a0001c0001t0002g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.700+2282A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481094 | |||||||
| chr12:21481128 | A | T | 1 | a0001c0001t0021g0023 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.700+2248T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481128 | |||||||
| chr12:21481133 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(252): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.700+2243A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481133 | |||||||
| chr12:21481164 | T | C | 1 | a0001c0001t0010g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.700+2212A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481164 | |||||||
| chr12:21481184 | G | A | 6 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+2192C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481184 | |||||||
| chr12:21481210 | A | G | 1 | a0003c0003t0038g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.700+2166T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481210 | |||||||
| chr12:21481224 | G | A | 16 | a0001c0001t0005g0234 a0001c0002t0008g0050 a0001c0002t0008g0232 others(13): Show |
18 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.700+2152C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481224 | |||||||
| chr12:21481391 | T | C | 2 | a0001c0002t0020g0056 a0001c0002t0020g0057 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.700+1985A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481391 | |||||||
| chr12:21481460 | A | C | 39 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(36): Show |
45 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.700+1916T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481460 | |||||||
| chr12:21481555 | C | G | 2 | a0003c0003t0006g0047 a0003c0003t0006g0249 |
3 | HG01243.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.700+1821G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481555 | |||||||
| chr12:21481563 | G | C | 40 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(37): Show |
46 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.700+1813C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481563 | |||||||
| chr12:21481569 | A | G | 1 | a0003c0003t0006g0047 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.700+1807T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481569 | |||||||
| chr12:21481589 | C | T | 6 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0088 others(3): Show |
9 | NA18943.hp1 NA18947.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.700+1787G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481589 | |||||||
| chr12:21481590 | G | A | 1 | a0001c0002t0003g0185 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.700+1786C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481590 | |||||||
| chr12:21481804 | A | T | 4 | a0001c0001t0002g0024 a0001c0001t0002g0074 a0001c0001t0026g0077 others(1): Show |
5 | NA18950.hp1 NA18991.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+1572T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481804 | |||||||
| chr12:21481856 | G | A | 16 | a0001c0001t0005g0234 a0001c0002t0008g0050 a0001c0002t0008g0232 others(13): Show |
18 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.700+1520C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481856 | |||||||
| chr12:21481957 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(66): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.700+1419T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21481957 | |||||||
| chr12:21482028 | G | GAAAAATG others(315): Show |
3 | a0001c0001t0013g0012 a0001c0001t0028g0202 a0001c0001t0028g0227 |
5 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+1347_700+1348i others(324): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482028 | |||||||
| chr12:21482028 | G | GAAAAATG others(316): Show |
1 | a0001c0001t0013g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.700+1347_700+1348i others(325): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482028 | |||||||
| chr12:21482267 | G | GA | 141 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(138): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.700+1108dupT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482267 | |||||||
| chr12:21482267 | G | GAA | 61 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(58): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.700+1107_700+1108d others(4): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482267 | |||||||
| chr12:21482298 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(74): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.700+1078C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482298 | |||||||
| chr12:21482367 | A | C | 2 | a0001c0001t0002g0121 a0003c0003t0040g0120 |
2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.700+1009T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482367 | |||||||
| chr12:21482403 | C | A | 1 | a0001c0001t0032g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.700+973G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482403 | |||||||
| chr12:21482446 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.700+930C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482446 | |||||||
| chr12:21482602 | G | T | 6 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.700+774C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482602 | |||||||
| chr12:21482655 | C | A | 1 | a0001c0001t0002g0016 | 3 | HG00423.hp2 HG02129.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.700+721G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482655 | |||||||
| chr12:21482671 | G | A | 40 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(37): Show |
47 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+705C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482671 | |||||||
| chr12:21482691 | G | A | 43 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(40): Show |
50 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.700+685C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482691 | |||||||
| chr12:21482736 | T | A | 1 | a0001c0001t0002g0106 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.700+640A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482736 | |||||||
| chr12:21482862 | G | C | 4 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(1): Show |
6 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.700+514C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482862 | |||||||
| chr12:21482955 | T | C | 1 | a0001c0002t0003g0186 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.700+421A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21482955 | |||||||
| chr12:21483073 | AT | A | 39 | a0001c0001t0001g0169 a0001c0001t0002g0162 a0001c0001t0002g0163 others(36): Show |
68 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.700+302delA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21483073 | |||||||
| chr12:21483085 | T | A | 3 | a0001c0005t0018g0240 a0001c0005t0018g0241 a0001c0005t0018g0242 |
3 | HG01891.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.700+291A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21483085 | |||||||
| chr12:21483197 | C | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0152 |
2 | NA19058.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.700+179G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 6/14 | chr12 | 21483197 | |||||||
| chr12:21483588 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.502-14T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21483588 | |||||||
| chr12:21483651 | C | T | 1 | a0003c0003t0038g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.502-77G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21483651 | |||||||
| chr12:21483677 | C | G | 3 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 |
3 | HG01884.hp1 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.502-103G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21483677 | |||||||
| chr12:21483736 | C | T | 3 | a0001c0005t0018g0240 a0001c0005t0018g0241 a0001c0005t0018g0242 |
3 | HG01891.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.502-162G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21483736 | |||||||
| chr12:21483949 | T | C | 1 | a0001c0001t0007g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.502-375A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21483949 | |||||||
| chr12:21484028 | T | C | 7 | a0001c0001t0005g0049 a0001c0001t0005g0223 a0001c0001t0005g0225 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.502-454A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484028 | |||||||
| chr12:21484202 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.502-628T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484202 | |||||||
| chr12:21484280 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.502-706G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484280 | |||||||
| chr12:21484291 | G | T | 60 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(57): Show |
102 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.502-717C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484291 | |||||||
| chr12:21484399 | C | A | 1 | a0001c0001t0007g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.502-825G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484399 | |||||||
| chr12:21484500 | C | A | 1 | a0001c0002t0003g0107 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.502-926G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484500 | |||||||
| chr12:21484690 | C | T | 3 | a0001c0001t0007g0013 a0001c0001t0007g0020 a0001c0001t0007g0058 |
6 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-1116G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484690 | |||||||
| chr12:21484702 | G | A | 3 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 |
3 | HG01884.hp1 HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.502-1128C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484702 | |||||||
| chr12:21484725 | A | G | 1 | a0001c0001t0047g0243 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.502-1151T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484725 | |||||||
| chr12:21484754 | G | GAT | 107 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(104): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.502-1182_502-1181d others(4): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484754 | |||||||
| chr12:21484913 | A | G | 1 | a0001c0001t0004g0042 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.502-1339T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484913 | |||||||
| chr12:21484952 | G | A | 3 | a0001c0005t0018g0240 a0001c0005t0018g0241 a0001c0005t0018g0242 |
3 | HG01891.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.502-1378C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21484952 | |||||||
| chr12:21485030 | A | C | 40 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(37): Show |
47 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.501+1449T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485030 | |||||||
| chr12:21485070 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.501+1409A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485070 | |||||||
| chr12:21485180 | T | G | 1 | a0001c0001t0002g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.501+1299A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485180 | |||||||
| chr12:21485184 | G | A | 1 | a0003c0003t0040g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.501+1295C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485184 | |||||||
| chr12:21485210 | C | CA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(86): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.501+1268dupT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485210 | |||||||
| chr12:21485318 | G | T | 177 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(174): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.501+1161C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485318 | |||||||
| chr12:21485330 | GA | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(84): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.501+1148delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485330 | |||||||
| chr12:21485346 | AAAAG | A | 16 | a0001c0001t0005g0234 a0001c0002t0008g0050 a0001c0002t0008g0232 others(13): Show |
18 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.501+1129_501+1132d others(6): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485346 | |||||||
| chr12:21485435 | A | C | 1 | a0003c0003t0038g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.501+1044T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485435 | |||||||
| chr12:21485481 | G | A | 1 | a0001c0002t0003g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.501+998C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485481 | |||||||
| chr12:21485548 | T | A | 6 | a0001c0001t0005g0226 a0001c0002t0015g0177 a0001c0005t0018g0240 others(3): Show |
6 | HG01074.hp1 HG01361.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+931A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485548 | |||||||
| chr12:21485548 | T | TA | 4 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+930_501+931ins others(1): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485548 | |||||||
| chr12:21485549 | T | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(255): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.501+930A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485549 | |||||||
| chr12:21485636 | C | T | 177 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(174): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.501+843G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485636 | |||||||
| chr12:21485646 | C | G | 4 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(1): Show |
6 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+833G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485646 | |||||||
| chr12:21485779 | G | A | 2 | a0001c0001t0006g0247 a0001c0001t0009g0248 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.501+700C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485779 | |||||||
| chr12:21485794 | T | A | 1 | a0001c0002t0003g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.501+685A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485794 | |||||||
| chr12:21485907 | G | A | 1 | a0001c0002t0008g0244 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+572C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485907 | |||||||
| chr12:21485912 | TA | T | 7 | a0001c0001t0002g0121 a0001c0001t0006g0246 a0001c0001t0006g0247 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.501+566delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21485912 | |||||||
| chr12:21486105 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.501+374C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21486105 | |||||||
| chr12:21486260 | T | C | 40 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(37): Show |
47 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.501+219A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21486260 | |||||||
| chr12:21486320 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.501+159T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21486320 | |||||||
| chr12:21486342 | C | T | 1 | a0002c0006t0022g0022 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.501+137G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21486342 | |||||||
| chr12:21486451 | TA | T | 41 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(38): Show |
48 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.501+27delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 5/14 | chr12 | 21486451 | |||||||
| chr12:21486594 | G | GA | 4 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 others(1): Show |
6 | HG00735.hp2 HG01346.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.395-10dupT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486594 | |||||||
| chr12:21486594 | GA | G | 107 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(104): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.395-10delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486594 | |||||||
| chr12:21486621 | T | A | 1 | a0001c0001t0016g0154 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.395-36A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486621 | |||||||
| chr12:21486655 | A | AC | 56 | a0001c0001t0001g0090 a0001c0001t0002g0009 a0001c0001t0002g0027 others(53): Show |
76 | HG01070.hp2 HG01074.hp1 HG01074.hp2 others(73): Show |
intron_variant | MODIFIER | c.395-71dupG | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486655 | |||||||
| chr12:21486656 | C | CCT | 18 | a0001c0001t0002g0087 a0001c0001t0004g0030 a0001c0001t0005g0046 others(15): Show |
24 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.395-72_395-71insAG | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486656 | |||||||
| chr12:21486656 | C | CCTT | 10 | a0001c0001t0005g0213 a0001c0001t0006g0199 a0001c0001t0006g0203 others(7): Show |
11 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.395-72_395-71insAA others(1): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486656 | |||||||
| chr12:21486656 | C | CCTTTTTT others(4): Show |
1 | a0001c0005t0018g0241 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.395-72_395-71insAA others(9): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486656 | |||||||
| chr12:21486656 | C | CCTTTTTT others(5): Show |
1 | a0001c0005t0018g0240 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.395-72_395-71insAA others(10): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486656 | |||||||
| chr12:21486656 | CG | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0123 others(31): Show |
40 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.395-72delC | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486656 | |||||||
| chr12:21486656 | CGT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0034 others(46): Show |
97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.395-73_395-72delAC | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486656 | |||||||
| chr12:21486656 | CGTTTTTT others(9): Show |
C | 1 | a0001c0001t0051g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.395-87_395-72delAA others(14): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486656 | |||||||
| chr12:21486657 | G | C | 81 | a0001c0001t0001g0028 a0001c0001t0001g0100 a0001c0001t0001g0130 others(78): Show |
139 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.395-72C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486657 | |||||||
| chr12:21486657 | G | T | 89 | a0001c0001t0001g0090 a0001c0001t0002g0009 a0001c0001t0002g0027 others(86): Show |
116 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.395-72C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486657 | |||||||
| chr12:21486658 | T | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0123 others(31): Show |
40 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.395-73A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486658 | |||||||
| chr12:21486659 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0034 others(46): Show |
97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.395-74A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486659 | |||||||
| chr12:21486673 | T | C | 1 | a0001c0001t0051g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.395-88A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486673 | |||||||
| chr12:21486687 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.395-102A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486687 | |||||||
| chr12:21486687 | T | TTTTTTTT others(5): Show |
1 | a0001c0005t0018g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.395-103_395-102ins others(12): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486687 | |||||||
| chr12:21486710 | G | GCCCAGGC others(1): Show |
6 | a0001c0001t0005g0234 a0001c0001t0006g0235 a0001c0002t0008g0050 others(3): Show |
7 | HG01884.hp2 HG02896.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.395-133_395-126dup others(8): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486710 | |||||||
| chr12:21486762 | C | T | 1 | a0003c0003t0006g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.395-177G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486762 | |||||||
| chr12:21486795 | C | T | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.395-210G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486795 | |||||||
| chr12:21486818 | C | G | 1 | a0001c0001t0005g0212 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.395-233G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486818 | |||||||
| chr12:21486930 | C | T | 17 | a0001c0001t0005g0234 a0001c0001t0006g0235 a0001c0002t0008g0050 others(14): Show |
19 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(16): Show |
intron_variant | MODIFIER | c.395-345G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21486930 | |||||||
| chr12:21487106 | T | TAAAC | 254 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(251): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.395-525_395-522dup others(4): Show |
RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487106 | |||||||
| chr12:21487280 | T | G | 41 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(38): Show |
48 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.395-695A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487280 | |||||||
| chr12:21487334 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.395-749C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487334 | |||||||
| chr12:21487337 | G | A | 4 | a0001c0001t0007g0062 a0001c0001t0030g0066 a0003c0003t0007g0064 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.395-752C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487337 | |||||||
| chr12:21487380 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(73): Show |
130 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.395-795C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487380 | |||||||
| chr12:21487549 | A | G | 1 | a0001c0001t0032g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.395-964T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487549 | |||||||
| chr12:21487701 | G | A | 1 | a0001c0001t0010g0157 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.395-1116C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487701 | |||||||
| chr12:21487811 | C | T | 41 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(38): Show |
48 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.395-1226G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487811 | |||||||
| chr12:21487859 | CT | C | 3 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 |
5 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1275delA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487859 | |||||||
| chr12:21487871 | C | T | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | NA18939.hp2 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.395-1286G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487871 | |||||||
| chr12:21487897 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.395-1312C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21487897 | |||||||
| chr12:21488110 | T | C | 3 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 |
5 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.395-1525A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488110 | |||||||
| chr12:21488113 | G | T | 6 | a0001c0001t0006g0203 a0001c0001t0006g0204 a0001c0001t0007g0013 others(3): Show |
9 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.395-1528C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488113 | |||||||
| chr12:21488185 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.395-1600A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488185 | |||||||
| chr12:21488243 | T | A | 39 | a0001c0001t0001g0169 a0001c0001t0002g0162 a0001c0001t0002g0163 others(36): Show |
68 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.395-1658A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488243 | |||||||
| chr12:21488516 | T | C | 1 | a0001c0001t0009g0210 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.394+1683A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488516 | |||||||
| chr12:21488613 | CG | C | 3 | a0001c0005t0018g0240 a0001c0005t0018g0241 a0001c0005t0018g0242 |
3 | HG01891.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394+1585delC | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488613 | |||||||
| chr12:21488614 | G | A | 1 | a0001c0002t0003g0159 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.394+1585C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488614 | |||||||
| chr12:21488621 | T | C | 1 | a0003c0003t0038g0119 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.394+1578A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488621 | |||||||
| chr12:21488649 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(251): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.394+1550G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488649 | |||||||
| chr12:21488702 | C | T | 6 | a0001c0001t0006g0203 a0001c0001t0006g0204 a0001c0001t0007g0013 others(3): Show |
9 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.394+1497G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488702 | |||||||
| chr12:21488871 | C | T | 1 | a0001c0001t0007g0070 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.394+1328G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488871 | |||||||
| chr12:21488950 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(74): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.394+1249G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21488950 | |||||||
| chr12:21489020 | A | G | 117 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(114): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.394+1179T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489020 | |||||||
| chr12:21489050 | C | A | 41 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(38): Show |
48 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.394+1149G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489050 | |||||||
| chr12:21489088 | C | T | 2 | a0001c0002t0003g0026 a0001c0002t0003g0083 |
3 | NA18963.hp2 NA18979.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.394+1111G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489088 | |||||||
| chr12:21489164 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.394+1035G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489164 | |||||||
| chr12:21489187 | T | A | 1 | a0001c0001t0002g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.394+1012A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489187 | |||||||
| chr12:21489248 | T | G | 1 | a0001c0001t0002g0110 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.394+951A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489248 | |||||||
| chr12:21489393 | A | AT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(77): Show |
134 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.394+805dupA | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489393 | |||||||
| chr12:21489519 | T | C | 3 | a0001c0001t0006g0203 a0001c0001t0006g0204 a0001c0001t0007g0065 |
3 | HG02717.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.394+680A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489519 | |||||||
| chr12:21489679 | T | G | 3 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 |
5 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+520A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489679 | |||||||
| chr12:21489692 | T | C | 2 | a0001c0001t0005g0238 a0001c0001t0052g0255 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.394+507A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489692 | |||||||
| chr12:21489768 | G | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0111 |
2 | HG01981.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.394+431C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21489768 | |||||||
| chr12:21490105 | T | C | 10 | a0001c0001t0002g0121 a0001c0001t0013g0012 a0001c0001t0013g0052 others(7): Show |
12 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.394+94A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 4/14 | chr12 | 21490105 | |||||||
| chr12:21490547 | G | T | 8 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(5): Show |
10 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-169C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490547 | |||||||
| chr12:21490600 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.215-222A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490600 | |||||||
| chr12:21490612 | T | A | 8 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(5): Show |
10 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-234A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490612 | |||||||
| chr12:21490643 | C | T | 2 | a0001c0002t0003g0039 a0001c0002t0003g0179 |
3 | NA18747.hp1 NA18971.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.215-265G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490643 | |||||||
| chr12:21490664 | C | T | 8 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(5): Show |
10 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-286G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490664 | |||||||
| chr12:21490665 | G | A | 8 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(5): Show |
10 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-287C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490665 | |||||||
| chr12:21490694 | T | A | 10 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(7): Show |
13 | HG00735.hp2 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.215-316A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490694 | |||||||
| chr12:21490829 | G | A | 8 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(5): Show |
10 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-451C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490829 | |||||||
| chr12:21490958 | T | G | 8 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(5): Show |
10 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.214+561A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21490958 | |||||||
| chr12:21491060 | T | C | 3 | a0001c0001t0006g0230 a0001c0002t0008g0198 a0001c0009t0049g0229 |
3 | HG02965.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.214+459A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21491060 | |||||||
| chr12:21491297 | T | C | 1 | a0001c0001t0007g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.214+222A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21491297 | |||||||
| chr12:21491375 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.214+144G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21491375 | |||||||
| chr12:21491383 | T | C | 2 | a0001c0001t0007g0071 a0003c0003t0038g0119 |
2 | NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.214+136A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21491383 | |||||||
| chr12:21491494 | C | CA | 7 | a0001c0001t0001g0038 a0001c0001t0002g0112 a0001c0001t0004g0040 others(4): Show |
11 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+24dupT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21491494 | |||||||
| chr12:21491494 | CA | C | 6 | a0001c0001t0001g0031 a0001c0001t0002g0073 a0001c0001t0007g0071 others(3): Show |
7 | HG02040.hp2 HG02055.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.214+24delT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 3/14 | chr12 | 21491494 | |||||||
| chr12:21491723 | G | A | 1 | a0001c0005t0018g0242 | 1 | HG01891.hp2 | splice_region_variant&intron_variant | LOW | c.17-7C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21491723 | |||||||
| chr12:21491732 | C | G | 8 | a0001c0001t0006g0246 a0001c0001t0006g0247 a0001c0001t0009g0248 others(5): Show |
10 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-16G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21491732 | |||||||
| chr12:21491733 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(63): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.17-17C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21491733 | |||||||
| chr12:21491792 | G | A | 16 | a0001c0001t0005g0234 a0001c0001t0006g0235 a0001c0002t0008g0050 others(13): Show |
18 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.17-76C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21491792 | |||||||
| chr12:21491798 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.17-82G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21491798 | |||||||
| chr12:21491888 | G | A | 39 | a0001c0001t0001g0169 a0001c0001t0002g0162 a0001c0001t0002g0163 others(36): Show |
68 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.17-172C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21491888 | |||||||
| chr12:21492299 | G | A | 40 | a0001c0001t0004g0030 a0001c0001t0004g0171 a0001c0001t0004g0172 others(37): Show |
47 | HG00099.hp2 HG00438.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.17-583C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492299 | |||||||
| chr12:21492339 | C | A | 1 | a0001c0001t0005g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.17-623G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492339 | |||||||
| chr12:21492459 | C | T | 1 | a0001c0001t0004g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.17-743G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492459 | |||||||
| chr12:21492746 | C | A | 3 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 |
5 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-1030G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492746 | |||||||
| chr12:21492752 | C | A | 1 | a0001c0001t0001g0041 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.17-1036G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492752 | |||||||
| chr12:21492838 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.17-1122T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492838 | |||||||
| chr12:21492858 | G | T | 5 | a0002c0004t0012g0256 a0002c0004t0012g0257 a0002c0004t0012g0258 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-1142C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492858 | |||||||
| chr12:21492861 | G | A | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.17-1145C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492861 | |||||||
| chr12:21492955 | C | G | 6 | a0001c0001t0006g0203 a0001c0001t0006g0204 a0001c0001t0007g0013 others(3): Show |
9 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-1239G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21492955 | |||||||
| chr12:21493034 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.17-1318T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493034 | |||||||
| chr12:21493204 | G | A | 2 | a0001c0001t0004g0042 a0001c0001t0042g0173 |
3 | HG01168.hp2 HG01169.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.17-1488C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493204 | |||||||
| chr12:21493246 | T | C | 2 | a0001c0001t0002g0121 a0003c0003t0040g0120 |
2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.17-1530A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493246 | |||||||
| chr12:21493395 | C | A | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.17-1679G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493395 | |||||||
| chr12:21493458 | A | G | 1 | a0001c0001t0032g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.17-1742T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493458 | |||||||
| chr12:21493469 | T | TA | 16 | a0001c0001t0005g0234 a0001c0001t0006g0235 a0001c0002t0008g0050 others(13): Show |
18 | HG01884.hp2 HG02630.hp1 HG02886.hp1 others(15): Show |
intron_variant | MODIFIER | c.17-1754dupT | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493469 | |||||||
| chr12:21493560 | C | A | 3 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0028g0202 |
5 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-1844G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493560 | |||||||
| chr12:21493628 | A | C | 18 | a0001c0001t0005g0201 a0001c0001t0013g0012 a0001c0001t0013g0052 others(15): Show |
21 | HG00735.hp2 HG01361.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.17-1912T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493628 | |||||||
| chr12:21493662 | G | A | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.17-1946C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493662 | |||||||
| chr12:21493946 | C | A | 1 | a0001c0001t0005g0237 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.17-2230G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21493946 | |||||||
| chr12:21494039 | C | T | 1 | a0001c0001t0007g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.17-2323G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494039 | |||||||
| chr12:21494089 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.17-2373C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494089 | |||||||
| chr12:21494222 | G | A | 3 | a0001c0001t0006g0199 a0001c0001t0014g0051 a0001c0001t0014g0251 |
4 | HG02615.hp1 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-2506C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494222 | |||||||
| chr12:21494385 | G | A | 2 | a0001c0001t0005g0238 a0001c0001t0052g0255 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.17-2669C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494385 | |||||||
| chr12:21494403 | T | C | 73 | a0001c0001t0001g0028 a0001c0001t0001g0090 a0001c0001t0001g0100 others(70): Show |
116 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.17-2687A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494403 | |||||||
| chr12:21494477 | T | C | 4 | a0001c0001t0007g0062 a0001c0001t0023g0021 a0003c0003t0007g0064 others(1): Show |
5 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-2761A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494477 | |||||||
| chr12:21494611 | G | T | 3 | a0001c0001t0013g0012 a0001c0001t0013g0052 a0001c0001t0032g0061 |
5 | HG01361.hp1 HG01516.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-2895C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494611 | |||||||
| chr12:21494627 | A | G | 1 | a0001c0002t0003g0176 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.17-2911T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494627 | |||||||
| chr12:21494780 | C | T | 2 | a0001c0001t0002g0175 a0001c0002t0003g0174 |
2 | HG03704.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.17-3064G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494780 | |||||||
| chr12:21494824 | A | G | 60 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0090 others(57): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.17-3108T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21494824 | |||||||
| chr12:21495012 | T | G | 14 | a0001c0001t0006g0199 a0001c0001t0006g0246 a0001c0001t0006g0247 others(11): Show |
15 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.17-3296A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495012 | |||||||
| chr12:21495046 | C | T | 5 | a0001c0001t0039g0194 a0001c0005t0018g0240 a0001c0005t0018g0241 others(2): Show |
5 | HG01891.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-3330G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495046 | |||||||
| chr12:21495073 | C | T | 4 | a0001c0001t0002g0121 a0001c0002t0003g0007 a0003c0003t0038g0119 others(1): Show |
8 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-3357G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495073 | |||||||
| chr12:21495136 | C | T | 50 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0049 others(47): Show |
57 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.17-3420G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495136 | |||||||
| chr12:21495137 | G | A | 3 | a0001c0001t0002g0113 a0001c0001t0039g0194 a0003c0003t0002g0195 |
3 | HG03098.hp1 NA18987.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.17-3421C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495137 | |||||||
| chr12:21495269 | C | T | 1 | a0001c0001t0041g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.17-3553G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495269 | |||||||
| chr12:21495319 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(255): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.17-3603T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495319 | |||||||
| chr12:21495362 | C | T | 1 | a0001c0001t0032g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.17-3646G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495362 | |||||||
| chr12:21495464 | C | T | 4 | a0001c0001t0002g0121 a0001c0002t0003g0007 a0003c0003t0038g0119 others(1): Show |
8 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-3748G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495464 | |||||||
| chr12:21495495 | C | T | 1 | a0001c0001t0007g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.17-3779G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495495 | |||||||
| chr12:21495521 | G | A | 24 | a0001c0001t0002g0175 a0001c0001t0002g0184 a0001c0001t0004g0017 others(21): Show |
43 | HG00621.hp2 HG00639.hp1 HG01361.hp2 others(40): Show |
intron_variant | MODIFIER | c.17-3805C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495521 | |||||||
| chr12:21495566 | G | C | 13 | a0001c0001t0005g0201 a0001c0001t0007g0013 a0001c0001t0007g0020 others(10): Show |
17 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.17-3850C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495566 | |||||||
| chr12:21495594 | A | G | 1 | a0001c0001t0032g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.17-3878T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495594 | |||||||
| chr12:21495716 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.16+3839C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495716 | |||||||
| chr12:21495752 | A | G | 13 | a0001c0001t0005g0201 a0001c0001t0007g0013 a0001c0001t0007g0020 others(10): Show |
17 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.16+3803T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495752 | |||||||
| chr12:21495766 | T | A | 1 | a0001c0002t0003g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.16+3789A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495766 | |||||||
| chr12:21495862 | G | C | 10 | a0001c0001t0007g0013 a0001c0001t0007g0020 a0001c0001t0007g0058 others(7): Show |
14 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.16+3693C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495862 | |||||||
| chr12:21495868 | C | T | 4 | a0001c0001t0007g0062 a0001c0001t0023g0021 a0003c0003t0007g0064 others(1): Show |
5 | HG01243.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+3687G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21495868 | |||||||
| chr12:21496011 | T | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(95): Show |
174 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.16+3544A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496011 | |||||||
| chr12:21496137 | T | C | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.16+3418A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496137 | |||||||
| chr12:21496226 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(95): Show |
174 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.16+3329A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496226 | |||||||
| chr12:21496237 | A | T | 1 | a0001c0001t0005g0200 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.16+3318T>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496237 | |||||||
| chr12:21496328 | G | C | 1 | a0001c0001t0002g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.16+3227C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496328 | |||||||
| chr12:21496388 | G | A | 10 | a0001c0001t0007g0013 a0001c0001t0007g0020 a0001c0001t0007g0058 others(7): Show |
14 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.16+3167C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496388 | |||||||
| chr12:21496452 | A | G | 7 | a0001c0001t0002g0121 a0001c0002t0003g0007 a0002c0004t0019g0262 others(4): Show |
11 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+3103T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496452 | |||||||
| chr12:21496605 | A | C | 63 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0090 others(60): Show |
108 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.16+2950T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496605 | |||||||
| chr12:21496608 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.16+2947T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496608 | |||||||
| chr12:21496620 | C | A | 12 | a0001c0001t0007g0013 a0001c0001t0007g0020 a0001c0001t0007g0058 others(9): Show |
16 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.16+2935G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496620 | |||||||
| chr12:21496631 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.16+2924T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496631 | |||||||
| chr12:21496703 | C | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(259): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.16+2852G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496703 | |||||||
| chr12:21496752 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.16+2803A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496752 | |||||||
| chr12:21496757 | G | A | 1 | a0001c0001t0001g0045 | 2 | NA18986.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.16+2798C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496757 | |||||||
| chr12:21496854 | C | T | 1 | a0001c0001t0002g0025 | 2 | NA18988.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.16+2701G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496854 | |||||||
| chr12:21496912 | C | A | 1 | a0001c0001t0005g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.16+2643G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21496912 | |||||||
| chr12:21497080 | C | T | 1 | a0001c0001t0007g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16+2475G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497080 | |||||||
| chr12:21497139 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18956.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.16+2416G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497139 | |||||||
| chr12:21497165 | T | C | 11 | a0001c0001t0006g0199 a0001c0001t0006g0246 a0001c0001t0006g0247 others(8): Show |
12 | HG01884.hp1 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.16+2390A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497165 | |||||||
| chr12:21497245 | T | C | 1 | a0001c0001t0036g0078 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.16+2310A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497245 | |||||||
| chr12:21497342 | T | G | 1 | a0001c0001t0032g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.16+2213A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497342 | |||||||
| chr12:21497433 | T | C | 14 | a0001c0001t0006g0199 a0001c0001t0006g0246 a0001c0001t0006g0247 others(11): Show |
15 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.16+2122A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497433 | |||||||
| chr12:21497510 | C | T | 4 | a0001c0001t0002g0024 a0001c0001t0002g0074 a0001c0001t0026g0077 others(1): Show |
5 | NA18950.hp1 NA18991.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+2045G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497510 | |||||||
| chr12:21497535 | G | A | 258 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(255): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.16+2020C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497535 | |||||||
| chr12:21497654 | A | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(258): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.16+1901T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497654 | |||||||
| chr12:21497682 | G | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(259): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.16+1873C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497682 | |||||||
| chr12:21497792 | C | G | 3 | a0002c0004t0019g0262 a0002c0004t0019g0263 a0002c0004t0019g0264 |
3 | HG02258.hp2 HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.16+1763G>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497792 | |||||||
| chr12:21497905 | C | A | 1 | a0001c0001t0004g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.16+1650G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497905 | |||||||
| chr12:21497922 | C | T | 63 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0090 others(60): Show |
108 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.16+1633G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21497922 | |||||||
| chr12:21498047 | C | T | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.16+1508G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498047 | |||||||
| chr12:21498265 | T | C | 1 | a0001c0002t0011g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.16+1290A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498265 | |||||||
| chr12:21498330 | C | T | 3 | a0001c0002t0011g0019 a0001c0002t0011g0054 a0001c0002t0011g0055 |
4 | HG04184.hp1 NA18962.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+1225G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498330 | |||||||
| chr12:21498333 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(167): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.16+1222C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498333 | |||||||
| chr12:21498340 | G | A | 1 | a0002c0004t0012g0261 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.16+1215C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498340 | |||||||
| chr12:21498426 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.16+1129G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498426 | |||||||
| chr12:21498526 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(95): Show |
174 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.16+1029C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498526 | |||||||
| chr12:21498531 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.16+1024G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498531 | |||||||
| chr12:21498586 | G | T | 1 | a0001c0001t0006g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.16+969C>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498586 | |||||||
| chr12:21498852 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0028 others(255): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.16+703T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498852 | |||||||
| chr12:21498888 | T | A | 1 | a0001c0001t0007g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16+667A>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498888 | |||||||
| chr12:21498969 | G | A | 1 | a0001c0001t0006g0252 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.16+586C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21498969 | |||||||
| chr12:21499013 | A | G | 1 | a0001c0001t0016g0118 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.16+542T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21499013 | |||||||
| chr12:21499084 | A | G | 1 | a0001c0002t0003g0007 | 5 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+471T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21499084 | |||||||
| chr12:21499407 | G | C | 1 | a0001c0001t0009g0253 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.16+148C>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21499407 | |||||||
| chr12:21499498 | A | G | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.16+57T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 2/14 | chr12 | 21499498 | |||||||
| chr12:21499707 | G | A | 60 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0090 others(57): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.-45-92C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21499707 | |||||||
| chr12:21499877 | C | T | 1 | a0001c0001t0004g0075 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-45-262G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21499877 | |||||||
| chr12:21500143 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-45-528T>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500143 | |||||||
| chr12:21500185 | A | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(103): Show |
186 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-45-570T>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500185 | |||||||
| chr12:21500188 | T | C | 1 | a0001c0001t0051g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-45-573A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500188 | |||||||
| chr12:21500218 | T | G | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | HG01433.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-45-603A>C | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500218 | |||||||
| chr12:21500429 | C | T | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-46+741G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500429 | |||||||
| chr12:21500641 | G | A | 1 | a0001c0002t0003g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-46+529C>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500641 | |||||||
| chr12:21500782 | C | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(102): Show |
185 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-46+388G>T | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500782 | |||||||
| chr12:21500823 | C | T | 10 | a0001c0001t0007g0013 a0001c0001t0007g0020 a0001c0001t0007g0058 others(7): Show |
14 | HG00280.hp2 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46+347G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21500823 | |||||||
| chr12:21501119 | T | C | 2 | a0001c0001t0039g0194 a0003c0003t0002g0195 |
2 | HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-46+51A>G | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21501119 | |||||||
| chr12:21501122 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-46+48G>A | RECQL | ENSG00000004700.16 | transcript | ENST00000444129.7 | protein_coding | 1/14 | chr12 | 21501122 |